Back to Multiple platform build/check report for BioC 3.20: simplified long |
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This page was generated on 2024-11-09 21:31 -0500 (Sat, 09 Nov 2024).
Hostname | OS | Arch (*) | R version | Installed pkgs |
---|---|---|---|---|
teran2 | Linux (Ubuntu 24.04.1 LTS) | x86_64 | 4.4.1 (2024-06-14) -- "Race for Your Life" | 4505 |
palomino8 | Windows Server 2022 Datacenter | x64 | 4.4.1 (2024-06-14 ucrt) -- "Race for Your Life" | 4506 |
lconway | macOS 12.7.1 Monterey | x86_64 | 4.4.1 (2024-06-14) -- "Race for Your Life" | 4538 |
kjohnson3 | macOS 13.6.5 Ventura | arm64 | 4.4.1 (2024-06-14) -- "Race for Your Life" | 4486 |
kunpeng2 | Linux (openEuler 22.03 LTS-SP1) | aarch64 | 4.4.1 (2024-06-14) -- "Race for Your Life" | 4493 |
Click on any hostname to see more info about the system (e.g. compilers) (*) as reported by 'uname -p', except on Windows and Mac OS X |
Package 1618/2289 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
PureCN 2.12.0 (landing page) Markus Riester
| teran2 | Linux (Ubuntu 24.04.1 LTS) / x86_64 | OK | OK | OK | |||||||||
palomino8 | Windows Server 2022 Datacenter / x64 | OK | OK | OK | OK | |||||||||
lconway | macOS 12.7.1 Monterey / x86_64 | OK | OK | OK | OK | |||||||||
kjohnson3 | macOS 13.6.5 Ventura / arm64 | OK | OK | OK | OK | |||||||||
kunpeng2 | Linux (openEuler 22.03 LTS-SP1) / aarch64 | OK | OK | OK | ||||||||||
To the developers/maintainers of the PureCN package: - Allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/PureCN.git to reflect on this report. See Troubleshooting Build Report for more information. - Use the following Renviron settings to reproduce errors and warnings. - If 'R CMD check' started to fail recently on the Linux builder(s) over a missing dependency, add the missing dependency to 'Suggests:' in your DESCRIPTION file. See Renviron.bioc for more information. |
Package: PureCN |
Version: 2.12.0 |
Command: /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:PureCN.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings PureCN_2.12.0.tar.gz |
StartedAt: 2024-11-09 10:18:38 -0500 (Sat, 09 Nov 2024) |
EndedAt: 2024-11-09 10:26:59 -0500 (Sat, 09 Nov 2024) |
EllapsedTime: 500.8 seconds |
RetCode: 0 |
Status: OK |
CheckDir: PureCN.Rcheck |
Warnings: 0 |
############################################################################## ############################################################################## ### ### Running command: ### ### /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:PureCN.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings PureCN_2.12.0.tar.gz ### ############################################################################## ############################################################################## * using log directory ‘/Users/biocbuild/bbs-3.20-bioc/meat/PureCN.Rcheck’ * using R version 4.4.1 (2024-06-14) * using platform: aarch64-apple-darwin20 * R was compiled by Apple clang version 14.0.0 (clang-1400.0.29.202) GNU Fortran (GCC) 12.2.0 * running under: macOS Ventura 13.6.7 * using session charset: UTF-8 * using option ‘--no-vignettes’ * checking for file ‘PureCN/DESCRIPTION’ ... OK * checking extension type ... Package * this is package ‘PureCN’ version ‘2.12.0’ * checking package namespace information ... OK * checking package dependencies ...Warning: unable to access index for repository https://CRAN.R-project.org/src/contrib: cannot open URL 'https://CRAN.R-project.org/src/contrib/PACKAGES' NOTE Package which this enhances but not available for checking: ‘genomicsdb’ * checking if this is a source package ... OK * checking if there is a namespace ... OK * checking for hidden files and directories ... OK * checking for portable file names ... OK * checking for sufficient/correct file permissions ... OK * checking whether package ‘PureCN’ can be installed ... OK * checking installed package size ... OK * checking package directory ... OK * checking ‘build’ directory ... OK * checking DESCRIPTION meta-information ... OK * checking top-level files ... OK * checking for left-over files ... OK * checking index information ... OK * checking package subdirectories ... OK * checking code files for non-ASCII characters ... OK * checking R files for syntax errors ... OK * checking whether the package can be loaded ... OK * checking whether the package can be loaded with stated dependencies ... OK * checking whether the package can be unloaded cleanly ... OK * checking whether the namespace can be loaded with stated dependencies ... OK * checking whether the namespace can be unloaded cleanly ... OK * checking dependencies in R code ... OK * checking S3 generic/method consistency ... OK * checking replacement functions ... OK * checking foreign function calls ... OK * checking R code for possible problems ... OK * checking Rd files ... OK * checking Rd metadata ... OK * checking Rd cross-references ... OK * checking for missing documentation entries ... OK * checking for code/documentation mismatches ... OK * checking Rd \usage sections ... OK * checking Rd contents ... OK * checking for unstated dependencies in examples ... OK * checking contents of ‘data’ directory ... OK * checking data for non-ASCII characters ... OK * checking data for ASCII and uncompressed saves ... OK * checking sizes of PDF files under ‘inst/doc’ ... OK * checking files in ‘vignettes’ ... OK * checking examples ... OK Examples with CPU (user + system) or elapsed time > 5s user system elapsed callAmplificationsInLowPurity 11.848 0.118 11.966 segmentationPSCBS 7.824 0.119 7.947 filterIntervals 6.814 0.119 6.935 runAbsoluteCN 5.458 0.107 5.565 * checking for unstated dependencies in ‘tests’ ... OK * checking tests ... Running ‘testthat.R’ OK * checking for unstated dependencies in vignettes ... OK * checking package vignettes ... OK * checking running R code from vignettes ... SKIPPED * checking re-building of vignette outputs ... SKIPPED * checking PDF version of manual ... OK * DONE Status: 1 NOTE See ‘/Users/biocbuild/bbs-3.20-bioc/meat/PureCN.Rcheck/00check.log’ for details.
PureCN.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### /Library/Frameworks/R.framework/Resources/bin/R CMD INSTALL PureCN ### ############################################################################## ############################################################################## * installing to library ‘/Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/library’ * installing *source* package ‘PureCN’ ... ** using staged installation ** R ** data ** inst ** byte-compile and prepare package for lazy loading ** help *** installing help indices ** building package indices ** installing vignettes ** testing if installed package can be loaded from temporary location ** testing if installed package can be loaded from final location ** testing if installed package keeps a record of temporary installation path * DONE (PureCN)
PureCN.Rcheck/tests/testthat.Rout
R version 4.4.1 (2024-06-14) -- "Race for Your Life" Copyright (C) 2024 The R Foundation for Statistical Computing Platform: aarch64-apple-darwin20 R is free software and comes with ABSOLUTELY NO WARRANTY. You are welcome to redistribute it under certain conditions. Type 'license()' or 'licence()' for distribution details. R is a collaborative project with many contributors. Type 'contributors()' for more information and 'citation()' on how to cite R or R packages in publications. Type 'demo()' for some demos, 'help()' for on-line help, or 'help.start()' for an HTML browser interface to help. Type 'q()' to quit R. > library(testthat) > library(PureCN) Loading required package: DNAcopy Loading required package: VariantAnnotation Loading required package: BiocGenerics Attaching package: 'BiocGenerics' The following objects are masked from 'package:stats': IQR, mad, sd, var, xtabs The following objects are masked from 'package:base': Filter, Find, Map, Position, Reduce, anyDuplicated, aperm, append, as.data.frame, basename, cbind, colnames, dirname, do.call, duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted, lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin, pmin.int, rank, rbind, rownames, sapply, saveRDS, setdiff, table, tapply, union, unique, unsplit, which.max, which.min Loading required package: MatrixGenerics Loading required package: matrixStats Attaching package: 'MatrixGenerics' The following objects are masked from 'package:matrixStats': colAlls, colAnyNAs, colAnys, colAvgsPerRowSet, colCollapse, colCounts, colCummaxs, colCummins, colCumprods, colCumsums, colDiffs, colIQRDiffs, colIQRs, colLogSumExps, colMadDiffs, colMads, colMaxs, colMeans2, colMedians, colMins, colOrderStats, colProds, colQuantiles, colRanges, colRanks, colSdDiffs, colSds, colSums2, colTabulates, colVarDiffs, colVars, colWeightedMads, colWeightedMeans, colWeightedMedians, colWeightedSds, colWeightedVars, rowAlls, rowAnyNAs, rowAnys, rowAvgsPerColSet, rowCollapse, rowCounts, rowCummaxs, rowCummins, rowCumprods, rowCumsums, rowDiffs, rowIQRDiffs, rowIQRs, rowLogSumExps, rowMadDiffs, rowMads, rowMaxs, rowMeans2, rowMedians, rowMins, rowOrderStats, rowProds, rowQuantiles, rowRanges, rowRanks, rowSdDiffs, rowSds, rowSums2, rowTabulates, rowVarDiffs, rowVars, rowWeightedMads, rowWeightedMeans, rowWeightedMedians, rowWeightedSds, rowWeightedVars Loading required package: GenomeInfoDb Loading required package: S4Vectors Loading required package: stats4 Attaching package: 'S4Vectors' The following object is masked from 'package:utils': findMatches The following objects are masked from 'package:base': I, expand.grid, unname Loading required package: IRanges Loading required package: GenomicRanges Loading required package: SummarizedExperiment Loading required package: Biobase Welcome to Bioconductor Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'. Attaching package: 'Biobase' The following object is masked from 'package:MatrixGenerics': rowMedians The following objects are masked from 'package:matrixStats': anyMissing, rowMedians Loading required package: Rsamtools Loading required package: Biostrings Loading required package: XVector Attaching package: 'Biostrings' The following object is masked from 'package:base': strsplit Attaching package: 'VariantAnnotation' The following object is masked from 'package:base': tabulate > > test_check("PureCN") WARN [2024-11-09 10:25:09] Attempted adding gene symbols to intervals. Heuristics have been used to pick symbols for overlapping genes. WARN [2024-11-09 10:25:09] Chromosome naming style of txdb file (UCSC) was different from interval file (Ensembl). WARN [2024-11-09 10:25:11] Attempted adding gene symbols to intervals. Heuristics have been used to pick symbols for overlapping genes. FATAL [2024-11-09 10:25:11] tumor.coverage.file and interval.file do not align. FATAL [2024-11-09 10:25:11] FATAL [2024-11-09 10:25:11] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:11] parameters (PureCN 2.12.0). WARN [2024-11-09 10:25:11] Cannot find all contig lengths while exporting interval file. INFO [2024-11-09 10:25:12] Processing seq1:1-21 (1/3)... INFO [2024-11-09 10:25:12] Processing seq1:1227-1247 (2/3)... INFO [2024-11-09 10:25:12] Processing seq2:594-614 (3/3)... WARN [2024-11-09 10:25:13] Large potential mis-calibration of on- and off-target log2 ratios: 0.26 FATAL [2024-11-09 10:25:13] Need either f or purity and ploidy. FATAL [2024-11-09 10:25:13] FATAL [2024-11-09 10:25:13] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:13] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:13] f not in expected range. FATAL [2024-11-09 10:25:13] FATAL [2024-11-09 10:25:13] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:13] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:13] coverage not in expected range (>=2) FATAL [2024-11-09 10:25:13] FATAL [2024-11-09 10:25:13] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:13] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:13] purity not in expected range. FATAL [2024-11-09 10:25:13] FATAL [2024-11-09 10:25:13] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:13] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:13] ploidy not in expected range. FATAL [2024-11-09 10:25:13] FATAL [2024-11-09 10:25:13] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:13] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:13] cell.fraction not in expected range. FATAL [2024-11-09 10:25:13] FATAL [2024-11-09 10:25:13] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:13] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:13] 576 on-target bins with low coverage in all samples. WARN [2024-11-09 10:25:13] You are likely not using the correct baits file! WARN [2024-11-09 10:25:13] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:13] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:13] Processing on-target regions... INFO [2024-11-09 10:25:14] Removing 930 intervals with low coverage in normalDB. INFO [2024-11-09 10:25:14] Removing 1 intervals with zero coverage in more than 3% of normalDB. INFO [2024-11-09 10:25:14] Tumor/normal noise ratio: 19.041 WARN [2024-11-09 10:25:14] Extensive noise in tumor compared to normals. INFO [2024-11-09 10:25:27] Tumor/normal noise ratio: 19.041 WARN [2024-11-09 10:25:27] Extensive noise in tumor compared to normals. INFO [2024-11-09 10:25:28] Using BiocParallel for parallel optimization. FATAL [2024-11-09 10:25:32] pvalue.cutoff not within expected range or format. FATAL [2024-11-09 10:25:32] FATAL [2024-11-09 10:25:32] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:32] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:32] pvalue.cutoff not within expected range or format. FATAL [2024-11-09 10:25:32] FATAL [2024-11-09 10:25:32] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:32] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:32] percentile.cutoff not in expected range (0 to 100). FATAL [2024-11-09 10:25:32] FATAL [2024-11-09 10:25:32] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:32] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:32] percentile.cutoff not in expected range (0 to 100). FATAL [2024-11-09 10:25:32] FATAL [2024-11-09 10:25:32] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:32] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:32] purity not within expected range or format. FATAL [2024-11-09 10:25:32] FATAL [2024-11-09 10:25:32] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:32] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:32] purity not within expected range or format. FATAL [2024-11-09 10:25:32] FATAL [2024-11-09 10:25:32] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:32] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:33] ------------------------------------------------------------ INFO [2024-11-09 10:25:33] PureCN 2.12.0 INFO [2024-11-09 10:25:33] ------------------------------------------------------------ INFO [2024-11-09 10:25:33] Loading coverage files... INFO [2024-11-09 10:25:33] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:25:33] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:33] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:33] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:25:33] Removing 22 small (< 5bp) intervals. INFO [2024-11-09 10:25:33] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:25:33] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:25:33] Removing 1724 low count (< 100 total reads) intervals. INFO [2024-11-09 10:25:33] Removing 6 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:25:33] Using 8050 intervals (8050 on-target, 0 off-target). INFO [2024-11-09 10:25:33] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:25:33] No interval.file provided. Cannot check for any GC-biases. INFO [2024-11-09 10:25:33] Loading VCF... INFO [2024-11-09 10:25:33] Found 127 variants in VCF file. INFO [2024-11-09 10:25:33] 127 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:25:33] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:25:33] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:25:33] Removing 1 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:33] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:25:33] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:25:33] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:25:33] Removing 1 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:25:33] Total size of targeted genomic region: 1.53Mb (2.33Mb with 50bp padding). INFO [2024-11-09 10:25:33] 1.2% of targets contain variants. INFO [2024-11-09 10:25:33] Removing 4 variants outside intervals. INFO [2024-11-09 10:25:33] Found SOMATIC annotation in VCF. INFO [2024-11-09 10:25:33] Setting somatic prior probabilities for somatic variants to 0.999000 or to 0.000100 otherwise. INFO [2024-11-09 10:25:33] Found SOMATIC annotation in VCF. Setting mapping bias to 0.972. INFO [2024-11-09 10:25:33] Excluding 0 novel or poor quality variants from segmentation. INFO [2024-11-09 10:25:33] Sample sex: ? INFO [2024-11-09 10:25:33] Segmenting data... INFO [2024-11-09 10:25:33] Loading pre-computed boundaries for DNAcopy... INFO [2024-11-09 10:25:33] Setting undo.SD parameter to 1.000000. INFO [2024-11-09 10:25:34] Setting prune.hclust.h parameter to 0.200000. INFO [2024-11-09 10:25:34] Found 59 segments with median size of 17.67Mb. INFO [2024-11-09 10:25:34] Using 121 variants. INFO [2024-11-09 10:25:34] Mean standard deviation of log-ratios: 0.34 (MAPD: 0.30) INFO [2024-11-09 10:25:34] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:25:34] Local optima: 0.63/1.9, 0.5/2 INFO [2024-11-09 10:25:34] Testing local optimum 1/2 at purity 0.63 and total ploidy 1.90... INFO [2024-11-09 10:25:34] Testing local optimum 2/2 at purity 0.50 and total ploidy 2.00... INFO [2024-11-09 10:25:35] Skipping 1 solutions that converged to the same optima. INFO [2024-11-09 10:25:35] Fitting variants with beta model for local optimum 1/2... INFO [2024-11-09 10:25:35] Fitting variants for purity 0.65, tumor ploidy 1.75 and contamination 0.01. INFO [2024-11-09 10:25:36] Optimized purity: 0.65 INFO [2024-11-09 10:25:36] Done. INFO [2024-11-09 10:25:36] ------------------------------------------------------------ INFO [2024-11-09 10:25:36] Estimating callable regions. FATAL [2024-11-09 10:25:36] exclude not a GRanges object. FATAL [2024-11-09 10:25:36] FATAL [2024-11-09 10:25:36] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:36] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:36] callable not a GRanges object. FATAL [2024-11-09 10:25:36] FATAL [2024-11-09 10:25:36] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:36] parameters (PureCN 2.12.0). WARN [2024-11-09 10:25:39] tumor.coverage.file and interval.file do not align. INFO [2024-11-09 10:25:39] No Gene column in interval.file. You won't get gene-level calls. FATAL [2024-11-09 10:25:39] No gc_bias column in interval.file. FATAL [2024-11-09 10:25:39] FATAL [2024-11-09 10:25:39] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:39] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:39] Provided coverage is zero, most likely due to a corrupt BAM file. FATAL [2024-11-09 10:25:39] FATAL [2024-11-09 10:25:39] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:39] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:40] No reptiming column in interval.file. INFO [2024-11-09 10:25:41] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.rds... INFO [2024-11-09 10:25:41] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.rds... INFO [2024-11-09 10:25:41] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.rds... INFO [2024-11-09 10:25:41] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.rds... INFO [2024-11-09 10:25:41] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.rds... INFO [2024-11-09 10:25:41] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.rds... FATAL [2024-11-09 10:25:41] Purity or Ploidy not numeric or in expected range. FATAL [2024-11-09 10:25:41] FATAL [2024-11-09 10:25:41] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:41] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:41] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.rds... INFO [2024-11-09 10:25:41] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.rds... FATAL [2024-11-09 10:25:41] 'Failed' column in FATAL [2024-11-09 10:25:41] /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad6f1c898e.csv FATAL [2024-11-09 10:25:41] not logical(1). FATAL [2024-11-09 10:25:41] FATAL [2024-11-09 10:25:41] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:41] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:42] 576 on-target bins with low coverage in all samples. WARN [2024-11-09 10:25:42] You are likely not using the correct baits file! WARN [2024-11-09 10:25:42] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:42] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:42] Processing on-target regions... INFO [2024-11-09 10:25:42] Removing 930 intervals with low coverage in normalDB. INFO [2024-11-09 10:25:42] Removing 1 intervals with zero coverage in more than 3% of normalDB. INFO [2024-11-09 10:25:43] 576 on-target bins with low coverage in all samples. WARN [2024-11-09 10:25:43] You are likely not using the correct baits file! WARN [2024-11-09 10:25:43] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:43] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:43] Processing on-target regions... INFO [2024-11-09 10:25:43] Removing 930 intervals with low coverage in normalDB. INFO [2024-11-09 10:25:43] Removing 1 intervals with zero coverage in more than 3% of normalDB. INFO [2024-11-09 10:25:44] 576 on-target bins with low coverage in all samples. WARN [2024-11-09 10:25:44] You are likely not using the correct baits file! WARN [2024-11-09 10:25:44] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:44] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:44] Processing on-target regions... INFO [2024-11-09 10:25:44] Removing 930 intervals with low coverage in normalDB. INFO [2024-11-09 10:25:44] Removing 1 intervals with zero coverage in more than 3% of normalDB. WARN [2024-11-09 10:25:44] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:44] Sample sex: NA WARN [2024-11-09 10:25:44] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:44] Sample sex: NA INFO [2024-11-09 10:25:44] 576 on-target bins with low coverage in all samples. WARN [2024-11-09 10:25:44] You are likely not using the correct baits file! WARN [2024-11-09 10:25:44] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:44] Allosome coverage missing, cannot determine sex. FATAL [2024-11-09 10:25:44] Length of normal.coverage.files and sex different FATAL [2024-11-09 10:25:44] FATAL [2024-11-09 10:25:44] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:44] parameters (PureCN 2.12.0). WARN [2024-11-09 10:25:46] Target intervals were not sorted. INFO [2024-11-09 10:25:46] 560 on-target bins with low coverage in all samples. WARN [2024-11-09 10:25:46] You are likely not using the correct baits file! WARN [2024-11-09 10:25:46] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:46] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:46] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:46] Processing on-target regions... INFO [2024-11-09 10:25:46] Removing 978 intervals with low coverage in normalDB. INFO [2024-11-09 10:25:46] Removing 11 intervals with zero coverage in more than 3% of normalDB. FATAL [2024-11-09 10:25:47] tumor.coverage.file and normalDB do not align. FATAL [2024-11-09 10:25:47] FATAL [2024-11-09 10:25:47] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:47] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:47] At least 2 normal.coverage.files required. FATAL [2024-11-09 10:25:47] FATAL [2024-11-09 10:25:47] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:47] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:47] ------------------------------------------------------------ INFO [2024-11-09 10:25:47] PureCN 2.12.0 INFO [2024-11-09 10:25:47] ------------------------------------------------------------ INFO [2024-11-09 10:25:47] Loading coverage files... INFO [2024-11-09 10:25:48] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:25:48] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:48] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:48] Removing 228 intervals with missing log.ratio. FATAL [2024-11-09 10:25:48] normalDB incompatible with this PureCN version. Please re-run FATAL [2024-11-09 10:25:48] NormalDB.R. FATAL [2024-11-09 10:25:48] FATAL [2024-11-09 10:25:48] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:48] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:48] normalDB incompatible with this PureCN version. Please re-run FATAL [2024-11-09 10:25:48] NormalDB.R. FATAL [2024-11-09 10:25:48] FATAL [2024-11-09 10:25:48] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:48] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:48] normal.coverage.files with _coverage.txt and _loess.txt suffix FATAL [2024-11-09 10:25:48] provided. Provide either only GC-normalized or raw coverage files! FATAL [2024-11-09 10:25:48] FATAL [2024-11-09 10:25:48] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:48] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:48] Removing 22 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:48] Removing 19 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:25:48] Base quality scores range from 24 to 35 (offset by 1) INFO [2024-11-09 10:25:48] Minimum number of supporting reads ranges from 2 to 9, depending on coverage and BQS. INFO [2024-11-09 10:25:48] Initial testing for significant sample cross-contamination: unlikely INFO [2024-11-09 10:25:48] Removing 45 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:25:48] Removing 22 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:48] Removing 19 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:25:48] Base quality scores range from 24 to 35 (offset by 1) INFO [2024-11-09 10:25:48] Minimum number of supporting reads ranges from 2 to 9, depending on coverage and BQS. INFO [2024-11-09 10:25:48] Initial testing for significant sample cross-contamination: unlikely INFO [2024-11-09 10:25:48] Removing 45 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:25:48] Removing 6 blacklisted variants. INFO [2024-11-09 10:25:48] Removing 22 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:48] Removing 19 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:25:48] Base quality scores range from 24 to 35 (offset by 1) INFO [2024-11-09 10:25:48] Minimum number of supporting reads ranges from 2 to 9, depending on coverage and BQS. INFO [2024-11-09 10:25:48] Initial testing for significant sample cross-contamination: unlikely INFO [2024-11-09 10:25:48] Removing 45 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. WARN [2024-11-09 10:25:48] MuTect stats file lacks contig and position columns. INFO [2024-11-09 10:25:48] Removing 22 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:48] Removing 19 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:25:48] Base quality scores range from 24 to 35 (offset by 1) INFO [2024-11-09 10:25:49] Minimum number of supporting reads ranges from 2 to 9, depending on coverage and BQS. INFO [2024-11-09 10:25:49] Initial testing for significant sample cross-contamination: unlikely INFO [2024-11-09 10:25:49] Removing 45 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. WARN [2024-11-09 10:25:49] MuTect stats file and VCF file do not align perfectly. Will remove 2325 unmatched variants. WARN [2024-11-09 10:25:49] MuTect stats file lacks failure_reasons column. Keeping all variants listed in stats file. INFO [2024-11-09 10:25:49] Removing 0 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:49] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:25:49] Base quality scores range from 31 to 33 (offset by 1) INFO [2024-11-09 10:25:49] Minimum number of supporting reads ranges from 3 to 4, depending on coverage and BQS. INFO [2024-11-09 10:25:49] Removing 0 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:25:49] Removing 22 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:49] Base quality scores range from 7 to 35 (offset by 1) INFO [2024-11-09 10:25:49] Minimum number of supporting reads ranges from 1 to 41, depending on coverage and BQS. INFO [2024-11-09 10:25:49] Initial testing for significant sample cross-contamination: unlikely INFO [2024-11-09 10:25:49] Removing 49 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:25:49] Removing 22 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:49] Base quality scores range from 7 to 35 (offset by 1) INFO [2024-11-09 10:25:49] Minimum number of supporting reads ranges from 1 to 41, depending on coverage and BQS. INFO [2024-11-09 10:25:49] Initial testing for significant sample cross-contamination: unlikely INFO [2024-11-09 10:25:49] Removing 49 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:25:49] Removing 22 non heterozygous (in matched normal) germline SNPs. WARN [2024-11-09 10:25:49] Many variants removed by min.base.quality (50) filter. You might want to lower the cutoff. FATAL [2024-11-09 10:25:49] No variants passed filter BQ. FATAL [2024-11-09 10:25:49] FATAL [2024-11-09 10:25:49] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:49] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:49] Found 11 variants in VCF file. WARN [2024-11-09 10:25:49] vcf.file has no DB info field for membership in germline databases. Found and used valid population allele frequency > 0.001000 instead. INFO [2024-11-09 10:25:49] 1 (9.1%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:25:50] Found 11 variants in VCF file. WARN [2024-11-09 10:25:50] vcf.file has no DB info field for membership in germline databases. Found and used valid population allele frequency > 0.001000 instead. INFO [2024-11-09 10:25:50] 1 (9.1%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:25:50] Found 11 variants in VCF file. WARN [2024-11-09 10:25:50] vcf.file has no DB or POP_AF info field for membership in germline databases. Guessing it based on available dbSNP ID. INFO [2024-11-09 10:25:50] 1 (9.1%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:25:50] Found 1000 variants in VCF file. INFO [2024-11-09 10:25:50] Removing 2 triallelic sites. WARN [2024-11-09 10:25:50] Having trouble guessing SOMATIC status... WARN [2024-11-09 10:25:50] DP FORMAT field contains NAs. Removing 44 variants. INFO [2024-11-09 10:25:50] 954 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:25:51] Found 12 variants in VCF file. INFO [2024-11-09 10:25:51] Removing 1 triallelic sites. WARN [2024-11-09 10:25:51] DP FORMAT field contains NAs. Removing 1 variants. WARN [2024-11-09 10:25:51] vcf.file has no DB info field for membership in germline databases. Found and used somatic status instead. INFO [2024-11-09 10:25:51] 8 (80.0%) variants annotated as likely germline (DB INFO flag). WARN [2024-11-09 10:25:51] BQ FORMAT field contains NAs. INFO [2024-11-09 10:25:51] Found 2331 variants in VCF file. INFO [2024-11-09 10:25:51] 2282 (97.9%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:25:51] Found 2331 variants in VCF file. INFO [2024-11-09 10:25:51] 2282 (97.9%) variants annotated as likely germline (DB INFO flag). WARN [2024-11-09 10:25:51] Did not find base quality scores, will use global error rate of 0.0010 instead. INFO [2024-11-09 10:25:51] Removing 21 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:25:51] Base quality scores range from 24 to 35 (offset by 1) INFO [2024-11-09 10:25:51] Initial testing for significant sample cross-contamination: unlikely INFO [2024-11-09 10:25:51] Removing 89 variants with AF < 0.030 or AF >= 0.970 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:25:51] Found 2331 variants in VCF file. INFO [2024-11-09 10:25:52] 2282 (97.9%) variants annotated as likely germline (DB INFO flag). WARN [2024-11-09 10:25:52] BQ FORMAT field contains NAs. WARN [2024-11-09 10:25:52] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:52] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:52] Mean coverages: chrX: 108.58, chrY: 108.58, chr1-22: 104.87. INFO [2024-11-09 10:25:52] Mean coverages: chrX: 108.58, chrY: 2.17, chr1-22: 104.87. INFO [2024-11-09 10:25:52] Mean coverages: chrX: 108.58, chrY: 5.17, chr1-22: 104.87. INFO [2024-11-09 10:25:52] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:25:52] No germline variants in VCF. FATAL [2024-11-09 10:25:52] No solution with id hello FATAL [2024-11-09 10:25:52] FATAL [2024-11-09 10:25:52] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:52] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:52] No solution with id 100 FATAL [2024-11-09 10:25:52] FATAL [2024-11-09 10:25:52] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:52] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:53] all.data and w have different lengths. FATAL [2024-11-09 10:25:53] FATAL [2024-11-09 10:25:53] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:53] parameters (PureCN 2.12.0). INFO [2024-11-09 10:25:53] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:53] No mappability scores provided. WARN [2024-11-09 10:25:53] No reptiming scores provided. INFO [2024-11-09 10:25:53] Calculating GC-content... INFO [2024-11-09 10:25:53] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:53] No mappability scores provided. WARN [2024-11-09 10:25:53] No reptiming scores provided. INFO [2024-11-09 10:25:53] Calculating GC-content... INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. INFO [2024-11-09 10:25:54] Removing 1 targets overlapping with exclude. WARN [2024-11-09 10:25:54] No mappability scores provided. WARN [2024-11-09 10:25:54] No reptiming scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... WARN [2024-11-09 10:25:54] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. FATAL [2024-11-09 10:25:54] off.target.padding must be negative. FATAL [2024-11-09 10:25:54] FATAL [2024-11-09 10:25:54] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:54] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:25:54] Interval coordinates should start at 1, not at 0 FATAL [2024-11-09 10:25:54] FATAL [2024-11-09 10:25:54] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:54] parameters (PureCN 2.12.0). WARN [2024-11-09 10:25:54] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. FATAL [2024-11-09 10:25:54] No off-target regions after filtering for mappability and FATAL [2024-11-09 10:25:54] off.target.padding FATAL [2024-11-09 10:25:54] FATAL [2024-11-09 10:25:54] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:54] parameters (PureCN 2.12.0). WARN [2024-11-09 10:25:54] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:54] No mappability scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... WARN [2024-11-09 10:25:54] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:54] Averaging reptiming into bins of size 200... INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:54] No mappability scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... WARN [2024-11-09 10:25:54] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:54] Splitting 6 large targets to an average width of 200. WARN [2024-11-09 10:25:54] No mappability scores provided. WARN [2024-11-09 10:25:54] No reptiming scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... WARN [2024-11-09 10:25:54] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:54] No mappability scores provided. WARN [2024-11-09 10:25:54] No reptiming scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. INFO [2024-11-09 10:25:54] Tiling off-target regions to an average width of 200000. WARN [2024-11-09 10:25:54] No mappability scores provided. WARN [2024-11-09 10:25:54] No reptiming scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... WARN [2024-11-09 10:25:54] Intervals contain off-target regions. Will not change intervals. WARN [2024-11-09 10:25:54] No mappability scores provided. WARN [2024-11-09 10:25:54] No reptiming scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:54] No reptiming scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... WARN [2024-11-09 10:25:54] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:54] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:54] No reptiming scores provided. INFO [2024-11-09 10:25:54] Calculating GC-content... WARN [2024-11-09 10:25:55] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:55] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:55] 1 intervals without mappability score (1 on-target). INFO [2024-11-09 10:25:55] Removing 1 intervals with low mappability score (<0.60). WARN [2024-11-09 10:25:55] No reptiming scores provided. INFO [2024-11-09 10:25:55] Calculating GC-content... WARN [2024-11-09 10:25:55] Found small target regions (< 100bp). Will resize them. INFO [2024-11-09 10:25:55] Splitting 5 large targets to an average width of 400. INFO [2024-11-09 10:25:55] Tiling off-target regions to an average width of 200000. WARN [2024-11-09 10:25:55] No reptiming scores provided. INFO [2024-11-09 10:25:55] Calculating GC-content... INFO [2024-11-09 10:25:55] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:55] No mappability scores provided. WARN [2024-11-09 10:25:55] No reptiming scores provided. INFO [2024-11-09 10:25:55] Calculating GC-content... WARN [2024-11-09 10:25:55] Chromosome naming style of interval file (Ensembl) was different from reference (UCSC). INFO [2024-11-09 10:25:55] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:55] No mappability scores provided. WARN [2024-11-09 10:25:55] No reptiming scores provided. INFO [2024-11-09 10:25:55] Calculating GC-content... FATAL [2024-11-09 10:25:55] Chromosome naming style of interval file unknown, should be UCSC. FATAL [2024-11-09 10:25:55] FATAL [2024-11-09 10:25:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:25:55] parameters (PureCN 2.12.0). WARN [2024-11-09 10:25:55] Chromosome naming style of interval file (Ensembl) was different from reference (UCSC). WARN [2024-11-09 10:25:55] Chromosome naming style of mappability file (Ensembl) was different from reference (UCSC). INFO [2024-11-09 10:25:55] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:55] No reptiming scores provided. INFO [2024-11-09 10:25:55] Calculating GC-content... WARN [2024-11-09 10:25:55] Found small target regions (< 60bp). Will resize them. INFO [2024-11-09 10:25:55] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:55] No mappability scores provided. WARN [2024-11-09 10:25:55] No reptiming scores provided. INFO [2024-11-09 10:25:55] Calculating GC-content... WARN [2024-11-09 10:25:55] Found small target regions (< 60bp). Will drop them. INFO [2024-11-09 10:25:55] Splitting 4 large targets to an average width of 400. WARN [2024-11-09 10:25:55] No mappability scores provided. WARN [2024-11-09 10:25:55] No reptiming scores provided. INFO [2024-11-09 10:25:55] Calculating GC-content... WARN [2024-11-09 10:25:56] Found small target regions (< 200bp). Will resize them. INFO [2024-11-09 10:25:56] Splitting 5 large targets to an average width of 400. WARN [2024-11-09 10:25:56] No mappability scores provided. WARN [2024-11-09 10:25:56] No reptiming scores provided. INFO [2024-11-09 10:25:56] Calculating GC-content... INFO [2024-11-09 10:25:56] Found 20 variants in VCF file. INFO [2024-11-09 10:25:56] 20 (100.0%) variants annotated as likely germline (DB INFO flag). WARN [2024-11-09 10:25:56] Did not find base quality scores, will use global error rate of 0.0010 instead. INFO [2024-11-09 10:25:56] Found 127 variants in VCF file. INFO [2024-11-09 10:25:56] 127 (100.0%) variants annotated as likely germline (DB INFO flag). WARN [2024-11-09 10:25:56] Did not find base quality scores, will use global error rate of 0.0010 instead. INFO [2024-11-09 10:25:56] ------------------------------------------------------------ INFO [2024-11-09 10:25:56] PureCN 2.12.0 INFO [2024-11-09 10:25:56] ------------------------------------------------------------ INFO [2024-11-09 10:25:56] Loading coverage files... INFO [2024-11-09 10:25:56] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:25:56] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:56] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:56] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:25:56] Removing 22 small (< 5bp) intervals. INFO [2024-11-09 10:25:56] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:25:56] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:25:56] Removing 1724 low count (< 100 total reads) intervals. INFO [2024-11-09 10:25:56] Removing 6 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:25:56] Using 8050 intervals (8050 on-target, 0 off-target). INFO [2024-11-09 10:25:56] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:25:56] No interval.file provided. Cannot check for any GC-biases. INFO [2024-11-09 10:25:56] Loading VCF... INFO [2024-11-09 10:25:56] Found 127 variants in VCF file. INFO [2024-11-09 10:25:56] 127 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:25:57] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:25:57] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:25:57] Removing 1 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:25:57] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:25:57] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:25:57] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:25:57] Removing 1 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:25:57] Total size of targeted genomic region: 1.53Mb (2.33Mb with 50bp padding). INFO [2024-11-09 10:25:57] 1.2% of targets contain variants. INFO [2024-11-09 10:25:57] Removing 4 variants outside intervals. INFO [2024-11-09 10:25:57] Found SOMATIC annotation in VCF. INFO [2024-11-09 10:25:57] Setting somatic prior probabilities for somatic variants to 0.999000 or to 0.000100 otherwise. INFO [2024-11-09 10:25:57] Found SOMATIC annotation in VCF. Setting mapping bias to 0.972. INFO [2024-11-09 10:25:57] Excluding 0 novel or poor quality variants from segmentation. INFO [2024-11-09 10:25:57] Sample sex: ? INFO [2024-11-09 10:25:57] Segmenting data... INFO [2024-11-09 10:25:57] Loading pre-computed boundaries for DNAcopy... INFO [2024-11-09 10:25:57] Setting undo.SD parameter to 1.000000. INFO [2024-11-09 10:25:57] Setting prune.hclust.h parameter to 0.200000. INFO [2024-11-09 10:25:57] Found 59 segments with median size of 17.67Mb. INFO [2024-11-09 10:25:57] Using 121 variants. INFO [2024-11-09 10:25:57] Mean standard deviation of log-ratios: 0.34 (MAPD: 0.30) INFO [2024-11-09 10:25:57] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:25:57] Local optima: 0.65/1.8, 0.52/2 INFO [2024-11-09 10:25:57] Testing local optimum 1/2 at purity 0.65 and total ploidy 1.80... INFO [2024-11-09 10:25:58] Testing local optimum 2/2 at purity 0.52 and total ploidy 2.00... INFO [2024-11-09 10:25:58] Skipping 1 solutions that converged to the same optima. INFO [2024-11-09 10:25:58] Fitting variants with beta model for local optimum 1/2... INFO [2024-11-09 10:25:58] Fitting variants for purity 0.65, tumor ploidy 1.75 and contamination 0.01. INFO [2024-11-09 10:25:59] Optimized purity: 0.65 INFO [2024-11-09 10:25:59] Done. INFO [2024-11-09 10:25:59] ------------------------------------------------------------ FATAL [2024-11-09 10:25:59] log.ratio NULL in .writeLogRatioFileGATK4 FATAL [2024-11-09 10:25:59] FATAL [2024-11-09 10:25:59] This runtime error might be caused by invalid input data or parameters. FATAL [2024-11-09 10:25:59] Please report bug (PureCN 2.12.0). INFO [2024-11-09 10:25:59] Loaded provided segmentation file example_seg.txt (format DNAcopy). INFO [2024-11-09 10:25:59] Re-centering provided segment means (offset -0.0033). INFO [2024-11-09 10:25:59] Loaded provided segmentation file example_gatk4_modelfinal.seg.gz (format GATK4). WARN [2024-11-09 10:25:59] Expecting numeric chromosome names in seg.file, assuming file is properly sorted. INFO [2024-11-09 10:25:59] Re-centering provided segment means (offset -0.0037). INFO [2024-11-09 10:25:59] 576 on-target bins with low coverage in all samples. WARN [2024-11-09 10:25:59] You are likely not using the correct baits file! WARN [2024-11-09 10:25:59] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:25:59] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:25:59] Processing on-target regions... INFO [2024-11-09 10:26:00] Removing 930 intervals with low coverage in normalDB. INFO [2024-11-09 10:26:00] Removing 1 intervals with zero coverage in more than 3% of normalDB. INFO [2024-11-09 10:26:00] ------------------------------------------------------------ INFO [2024-11-09 10:26:00] PureCN 2.12.0 INFO [2024-11-09 10:26:00] ------------------------------------------------------------ INFO [2024-11-09 10:26:00] Using BiocParallel for parallel optimization. INFO [2024-11-09 10:26:00] Loading coverage files... INFO [2024-11-09 10:26:00] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:00] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:00] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:00] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:00] Removing 705 intervals excluded in normalDB. INFO [2024-11-09 10:26:00] normalDB provided. Setting minimum coverage for segmentation to 0.0015X. INFO [2024-11-09 10:26:00] Removing 1066 low count (< 100 total reads) intervals. INFO [2024-11-09 10:26:00] Using 8050 intervals (8050 on-target, 0 off-target). INFO [2024-11-09 10:26:00] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:00] No interval.file provided. Cannot check for any GC-biases. INFO [2024-11-09 10:26:00] Sample sex: ? INFO [2024-11-09 10:26:00] Segmenting data... INFO [2024-11-09 10:26:00] Interval weights found, will use weighted CBS. INFO [2024-11-09 10:26:00] Loading pre-computed boundaries for DNAcopy... INFO [2024-11-09 10:26:00] Setting undo.SD parameter to 1.000000. Setting multi-figure configuration INFO [2024-11-09 10:26:01] Found 52 segments with median size of 29.35Mb. INFO [2024-11-09 10:26:01] Mean standard deviation of log-ratios: 0.34 (MAPD: 0.30) INFO [2024-11-09 10:26:01] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:26:01] Local optima: 0.65/1.8, 0.52/2 INFO [2024-11-09 10:26:01] Skipping 1 solutions that converged to the same optima. INFO [2024-11-09 10:26:01] Done. INFO [2024-11-09 10:26:01] ------------------------------------------------------------ INFO [2024-11-09 10:26:01] Reading /var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107adaf4a3e.rds... FATAL [2024-11-09 10:26:01] runAbsoluteCN was run without a VCF file. FATAL [2024-11-09 10:26:01] FATAL [2024-11-09 10:26:01] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:01] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:01] runAbsoluteCN was run without a VCF file. FATAL [2024-11-09 10:26:01] FATAL [2024-11-09 10:26:01] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:01] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:01] ------------------------------------------------------------ INFO [2024-11-09 10:26:01] PureCN 2.12.0 INFO [2024-11-09 10:26:02] ------------------------------------------------------------ INFO [2024-11-09 10:26:02] Loading coverage files... INFO [2024-11-09 10:26:02] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:02] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:02] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:02] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:02] Removing 705 intervals excluded in normalDB. INFO [2024-11-09 10:26:02] normalDB provided. Setting minimum coverage for segmentation to 0.0015X. INFO [2024-11-09 10:26:02] Removing 1066 low count (< 100 total reads) intervals. INFO [2024-11-09 10:26:02] Using 8050 intervals (8050 on-target, 0 off-target). INFO [2024-11-09 10:26:02] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:02] No interval.file provided. Cannot check for any GC-biases. INFO [2024-11-09 10:26:02] Sample sex: ? INFO [2024-11-09 10:26:02] Segmenting data... INFO [2024-11-09 10:26:02] Interval weights found, will use weighted PSCBS. FATAL [2024-11-09 10:26:02] segmentationPSCBS requires VCF file. FATAL [2024-11-09 10:26:02] FATAL [2024-11-09 10:26:02] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:02] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] Loading coverage files... FATAL [2024-11-09 10:26:04] Need a normal coverage file if log.ratio and seg.file are not provided. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] min.ploidy or max.ploidy not within expected range. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] min.ploidy or max.ploidy not within expected range. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] test.num.copy not within expected range. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ WARN [2024-11-09 10:26:04] test.num.copy outside recommended range. FATAL [2024-11-09 10:26:04] max.non.clonal not within expected range or format. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ WARN [2024-11-09 10:26:04] test.num.copy outside recommended range. FATAL [2024-11-09 10:26:04] max.non.clonal not within expected range or format. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] test.purity not within expected range. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] Loading coverage files... FATAL [2024-11-09 10:26:04] Tumor and normal are identical. This won't give any meaningful results FATAL [2024-11-09 10:26:04] and I'm stopping here. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] Loading coverage files... FATAL [2024-11-09 10:26:04] Length of log.ratio different from tumor coverage. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] prior.purity must have the same length as test.purity. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] min.gof not within expected range or format. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] prior.purity not within expected range or format. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] prior.purity must add to 1. Sum is 1.5 FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] max.homozygous.loss not within expected range or format. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] prior.K not within expected range or format. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] prior.contamination not within expected range or format. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] Iterations not in the expected range from 10 to 250. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ FATAL [2024-11-09 10:26:04] Iterations not in the expected range from 10 to 250. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] Loading coverage files... FATAL [2024-11-09 10:26:04] Missing tumor.coverage.file requires seg.file or log.ratio and FATAL [2024-11-09 10:26:04] interval.file. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] PureCN 2.12.0 INFO [2024-11-09 10:26:04] ------------------------------------------------------------ INFO [2024-11-09 10:26:04] Loading coverage files... FATAL [2024-11-09 10:26:04] Interval files in normal and tumor different. FATAL [2024-11-09 10:26:04] FATAL [2024-11-09 10:26:04] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:04] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:05] ------------------------------------------------------------ INFO [2024-11-09 10:26:05] PureCN 2.12.0 INFO [2024-11-09 10:26:05] ------------------------------------------------------------ INFO [2024-11-09 10:26:05] Loading coverage files... INFO [2024-11-09 10:26:05] Mean target coverages: 0X (tumor) 99X (normal). WARN [2024-11-09 10:26:05] Large difference in coverage of tumor and normal. FATAL [2024-11-09 10:26:05] No finite intervals. FATAL [2024-11-09 10:26:05] FATAL [2024-11-09 10:26:05] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:05] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:05] ------------------------------------------------------------ INFO [2024-11-09 10:26:05] PureCN 2.12.0 INFO [2024-11-09 10:26:05] ------------------------------------------------------------ INFO [2024-11-09 10:26:05] Loading coverage files... INFO [2024-11-09 10:26:05] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:05] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:05] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:05] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:05] Removing 22 small (< 5bp) intervals. INFO [2024-11-09 10:26:05] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:26:05] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:26:05] Removing 1724 low count (< 100 total reads) intervals. INFO [2024-11-09 10:26:05] Removing 6 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:26:05] Using 8050 intervals (8050 on-target, 0 off-target). INFO [2024-11-09 10:26:05] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:05] No interval.file provided. Cannot check for any GC-biases. INFO [2024-11-09 10:26:05] Loading VCF... INFO [2024-11-09 10:26:05] Found 127 variants in VCF file. INFO [2024-11-09 10:26:05] 127 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:26:05] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:26:05] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:26:05] Removing 1 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:26:05] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:26:05] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:26:05] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:26:05] Removing 1 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. Error in FileForFormat(resource(con), fileFormat(con)) : Format 'txt' unsupported In addition: Warning messages: 1: In for (i in seq_len(n)) { : closing unused connection 5 (/var/folders/r0/l4fjk6cj5xj0j3brt4bplpl40000gt/T//RtmpBUOXhJ/file107ad17e3b548.tsv) 2: In for (i in seq_len(n)) { : closing unused connection 4 (/Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/library/PureCN/extdata/example_gatk4_denoised_cr.tsv.gz) FATAL [2024-11-09 10:26:05] Could not import snp.blacklist FATAL [2024-11-09 10:26:05] /Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/library/PureCN/extdata/example_normal.txt.gz:Error FATAL [2024-11-09 10:26:05] in FileForFormat(resource(con), fileFormat(con)) : Format 'txt' FATAL [2024-11-09 10:26:05] unsupported FATAL [2024-11-09 10:26:05] FATAL [2024-11-09 10:26:05] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:05] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:05] ------------------------------------------------------------ INFO [2024-11-09 10:26:05] PureCN 2.12.0 INFO [2024-11-09 10:26:05] ------------------------------------------------------------ INFO [2024-11-09 10:26:05] Loading coverage files... INFO [2024-11-09 10:26:05] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:05] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:05] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:05] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:05] Removing 22 small (< 5bp) intervals. INFO [2024-11-09 10:26:05] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:26:05] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:26:05] Removing 233 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:26:05] Using 9547 intervals (9547 on-target, 0 off-target). INFO [2024-11-09 10:26:05] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:05] No interval.file provided. Cannot check for any GC-biases. INFO [2024-11-09 10:26:05] Loading VCF... INFO [2024-11-09 10:26:06] Found 127 variants in VCF file. INFO [2024-11-09 10:26:06] 127 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:26:06] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:26:06] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:26:06] Removing 1 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:26:06] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:26:06] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:26:06] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:26:06] Removing 1 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:26:06] Total size of targeted genomic region: 1.63Mb (2.58Mb with 50bp padding). INFO [2024-11-09 10:26:06] 1.0% of targets contain variants. INFO [2024-11-09 10:26:06] Removing 2 variants outside intervals. INFO [2024-11-09 10:26:06] Found SOMATIC annotation in VCF. INFO [2024-11-09 10:26:06] Setting somatic prior probabilities for somatic variants to 0.999000 or to 0.000100 otherwise. INFO [2024-11-09 10:26:06] Found SOMATIC annotation in VCF. Setting mapping bias to 0.973. INFO [2024-11-09 10:26:06] Excluding 0 novel or poor quality variants from segmentation. INFO [2024-11-09 10:26:06] Sample sex: ? INFO [2024-11-09 10:26:06] Segmenting data... INFO [2024-11-09 10:26:06] Loading pre-computed boundaries for DNAcopy... INFO [2024-11-09 10:26:06] Setting undo.SD parameter to 1.000000. INFO [2024-11-09 10:26:06] Setting prune.hclust.h parameter to 0.200000. INFO [2024-11-09 10:26:06] Found 54 segments with median size of 24.88Mb. INFO [2024-11-09 10:26:06] Using 123 variants. INFO [2024-11-09 10:26:06] Mean standard deviation of log-ratios: 0.37 (MAPD: 0.32) INFO [2024-11-09 10:26:06] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:26:07] Local optima: 0.62/1.9, 0.3/1.9, 0.32/2 INFO [2024-11-09 10:26:07] Testing local optimum 1/3 at purity 0.62 and total ploidy 1.90... INFO [2024-11-09 10:26:07] Testing local optimum 2/3 at purity 0.30 and total ploidy 1.90... INFO [2024-11-09 10:26:07] Recalibrating log-ratios... INFO [2024-11-09 10:26:07] Testing local optimum 2/3 at purity 0.30 and total ploidy 1.90... INFO [2024-11-09 10:26:07] Recalibrating log-ratios... INFO [2024-11-09 10:26:07] Testing local optimum 2/3 at purity 0.30 and total ploidy 1.90... INFO [2024-11-09 10:26:07] Recalibrating log-ratios... INFO [2024-11-09 10:26:07] Testing local optimum 2/3 at purity 0.30 and total ploidy 1.90... INFO [2024-11-09 10:26:07] Testing local optimum 3/3 at purity 0.32 and total ploidy 2.00... INFO [2024-11-09 10:26:07] Recalibrating log-ratios... INFO [2024-11-09 10:26:07] Testing local optimum 3/3 at purity 0.32 and total ploidy 2.00... INFO [2024-11-09 10:26:08] Recalibrating log-ratios... INFO [2024-11-09 10:26:08] Testing local optimum 3/3 at purity 0.32 and total ploidy 2.00... INFO [2024-11-09 10:26:08] Recalibrating log-ratios... INFO [2024-11-09 10:26:08] Testing local optimum 3/3 at purity 0.32 and total ploidy 2.00... INFO [2024-11-09 10:26:08] Skipping 1 solutions that converged to the same optima. INFO [2024-11-09 10:26:08] Skipping 1 solutions exceeding max.non.clonal (0.20): 0.3/1.9 (purity/tumor ploidy) INFO [2024-11-09 10:26:08] Fitting variants with beta model for local optimum 1/3... INFO [2024-11-09 10:26:08] Fitting variants for purity 0.65, tumor ploidy 1.74 and contamination 0.01. INFO [2024-11-09 10:26:09] Optimized purity: 0.65 INFO [2024-11-09 10:26:09] Done. INFO [2024-11-09 10:26:09] ------------------------------------------------------------ INFO [2024-11-09 10:26:09] ------------------------------------------------------------ INFO [2024-11-09 10:26:09] PureCN 2.12.0 INFO [2024-11-09 10:26:09] ------------------------------------------------------------ INFO [2024-11-09 10:26:09] Loading coverage files... INFO [2024-11-09 10:26:09] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:09] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:09] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:09] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:09] Removing 22 small (< 5bp) intervals. INFO [2024-11-09 10:26:09] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:26:09] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:26:09] Removing 1724 low count (< 100 total reads) intervals. INFO [2024-11-09 10:26:09] Removing 6 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:26:09] Using 8050 intervals (8050 on-target, 0 off-target). INFO [2024-11-09 10:26:09] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:09] No interval.file provided. Cannot check for any GC-biases. INFO [2024-11-09 10:26:09] Loading VCF... INFO [2024-11-09 10:26:09] Found 127 variants in VCF file. WARN [2024-11-09 10:26:09] DP FORMAT field contains NAs. Removing 3 variants. WARN [2024-11-09 10:26:09] DB INFO flag contains NAs INFO [2024-11-09 10:26:09] 119 (96.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:26:09] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:26:09] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:26:09] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:26:09] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:26:09] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:26:09] Removing 1 variants with AF < 0.030 or AF >= 0.970 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:26:09] Total size of targeted genomic region: 1.53Mb (2.33Mb with 50bp padding). INFO [2024-11-09 10:26:09] 1.2% of targets contain variants. INFO [2024-11-09 10:26:09] Setting somatic prior probabilities for likely germline hits to 0.000500 or to 0.500000 otherwise. INFO [2024-11-09 10:26:09] Excluding 5 novel or poor quality variants from segmentation. INFO [2024-11-09 10:26:09] Sample sex: ? INFO [2024-11-09 10:26:09] Segmenting data... INFO [2024-11-09 10:26:09] Loading pre-computed boundaries for DNAcopy... INFO [2024-11-09 10:26:09] Setting undo.SD parameter to 1.000000. Setting multi-figure configuration INFO [2024-11-09 10:26:10] Setting prune.hclust.h parameter to 0.200000. INFO [2024-11-09 10:26:10] Found 59 segments with median size of 17.67Mb. INFO [2024-11-09 10:26:10] Using 123 variants. INFO [2024-11-09 10:26:10] Mean standard deviation of log-ratios: 0.34 (MAPD: 0.30) INFO [2024-11-09 10:26:10] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:26:10] Local optima: 0.62/1.9, 0.3/1.9, 0.32/2 INFO [2024-11-09 10:26:10] Testing local optimum 1/3 at purity 0.62 and total ploidy 1.90... INFO [2024-11-09 10:26:10] Testing local optimum 2/3 at purity 0.30 and total ploidy 1.90... INFO [2024-11-09 10:26:10] Recalibrating log-ratios... INFO [2024-11-09 10:26:10] Testing local optimum 2/3 at purity 0.30 and total ploidy 1.90... INFO [2024-11-09 10:26:11] Recalibrating log-ratios... INFO [2024-11-09 10:26:11] Testing local optimum 2/3 at purity 0.30 and total ploidy 1.90... INFO [2024-11-09 10:26:11] Recalibrating log-ratios... INFO [2024-11-09 10:26:11] Testing local optimum 2/3 at purity 0.30 and total ploidy 1.90... INFO [2024-11-09 10:26:11] Testing local optimum 3/3 at purity 0.32 and total ploidy 2.00... INFO [2024-11-09 10:26:11] Recalibrating log-ratios... INFO [2024-11-09 10:26:11] Testing local optimum 3/3 at purity 0.32 and total ploidy 2.00... INFO [2024-11-09 10:26:11] Recalibrating log-ratios... INFO [2024-11-09 10:26:11] Testing local optimum 3/3 at purity 0.32 and total ploidy 2.00... INFO [2024-11-09 10:26:11] Recalibrating log-ratios... INFO [2024-11-09 10:26:11] Testing local optimum 3/3 at purity 0.32 and total ploidy 2.00... INFO [2024-11-09 10:26:11] Skipping 2 solutions exceeding max.non.clonal (0.20): 0.3/1.9, 0.35/1.61 (purity/tumor ploidy) INFO [2024-11-09 10:26:11] Fitting variants with beta model for local optimum 1/3... INFO [2024-11-09 10:26:11] Fitting variants for purity 0.65, tumor ploidy 1.75 and contamination 0.01. INFO [2024-11-09 10:26:12] Optimized purity: 0.65 INFO [2024-11-09 10:26:12] Done. INFO [2024-11-09 10:26:12] ------------------------------------------------------------ INFO [2024-11-09 10:26:12] ------------------------------------------------------------ INFO [2024-11-09 10:26:12] PureCN 2.12.0 INFO [2024-11-09 10:26:12] ------------------------------------------------------------ INFO [2024-11-09 10:26:12] Loading coverage files... INFO [2024-11-09 10:26:12] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:12] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:12] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:12] No Gene column in interval.file. You won't get gene-level calls. INFO [2024-11-09 10:26:12] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:12] Removing 15 low/high GC targets. INFO [2024-11-09 10:26:12] Removing 21 small (< 5bp) intervals. INFO [2024-11-09 10:26:12] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:26:12] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:26:12] Removing 1718 low count (< 100 total reads) intervals. INFO [2024-11-09 10:26:12] Removing 6 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:26:12] Removing 36 low mappability intervals. INFO [2024-11-09 10:26:12] Using 8006 intervals (8006 on-target, 0 off-target). INFO [2024-11-09 10:26:12] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:12] AT/GC dropout: 1.01 (tumor), 1.03 (normal), 0.98 (coverage log-ratio). INFO [2024-11-09 10:26:12] Loading VCF... INFO [2024-11-09 10:26:13] Found 127 variants in VCF file. INFO [2024-11-09 10:26:13] 127 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:26:13] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:26:13] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:26:13] Removing 1 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:26:13] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:26:13] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:26:13] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:26:13] Removing 1 variants with AF < 0.030 or AF >= Inf or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:26:13] Total size of targeted genomic region: 1.51Mb (2.31Mb with 50bp padding). INFO [2024-11-09 10:26:13] 1.2% of targets contain variants. INFO [2024-11-09 10:26:13] Removing 11 variants outside intervals. INFO [2024-11-09 10:26:13] Found SOMATIC annotation in VCF. INFO [2024-11-09 10:26:13] Setting somatic prior probabilities for somatic variants to 0.999000 or to 0.000100 otherwise. INFO [2024-11-09 10:26:13] Found SOMATIC annotation in VCF. Setting mapping bias to 0.970. INFO [2024-11-09 10:26:13] Excluding 0 novel or poor quality variants from segmentation. INFO [2024-11-09 10:26:13] Sample sex: ? INFO [2024-11-09 10:26:13] Segmenting data... INFO [2024-11-09 10:26:13] MAPD of 114 allelic fractions: 0.14 (0.15 adjusted). INFO [2024-11-09 10:26:13] Using unweighted PSCBS. INFO [2024-11-09 10:26:13] Setting undo.SD parameter to 1.000000. INFO [2024-11-09 10:26:18] Setting prune.hclust.h parameter to 0.200000. INFO [2024-11-09 10:26:18] Found 71 segments with median size of 27.72Mb. INFO [2024-11-09 10:26:18] Using 114 variants. INFO [2024-11-09 10:26:18] Mean standard deviation of log-ratios: 0.34 (MAPD: 0.30) INFO [2024-11-09 10:26:18] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:26:18] Local optima: 0.65/1.8, 0.38/2.2 INFO [2024-11-09 10:26:18] Testing local optimum 1/2 at purity 0.65 and total ploidy 1.80... INFO [2024-11-09 10:26:18] Recalibrating log-ratios... INFO [2024-11-09 10:26:18] Testing local optimum 1/2 at purity 0.65 and total ploidy 1.80... INFO [2024-11-09 10:26:18] Recalibrating log-ratios... INFO [2024-11-09 10:26:18] Testing local optimum 1/2 at purity 0.65 and total ploidy 1.80... INFO [2024-11-09 10:26:18] Recalibrating log-ratios... INFO [2024-11-09 10:26:18] Testing local optimum 1/2 at purity 0.65 and total ploidy 1.80... INFO [2024-11-09 10:26:18] Testing local optimum 2/2 at purity 0.38 and total ploidy 2.20... INFO [2024-11-09 10:26:18] Skipping 1 solutions exceeding max.non.clonal (0.20): 0.65/2.04 (purity/tumor ploidy) INFO [2024-11-09 10:26:18] Fitting variants with beta model for local optimum 2/2... INFO [2024-11-09 10:26:19] Fitting variants for purity 0.40, tumor ploidy 2.53 and contamination 0.01. INFO [2024-11-09 10:26:19] Optimized purity: 0.40 INFO [2024-11-09 10:26:19] Done. INFO [2024-11-09 10:26:19] ------------------------------------------------------------ FATAL [2024-11-09 10:26:19] This function requires gene-level calls. Please add a column 'Gene' FATAL [2024-11-09 10:26:19] containing gene symbols to the interval.file. FATAL [2024-11-09 10:26:19] FATAL [2024-11-09 10:26:19] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:19] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:20] ------------------------------------------------------------ INFO [2024-11-09 10:26:20] PureCN 2.12.0 INFO [2024-11-09 10:26:20] ------------------------------------------------------------ INFO [2024-11-09 10:26:20] Loading coverage files... INFO [2024-11-09 10:26:20] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:20] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:20] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:20] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:20] Removing 22 small (< 5bp) intervals. INFO [2024-11-09 10:26:20] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:26:20] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:26:20] Removing 1724 low count (< 100 total reads) intervals. INFO [2024-11-09 10:26:20] Removing 6 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:26:20] Using 8050 intervals (8050 on-target, 0 off-target). INFO [2024-11-09 10:26:20] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:20] No interval.file provided. Cannot check for any GC-biases. INFO [2024-11-09 10:26:20] Loading VCF... INFO [2024-11-09 10:26:20] Found 127 variants in VCF file. INFO [2024-11-09 10:26:20] 127 (100.0%) variants annotated as likely germline (DB INFO flag). FATAL [2024-11-09 10:26:20] Different chromosome names in coverage and VCF. FATAL [2024-11-09 10:26:20] FATAL [2024-11-09 10:26:20] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:20] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:20] ------------------------------------------------------------ INFO [2024-11-09 10:26:20] PureCN 2.12.0 INFO [2024-11-09 10:26:20] ------------------------------------------------------------ INFO [2024-11-09 10:26:20] Loading coverage files... INFO [2024-11-09 10:26:20] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:20] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:20] Allosome coverage missing, cannot determine sex. FATAL [2024-11-09 10:26:20] tumor.coverage.file and interval.file do not align. FATAL [2024-11-09 10:26:20] FATAL [2024-11-09 10:26:20] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:20] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:20] ------------------------------------------------------------ INFO [2024-11-09 10:26:20] PureCN 2.12.0 INFO [2024-11-09 10:26:20] ------------------------------------------------------------ INFO [2024-11-09 10:26:20] Loading coverage files... INFO [2024-11-09 10:26:20] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:21] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:21] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:21] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:21] Removing 15 low/high GC targets. INFO [2024-11-09 10:26:21] Removing 21 small (< 5bp) intervals. INFO [2024-11-09 10:26:21] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:26:21] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:26:21] Removing 1718 low count (< 100 total reads) intervals. INFO [2024-11-09 10:26:21] Removing 6 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:26:21] Removing 36 low mappability intervals. INFO [2024-11-09 10:26:21] Using 8006 intervals (8006 on-target, 0 off-target). INFO [2024-11-09 10:26:21] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:21] AT/GC dropout: 1.01 (tumor), 1.03 (normal), 0.98 (coverage log-ratio). INFO [2024-11-09 10:26:21] Loading VCF... INFO [2024-11-09 10:26:21] Found 127 variants in VCF file. INFO [2024-11-09 10:26:21] 127 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:26:21] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:26:21] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:26:21] Removing 1 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:26:21] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:26:21] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:26:21] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:26:21] Removing 1 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:26:21] Total size of targeted genomic region: 1.51Mb (2.31Mb with 50bp padding). INFO [2024-11-09 10:26:21] 1.2% of targets contain variants. INFO [2024-11-09 10:26:21] Removing 11 variants outside intervals. INFO [2024-11-09 10:26:21] Found SOMATIC annotation in VCF. INFO [2024-11-09 10:26:21] Setting somatic prior probabilities for somatic variants to 0.999000 or to 0.000100 otherwise. INFO [2024-11-09 10:26:21] Found SOMATIC annotation in VCF. Setting mapping bias to 0.970. INFO [2024-11-09 10:26:21] Excluding 0 novel or poor quality variants from segmentation. INFO [2024-11-09 10:26:21] Sample sex: ? INFO [2024-11-09 10:26:21] Segmenting data... INFO [2024-11-09 10:26:21] Loading pre-computed boundaries for DNAcopy... INFO [2024-11-09 10:26:21] Setting undo.SD parameter to 1.000000. INFO [2024-11-09 10:26:22] Setting prune.hclust.h parameter to 0.200000. INFO [2024-11-09 10:26:22] Found 59 segments with median size of 17.67Mb. INFO [2024-11-09 10:26:22] Using 114 variants. INFO [2024-11-09 10:26:22] Mean standard deviation of log-ratios: 0.34 (MAPD: 0.30) INFO [2024-11-09 10:26:22] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:26:22] Local optima: 0.63/1.9 INFO [2024-11-09 10:26:22] Testing local optimum 1/1 at purity 0.63 and total ploidy 1.90... INFO [2024-11-09 10:26:22] Fitting variants with beta model for local optimum 1/1... INFO [2024-11-09 10:26:22] Fitting variants for purity 0.65, tumor ploidy 1.75 and contamination 0.01. INFO [2024-11-09 10:26:23] Optimized purity: 0.65 INFO [2024-11-09 10:26:23] Done. INFO [2024-11-09 10:26:23] ------------------------------------------------------------ INFO [2024-11-09 10:26:23] ------------------------------------------------------------ INFO [2024-11-09 10:26:23] PureCN 2.12.0 INFO [2024-11-09 10:26:23] ------------------------------------------------------------ INFO [2024-11-09 10:26:23] Loading coverage files... INFO [2024-11-09 10:26:23] Mean target coverages: 112X (tumor) 99X (normal). WARN [2024-11-09 10:26:23] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:23] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:23] Removing 228 intervals with missing log.ratio. INFO [2024-11-09 10:26:23] Removing 15 low/high GC targets. INFO [2024-11-09 10:26:23] Removing 21 small (< 5bp) intervals. INFO [2024-11-09 10:26:23] Removing 19 intervals with low total coverage in normal (< 150.00 reads). WARN [2024-11-09 10:26:23] No normalDB provided. Provide one for better results. INFO [2024-11-09 10:26:23] Removing 1718 low count (< 100 total reads) intervals. INFO [2024-11-09 10:26:23] Removing 6 low coverage (< 15.0000X) intervals. INFO [2024-11-09 10:26:24] Removing 36 low mappability intervals. INFO [2024-11-09 10:26:24] Using 8006 intervals (8006 on-target, 0 off-target). INFO [2024-11-09 10:26:24] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:24] AT/GC dropout: 1.01 (tumor), 1.03 (normal), 0.98 (coverage log-ratio). INFO [2024-11-09 10:26:24] Loading VCF... INFO [2024-11-09 10:26:24] Found 127 variants in VCF file. INFO [2024-11-09 10:26:24] 127 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:26:24] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:26:24] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:26:24] Removing 1 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:26:24] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:26:24] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:26:24] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:26:24] Removing 1 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:26:24] Total size of targeted genomic region: 1.51Mb (2.31Mb with 50bp padding). INFO [2024-11-09 10:26:24] 1.2% of targets contain variants. INFO [2024-11-09 10:26:24] Removing 11 variants outside intervals. INFO [2024-11-09 10:26:24] Found SOMATIC annotation in VCF. INFO [2024-11-09 10:26:24] Setting somatic prior probabilities for somatic variants to 0.999000 or to 0.000100 otherwise. INFO [2024-11-09 10:26:24] Found SOMATIC annotation in VCF. Setting mapping bias to 0.970. INFO [2024-11-09 10:26:24] Excluding 0 novel or poor quality variants from segmentation. INFO [2024-11-09 10:26:24] Sample sex: ? INFO [2024-11-09 10:26:24] Segmenting data... INFO [2024-11-09 10:26:24] Loading pre-computed boundaries for DNAcopy... INFO [2024-11-09 10:26:24] Setting undo.SD parameter to 1.000000. INFO [2024-11-09 10:26:24] Setting prune.hclust.h parameter to 0.200000. INFO [2024-11-09 10:26:24] Found 59 segments with median size of 17.67Mb. INFO [2024-11-09 10:26:24] Using 114 variants. INFO [2024-11-09 10:26:24] Mean standard deviation of log-ratios: 0.34 (MAPD: 0.30) INFO [2024-11-09 10:26:24] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:26:25] Local optima: 0.63/1.9 INFO [2024-11-09 10:26:25] Testing local optimum 1/1 at purity 0.63 and total ploidy 1.90... INFO [2024-11-09 10:26:25] Fitting variants with beta model for local optimum 1/1... WARN [2024-11-09 10:26:25] Some gene symbols found on multiple chromosomes. Use of approved symbols suggested. INFO [2024-11-09 10:26:25] Fitting variants for purity 0.65, tumor ploidy 1.75 and contamination 0.01. INFO [2024-11-09 10:26:26] Optimized purity: 0.65 INFO [2024-11-09 10:26:26] Done. INFO [2024-11-09 10:26:26] ------------------------------------------------------------ FATAL [2024-11-09 10:26:26] chr1 not valid chromosome name(s). Valid names are: FATAL [2024-11-09 10:26:26] 1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22 FATAL [2024-11-09 10:26:26] FATAL [2024-11-09 10:26:26] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:26] parameters (PureCN 2.12.0). INFO [2024-11-09 10:26:26] ------------------------------------------------------------ INFO [2024-11-09 10:26:26] PureCN 2.12.0 INFO [2024-11-09 10:26:26] ------------------------------------------------------------ INFO [2024-11-09 10:26:26] Loading coverage files... WARN [2024-11-09 10:26:26] Provided sampleid (Sample2) does not match Sample1 found in segmentation. WARN [2024-11-09 10:26:26] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:26] Allosome coverage missing, cannot determine sex. INFO [2024-11-09 10:26:26] Removing 10 intervals with missing log.ratio. INFO [2024-11-09 10:26:26] Using 10039 intervals (10039 on-target, 0 off-target). INFO [2024-11-09 10:26:26] No off-target intervals. If this is hybrid-capture data, consider adding them. INFO [2024-11-09 10:26:26] Loading VCF... INFO [2024-11-09 10:26:26] Found 127 variants in VCF file. INFO [2024-11-09 10:26:26] 127 (100.0%) variants annotated as likely germline (DB INFO flag). INFO [2024-11-09 10:26:26] LIB-02240e4 is tumor in VCF file. INFO [2024-11-09 10:26:26] No homozygous variants in VCF, provide unfiltered VCF. INFO [2024-11-09 10:26:26] Removing 1 non heterozygous (in matched normal) germline SNPs. INFO [2024-11-09 10:26:26] Removing 0 low quality variants with non-offset BQ < 25. INFO [2024-11-09 10:26:26] Base quality scores range from 29 to 35 (offset by 1) INFO [2024-11-09 10:26:26] Minimum number of supporting reads ranges from 2 to 5, depending on coverage and BQS. INFO [2024-11-09 10:26:26] Removing 1 variants with AF < 0.030 or AF >= 1.000 or insufficient supporting reads or depth < 15. INFO [2024-11-09 10:26:26] Total size of targeted genomic region: 1.71Mb (2.70Mb with 50bp padding). INFO [2024-11-09 10:26:26] 1.0% of targets contain variants. INFO [2024-11-09 10:26:26] Removing 0 variants outside intervals. INFO [2024-11-09 10:26:26] Found SOMATIC annotation in VCF. INFO [2024-11-09 10:26:26] Setting somatic prior probabilities for somatic variants to 0.999000 or to 0.000100 otherwise. INFO [2024-11-09 10:26:26] Found SOMATIC annotation in VCF. Setting mapping bias to 0.976. INFO [2024-11-09 10:26:26] Excluding 0 novel or poor quality variants from segmentation. INFO [2024-11-09 10:26:26] Sample sex: ? INFO [2024-11-09 10:26:26] Segmenting data... INFO [2024-11-09 10:26:26] Loaded provided segmentation file example_seg.txt (format DNAcopy). WARN [2024-11-09 10:26:26] Provided sampleid (Sample2) does not match Sample1 found in segmentation. INFO [2024-11-09 10:26:26] Re-centering provided segment means (offset -0.0033). INFO [2024-11-09 10:26:26] Loading pre-computed boundaries for DNAcopy... INFO [2024-11-09 10:26:26] Setting undo.SD parameter to 0.000000. Setting multi-figure configuration INFO [2024-11-09 10:26:26] Setting prune.hclust.h parameter to 0.200000. INFO [2024-11-09 10:26:27] Found 54 segments with median size of 24.88Mb. INFO [2024-11-09 10:26:27] Using 125 variants. INFO [2024-11-09 10:26:27] Mean standard deviation of log-ratios: 0.40 (MAPD: 0.00) INFO [2024-11-09 10:26:27] 2D-grid search of purity and ploidy... INFO [2024-11-09 10:26:27] Local optima: 0.6/1.9 INFO [2024-11-09 10:26:27] Testing local optimum 1/1 at purity 0.60 and total ploidy 1.90... INFO [2024-11-09 10:26:27] Fitting variants with beta model for local optimum 1/1... INFO [2024-11-09 10:26:27] Fitting variants for purity 0.65, tumor ploidy 1.74 and contamination 0.01. INFO [2024-11-09 10:26:28] Optimized purity: 0.65 INFO [2024-11-09 10:26:28] Done. INFO [2024-11-09 10:26:28] ------------------------------------------------------------ WARN [2024-11-09 10:26:28] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:28] Allosome coverage missing, cannot determine sex. Setting multi-figure configuration FATAL [2024-11-09 10:26:30] Segmentation file expected with colnames ID, chrom, loc.start, loc.end, FATAL [2024-11-09 10:26:30] num.mark, seg.mean FATAL [2024-11-09 10:26:30] FATAL [2024-11-09 10:26:30] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:30] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:30] seg.file contains multiple samples and sampleid missing. FATAL [2024-11-09 10:26:30] FATAL [2024-11-09 10:26:30] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:30] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:30] seg.file contains multiple samples and sampleid does not match any. FATAL [2024-11-09 10:26:30] FATAL [2024-11-09 10:26:30] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:30] parameters (PureCN 2.12.0). WARN [2024-11-09 10:26:30] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:30] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:33] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:33] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:33] Provided sampleid (example_tumor.txt.gz) does not match Sample1 found in segmentation. WARN [2024-11-09 10:26:34] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:34] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:34] No normalDB provided. Provide one for better results. WARN [2024-11-09 10:26:36] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:36] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:37] Provided sampleid (Sample.1) does not match Sample1 found in segmentation. Setting multi-figure configuration WARN [2024-11-09 10:26:39] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:39] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:39] No normalDB provided. Provide one for better results. WARN [2024-11-09 10:26:40] Sampleid looks like a normal in VCF, not like a tumor. WARN [2024-11-09 10:26:42] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:42] Allosome coverage missing, cannot determine sex. FATAL [2024-11-09 10:26:42] normalDB not a valid normalDB object. Use createNormalDatabase to FATAL [2024-11-09 10:26:42] create one. FATAL [2024-11-09 10:26:42] FATAL [2024-11-09 10:26:42] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:42] parameters (PureCN 2.12.0). WARN [2024-11-09 10:26:42] You are likely not using the correct baits file! WARN [2024-11-09 10:26:42] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:42] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:43] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:43] Allosome coverage missing, cannot determine sex. FATAL [2024-11-09 10:26:43] normalDB appears to be empty. FATAL [2024-11-09 10:26:43] FATAL [2024-11-09 10:26:43] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:43] parameters (PureCN 2.12.0). WARN [2024-11-09 10:26:43] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:43] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:43] Intervals in coverage and interval.file have conflicting on/off-target annotation. WARN [2024-11-09 10:26:46] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:46] Allosome coverage missing, cannot determine sex. FATAL [2024-11-09 10:26:46] Seqlevels missing in provided segmentation: 6 FATAL [2024-11-09 10:26:46] FATAL [2024-11-09 10:26:46] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:46] parameters (PureCN 2.12.0). sh: gatk: command not found WARN [2024-11-09 10:26:47] Cannot find gatk binary in path. WARN [2024-11-09 10:26:47] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:47] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:47] No normalDB provided. Provide one for better results. FATAL [2024-11-09 10:26:47] segmentationHclust requires an input segmentation. FATAL [2024-11-09 10:26:47] FATAL [2024-11-09 10:26:47] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:47] parameters (PureCN 2.12.0). WARN [2024-11-09 10:26:47] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:47] Allosome coverage missing, cannot determine sex. WARN [2024-11-09 10:26:47] No normalDB provided. Provide one for better results. FATAL [2024-11-09 10:26:55] The normal.panel.vcf.file contains only a single sample. FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:55] mapping.bias.file must be a file with *.rds suffix. FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). Failed with error: 'there is no package called 'genomicsdb'' FATAL [2024-11-09 10:26:55] min.normals (0) must be >= 1. FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:55] min.normals (10) cannot be larger than min.normals.assign.betafit (3). FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:55] min.normals.assign.betafit (10) cannot be larger than FATAL [2024-11-09 10:26:55] min.normals.betafit (7). FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:55] min.normals.betafit (20) cannot be larger than FATAL [2024-11-09 10:26:55] min.normals.position.specific.fit (10). FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:55] min.betafit.rho not within expected range or format. FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:55] max.betafit.rho not within expected range or format. FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). FATAL [2024-11-09 10:26:55] min.betafit.rho (0.9) cannot be larger than max.betafit.rho (0.2). FATAL [2024-11-09 10:26:55] FATAL [2024-11-09 10:26:55] This is most likely a user error due to invalid input data or FATAL [2024-11-09 10:26:55] parameters (PureCN 2.12.0). [ FAIL 0 | WARN 13 | SKIP 2 | PASS 404 ] ══ Skipped tests (2) ═══════════════════════════════════════════════════════════ • gatk binary > 4.1.7.0 required (1): 'test_segmentation.R:25:4' • genomicsdb required (1): 'test_setMappingBiasVcf.R:45:5' [ FAIL 0 | WARN 13 | SKIP 2 | PASS 404 ] > > proc.time() user system elapsed 121.359 4.036 114.691
PureCN.Rcheck/PureCN-Ex.timings
name | user | system | elapsed | |
adjustLogRatio | 0.718 | 0.013 | 0.733 | |
annotateTargets | 2.346 | 0.066 | 2.415 | |
bootstrapResults | 0.582 | 0.014 | 0.597 | |
calculateBamCoverageByInterval | 0.061 | 0.002 | 0.064 | |
calculateLogRatio | 0.193 | 0.010 | 0.203 | |
calculateMappingBiasGatk4 | 0.000 | 0.001 | 0.000 | |
calculateMappingBiasVcf | 0.590 | 0.017 | 0.607 | |
calculatePowerDetectSomatic | 0.431 | 0.005 | 0.436 | |
calculateTangentNormal | 0.899 | 0.040 | 0.939 | |
callAlterations | 0.053 | 0.002 | 0.055 | |
callAlterationsFromSegmentation | 0.474 | 0.011 | 0.489 | |
callAmplificationsInLowPurity | 11.848 | 0.118 | 11.966 | |
callCIN | 0.080 | 0.002 | 0.082 | |
callLOH | 0.070 | 0.002 | 0.072 | |
callMutationBurden | 0.535 | 0.010 | 0.546 | |
centromeres | 0.000 | 0.001 | 0.001 | |
correctCoverageBias | 0.524 | 0.008 | 0.532 | |
createCurationFile | 0.143 | 0.003 | 0.146 | |
createNormalDatabase | 0.770 | 0.006 | 0.776 | |
filterIntervals | 6.814 | 0.119 | 6.935 | |
filterVcfBasic | 0.202 | 0.002 | 0.204 | |
filterVcfMuTect | 0.215 | 0.001 | 0.217 | |
filterVcfMuTect2 | 0.207 | 0.001 | 0.216 | |
findFocal | 3.920 | 0.022 | 3.943 | |
getSexFromCoverage | 0.087 | 0.004 | 0.091 | |
getSexFromVcf | 0.080 | 0.004 | 0.083 | |
plotAbs | 0.082 | 0.003 | 0.086 | |
poolCoverage | 0.183 | 0.009 | 0.192 | |
predictSomatic | 0.156 | 0.002 | 0.157 | |
preprocessIntervals | 0.215 | 0.003 | 0.219 | |
processMultipleSamples | 0.808 | 0.013 | 0.821 | |
readAllelicCountsFile | 0.193 | 0.000 | 0.194 | |
readCoverageFile | 0.074 | 0.002 | 0.076 | |
readCurationFile | 0.083 | 0.002 | 0.085 | |
readIntervalFile | 0.060 | 0.000 | 0.061 | |
readLogRatioFile | 0.008 | 0.000 | 0.009 | |
readSegmentationFile | 0.002 | 0.000 | 0.002 | |
runAbsoluteCN | 5.458 | 0.107 | 5.565 | |
segmentationCBS | 2.512 | 0.021 | 2.533 | |
segmentationGATK4 | 0.001 | 0.000 | 0.001 | |
segmentationHclust | 4.701 | 0.060 | 4.762 | |
segmentationPSCBS | 7.824 | 0.119 | 7.947 | |
setMappingBiasVcf | 0.113 | 0.004 | 0.117 | |
setPriorVcf | 0.087 | 0.003 | 0.090 | |