Chapter 7 Lawlor human pancreas (SMARTer)
7.1 Introduction
This performs an analysis of the Lawlor et al. (2017) dataset, consisting of human pancreas cells from various donors.
7.3 Quality control
library(scater)
stats <- perCellQCMetrics(sce.lawlor,
subsets=list(Mito=which(rowData(sce.lawlor)$SEQNAME=="MT")))
qc <- quickPerCellQC(stats, percent_subsets="subsets_Mito_percent",
batch=sce.lawlor$`islet unos id`)
sce.lawlor <- sce.lawlor[,!qc$discard]colData(unfiltered) <- cbind(colData(unfiltered), stats)
unfiltered$discard <- qc$discard
gridExtra::grid.arrange(
plotColData(unfiltered, x="islet unos id", y="sum", colour_by="discard") +
scale_y_log10() + ggtitle("Total count") +
theme(axis.text.x = element_text(angle = 90)),
plotColData(unfiltered, x="islet unos id", y="detected",
colour_by="discard") + scale_y_log10() + ggtitle("Detected features") +
theme(axis.text.x = element_text(angle = 90)),
plotColData(unfiltered, x="islet unos id", y="subsets_Mito_percent",
colour_by="discard") + ggtitle("Mito percent") +
theme(axis.text.x = element_text(angle = 90)),
ncol=2
)
Figure 7.1: Distribution of each QC metric across cells from each donor of the Lawlor pancreas dataset. Each point represents a cell and is colored according to whether that cell was discarded.
Figure 7.2: Percentage of mitochondrial reads in each cell in the 416B dataset compared to the total count. Each point represents a cell and is colored according to whether that cell was discarded.
## low_lib_size low_n_features high_subsets_Mito_percent
## 9 5 25
## discard
## 347.4 Normalization
library(scran)
set.seed(1000)
clusters <- quickCluster(sce.lawlor)
sce.lawlor <- computeSumFactors(sce.lawlor, clusters=clusters)
sce.lawlor <- logNormCounts(sce.lawlor)## Min. 1st Qu. Median Mean 3rd Qu. Max.
## 0.295 0.781 0.963 1.000 1.182 2.629plot(librarySizeFactors(sce.lawlor), sizeFactors(sce.lawlor), pch=16,
xlab="Library size factors", ylab="Deconvolution factors", log="xy")
Figure 7.3: Relationship between the library size factors and the deconvolution size factors in the Lawlor pancreas dataset.
7.5 Variance modelling
Using age as a proxy for the donor.
dec.lawlor <- modelGeneVar(sce.lawlor, block=sce.lawlor$`islet unos id`)
chosen.genes <- getTopHVGs(dec.lawlor, n=2000)par(mfrow=c(4,2))
blocked.stats <- dec.lawlor$per.block
for (i in colnames(blocked.stats)) {
current <- blocked.stats[[i]]
plot(current$mean, current$total, main=i, pch=16, cex=0.5,
xlab="Mean of log-expression", ylab="Variance of log-expression")
curfit <- metadata(current)
curve(curfit$trend(x), col='dodgerblue', add=TRUE, lwd=2)
}
Figure 7.4: Per-gene variance as a function of the mean for the log-expression values in the Lawlor pancreas dataset. Each point represents a gene (black) with the mean-variance trend (blue) fitted separately for each donor.
7.7 Clustering
snn.gr <- buildSNNGraph(sce.lawlor, use.dimred="PCA")
colLabels(sce.lawlor) <- factor(igraph::cluster_walktrap(snn.gr)$membership)##
## Acinar Alpha Beta Delta Ductal Gamma/PP None/Other Stellate
## 1 1 0 1 13 2 16 2 0
## 2 0 0 75 1 0 0 0 0
## 3 0 161 1 0 0 1 2 0
## 4 0 1 0 1 0 0 5 19
## 5 22 0 0 0 0 0 0 0
## 6 0 0 174 4 1 0 1 0
## 7 0 76 1 0 0 0 0 0
## 8 0 0 0 1 20 0 2 0##
## ACCG268 ACCR015A ACEK420A ACEL337 ACHY057 ACIB065 ACIW009 ACJV399
## 1 8 2 2 4 4 4 9 2
## 2 13 3 2 33 3 2 4 16
## 3 36 23 14 13 14 14 21 30
## 4 7 1 0 1 0 4 9 4
## 5 0 2 13 0 0 0 5 2
## 6 34 10 4 39 7 23 24 39
## 7 33 12 0 5 6 7 4 10
## 8 1 1 2 1 2 1 12 3gridExtra::grid.arrange(
plotTSNE(sce.lawlor, colour_by="label"),
plotTSNE(sce.lawlor, colour_by="islet unos id"),
ncol=2
)
Figure 5.3: Obligatory \(t\)-SNE plots of the Lawlor pancreas dataset. Each point represents a cell that is colored by cluster (left) or batch (right).
Session Info
R Under development (unstable) (2024-10-21 r87258)
Platform: x86_64-pc-linux-gnu
Running under: Ubuntu 24.04.1 LTS
Matrix products: default
BLAS: /home/biocbuild/bbs-3.21-bioc/R/lib/libRblas.so
LAPACK: /usr/lib/x86_64-linux-gnu/lapack/liblapack.so.3.12.0
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_GB LC_COLLATE=C
[5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
[7] LC_PAPER=en_US.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
time zone: America/New_York
tzcode source: system (glibc)
attached base packages:
[1] stats4 stats graphics grDevices utils datasets methods
[8] base
other attached packages:
[1] BiocSingular_1.23.0 scran_1.35.0
[3] scater_1.35.0 ggplot2_3.5.1
[5] scuttle_1.17.0 ensembldb_2.31.0
[7] AnnotationFilter_1.31.0 GenomicFeatures_1.59.1
[9] AnnotationDbi_1.69.0 AnnotationHub_3.15.0
[11] BiocFileCache_2.15.0 dbplyr_2.5.0
[13] scRNAseq_2.21.0 SingleCellExperiment_1.29.1
[15] SummarizedExperiment_1.37.0 Biobase_2.67.0
[17] GenomicRanges_1.59.0 GenomeInfoDb_1.43.0
[19] IRanges_2.41.0 S4Vectors_0.45.1
[21] BiocGenerics_0.53.1 generics_0.1.3
[23] MatrixGenerics_1.19.0 matrixStats_1.4.1
[25] BiocStyle_2.35.0 rebook_1.17.0
loaded via a namespace (and not attached):
[1] jsonlite_1.8.9 CodeDepends_0.6.6 magrittr_2.0.3
[4] ggbeeswarm_0.7.2 gypsum_1.3.0 farver_2.1.2
[7] rmarkdown_2.29 BiocIO_1.17.0 zlibbioc_1.53.0
[10] vctrs_0.6.5 memoise_2.0.1 Rsamtools_2.23.0
[13] RCurl_1.98-1.16 htmltools_0.5.8.1 S4Arrays_1.7.1
[16] curl_6.0.0 BiocNeighbors_2.1.0 Rhdf5lib_1.29.0
[19] SparseArray_1.7.1 rhdf5_2.51.0 sass_0.4.9
[22] alabaster.base_1.7.1 bslib_0.8.0 alabaster.sce_1.7.0
[25] httr2_1.0.6 cachem_1.1.0 GenomicAlignments_1.43.0
[28] igraph_2.1.1 mime_0.12 lifecycle_1.0.4
[31] pkgconfig_2.0.3 rsvd_1.0.5 Matrix_1.7-1
[34] R6_2.5.1 fastmap_1.2.0 GenomeInfoDbData_1.2.13
[37] digest_0.6.37 colorspace_2.1-1 dqrng_0.4.1
[40] irlba_2.3.5.1 ExperimentHub_2.15.0 RSQLite_2.3.7
[43] beachmat_2.23.0 labeling_0.4.3 filelock_1.0.3
[46] fansi_1.0.6 httr_1.4.7 abind_1.4-8
[49] compiler_4.5.0 bit64_4.5.2 withr_3.0.2
[52] BiocParallel_1.41.0 viridis_0.6.5 DBI_1.2.3
[55] HDF5Array_1.35.1 alabaster.ranges_1.7.0 alabaster.schemas_1.7.0
[58] rappdirs_0.3.3 DelayedArray_0.33.1 bluster_1.17.0
[61] rjson_0.2.23 tools_4.5.0 vipor_0.4.7
[64] beeswarm_0.4.0 glue_1.8.0 restfulr_0.0.15
[67] rhdf5filters_1.19.0 grid_4.5.0 Rtsne_0.17
[70] cluster_2.1.6 gtable_0.3.6 metapod_1.15.0
[73] ScaledMatrix_1.15.0 utf8_1.2.4 XVector_0.47.0
[76] ggrepel_0.9.6 BiocVersion_3.21.1 pillar_1.9.0
[79] limma_3.63.2 dplyr_1.1.4 lattice_0.22-6
[82] rtracklayer_1.67.0 bit_4.5.0 tidyselect_1.2.1
[85] locfit_1.5-9.10 Biostrings_2.75.1 knitr_1.49
[88] gridExtra_2.3 bookdown_0.41 ProtGenerics_1.39.0
[91] edgeR_4.5.0 xfun_0.49 statmod_1.5.0
[94] UCSC.utils_1.3.0 lazyeval_0.2.2 yaml_2.3.10
[97] evaluate_1.0.1 codetools_0.2-20 tibble_3.2.1
[100] alabaster.matrix_1.7.0 BiocManager_1.30.25 graph_1.85.0
[103] cli_3.6.3 munsell_0.5.1 jquerylib_0.1.4
[106] Rcpp_1.0.13-1 dir.expiry_1.15.0 png_0.1-8
[109] XML_3.99-0.17 parallel_4.5.0 blob_1.2.4
[112] bitops_1.0-9 viridisLite_0.4.2 alabaster.se_1.7.0
[115] scales_1.3.0 purrr_1.0.2 crayon_1.5.3
[118] rlang_1.1.4 cowplot_1.1.3 KEGGREST_1.47.0 References
Lawlor, N., J. George, M. Bolisetty, R. Kursawe, L. Sun, V. Sivakamasundari, I. Kycia, P. Robson, and M. L. Stitzel. 2017. “Single-cell transcriptomes identify human islet cell signatures and reveal cell-type-specific expression changes in type 2 diabetes.” Genome Res. 27 (2): 208–22.