### R code from vignette source 'DesignSignatures.Rnw'

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### code chunk number 1: DesignSignatures.Rnw:46-48
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options(continue=" ")
options(width=80)


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### code chunk number 2: startup
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library(DECIPHER)


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### code chunk number 3: expr1
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# specify the path to your sequence file:
fas <- "<<path to FASTA file>>"
# OR find the example sequence file used in this tutorial:
fas <- system.file("extdata", "IDH2.fas", package="DECIPHER")


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### code chunk number 4: expr2 (eval = FALSE)
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## # specify a path for where to write the sequence database
## dbConn <- "<<path to write sequence database>>"
## # OR create the sequence database in memory
## dbConn <- dbConnect(dbDriver("SQLite"), ":memory:")
## N <- Seqs2DB(fas, "FASTA", dbConn, "")
## N # number of sequences in the database


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### code chunk number 5: expr3 (eval = FALSE)
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## # if each sequence belongs to its own group,
## # then identify the sequences with a number:
## desc <- as.character(seq_len(N)) # N is the number of sequences
## # OR get the FASTA record description:
## desc <- dbGetQuery(dbConn, "select description from Seqs")$description
## # show the unique descriptors:
## unique(desc)


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### code chunk number 6: expr4 (eval = FALSE)
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## Add2DB(data.frame(identifier=desc, stringsAsFactors=FALSE), dbConn)


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### code chunk number 7: expr5a (eval = FALSE)
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## # Designing primers for sequencing experiments:
## TYPE <- "sequence"
## MIN_SIZE <- 300 # base pairs
## MAX_SIZE <- 700
## RESOLUTION <- 5 # k-mer signature
## LEVELS <- 5 # max number of each k-mer


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### code chunk number 8: expr5b (eval = FALSE)
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## # Designing primers for community fingerprinting (FLP):
## TYPE <- "length"
## # it is important to have a width range of lengths
## MIN_SIZE <- 200 # base pairs
## MAX_SIZE <- 1400
## # define bin boundaries for distinguishing length,
## # the values below require high-resolution, but
## # the bin boundaries can be redefined for lower
## # resolution experiments such as gel runs
## RESOLUTION <- c(seq(200, 700, 3),
##                 seq(705, 1000, 5),
##                 seq(1010, 1400, 10))
## LEVELS <- 2 # presence/absence of the length


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### code chunk number 9: expr5c (eval = FALSE)
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## # Designing primers for high resolution melting (HRM):
## TYPE <- "melt"
## MIN_SIZE <- 55 # base pairs
## MAX_SIZE <- 400
## # the recommended values for resolution
## RESOLUTION <- seq(75, 100, 0.25) # degrees Celsius
## LEVELS <- 10


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### code chunk number 10: expr6 (eval = FALSE)
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## ENZYMES <- NULL # required for sequencing
## # OR select restriction enzymes to consider
## data(RESTRICTION_ENZYMES) # load available enzymes
## # for this tutorial we will use the enzyme MslI
## ENZYMES <- RESTRICTION_ENZYMES["MslI"]
## ENZYMES


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### code chunk number 11: expr7 (eval = FALSE)
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## primers <- DesignSignatures(dbConn,
##                             type=TYPE,
##                             minProductSize=MIN_SIZE,
##                             maxProductSize=MAX_SIZE,
##                             resolution=RESOLUTION,
##                             levels=LEVELS,
##                             enzymes=ENZYMES)


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### code chunk number 12: expr8 (eval = FALSE)
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## primers[which.max(primers$score),] # best primers without digestion


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### code chunk number 13: expr9 (eval = FALSE)
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## primers[which.max(primers$digest_score),] # best primers with digestion


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### code chunk number 14: expr9 (eval = FALSE)
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## PSET <- 1 # examine the top scoring primer set overall
## 
## # select the first sequence from each group
## dna <- SearchDB(dbConn,
##                 remove="all",
##                 nameBy="identifier",
##                 clause="row_names =
##                         (select min(row_names) from Seqs as S
##                          where S.identifier = Seqs.identifier)",
##                 verbose=FALSE)
## 
## f_primer <- DNAStringSet(primers$forward_primer[PSET])
## r_primer <- DNAStringSet(primers$reverse_primer[PSET])
## patterns <- c(f_primer,
##               reverseComplement(r_primer),
##               DNAStringSet(gsub("[^A-Z]", "", ENZYMES)))
## 
## BrowseSeqs(dna,
##            patterns=patterns)


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### code chunk number 15: expr10 (eval = FALSE)
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## PSET <- which.max(primers$score) # top scoring without digestion
## 
## f_primer <- DNAString(primers$forward_primer[PSET])
## r_primer <- DNAString(primers$reverse_primer[PSET])
## r_primer <- reverseComplement(r_primer)
## 
## ids <- dbGetQuery(dbConn, "select distinct identifier from Seqs")
## ids <- ids$identifier
## 
## if (TYPE=="sequence") {
##     signatures <- matrix(0, nrow=4^RESOLUTION, ncol=length(ids))
## } else if (TYPE=="melt") {
##     signatures <- matrix(0, nrow=length(RESOLUTION), ncol=length(ids))
## } else { # TYPE=="length"
##     signatures <- matrix(0, nrow=length(RESOLUTION) - 1, ncol=length(ids))
## }
## colnames(signatures) <- abbreviate(ids, 15)
## 
## for (i in seq_along(ids)) {
##     dna <- SearchDB(dbConn, identifier=ids[i], remove="all", verbose=FALSE)
##     amplicons <- matchLRPatterns(f_primer, r_primer,
##                                  MAX_SIZE, unlist(dna),
##                                  max.Lmismatch=2, max.Rmismatch=2,
##                                  Lfixed="subject", Rfixed="subject")
##     amplicons <- as(amplicons, "DNAStringSet")
##     if (length(amplicons)==0)
##         next
##     
##     if (TYPE=="sequence") {
##         signature <- oligonucleotideFrequency(amplicons, RESOLUTION)
##         signatures[, i] <- colMeans(signature)
##     } else if (TYPE=="melt") {
##         signature <- MeltDNA(amplicons, "melt curves", RESOLUTION)
##         # weight melting curves by their amlicon's width
##         signature <- t(signature)*width(amplicons)
##         signatures[, i] <- colSums(signature)/sum(width(amplicons))
##     } else { # TYPE=="length"
##         signature <- .bincode(width(amplicons), RESOLUTION)
##         for (j in signature[which(!is.na(signature))])
##             signatures[j, i] <- signatures[j, i] + 1/length(signature)
##     }
## }
## 
## if (TYPE=="sequence") {
##     d <- dist(t(signatures), "minkowski", p=1) # L1-Norm
##     Treeline(myDistMatrix=as.matrix(d), method="UPGMA", showPlot=TRUE)
##     mtext(paste(RESOLUTION, "-mer Profile Distance", sep=""),
##         side=2, padj=-4)
## } else if (TYPE=="melt") {
##     matplot(RESOLUTION, signatures, type="l",
##         xlab="Temperature (degrees Celsius)", ylab="Average Helicity")
## } else { # TYPE=="length"
##     if (length(ids) > 20) {
##         plot(NA,
##             xlim=c(0.5, length(ids) + 0.5), ylim=range(RESOLUTION),
##             xlab="Group Index", ylab="Amplicon Length",
##             yaxs="i", xaxs="i")
##         axis(1, at=1:length(ids), labels=FALSE, tck=-0.01)
##     } else {
##         plot(NA,
##             xlim=c(0.5, length(ids) + 0.5), ylim=range(RESOLUTION),
##             xlab="", ylab="Amplicon Length",
##             yaxs="i", xaxs="i", xaxt="n")
##         axis(1, at=1:length(ids), labels=abbreviate(ids, 7), las=2)
##     }
##     xaxs <- RESOLUTION[-1] - diff(RESOLUTION)/2 # average lengths
##     for (i in seq_along(ids)) {
##         w <- which(signatures[, i] > 0)
##         if (length(w) > 0)
##             segments(i - 0.45, xaxs[w], i + 0.45, xaxs[w], lwd=2)
##     }
## }


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### code chunk number 16: expr11 (eval = FALSE)
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## PSET <- which.max(primers$digest_score) # top scoring with digestion
## 
## f_primer <- DNAString(primers$forward_primer[PSET])
## r_primer <- DNAString(primers$reverse_primer[PSET])
## r_primer <- reverseComplement(r_primer)
## enzyme <- RESTRICTION_ENZYMES[primers$enzyme[PSET]]
## 
## signatures[] <- 0 # initialize the results matrix used previously
## for (i in seq_along(ids)) {
##     dna <- SearchDB(dbConn, identifier=ids[i], remove="all", verbose=FALSE)
##     amplicons <- matchLRPatterns(f_primer, r_primer,
##                                  MAX_SIZE, unlist(dna),
##                                  max.Lmismatch=2, max.Rmismatch=2,
##                                  Lfixed="subject", Rfixed="subject")
##     amplicons <- as(amplicons, "DNAStringSet")
##     if (length(amplicons)==0)
##         next
##     digested <- DigestDNA(enzyme, amplicons, strand="top")
##     digested <- unlist(digested) # convert to DNAStringSet
##     
##     if (TYPE=="melt") {
##         signature <- MeltDNA(digested, "melt curves", RESOLUTION)
##         # weight melting curves by their fragment's width
##         signature <- t(signature)*width(digested)
##         signatures[, i] <- colSums(signature)/sum(width(digested))
##     } else { # TYPE=="length"
##         signature <- .bincode(width(digested), RESOLUTION)
##         for (j in signature[which(!is.na(signature))])
##             signatures[j, i] <- signatures[j, i] + 1/length(signature)
##     }
## }
## 
## if (TYPE=="melt") {
##     matplot(RESOLUTION, signatures, type="l",
##         xlab="Temperature (degrees Celsius)", ylab="Average Helicity")
## } else { # TYPE=="length"
##     if (length(ids) > 20) {
##         plot(NA,
##             xlim=c(0.5, length(ids) + 0.5), ylim=range(RESOLUTION),
##             xlab="Group Index", ylab="Amplicon Length",
##             yaxs="i", xaxs="i")
##         axis(1, at=1:length(ids), labels=FALSE, tck=-0.01)
##     } else {
##         plot(NA,
##             xlim=c(0.5, length(ids) + 0.5), ylim=range(RESOLUTION),
##             xlab="", ylab="Amplicon Length",
##             yaxs="i", xaxs="i", xaxt="n")
##         axis(1, at=1:length(ids), labels=abbreviate(ids, 7), las=2)
##     }
##     xaxs <- RESOLUTION[-1] - diff(RESOLUTION)/2 # average lengths
##     for (i in seq_along(ids)) {
##         w <- which(signatures[, i] > 0)
##         if (length(w) > 0)
##             segments(i - 0.45, xaxs[w], i + 0.45, xaxs[w], lwd=2)
##     }
## }
## zzz <- dbDisconnect(dbConn)


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### code chunk number 17: sessinfo
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toLatex(sessionInfo(), locale=FALSE)