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Changeset 3:79212a309499 (2020-07-14)

Previous changeset 2:1c9715cef808 (2020-03-16) Next changeset 4:5b5a7af9fbb4 (2021-02-01)

Commit message:
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/dada2 commit 8533fe71d1d50f09348da2dc34941724407a1ffe"

modified:
macros.xml
static/images/pairpipe.png
static/images/pairpipe.svg
test-data/gentest.R

removed:
test-data/learnErrors.pdf
test-data/learnErrors_R1.pdf

diff -r 1c9715cef808 -r 79212a309499 macros.xml
--- a/macros.xml Mon Mar 16 08:03:24 2020 -0400
+++ b/macros.xml Tue Jul 14 07:39:34 2020 -0400

@@ -7,7 +7,7 @@
         </requirements>
     </xml>

-    <token name="@DADA2_VERSION@">1.14</token>
+    <token name="@DADA2_VERSION@">1.16</token>
     <token name="@WRAPPER_VERSION@">0</token>

     <xml name="version_command">
@@ -124,6 +124,9 @@

.. image:: pairpipe.png

+Note: In particular for the analysis of paired collections the collections should be sorted lexicographical
+before the analysis.
+
For single end data you the steps "Unzip collection" and "mergePairs" are not necessary.

More information may be found on the dada2 homepage:: https://benjjneb.github.io/dada2/index.html (in particular tutorials) or the documentation of dada2's R package https://bioconductor.org/packages/release/bioc/html/dada2.html (in particular the pdf which contains the full documentation of all parameters)

diff -r 1c9715cef808 -r 79212a309499 static/images/pairpipe.png

Binary file static/images/pairpipe.png has changed

diff -r 1c9715cef808 -r 79212a309499 static/images/pairpipe.svg
--- a/static/images/pairpipe.svg Mon Mar 16 08:03:24 2020 -0400
+++ b/static/images/pairpipe.svg Tue Jul 14 07:39:34 2020 -0400

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style="stroke:#000000;marker-end:url(#id2);stroke-width:0.93333333;stroke-miterlimit:4;stroke-dasharray:none"\n d="m 1167.5598,116.5 h 42"\n id="path5593"\n inkscape:connector-curvature="0"\n@@ -494,8 +494,8 @@\n sodipodi:nodetypes="cc"\n inkscape:connector-curvature="0"\n id="path5557"\n- d="m 255.55976,114.5 h 42"\n- style="stroke:#000000;marker-end:url(#id2)" />\n+ d="m 283.77925,110.5 h 33.78051"\n+ style="stroke:#000000;stroke-width:0.93333333;marker-end:url(#id2);stroke-miterlimit:4;stroke-dasharray:none" />\n <g\n id="g5364"\n transform="translate(-1226.0934,-496.75423)">\n@@ -524,7 +524,7 @@\n sodipodi:role="line">and addSpecies</tspan></text>\n </g>\n <path\n- style="stroke:#000000;marker-end:url(#id2)"\n+ style="stroke:#000000;marker-end:url(#id2);stroke-width:0.93333333;stroke-miterlimit:4;stroke-dasharray:none"\n d="m 545.55976,90.499996 h 42"\n id="path5573"\n inkscape:connector-curvature="0"\n@@ -534,21 +534,21 @@\n inkscape:connector-curvature="0"\n id="path5575"\n d="m 545.55976,150.5 h 42"\n- style="stroke:#000000;marker-end:url(#id2)" />\n+ style="stroke:#000000;marker-end:url(#id2);stroke-width:0.93333333;stroke-miterlimit:4;stroke-dasharray:none" />\n <path\n sodipodi:nodetypes="cc"\n inkscape:connector-curvature="0"\n id="path5597"\n d="m 645.55976,90.499996 555.87494,-54.3773"\n- style="fill:none;fill-rule:evenodd;stroke:#000000;stroke-width:1px;stroke-linecap:butt;stroke-linejoin:miter;stroke-opacity:1;marker-end:url(#id2)" />\n+ style="fill:none;fill-rule:evenodd;stroke:#000000;stroke-width:0.93333333;stroke-linecap:butt;stroke-linejoin:miter;stroke-opacity:1;marker-end:url(#id2);stroke-miterlimit:4;stroke-dasharray:none" />\n <path\n- style="fill:none;fill-rule:evenodd;stroke:#000000;stroke-width:1px'..b'd="path1293"\n inkscape:connector-curvature="0"\n@@ -886,26 +850,78 @@\n inkscape:connector-curvature="0"\n sodipodi:nodetypes="cc" />\n <path\n- 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diff -r 1c9715cef808 -r 79212a309499 test-data/gentest.R
--- a/test-data/gentest.R Mon Mar 16 08:03:24 2020 -0400
+++ b/test-data/gentest.R Tue Jul 14 07:39:34 2020 -0400

[

b'@@ -1,192 +1,186 @@\n-library(dada2, quietly=T)\n-library(ggplot2, quietly=T)\n+library(dada2, quietly = T)\n+library(ggplot2, quietly = T)\n \n-sample.names <- c(\'F3D0_S188_L001\', \'F3D141_S207_L001\')\n-fwd <- c(\'F3D0_S188_L001_R1_001.fastq.gz\', \'F3D141_S207_L001_R1_001.fastq.gz\')\n-rev <- c(\'F3D0_S188_L001_R2_001.fastq.gz\', \'F3D141_S207_L001_R2_001.fastq.gz\')\n+sample_names <- c("F3D0_S188_L001", "F3D141_S207_L001")\n+fwd <- c("F3D0_S188_L001_R1_001.fastq.gz", "F3D141_S207_L001_R1_001.fastq.gz")\n+rev <- c("F3D0_S188_L001_R2_001.fastq.gz", "F3D141_S207_L001_R2_001.fastq.gz")\n \n-filt.fwd <- c(\'filterAndTrim_F3D0_R1.fq.gz\', \'filterAndTrim_F3D141_R1.fq.gz\')\n-filt.rev <- c(\'filterAndTrim_F3D0_R2.fq.gz\', \'filterAndTrim_F3D141_R2.fq.gz\')\n+filt_fwd <- c("filterAndTrim_F3D0_R1.fq.gz", "filterAndTrim_F3D141_R1.fq.gz")\n+filt_rev <- c("filterAndTrim_F3D0_R2.fq.gz", "filterAndTrim_F3D141_R2.fq.gz")\n \n print("filterAndTrim")\n \n-for(i in 1:length(fwd)){\n-\tftout <- filterAndTrim(fwd[i], filt.fwd[i], rev[i], filt.rev[i])\n- b <- paste(strsplit(fwd[i], ".", fixed=T)[[1]][1], "tab", sep=".")\n- write.table(ftout, b, quote=F, sep="\\t", col.names=NA)\n+for (i in seq_len(fwd)) {\n+ ftout <- dada2::filterAndTrim(fwd[i], filt_fwd[i], rev[i], filt_rev[i])\n+ b <- paste(strsplit(fwd[i], ".", fixed = T)[[1]][1], "tab", sep = ".")\n+ write.table(ftout, b, quote = F, sep = "\\t", col.names = NA)\n }\n \n # In the test only the 1st data set is used\n t <- data.frame()\n-t <- rbind(t, ftout[1,])\n+t <- rbind(t, ftout[1, ])\n colnames(t) <- colnames(ftout)\n rownames(t) <- rownames(ftout)[1]\n-write.table(t, "filterAndTrim.tab", quote=F, sep="\\t", col.names=NA)\n+write.table(t, "filterAndTrim.tab", quote = F, sep = "\\t", col.names = NA)\n \n-names(fwd) <- sample.names\n-names(rev) <- sample.names\n-names(filt.fwd) <- sample.names\n-names(filt.rev) <- sample.names\n+names(fwd) <- sample_names\n+names(rev) <- sample_names\n+names(filt_fwd) <- sample_names\n+names(filt_rev) <- sample_names\n \n # Plot quality profile (just for one file, Galaxy compares with sim_size)\n print("plots")\n-qp <- plotQualityProfile(fwd)\n-ggsave(\'qualityProfile_fwd.pdf\', qp, width = 20,height = 15,units = c("cm"))\n-qp <- plotQualityProfile(rev)\n-ggsave(\'qualityProfile_rev.pdf\', qp, width = 20,height = 15,units = c("cm"))\n-qp <- plotQualityProfile(fwd[1])\n-ggsave(\'qualityProfile.pdf\', qp, width = 20,height = 15,units = c("cm"))\n+qp <- dada2::plotQualityProfile(fwd)\n+ggsave("qualityProfile_fwd.pdf", qp, width = 20, height = 15, units = c("cm"))\n+qp <- dada2::plotQualityProfile(rev)\n+ggsave("qualityProfile_rev.pdf", qp, width = 20, height = 15, units = c("cm"))\n+qp <- dada2::plotQualityProfile(fwd[1])\n+ggsave("qualityProfile.pdf", qp, width = 20, height = 15, units = c("cm"))\n \n # Plot complexity (just for one file, Galaxy compares with sim_size)\n \n-cp <- plotComplexity(fwd)\n-ggsave(\'complexity_fwd.pdf\', cp, width = 20,height = 15,units = c("cm"))\n-cp <- plotComplexity(rev)\n-ggsave(\'complexity_rev.pdf\', cp, width = 20,height = 15,units = c("cm"))\n-cp <- plotComplexity(fwd[1])\n-ggsave(\'complexity.pdf\', cp, width = 20,height = 15,units = c("cm"))\n+cp <- dada2::plotComplexity(fwd)\n+ggsave("complexity_fwd.pdf", cp, width = 20, height = 15, units = c("cm"))\n+cp <- dada2::plotComplexity(rev)\n+ggsave("complexity_rev.pdf", cp, width = 20, height = 15, units = c("cm"))\n+cp <- dada2::plotComplexity(fwd[1])\n+ggsave("complexity.pdf", cp, width = 20, height = 15, units = c("cm"))\n \n \n # learn Errors\n print("learnErrors")\n-err.fwd <- learnErrors(filt.fwd) \n-saveRDS(err.fwd, file=\'learnErrors_R1.Rdata\')\n-plot <- plotErrors(err.fwd)\n-ggsave(\'learnErrors_R1.pdf\', plot, width = 20,height = 15,units = c("cm"))\n+err_fwd <- dada2::learnErrors(filt_fwd)\n+saveRDS(err_fwd, file = "learnErrors_R1.Rdata")\n+plot <- dada2::plotErrors(err_fwd)\n+ggsave("learnErrors_R1.pdf", plot, width = 20, height = 15, units = c("cm"))\n \n-err.rev <- learnErrors(filt.rev) \n-saveRDS(err.rev, file=\'learnErrors_R2.Rdata\')\n-plot <- plotErrors(err.rev)\n-ggsav'..b' "seqCounts_filter.tab", quote = F, sep = "\\t", row.names = F, col.names = T)\n \n-samples = list()\n-samples[["F3D0_S188_L001_R1_001.tab"]] <- read.table("F3D0_S188_L001_R1_001.tab", header=T, sep="\\t", row.names=1)\n-samples[["F3D141_S207_L001_R1_001.tab"]] <- read.table("F3D141_S207_L001_R1_001.tab", header=T, sep="\\t", row.names=1)\n+samples <- list()\n+samples[["F3D0_S188_L001_R1_001.tab"]] <- read.table("F3D0_S188_L001_R1_001.tab", header = T, sep = "\\t", row.names = 1)\n+samples[["F3D141_S207_L001_R1_001.tab"]] <- read.table("F3D141_S207_L001_R1_001.tab", header = T, sep = "\\t", row.names = 1)\n dname <- "filter"\n tdf <- samples[["F3D0_S188_L001_R1_001.tab"]]\n tdf <- rbind(tdf, samples[["F3D141_S207_L001_R1_001.tab"]])\n-names(tdf) <- paste( dname, names(tdf) )\n-tdf <- cbind( data.frame(samples=names( samples )), tdf)\n-write.table(tdf, "seqCounts_filter_both.tab", quote=F, sep="\\t", row.names = F, col.names = T)\n+names(tdf) <- paste(dname, names(tdf))\n+tdf <- cbind(data.frame(samples = names(samples)), tdf)\n+write.table(tdf, "seqCounts_filter_both.tab", quote = F, sep = "\\t", row.names = F, col.names = T)\n \n print("seqCounts dada")\n-samples = list()\n-samples[["dada_F3D0_S188_L001_R1.Rdata"]] <- readRDS(\'dada_F3D0_S188_L001_R1.Rdata\')\n-samples[["dada_F3D141_S207_L001_R1.Rdata"]] <- readRDS(\'dada_F3D141_S207_L001_R1.Rdata\')\n+samples <- list()\n+samples[["dada_F3D0_S188_L001_R1.Rdata"]] <- readRDS("dada_F3D0_S188_L001_R1.Rdata")\n+samples[["dada_F3D141_S207_L001_R1.Rdata"]] <- readRDS("dada_F3D141_S207_L001_R1.Rdata")\n dname <- "dadaF"\n-tdf <- data.frame( samples = names(samples) )\n-tdf[[ dname ]] <- sapply(samples, getN)\n-write.table(tdf, "seqCounts_dadaF.tab", quote=F, sep="\\t", row.names = F, col.names = T)\n+tdf <- data.frame(samples = names(samples))\n+tdf[[dname]] <- sapply(samples, get_n)\n+write.table(tdf, "seqCounts_dadaF.tab", quote = F, sep = "\\t", row.names = F, col.names = T)\n \n print("seqCounts mp")\n-samples = list()\n-samples[["mergePairs_F3D0_S188_L001.Rdata"]] <- readRDS(\'mergePairs_F3D0_S188_L001.Rdata\')\n-samples[["mergePairs_F3D141_S207_L001.Rdata"]] <- readRDS(\'mergePairs_F3D141_S207_L001.Rdata\')\n+samples <- list()\n+samples[["mergePairs_F3D0_S188_L001.Rdata"]] <- readRDS("mergePairs_F3D0_S188_L001.Rdata")\n+samples[["mergePairs_F3D141_S207_L001.Rdata"]] <- readRDS("mergePairs_F3D141_S207_L001.Rdata")\n dname <- "merge"\n-tdf <- data.frame( samples = names(samples) )\n-tdf[[ dname ]] <- sapply(samples, getN)\n-write.table(tdf, "seqCounts_merge.tab", quote=F, sep="\\t", row.names = F, col.names = T)\n+tdf <- data.frame(samples = names(samples))\n+tdf[[dname]] <- sapply(samples, get_n)\n+write.table(tdf, "seqCounts_merge.tab", quote = F, sep = "\\t", row.names = F, col.names = T)\n \n print("seqCounts st")\n-samples = list()\n-samples <- t(as.matrix( read.table("makeSequenceTable.tab", header=T, sep="\\t", row.names=1) ))\n+samples <- list()\n+samples <- t(as.matrix(read.table("makeSequenceTable.tab", header = T, sep = "\\t", row.names = 1)))\n dname <- "seqtab"\n-tdf <- data.frame( samples = row.names(samples) )\n-tdf[[ dname ]] <- rowSums(samples)\n-write.table(tdf, "seqCounts_seqtab.tab", quote=F, sep="\\t", row.names = F, col.names = T)\n+tdf <- data.frame(samples = row.names(samples))\n+tdf[[dname]] <- rowSums(samples)\n+write.table(tdf, "seqCounts_seqtab.tab", quote = F, sep = "\\t", row.names = F, col.names = T)\n \n print("seqCounts rb")\n-samples = list()\n-samples <- t(as.matrix( read.table("removeBimeraDenovo.tab", header=T, sep="\\t", row.names=1) ))\n+samples <- list()\n+samples <- t(as.matrix(read.table("removeBimeraDenovo.tab", header = T, sep = "\\t", row.names = 1)))\n dname <- "nochim"\n-tdf <- data.frame( samples = row.names(samples) )\n-tdf[[ dname ]] <- rowSums(samples)\n-write.table(tdf, "seqCounts_nochim.tab", quote=F, sep="\\t", row.names = F, col.names = T)\n-\n+tdf <- data.frame(samples = row.names(samples))\n+tdf[[dname]] <- rowSums(samples)\n+write.table(tdf, "seqCounts_nochim.tab", quote = F, sep = "\\t", row.names = F, col.names = T)\n'

diff -r 1c9715cef808 -r 79212a309499 test-data/learnErrors.pdf

Binary file test-data/learnErrors.pdf has changed

diff -r 1c9715cef808 -r 79212a309499 test-data/learnErrors_R1.pdf

Binary file test-data/learnErrors_R1.pdf has changed