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author | lparsons |
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date | Thu, 16 Jul 2015 17:35:52 -0400 |
parents | a51942c74761 |
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<tool id="sam_stats" name="sam-stats" version="1.38.763"> <description> - Compute statistics from SAM or BAM files</description> <requirements> <requirement type="package" version="1.1.2-806">ea-utils</requirement> </requirements> <stdio> <exit_code range="1:" level="fatal" description="Unknown error occurred" /> </stdio> <command><![CDATA[ sam-stats $trackMultAlign $reportAllChr #if $rnaSeqStats: -R $rnaSeqStatsFile #end if #if $input.extension == "bam": -B #end if -S $histBinSize $input > $samStats ]]> </command> <inputs> <param format="sam, bam" name="input" type="data" label="SAM/BAM File" /> <param name="trackMultAlign" type="boolean" value="False" truevalue="-D" falsevalue="" label="Keep track of multiple alignments (slower!)" /> <param name="reportAllChr" type="boolean" value="False" truevalue="-A" falsevalue="" label="Report all chr sigs, even if there are more than 1000" /> <!-- <param name="numReadsSubsample" type="integer" value="1000000" min="1" max="1000000" label="Number of reads to sample for per-base statistics (max 1,000,000)" /> --> <param name="histBinSize" type="integer" value="30" min="1" label="Number of bins per chromosome for reads by chromosome "histogram"" /> <param name="rnaSeqStats" type="boolean" value="False" label="Output RNA-Seq statistics (coverage, 3 prime bias, etc.)" /> </inputs> <outputs> <data format="tabular" name="samStats" label="${tool.name} on ${on_string}"/> <data format="tabular" name="rnaSeqStatsFile" label="${tool.name} on ${on_string} (RNA-Seq Stats)"> <filter>rnaSeqStats</filter> </data> </outputs> <tests> <test> <param name="input" value="test.sam" /> <output name="samStats" file="testout.txt" /> </test> </tests> <help><![CDATA[ Overview -------- sam-stats computes varius statics on SAM/BAM alignment files. Complete Stats:: <STATS> : mean, max, stdev, median, Q1 (25 percentile), Q3 reads : # of entries in the sam file, might not be # reads phred : phred scale used bsize : # reads used for qual stats mapped reads : number of aligned reads (unique probe id sequences) mapped bases : total of the lengths of the aligned reads forward : number of forward-aligned reads reverse : number of reverse-aligned reads snp rate : mismatched bases / total bases ins rate : insert bases / total bases del rate : deleted bases / total bases pct mismatch : percent of reads that have mismatches len <STATS> : read length stats, ignored if fixed-length mapq <STATS> : stats for mapping qualities insert <STATS> : stats for insert sizes <CHR> : percentage of mapped bases per chr, followed by a signature Subsampled stats (1M reads max):: base qual <STATS> : stats for base qualities A,T,C,G : base percentages Meaning of the per-chromosome signature: A ascii-histogram of mapped reads by chromosome position. It is only output if the original SAM/BAM has a header. The values are the log2 of the # of mapped reads at each position + ascii '0'. See http://code.google.com/p/ea-utils/wiki/SamStatsDetails for more information on each stat, how it's calculated and what it means. This tool uses the sam-stats program that is part of the ea-utils suite. See http://code.google.com/p/ea-utils/wiki/SamStats for details. ]]> </help> <citations> <citation type="bibtex"> @article{aronesty_comparison_2013, title = {Comparison of {Sequencing} {Utility} {Programs}}, volume = {7}, issn = {18750362}, url = {http://benthamopen.com/ABSTRACT/TOBIOIJ-7-1}, doi = {10.2174/1875036201307010001}, language = {en}, number = {1}, urldate = {2015-07-10}, journal = {The Open Bioinformatics Journal}, author = {Aronesty, Erik}, month = jan, year = {2013}, pages = {1--8} } </citation> </citations> </tool>