Difference between revisions of "Qualimap"

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* optparse (available from CRAN)
 
* optparse (available from CRAN)
 
* NOISeq, Repitools, Rsamtools, GenomicFeatures, rtracklayer (available from Bioconductor)
 
* NOISeq, Repitools, Rsamtools, GenomicFeatures, rtracklayer (available from Bioconductor)
 +
 +
= Usage =
 +
 +
On its own, the GUI will be launched.
 +
 +
However if you launch
 +
 +
qualimap bamqc -bam <bamfile> -outfile <youpdfname.pdf>
 +
 +
it seems to know it should behave in command-line fashion
 +
 +
Typical output (truncated)
 +
Processed 400 out of 403 windows...
 +
Total processed windows:403
 +
Number of reads: 790595
 +
Number of valid reads: 72116
 +
Number of correct strand reads:0
 +
 +
Inside of regions...
 +
Num mapped reads: 72116
 +
Num mapped first of pair: 36084
 +
Num mapped second of pair: 36032
 +
Num singletons: 1216
 +
Time taken to analyze reads: 159
 +
Computing descriptors...
 +
numberOfMappedBases: 14882078
 +
referenceSize: 3359974
 +
numberOfSequencedBases: 14876535
 +
numberOfAs: 4618823
 +
Computing per chromosome statistics...
 +
Computing histograms...
 +
Overall analysis time: 160
 +
end of bam qc
 +
Computing report...
 +
Writing PDF report...
 +
PDF file created successfully
 +
 +
However, it may not output a PDF file. That was one experience anyway.
  
 
= Links=  
 
= Links=  
  
 
* [http://qualimap.bioinfo.cipf.es/doc_html/intro.html#citing-qualimap homepage]
 
* [http://qualimap.bioinfo.cipf.es/doc_html/intro.html#citing-qualimap homepage]

Revision as of 00:01, 28 April 2017

Introduction

Inspecting bam files for quality. Comes from same home as Blast2Go, the famous functional annotation system, in CIPF, Valencia, Spain.

Installation

Has a number of dependencies:

  • optparse (available from CRAN)
  • NOISeq, Repitools, Rsamtools, GenomicFeatures, rtracklayer (available from Bioconductor)

Usage

On its own, the GUI will be launched.

However if you launch

qualimap bamqc -bam <bamfile> -outfile <youpdfname.pdf>

it seems to know it should behave in command-line fashion

Typical output (truncated)
Processed 400 out of 403 windows...
Total processed windows:403
Number of reads: 790595
Number of valid reads: 72116
Number of correct strand reads:0

Inside of regions...
Num mapped reads: 72116
Num mapped first of pair: 36084
Num mapped second of pair: 36032
Num singletons: 1216
Time taken to analyze reads: 159
Computing descriptors...
numberOfMappedBases: 14882078
referenceSize: 3359974
numberOfSequencedBases: 14876535
numberOfAs: 4618823
Computing per chromosome statistics...
Computing histograms...
Overall analysis time: 160
end of bam qc
Computing report...
Writing PDF report...
PDF file created successfully

However, it may not output a PDF file. That was one experience anyway.

Links