From: Heng Li <lh...@sa...> - 2009-12-15 21:02:24
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Do you have some small example files that trigger the bug? Many thanks, Heng On Tue, Dec 15, 2009 at 08:58:28PM +0000, Gerton Lunter wrote: > Hi all, > > There seems to be a bug in samtools sort. In most examples I looked > at the bulk of the data seems fine, but the last dozen or so lines > are out of order. > > In another example I found one out-of-order read within an otherwise > sorted lot, again followed by a few dozen lines out of order. > > See below for the output of: samtools view SRR004781_PE.bam | awk > '{print $3}' | uniq -c. Note the two reads mapped to chromosome 1 > within the chromosome 7 reads. > The bam file was sorted using "samtools sort -m 750000000". > > Any ideas? > Cheers > > Gerton. > > > > > ------------------------------------------------------------------------------ > This SF.Net email is sponsored by the Verizon Developer Community > Take advantage of Verizon's best-in-class app development support > A streamlined, 14 day to market process makes app distribution fast and easy > Join now and get one step closer to millions of Verizon customers > http://p.sf.net/sfu/verizon-dev2dev > _______________________________________________ > Samtools-devel mailing list > Sam...@li... > https://lists.sourceforge.net/lists/listinfo/samtools-devel -- The Wellcome Trust Sanger Institute is operated by Genome Research Limited, a charity registered in England with number 1021457 and a company registered in England with number 2742969, whose registered office is 215 Euston Road, London, NW1 2BE. |