![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Normal size of .sam output file from Tophat | GiladZil | RNA Sequencing | 0 | 07-04-2011 09:02 AM |
wig file generated by MACS doesn`t fit input sam | tujchl | Bioinformatics | 2 | 06-16-2011 01:23 AM |
MRNM problem for the .sam output file of tophat | Gangcai | Bioinformatics | 4 | 08-13-2010 10:19 AM |
Cufflinks sample file(test_data.sam) output | snp_analyser | Bioinformatics | 0 | 06-07-2010 07:38 AM |
bwasw: get SAM output containing all hits per query? | bbimber | Bioinformatics | 1 | 04-22-2010 06:10 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: Wageningen, Netherlands Join Date: Sep 2012
Posts: 19
|
![]()
When running BWA I get normal total number of reads (the same as in the input file).
But when running BWASW alignment I get this: (that's from samtools flagstat) 56125 + 0 in total (QC-passed reads + QC-failed reads) 0 + 0 duplicates 30118 + 0 mapped (53.66%:-nan%) 0 + 0 paired in sequencing 0 + 0 read1 0 + 0 read2 0 + 0 properly paired (-nan%:-nan%) 0 + 0 with itself and mate mapped 0 + 0 singletons (-nan%:-nan%) 0 + 0 with mate mapped to a different chr 0 + 0 with mate mapped to a different chr (mapQ>=5) My input number of reads loaded to BWA was 45997. How come I got over 80k? |
![]() |
![]() |
![]() |
#2 |
Member
Location: Gothenburg/Uppsala, Sweden Join Date: Oct 2010
Posts: 82
|
![]()
BWA-SW performs local alignment and can output several alignments per input read/sequence. So a given read or different parts of a read can be aligned to different places, which are all included in the output file.
|
![]() |
![]() |
![]() |
#3 |
Member
Location: Wageningen, Netherlands Join Date: Sep 2012
Posts: 19
|
![]()
I also heard that with extremely long reads bwa-sw can give not very reliable output. Is there any sense in browsing reads up to a given length, or it will change nothing, at will only consume my time.
|
![]() |
![]() |
![]() |
Thread Tools | |
|
|