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Thread | Thread Starter | Forum | Replies | Last Post |
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tophat - cannot view sam output in samtools tview | lmilne | Bioinformatics | 2 | 12-01-2009 01:13 PM |
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#1 |
Member
Location: germany Join Date: Dec 2009
Posts: 15
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Hi,
When I try to use "samtools view" to creat .bam file from .sam, I get these error msg. The .sam file is created by mapping raw illumina reads with tophat. samtools view -bS -t index.fa.fai -o accepted_hits.bam accepted_hits.sam The tag [ID] required for [PG] not present. [sam_header_read2] 7409 sequences loaded. Parse error at line 8263: CIGAR and sequence length are inconsistent This #line 8263 is like this: head -n 8263 accepted_hits.sam |tail -n 1 HWI-EAS210R:5:55:1018:1930#0 0 SL1.00sc00002 428427 0 36M92N36M473N536870911M * 0 0 CTCATCTCTCATCTCAGAGAGGTCCTCCAGGAGCAGGAATATAAGTTGGATCAAGTACGCAATCATCTTCA XXQZXR^Ta\[a\ZVZ^ZYXWWYPSUMSSQXZTO^ZZPV_\`_U\VYY[W^G\SJSTTRTUTXFTTQTYVS NM:i:0 XS:A:+ NS:i:0 Anybody could explain me why Samtools gave such error msg? ![]() Thanks! ![]() |
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#2 |
Member
Location: germany Join Date: Dec 2009
Posts: 15
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I think the problem is caused by:
36M92N36M473N536870911M But, I don't know how could it occur? |
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#3 |
Member
Location: germany Join Date: Dec 2009
Posts: 15
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I think the solution could be:
reformat the raw .fastq file. Maybe, somewhere is not Tab, but space. then, 536870911M will not occur. |
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