![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Bowtie --sam option - includes non-aligned reads? | ledsall | Bioinformatics | 3 | 02-24-2013 01:31 AM |
From sam file, how to the mate aligned or not? | fabrice | Bioinformatics | 2 | 08-09-2011 11:37 AM |
Base Quality values in BAM file | donniemarco | Bioinformatics | 2 | 06-22-2011 11:06 AM |
Right way to convert splice-aligned Solexa reads (s_?_export.txt) to SAM format | jorgebm | Bioinformatics | 0 | 09-23-2010 07:58 AM |
Question on SAMtools variations calling of a BFAST-aligned SAM file? | Ling | Bioinformatics | 4 | 02-02-2010 07:26 PM |
![]() |
|
Thread Tools |
![]() |
#1 |
Junior Member
Location: Seattle WA Join Date: Nov 2009
Posts: 5
|
![]()
Hi,
I am mapping ABI solid reads using bwa, and then converting to a sam file and ultimately to a .pilup file using samtools. I am trying to understand the quality values in the sam file. For the unmapped reads the quality values agree with those in the fastq file, but for the mapped reads, I can see no relationship between the quality values in the .sam file and those in the .fastq file, or the mapping quality. I bring this up because I am trying to write my own snp filter, and don't know whether I can trust the reported quality values. I would appreciate any help on this. Arnold Kas |
![]() |
![]() |
![]() |
#2 | |
Nils Homer
Location: Boston, MA, USA Join Date: Nov 2008
Posts: 1,285
|
![]() Quote:
Briefly, let X and Y be indicators whether or not the first and second colors encoding a base are aligned as errors. Let A and B the color qualities (log probabilities) of the two colors respectively. Then the returned base quality is: Code:
if(1==X && 1==Y) { return (A + B + 10); } else if(1==X && 0==Y) { return (A - B); } else if(0==X && 1==Y) { return (B - A); } else { return 0; } |
|
![]() |
![]() |
![]() |
#3 |
Junior Member
Location: Seattle WA Join Date: Nov 2009
Posts: 5
|
![]()
Perfect. Thanks.
|
![]() |
![]() |
![]() |
Thread Tools | |
|
|