Different Qualities In Bam And Pileup Files
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11.6 years ago
Mus Musculus ▴ 20

I have such a problem. I run samtools this way: mpileup -f <ref.fasta -l contigs.list input.bam > output.pileup Input reads have good base quality, but in pileup file at SNP positions I have poor base quality. I mean, for example

AAAATTTTG - reference

AAACTTTT     qqqqqqqq

AACTTTTG     qqqqqqqq

In pileup file base quality at snp posiiton: !! base quality at ordinary place: qq It occurs not always, not at all snp postions but very often. Thanks.

samtools snp • 4.0k views
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Did you convert your base qualities at any point? Did you specify illumina quality?

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Reads are actually SOLiD data. And we didn't convert anything.

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11.6 years ago
Andreas ★ 2.5k

As Istvan correctly pointed out, your data looks odd.

But anyway, if you see differences between the quality scores in a pileup (samtools mpileup) and the actual sequences (samtools view), then this is very likely due to samtools automatic BAQ computation, which can downgrade quality scores if a misalignment is likely. BAQ is switched on by default, but you can disable it with mpileup's -B option (not recommended though). See Li, 2001.

Andreas

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I experienced something similar a while ago and BAQ was the cause. So even if the qualities require conversion, don't be surprise if there are still differences.

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Thank you, Andreas. The problem was in BAQ computation. It underestimates qualities. With regards our data, they were fine. Text below is just a part of sam file: some insignificant for my question fields were dropped.

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11.6 years ago
Mus Musculus ▴ 20

View from bam file:

278_1780_882_F36004GAAAGGACGGAGTGAACGAACTGATGGTTAACAAAGGCqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
1277_1512_1769_F36013GAGTGAACGAACTGATGGTTAACAAAGGCCTCATCAAGGAqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
405_1727_636_F36014AGTGAACGAACTGATGGTTAACAAAGGCCTCATCAAGGAATACCGTGAqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
235_427_1021_F36017GAACGAACTGATGGTTAACAAAGGCCTCATCAAGGAATACCGTGAqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
561_1318_1376_F36023ACTGATGGTTAACAAAGGCCTCATCAAGGAATACCGTGACTTTACCGAqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
1806_1724_117_F36024CTGATGGTTAACAAAGGCCTCATCAAGGAATACCGTGACTTTACCGqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
282_1435_1468_F36025TGATGGTTAACAAAGGCCTCATCAAGGAATACCGTGACTTTACCqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
1271_1653_1368_F36026GATGGTTAACAAAGGCCTCATCAAGGAATACCGTGACTTTACCGAGCGqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
2340_30_76_F36026GATGGTTAACAAAGGCCTCATCAAGGAATACCGTGACTTTACCGAGCqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
1008_1283_1513_F36052AATACCGTGACTTTACCGAGCGTTGCTTCCAGGACATTACTCCCGAGGqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
1967_902_850_F36054TACCGTGACTTTACCGAGCGTTGCTTCCAGGACATTACTCCCGAGqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
248_393_300_F36059TGCATTTACCGAGCGTTGCTTCCAGGACATTACTCqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq
1546_1682_68_F36059TGACTTTACCGAGCGTTGCTTCCAGGACATTACTCCCGAGGAGCAGCAq!!qqqq!!qqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqqq

Position in pileup file:

gi|260081398|gb|ACBX02000015.1|6034C12 .AAaaAAaaAAA      !!!!!!!!!!!!
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please edit and add this to the main post then delete it. Right now you have listed it as an answer and people think your problem has been solved.

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11.6 years ago

The q is not a valid quality in the Sanger encoding. At the same time what you are listing is not a valid BAM file

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q is ascii 123. Illumina and I think Solid range quality from 64 ... 126. So it looks like you need to convert your quality scores to PHRED scale. If I remember correctly both BWA and Bowtie can be told to convert quality ranges of the FASTQ. Then again I have never worked with solid data.

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Current (two year old) Illumina and Solid systems use Sanger (+33) encodings. Older Illumina were indeed on the +64 scale (not sure about Solid) but even on that scale the reported quality measures typically end at 41 (it does not use the entire scale). The q would account for a quality of 49 so that makes it a bit suspicious value even on the older scale. Then tools may exhibit strange behaviors once they get codes that are outside of the expected range - there is little error checking - perhaps rightfully so as typically it would mean billions of wasted checks.

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