Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

Phred-scaled quality scores Follow

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    Mahmoud Al-Bassam

    Thank you for the explanation. Super grateful! 

     

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    Roller, Eric

    If there is 50/50 chance that the variant is present, what should the QUAL be?

    I would expect -10log10(0.5) = ~3
    But if you are normalizing similar to how your PL values are normalized then this may end up being
    -10log10(0.5/0.5) = 0

    Which one does GATK report and can you confirm if this is compliant with the VCF spec:
    QUAL — quality: Phred-scaled quality score for the assertion made in ALT. i.e. −10log10 prob(call in ALT is wrong). If ALT is ‘.’ (no variant) then this is −10log10 prob(variant), and if ALT is not ‘.’ this is −10log10 prob(no variant). If unknown, the MISSING value must be specified. (Float)

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