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

AnalyzeCovariates were stopped.

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    Gökalp Çelik

    Hi E Ra

    We don't see any error messages in those logs. Can you elaborate more on the error message the you are receiving?

    Regards. 

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    E Ra

    Hello,

    Sorry for the confusion. I just noticed that I could generate a BSQRplot01.pdf file for each sample. It is actually GATK BaseRecalibration report that contains graphs. My questions would rather be where I could find info that allows me to interpret those graphs.

    Thank you!

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    Gökalp Çelik

    Hi again.

    We have a very brief slide for that. Basically the aim is to get recalibrated scores to align perfectly with the dotted line. If that's the case your recalibration went perfectly. If not there is still room to improve by adding more variant sites. But sometimes due to the amount of reads and covered regions you have recalibration may not work properly. In that case there is really not much to do as the whole recalibration needs as much data as possible to work.

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    E Ra

    Hi Gökalp

    That helps. Thank you very much for the answer.

     

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