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

WARN InbreedingCoeff - InbreedingCoeff will not be calculated at position chr1:40 and possibly subsequent; at least 10 samples must have called genotypes

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    Dina Tzur

    In addition, I ran HaplotypeCaller once more on the same file and received a different output file from previous times. A much larger file ..

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    Genevieve Brandt (she/her)

    Hi Dina Tzur,

    The warning you have identified here is not a problem for HaplotypeCaller. The only thing it indicates is that you have fewer than 10 samples in this bam. There might be another error message at the bottom of the program log indicating if there are any issues. 

    Best,

    Genevieve

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    Dina Tzur

    Hi Genevieve Brandt,

    Thanks!

    Dinna

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