Hi All,
What is the best way to check if a variant at a specific location is well covered in the 1000 genomes. The way that I am pulling this information is by slicing the bam files and viewing the reads in IGV. Is this information summarized for all the samples in the 1000 genomes project?
thanks
What is the best way to check if a variant at a specific location is well covered in the 1000 genomes. The way that I am pulling this information is by slicing the bam files and viewing the reads in IGV. Is this information summarized for all the samples in the 1000 genomes project?
thanks
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