Thanks Jeremy
Hi,
Does anyone know what coverage the GIAB truth set is for NA12878?
I was wanting to download the vcf from here GIAB truthset vcf but it would be good to know what the mean coverage is.
I have read this paper Best practices for benchmarking germline small-variant calls in human genomes and this paper Extensive sequencing of seven human genomes to characterize benchmark reference materials but I can't seem to find the info anywhere.
1 answer
The truthset is an amalgam or consensus of at least 3 different sequencing technologies (Complete Genomics, 10X, Illumina). I'm not sure coverage is easily interpretable.
In spot checking at the HG002_GIAB_highconf_CG-IllFB-IllGATKHC-Ion-Solid-10X_CHROM1-22_v3.3_highconf.vcf.gz VCF itself, the depth is usually over 300X.
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