Whole genome sequencing for $330 including interpretation
Originally shared by Ward Plunet
Whole genome sequencing for $330 including interpretation
If you can live with 2 time coverage, higher price for higher level of coverage.
They provide the following:
BAM file (roughly 50 GB)
variant summary reports from SnpEff and VEP
autosomal and chrX variant identification (as two VCF files):
novel variants (annotated with SnpEff and VEP)
results for a set of over 100 million known SNPs from dbSNP build 142
mtDNA sequence (as FASTA file)
Y-DNA analysis (for males)
Whole genome sequencing for $330 including interpretation
If you can live with 2 time coverage, higher price for higher level of coverage.
They provide the following:
BAM file (roughly 50 GB)
variant summary reports from SnpEff and VEP
autosomal and chrX variant identification (as two VCF files):
novel variants (annotated with SnpEff and VEP)
results for a set of over 100 million known SNPs from dbSNP build 142
mtDNA sequence (as FASTA file)
Y-DNA analysis (for males)
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