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There appears to be no "E_Multiple_observations" entries for GRCh38 1000genomes phase3 vcfs. I checked phase3 vcfs for release91 and release99 from ENSEMBL.
Is there an alternative method to generate the SNP positions for GRCh38 since I want to use ascatNGS for GRCh38 aligned bams.
The text was updated successfully, but these errors were encountered:
There appears to be no "E_Multiple_observations" entries for GRCh38 1000genomes phase3 vcfs. I checked phase3 vcfs for release91 and release99 from ENSEMBL.
Is there an alternative method to generate the SNP positions for GRCh38 since I want to use ascatNGS for GRCh38 aligned bams.
The text was updated successfully, but these errors were encountered: