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In the paper or script description for XPCLR, only the variant type of SNPs was introduced, thus I'm not sure if the method is equally applicable to other types of variants like indels, SVs, etc.
The text was updated successfully, but these errors were encountered:
In the paper or script description for XPCLR, only the variant type of SNPs was introduced, thus I'm not sure if the method is equally applicable to other types of variants like indels, SVs, etc.
The text was updated successfully, but these errors were encountered: