Monopogen
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SNP calling for the X chromosome
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Hi,
Thank you for developing this great tool! I have a question regarding calling X chromosomal SNPs in female samples. Given that X chromosome inactivation occurs randomly, single-cell data should contain reads from both X chromosomes across the cell population.
Is it possible to call germline variants for the X chromosome in this context?
I appreciate your help and look forward to your insights.
Best regards, Tim