Hi, I've gone through your articles describing the variant calling on cohort samples.
Could you please publish and article describing your experience, best practices, nuances and things to look out for in the results when calling variants from samples from multiple batches, where the sequencing kits/builds don't necessary match.
A simple example would be- I have sequenced a set of case samples on the latest hg38 based kit (ex. SureSelect Exon V7). And I want to call them with publicly available controls (e.g. an older hg19 based capture kit).
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