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Thank you for your pipeline first. I am confused about the output. For example, if "normal_sample" and "tumor_sample" are used as input. The merged vcf file will have four heads named tumor _sample, normal_sample, TUMOR, and NORMAL. Which one should I refer to if I want to know the mutations in the "tumor_sample". And what's the meaning of "TUMOR" and "NORMAL"? They have more mutations and don't seem to be duplicates of other columns.
The text was updated successfully, but these errors were encountered:
Thank you for your pipeline first. I am confused about the output. For example, if "normal_sample" and "tumor_sample" are used as input. The merged vcf file will have four heads named tumor _sample, normal_sample, TUMOR, and NORMAL. Which one should I refer to if I want to know the mutations in the "tumor_sample". And what's the meaning of "TUMOR" and "NORMAL"? They have more mutations and don't seem to be duplicates of other columns.
The text was updated successfully, but these errors were encountered: