Frequencies of different mutation types in somatic tissues and oocytes.
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p-Values were corrected for multiple testing (separately for mother versus pup comparisons for different mutations types, mother versus pup comparisons of Ti and Tv, and CpG versus nonCpG comparisons) using the method of Benjamini–Hochberg to control the false discovery rate. The “nt sequenced (type)” is the number of sequenced nucleotides that can effectively lead to the observed mutation type. Ti, transition; Tv, transversion. (XLSX)
创建时间：
2020-07-15
