Analysis of strand-biased mutation accumulation.
收藏Figshare2020-07-15 更新2026-04-28 收录
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p-Values for differences in mutation frequencies of the two complementary mutation types (strand bias) were calculated with FET and corrected for multiple testing 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. FET, Fisher’s exact test. (XLSX)
创建时间：
2020-07-15
