Additional file 1 of Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms
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Additional file 1. Table S1: Whole-genome sequencing data of NA12878 based on four sequencing platforms. Table S2: Number and length statistics of all 50 CNV sets. Table S3: Regional distribution of all 50 CNV sets across the genome. Table S4: List of the complete CNV benchmark of NA12878. Table S5: CNV detection tools using whole-genome sequencing data.
创建时间：
2020-11-11
