Healthy and cancer individuals from Long-read sequencing reveals aberrant fragmentation patterns and origins of circulating DNA in cancer
收藏NIAID Data Ecosystem2026-05-02 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP505089
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Level 1: BAM files before filtering steps were modified by replacing all single-nucleotide variants with the base in the reference genome hg38, and all insertion variants with Ns (see Methods). This allows all fragmentomic analysis to be performed without exposing any personally identifying genetic variants. These are listed as anonymized BAM files.
创建时间：
2025-04-30
