ena-DATASET-MUG-25-01-2021-19:08:23:000-259 - samples
收藏NIAID Data Ecosystem2026-03-12 收录
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资源简介：
Paired end shallow whole genome sequencing (sWGS) data for the identification of somatic copy number alterations (SCNA) and the estimation of tumor fraction and ploidy sorted malignant CD3+/Vb+ T-cells and corresponding CD19+ non-malignant B-cellsEGA dataset EGAD00001006901
创建时间：
2021-02-01
