Ena-DATASET-MUG-25-01-2021-19:08:23:000-259 - samples

ABSTRACT: 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-cells

PROVIDER: EGAD00001006901 | EGA |

REPOSITORIES: EGA