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Ena-DATASET-MUG-04-05-2020-16:04:36:243-580 - samples

ABSTRACT: Paired end (47/98) and single end (51/98) shallow whole genome sequencing (sWGS) data for the identification of somatic copy number alterations (SCNA) and the estimation of tumor fractions in plasma DNA of colorectal cancer (CRC) patients.

PROVIDER: EGAD00001006101 | EGA |

REPOSITORIES: EGA

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