ctDNA whole exome genome sequencing dataset
Dataset contains all available exome sequencing paired-end fastq files from our study "A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomes"
- 310 samples
- DAC: EGAC00001003111
- Technology: Illumina NovaSeq 6000
- HMB DUO:0000006 (version: 2021-02-23)health or medical or biomedical researchThis data use permission indicates that use is allowed for health/medical/biomedical purposes; does not include the study of population origins or ancestry.
- NCU DUO:0000046 (version: 2021-02-23)non-commercial use onlyThis data use modifier indicates that use of the data is limited to not-for-profit use.
Dataset contains all available exome sequencing paired-end fastq files from our study, "A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomes".
Please fill out the following data access agreement form: https://docs.google.com/forms/d/e/1FAIpQLScy4KzxU8JA_3gU3hmHgZYE7mVgvBKYmpZkwBB0vASA9zqAQQ/viewform?usp=sf_link
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| Cancer Genomics |