Study
Defective homologous recombination in HCC
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001006599 | Other |
Study Description
Backgrounds and Aims: We performed an in-depth examination of pathogenic germline (PGVs) and somatic variants in DNA damage response (DDR) genes in hepatocellular carcinoma (HCC) to explore their clinical and genomic impacts.
Approach and Results: We used a merged whole exome or RNA sequencing dataset derived from in-house (n=230) and TCGA (n=362) databases of multiethnic HCC samples.
Study Datasets 1 dataset.
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples |
|---|---|---|---|
| EGAD00001009410 |
Germline variants calls were defined using the sequenced reads derived from 230 patients with hepatocellular carcinoma.
This dataset is comprised of one aggregated vcf file.
|
230 |
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