Study
Application of Hi-C sequencing to detect structural variants in B-cell acute lymphoblastic leukemia
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001005605 | Other |
Study Description
Large structural variants are easily detected by Hi-C sequencing as strong, distant signals on a Hi-C contact map. Translocations are frequently evident in B-ALL and accurate identification of these translocations can guide clinical treatment options. Here were apply shallow Hi-C sequencing as an unbiased, cost-effective approach to identify translocations among B-ALL patients.
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 |
|---|---|---|---|
| EGAD00001008125 |
Hi-C sequencing data includes 5 samples collected from 4 B-ALL patients.
|
NextSeq 500 | 5 |
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