Study
Single cell sequencing: Capturing the origin and dynamics of chromosomal copy-number heterogeneity
| Study ID | Alternative Stable ID | Type |
|---|---|---|
| EGAS00001003812 | Other |
Study Description
Shallow whole-genome sequencing of single cells from individual clonal (patient-derived colorectal cancer) organoids was performed to investigate the degree of copy-number heterogeneity that emerges and propagates during clonal organoid outgrowth of a single cancerous cell. Selected single cells were sequenced with higher coverage. In addition, daughter cells were isolated to directly link mitotic chromatin errors to chromosomal copy number changes.
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 |
|---|---|---|---|
| EGAD00001005422 |
Dataset contains 854 single cell sequenced colorectal cancer organoids.
|
854 |
Who archives the data?
