| 项目编号 |
PRJCA022267 |
| 项目标题 |
Shallow whole-genome sequencing for identifying copy number abnormalities in multiple myelom complements conventional cytogenetic analyses |
| 涉及领域 |
Medical |
| 数据类型 |
Whole genome sequencing
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| 物种名称 |
Homo sapiens
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| 描述信息 |
Background: Multiple myeloma (MM) is a malignant neoplasm of plasma cells leading to bone destruction and marrow failure. Prognosis and management of MM rely on cytogenetic determination of copy number abnormalities (CNAs). Nevertheless, chromosome abnormality analysis is difficult due to the presence of few plasma cells and their low proliferative activity. |
| 样品范围 |
Multiisolate |
| 发布日期 |
2023-12-23 |
| 项目资金来源 |
| 机构 |
项目类型 |
授权项目ID |
授权项目名称 |
| No funding support
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| 提交者 |
Mao
Mao (maomao@seekin.onaliyun.com)
|
| 提交单位 |
Shenzhen SeekIn Inc |
| 提交日期 |
2023-12-21 |
