Purpose: We evaluated the value of copy number variation sequencing (CNV-seq) for analyzing chromosomal abnormalities (CA) in spontaneous abortion specimens.
| Accession | PRJNA961959 |
| Data Type | Raw sequence reads |
| Scope | Multispecies |
| Submission | Registration date: 26-Apr-2023
- Fujian Provincial Maternity and Child Health Hospital
- Dai Yifang
|
Project Data:
| Resource Name | Number
of Links |
|---|
| Sequence data |
| SRA Experiments | 650 |
| Other datasets |
| BioSample | 650 |