The data are derived from amplicons sequencing of genomic DNA samples after genome editing experiments. Sequencing reads were used to quantify genome editing efficiency and effect of variants.
| Accession | PRJNA759404 |
| Data Type | Raw sequence reads |
| Scope | Multispecies |
| Publications | Niu Y et al., "Multiparametric and accurate functional analysis of genetic sequence variants using CRISPR-Select.", Nat Genet, 2022 Dec;54(12):1983-1993 |
| Submission | Registration date: 1-Sep-2021
BRIC |
| Relevance | Medical |
Project Data:
| Resource Name | Number
of Links |
|---|
| Sequence data |
| SRA Experiments | 486 |
| Publications |
| PubMed | 1 |
| PMC | 1 |
| Other datasets |
| BioSample | 486 |