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SNV identification from single-cell RNA sequencing data
Integrating single-cell RNA sequencing (scRNA-seq) data with genotypes obtained from DNA sequencing studies facilitates the detection of functional genetic variants underlying cell type-specific gene expression variation. Unfortunately, most existing scRNA-seq studies do not come with DNA sequencing...
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| Publicat a: | Hum Mol Genet |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7279618/ https://ncbi.nlm.nih.gov/pubmed/31504520 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddz207 |
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