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scSNV: accurate dscRNA-seq SNV co-expression analysis using duplicate tag collapsing
Identifying single nucleotide variants has become common practice for droplet-based single-cell RNA-seq experiments; however, presently, a pipeline does not exist to maximize variant calling accuracy. Furthermore, molecular duplicates generated in these experiments have not been utilized to optimall...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Genome Biol |
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| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BioMed Central
2021
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8103760/ https://ncbi.nlm.nih.gov/pubmed/33962667 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-021-02364-5 |
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