A carregar...
Monovar: single nucleotide variant detection in single cells
Current variant callers are not suitable for single-cell DNA sequencing (SCS) as they do not account for allelic dropout, false-positive errors, and coverage non-uniformity. We developed Monovar, a novel statistical method for detecting and genotyping single nucleotide variants in SCS data. Evaluati...
Na minha lista:
| Publicado no: | Nat Methods |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4887298/ https://ncbi.nlm.nih.gov/pubmed/27088313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nmeth.3835 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|