A carregar...
Detection of somatic structural variants from short-read next-generation sequencing data
Somatic structural variants (SVs), which are variants that typically impact >50 nucleotides, play a significant role in cancer development and evolution but are notoriously more difficult to detect than small variants from short-read next-generation sequencing (NGS) data. This is due to a combina...
Na minha lista:
| Publicado no: | Brief Bioinform |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8138798/ https://ncbi.nlm.nih.gov/pubmed/32379294 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbaa056 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|