Cargando...
Gencore: an efficient tool to generate consensus reads for error suppressing and duplicate removing of NGS data
BACKGROUND: Removing duplicates might be considered as a well-resolved problem in next-generation sequencing (NGS) data processing domain. However, as NGS technology gains more recognition in clinical application, researchers start to pay more attention to its sequencing errors, and prefer to remove...
Gardado en:
| Publicado en: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2019
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6933617/ https://ncbi.nlm.nih.gov/pubmed/31881822 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-019-3280-9 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|