Carregant...
An evaluation of copy number variation detection tools for cancer using whole exome sequencing data
BACKGROUND: Recently copy number variation (CNV) has gained considerable interest as a type of genomic/genetic variation that plays an important role in disease susceptibility. Advances in sequencing technology have created an opportunity for detecting CNVs more accurately. Recently whole exome sequ...
Guardat en:
| Publicat a: | BMC Bioinformatics |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2017
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5452530/ https://ncbi.nlm.nih.gov/pubmed/28569140 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1705-x |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|