Chargement en cours...
HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data
Copy number variation (CNV) is a genomic mutation that plays an important role in tumor evolution and tumor genesis. Accurate detection of CNVs from next-generation sequencing (NGS) data is still a challenging task due to artifacts such as uneven mapped reads and unbalanced amplitudes of gains and l...
Enregistré dans:
| Publié dans: | Front Genet |
|---|---|
| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Frontiers Media S.A.
2021
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8215577/ https://ncbi.nlm.nih.gov/pubmed/34163521 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.642473 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|