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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...
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| Publicado en: | Front Genet |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Frontiers Media S.A.
2021
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| Assuntos: | |
| Acceso en liña: | 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 |
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