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Preprocessing Sequence Coverage Data for More Precise Detection of Copy Number Variations
Copy number variation (CNV) is a type of genomic/genetic variation that plays an important role in phenotypic diversity, evolution, and disease susceptibility. Next generation sequencing (NGS) technologies have created an opportunity for more accurate detection of CNVs with higher resolution. Howeve...
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| Publicado no: | IEEE/ACM Trans Comput Biol Bioinform |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7278033/ https://ncbi.nlm.nih.gov/pubmed/30222580 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1109/TCBB.2018.2869738 |
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