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CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing
High-throughput DNA sequencing enables detection of copy number variations (CNVs) on the genome-wide scale with finer resolution compared to array-based methods but suffers from biases and artifacts that lead to false discoveries and low sensitivity. We describe CODEX2, as a statistical framework fo...
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| Publicado no: | Genome Biol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6260772/ https://ncbi.nlm.nih.gov/pubmed/30477554 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-018-1578-y |
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