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cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data
Recent advances in sequencing technologies provide the means for identifying copy number variation (CNV) at an unprecedented resolution. A single next-generation sequencing experiment offers several features that can be used to detect CNV, yet current methods do not incorporate all available signatu...
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| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4056371/ https://ncbi.nlm.nih.gov/pubmed/23259578 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2012-13-12-r120 |
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