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PennCNV in whole-genome sequencing data
BACKGROUND: The use of high-throughput sequencing data has improved the results of genomic analysis due to the resolution of mapping algorithms. Although several tools for copy-number variation calling in whole genome sequencing have been published, the noisy nature of sequencing data is still a lim...
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| Pubblicato in: | BMC Bioinformatics |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5629549/ https://ncbi.nlm.nih.gov/pubmed/28984186 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1802-x |
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