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SubPatCNV: approximate subspace pattern mining for mapping copy-number variations
BACKGROUND: Many DNA copy-number variations (CNVs) are known to lead to phenotypic variations and pathogenesis. While CNVs are often only common in a small number of samples in the studied population or patient cohort, previous work has not focused on customized identification of CNV regions that on...
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| Yayımlandı: | BMC Bioinformatics |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4305219/ https://ncbi.nlm.nih.gov/pubmed/25591662 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-014-0426-7 |
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