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Penalized weighted low-rank approximation for robust recovery of recurrent copy number variations
BACKGROUND: Copy number variation (CNV) analysis has become one of the most important research areas for understanding complex disease. With increasing resolution of array-based comparative genomic hybridization (aCGH) arrays, more and more raw copy number data are collected for multiple arrays. It...
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Gepubliceerd in: | BMC Bioinformatics |
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Hoofdauteur: | |
Formaat: | Artigo |
Taal: | Inglês |
Gepubliceerd in: |
BioMed Central
2015
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Onderwerpen: | |
Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4676147/ https://ncbi.nlm.nih.gov/pubmed/26652207 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0835-2 |
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