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Reducing system noise in copy number data using principal components of self-self hybridizations
Genomic copy number variation underlies genetic disorders such as autism, schizophrenia, and congenital heart disease. Copy number variations are commonly detected by array based comparative genomic hybridization of sample to reference DNAs, but probe and operational variables combine to create corr...
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| Autori principali: | , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
National Academy of Sciences
2012
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3271883/ https://ncbi.nlm.nih.gov/pubmed/22207624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1106233109 |
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