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A comparison of genomic copy number calls by Partek Genomics Suite, Genotyping Console and Birdsuite algorithms to quantitative PCR
BACKGROUND: Copy number variants are >1 kb genomic amplifications or deletions that can be identified using array platforms. However, arrays produce substantial background noise that contributes to high false discovery rates of variants. We hypothesized that quantitative PCR could finitely determ...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2011
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3084167/ https://ncbi.nlm.nih.gov/pubmed/21489293 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-0381-4-8 |
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