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An accessible GenePattern notebook for the copy number variation analysis of Illumina Infinium DNA methylation arrays
Illumina Infinium DNA methylation arrays are a cost-effective technology to measure DNA methylation at CpG sites genome-wide and across cohorts of normal and cancer samples. While copy number alterations are commonly inferred from array-CGH, SNP arrays, or whole-genome DNA sequencing, Illumina Infin...
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| Pubblicato in: | F1000Res |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
F1000 Research Limited
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6498745/ https://ncbi.nlm.nih.gov/pubmed/31105932 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.16338.1 |
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