Integration of Copy Number and Methylation Data Identified from the Illumina® Infinium HumanMethylation450 BeadChip Array

<p>Integration of genomic data and epigenomic data as a means for understanding complex genomic regulatory mechanisms is gaining in popularity. In this webinar, we will show you how to use Partek® Genomics Suite® to identify copy number regions from the Illumina® Infinium HumanMethylation450 BeadChip array and merge the results with differentially methylated regions detected using the same arrays.</p>
Learn to
Import Illumina .idat files and normalize the data
Detect differentially methylated regions
Remove probes with SNP in the vicinity of the query site
Visualize the methylation signature
Create a list of genes regulated by differential methylation
Identify copy number regions
Find copy number regions shared across study samples
Integrate the copy number data with methylation data

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