CD Genomics provides a number of options for those looking to perform copy number variation (CNV) analysis on several different microarray platforms depending on the organism, starting material and size of your project. http://www.cd-genomics.com/CNV-Analysis-Service.html
Expanding the Genetic Basis of Copy Number Variation in Familial Breast Cancer. READ MORE: https://www.worldnewsmd.com/Article/Oncology/Copy-Number-Variation-In-Familial-Breast-Cancer #BreastCAncer #RepairDNA #ClinicalTrials
The Broad Institute plans to develop and roll out GATK4, the next generation version of Genome Analysis Toolkit. The new service will include cancer, structural variation, copy number variation and related functionality.