comprehensive, all-in-one detection of genome-wide cnvs, copy-neutral loh (cnloh), snps, and indels in one target enrichment capture.study both cnvs and mutations for your constitutional studies using......
oneseq cnv backbone + sureselect custom panels 产品详情
cnv backbone (comprised of 300 kb functional copy number resolution genome-wide, with higher resolution of 25−50 kb in disease associated clingen regions, and cnloh as small as 5 mb)add up to 12 mb of your gene targets via suredesignfor copy number determination, experimental dna samples are run side by side with a human reference dna sampleproviding you the flexibility you need, oneseq’s custom solution lets you add your targeted regions of interest to the cnv backbonefor larger designs, please contact your local agilent representative for more information