OneSeq CNV Backbone + SureSelect Custom Panels

OneSeq CNV Backbone + SureSelect Custom Panels

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2021-01-05 14:01:37
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安捷伦科技公司中国总部

安捷伦科技公司中国总部

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产品简介

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......

详细介绍

  • 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 SureDesign
  • For copy number determination, experimental DNA samples are run side by side with a human reference DNA sample
  • Providing you the flexibility you need, OneSeq’s custom solution lets you add your targeted regions of interest to the CNV backbone
  • For larger designs, please contact your local Agilent representative for more information
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