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"Many types of working are under caused by either inherited or DE novo genomic abnormalities to as single - nucleotide variants (SNVs), copy number variations (CNVs), and/or chromosomal translocations."
- En Publication Part Number: 5994-3099
- Created: 23 Feb 2021
- 161 KB
This application note focuses on using open source software, BSmooth, to detect DMRs in SureSelect Methyl - Seq data and independently validate these high value DMRs
- En Publication Part Number: 5991-5298
- Created: 4 May 2016
- 737 KB
The 188bet博金宝官方网站Agilent HaloPlex target enrichment system was 2 to prepare DNA libraries derived from FFPE tissues for NGS sequencing.
- Created: Aug 28, 2015
- 627 KB
This technical summary introduced in the 4200 TapeStation system with high sensitivity RNA ScreenTape DV200 simplifying analysis of the evaluation.
- ZHCN Publication Part Number: 5991-8355
- Created: 09 May 2018
- 679 KB
This techn188bet博金宝官方网站ical overview on the Agilent 2100 bioanalyzer system are introduced using Nano and DV200 DV200 RNA RNA Pico DV200 simplifying analysis of the evaluation.
- ZHCN Publication Part Number: 5991-8287
- Created: 09 May 2018
- 282 KB
188bet博金宝官方网站Agilent SureSelect XT HumanMethyl - Seq を with い た 1 salt base の resolution で の DNA メ チ ル quantitative analysis
- Jajp Publication Part Number: 5991-0166
- Created: 6 Apr 2013
- 3 MB