Hopkins Team Develops Method to Improve Rare Mutation Detection for Early Cancer Dx
June 01, 2011
Hopkins Team Develops Method to Improve Rare Mutation Detection for Early Cancer Dx
The next step in developing Safe-SeqS is to validate the method in a large number of samples from patients with a variety of cancer types as well as normal controls.
Full-text access for premium subscribers only.
Existing premium subscribers login here.
New to GenomeWeb? Register here quickly.
New to GenomeWeb? Register here quickly.
Related Stories
- NHGRI's ClinSeq Study Finds Clinically Relevant Results, but Challenges Remain
May 24, 2011 / Clinical Sequencing News - Cancer Sequencing Papers of Note
March 16, 2011 / Clinical Sequencing News - Hopkins-Led Team Sees Clinical Promise for WGS Method to Detect Chromosomal Alterations in Plasma
December 5, 2012 / Clinical Sequencing News - Cancer-related Chromosomal Changes Detected by Blood-based DNA Sequencing
November 28, 2012 / GenomeWeb Daily News - UW Team Says 'Duplex Sequencing' Method Offers Millions-Fold Improvement in Error Rate
August 21, 2012 / In Sequence