Current Issue

Sponsored
Keywords

Sequencing - Related Content

Moving Genomics Closer to the Clinic
May 16, 2013
Foundation Medicine and Memorial Sloan-Kettering Cancer Center are working to translate genomic information into personalized cancer treatment.
Your Genes, Your Choice?
May 9, 2013
Critics say the American College of Medical Genetics and Genomics’ recent recommendations for reporting incidental clinical sequencing results undermine patient autonomy.
Detecting Acquired Drug Resistance in Cancer
April 30, 2013
New methods allow noninvasive analysis in blood plasma.
Arrivederci, GINA
February 4, 2013
New rules on protecting genetic privacy are under way, as study rekindles debate over sharing vs. protecting data.
10 Predictions That Will Transform Healthcare
January 22, 2013
Peer into GEN's crystal ball for a glimpse of what's to come.

NANOTECHNOLOGISTS CREATE ARTIFICIAL PORE
- Interview with Peixuan Guo, Ph.D., Director of the NIH Nanomedicine Development Center at the University of Cincinnati, Endowed Chair, and Professor of Biomedical Engineering
ALUMINUM OXIDE NANOPORE FOR DNA ANALYSIS
- Interview with Bala Murali Venkatesan, Fourth-Year Graduate Student, Department of Electrical and Computer Engineering Department, University of Illinois at Urbana-Champaign
Richard A. Gibbs, Ph.D.
- from the Baylor College of Medicine, talks with GEN's Editor-in-Chief John Sterling about frontiers in DNA sequencing.

	DNASTAR Sequence Analysis Software Lasergene 10 is a Sanger and next-generation sequence analysis and assembly software upgrade with new features to its desktop software suite for molecular biologists. Among other changes, Lasergene 10 introduces SeqNinja, a tool for manipulating an
	Roche Sequencing Assays GS GType TET2/CBL/KRAS and the GS GType RUNX1 primer sets are designed for comprehensive genetic variation detection in four key human genes using the 454 GS Junior and GS FLX Systems. The sequence-based assays offer a solution for cancer researche
	Integrated DNA Technologies (IDT) Capture Oligonucleotides xGen™ Lockdown™ probes are individually synthesized 60–120 nucleotide 5’-biotinylated capture oligonucleotides designed to enable high-depth sequencing and analysis of specific regions of the genome. xGen Lockdown probes work well for target enrich
	GenoLogics Life Sciences Software LIMS for NGS Specifically designed for sequencing, Clarity LIMS is a lab management system that combines information management essentials for CLIA-certified and regulated labs with an easy-to-navigate interface. Clarity LIMS can offer support for clinical lab
	Beckman Coulter NGS Fragment Library Prep SPRIselect utilizes SPRI (Solid Phase Reversible Immobilization)-based chemistry to simplify genomic DNA size selection for next-generation sequencing fragment library preparation. Following shearing, the library construction process requires size