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Sequencing - Related Content

Point of View: Genome 2.0: First Form, Now Function
An Effort on the Size and Scale of the HGP Is Needed to Figure Out What Variation Means
BioMarket Trends: DNA Sequencing: Coming to a Clinic Near You
High-Sensitivity, High-Throughput, and Unbiased Nature Will Drive Adoption in the Clinic
Insight & Intelligence™: Acquired Drug Resistance in Cancer
New Methods Allow Non-invasive Analysis in Blood Plasma
BioPerspectives: Avoiding “Incidental” Damages
Presidential panel, ACMG, and experts struggle with what patients should learn, and how.
Feature Articles: Comparative Genomics: Insights into Disease Susceptibility

Chips By Choice
June 12, 2013
The technology that was slated to make microarrays obsolete has actually helped make them better.
Metagenomics May Hold Key to Novel Antibiotic Discovery
June 6, 2013
This relatively new science has the potential to fill a technological void.
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.

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.

	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
	Agilent Technologies Exome Sample Prep SureSelect Human All-Exon V5 and V5 + UTRs for next-generation sequencing produce exome samples ready for sequencing the next day. They also provide good sequencing efficiencies as well as coverage of current genomics databases including RefSeq, CC

Bioinformatic Analysis of Next Generation Sequencing Data
2013 July 9 - July 12 Bethesda, MD, UNITED STATES
Sequencing Strategies for Success
2013 August 19 - August 20 Providence, RI, UNITED STATES
Single-Cell Sequencing
2013 August 20 - August 21 Providence, RI, UNITED STATES
Consumer Genetics Conference
2013 September 25 - September 27 Boston, MA, UNITED STATES