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Next-Generation Sequencing - Related Content

BioMarket Trends: DNA Sequencing: Coming to a Clinic Near You
High-Sensitivity, High-Throughput, and Unbiased Nature Will Drive Adoption in the Clinic
Feature Articles: Creative Approaches to Next-Gen Sequencing
BioPerspectives: Next-Generation Sequencing in the Clinic
Elaine Mardis, Ph.D., co-director of the Genome Institute at Washington University, discusses NGS and its future.
BioPerspectives: Unveiling Biological Complexity with SMRT Sequencing
Single molecule, real-time DNA sequencing can help scientists close genomes, study linked variants, and detect base modifications.
BioPerspectives: Next-Generation Sequencing vs. Microarrays
Is it time to switch?

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.
Illumina, Complete Genomics Prepare for Legal Battle over Sequencing IP
March 29, 2012
Illumina filed the case stating that the Complete Genomics Analysis Platform infringes on three of its patents.
U.K. Groups Grapple with Ethical Issues Linked to Clinical Sequencing
March 13, 2012
Questions cover data dissemination, bioinformatics, and more education.
Will Roche Really Drop Illumina and Seek out Another Sequencing Firm?
March 12, 2012
Oxford Nanopore and PacBio both have exciting technologies, but Illumina remains market leader.
Roche, Illumina Duke It Out in Potential $5.7B Takeover Deal
March 1, 2012
Roche’s hostile $44.50 per share bid could also spark additional sequencing acquisition wars.

A New Tool for Personal Genomics
Gholson Lyon, M.D., Ph.D., Senior Scientist, Principal Investigator, Center for Applied Genomics, The Children’s Hospital of Philadelphia
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.

	Interactive Biosoftware Next-Gen Sequencing Software Alamut HT is a human genomic variation annotation and interpretation solution. As a high-throughput annotation engine for next-generation sequencing (NGS), it is designed for intensive variant analysis workflows. This software enriches raw NGS vari
	Advanced Analytical DNA Fragment Analysis The new Fragment Analyzer™ can provide a high-throughput alternative to lab-on-a-chip methods for qualifying DNA fragments prior to next-gen sequencing runs. The Fragment Analyzer can help labs under pressure from increasing sample workloads. No fl
	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
	New England BioLabs DNA Library Prep The NEBNext® Ultra DNA Library Prep Kit for Illumina® contains enzymes and buffers that can convert a small amount of DNA input into indexed libraries for next-generation sequencing on the Illumina platform. The workflow of NEBNext Ultra

Bioinformatic Analysis of Next Generation Sequencing Data
2013 July 9 - July 12 Bethesda, MD, UNITED STATES
Applying Next Generation Sequencing
2013 August 19 - August 21 Providence, RI, UNITED STATES
Next Generation Dx Summit
2013 August 20 - August 22 Washington, DC, UNITED STATES
NGS for Cancer Development
2013 September 24 - September 26 Boston, MA, UNITED STATES
Next Generation Sequencing Asia Congress
2013 October 8 - October 9 Singapore, , SINGAPORE