Next-Generation Sequencing – News and Features

News
FDA Utilizes the Rosetta Syllego™ System to Manage GWA Study Data Submitted through VXDS Program
The Syllego system will provide a single repository for easy access to genotyping data used in genome-wide association studies.

News
BioNanomatrix Announces Issuance of Key Nanofluidics Patent Enabling Single Molecule Whole Genome Analysis
The patent covers integration of nanofluidic channels into sample analysis systems.

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Sequenom to Develop Third-Generation Nanopore-Based Single Molecule Sequencing Technology
Sequenom acquires rights to DNA and RNA readout technology that holds potential for cost-effective and ultra rapid human genome sequencing.

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BioNanomatrix and Complete Genomics Receive $8.8 Million NIST-ATP Award to Develop Sequencing Platform for $100 Genome
Project combines novel gene sequencing chemistry and advanced nanofluidic technology to sequence entire human genome in eight hours at a cost of $100.

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Sequenom to Develop Third-Generation Nanopore-Based Single Molecule Sequencing Technology
Company Acquires Rights to DNA and RNA Readout Technology That Holds Potential for Cost-Effective and Ultra Rapid Human Genome Sequencing

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ZS Genetics and the University of New Hampshire Sign Long-Term Development Contract
The agreement supports the development of technology and intellectual property for ZS Genetics’ radically different genetic analysis technology.

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First Individual Diploid Human Genome Published by Researchers at J. Craig Venter Institute
Sequence reveals that human to human variation is substantially greater than earlier estimates.

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University of Washington, Fred Hutchinson Cancer Research Center to Coordinate NHGRI Disease Studies
UW and FHCRC awarded a four-year $4.8 million contract to coordinate activities for several whole-genome studies of human disease across the U.S.

News
Applied Biosystems Announces Software Development Initiative for Next-Generation Sequencing
Software Development Community expected to facilitate the advancement of bioinformatics applications for the SOLiD™ system and other sequencing platforms.

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Quest Introduces ClariSure™ Test for Identifying Chromosome Abnormalities in Children
The molecular diagnostic test is designed to detect chromosome abnormalities associated with 85 developmental disorders affecting children.
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