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Optimized ChIP Protocols for qPCR and Sequencing
Thursday, June 18, 2015
Protocols developed using proprietary solid state chromatin immunoprecipitation technology.

Highly Efficient ChIP Assay Kit for FFPE Samples
Thursday, June 18, 2015
New Chromatrap® FFPE ChIP kit provides sufficient DNA to perform library preps for ChIP-seq assays.

Bioo Scientific Releases Automated NEXTflex Protocols
Thursday, June 11, 2015
Company has developed and optimized automation protocols for the Sciclone NGS workstation.

New Database of Ethnically and Phenotypically Diverse Whole Genome Information
Tuesday, June 09, 2015
QIAGEN and Inova Translational Medicine Institute have announced the launch of Inova Genomes, a unique compendium of ethnically, phenotypically, and ancestrally diverse whole-genome sequencing data for researchers seeking to accelerate cohort analysis programs or improve success rates in diagnostic odyssey cases.

Manchester First to Adopt Congenica's Sapientia Technology for Clinical Service
Monday, June 08, 2015
Manchester Centre for Genomic Medicine becomes the first NHS genetics service in the country to use genome DNA sequence analysis supported by Sapientia, a technology developed by Cambridge, UK based Congenica.

Agilent Releases New Target-Enrichment Solutions for Disease Research
Friday, June 05, 2015
Products address current limitations of exome sequencing.

New Single-Cell T-cell Receptor Assay
Wednesday, June 03, 2015
New assay for immunology and immuno-oncology research available from Cellular Research.

Fluxion Biosciences and Swift Biosciences Announce New Workflow
Friday, May 29, 2015
Jointly developed next-generation sequencing workflow for somatic mutation detection from liquid biopsy samples.

PrimePCR™ Assays Used to Create qPCR Reference Data for FDA-Led Sequencing Project
Tuesday, May 19, 2015
Biogazelle recently used Bio-Rad Laboratories’ PrimePCR Real-Time PCR Assays in a global analysis of NGS reproducibility that was published in Nature Biotechnology.

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Scientific News
Shining A Light On Bladder Cancer
Researchers scrutinize patterns of mutations in bladder tumor genomes, gleaning insights into the roles of DNA repair and tobacco-related DNA damage.
Monovar Drills Down Into Cancer Genome
Rice, MD Anderson develop program to ID mutations in single cancer cells.
Five New Breast Cancer Genes Found
Discovery of mutations paves the way for personalised treatment of breast cancer.
New Neurodevelopmental Syndrome Identified
Study pinpoints underlying genetic mutations, raising hopes for targeted therapies.
Uncovering Hidden Genomic Alterations that Drive Cancers
Tested on large tumor genomics database, REVEALER method allows researchers to connect genomics to cell function.
Gene Behind Rare Childhood Syndrome Identified
Online activism by one patient’s mother spurred research collaboration which led to the identification of a new genetic syndrome.
Resilience Project Identifies Rare Unaffected Individuals
Researchers from Mount Sinai and Sage Bionetworks report analysis of nearly 600,000 genomes for resilience project.
Rare DNA Will Have Nowhere To Hide
Two National Institutes of Health grants back Rice University effort to develop new diagnostics.
Virus Causing Tilapia Die-Offs Identified
Discovery of the virus causing Tilapia die-offs in Israel and Ecuador points the way to protecting a fish that feeds multitudes.
Children With Cancer To Get New Gene Test
Pilot study will sequence 81 cancer genes in children’s tumours to help personalise cancer treatment.
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