Skip to main content
Premium Trial:

Request an Annual Quote

Harvard Medical School, Partners HealthCare and Affymetrix, University of Cambridge, UK, Cancer Research UK and Perlegen, and Applied Biosystems and Celera Genomics


Harvard/Partners Center for Genetics and Genomics Will Use Affy Arrays in Atherosclerosis Genotyping Study

The Center for Genetics and Genomics of Harvard Medical School and Partners HealthCare will use Affymetrix’s GeneChip Human Mapping microarrays in a genotyping study of atherosclerosis, the two institutions said this week.

HPCGG will obtain the arrays by the end of June under an early access program. In the study, which is funded by the Reynolds Foundation, researchers will genotype more than 1,200 patient samples from the Women’s Health Study, an ongoing NIH study of cardiovascular disease in which 38,000 women participate.

The Human Mapping array is capable of scanning up to 500,000 SNPs, according to Affymetrix.

U. of Cambridge, Cancer Research UK, Perlegen Team Up for Breast Cancer Genotyping Study

Researchers at the University of Cambridge, UK, Cancer Research UK and its technology transfer arm, and Perlegen Sciences will collaborate in a genotyping study to find genetic variations associated with breast cancer, the institutions said this week.

Cancer Research UK provides the funding for the project.

Perlegen Sciences will determine over 200 million genotypes in DNA samples collected from breast cancer patients in the UK and healthy women enrolled in the European Prospective Investigation of Cancer study. Initial results will be validated by Cambridge researchers, who plan to analyze several thousand additional samples.

ABI Restructures Its Marketing, Distribution Pact With Celera

Applera’s board has said Applied Biosystems and Celera Genomics can restructure their 10-year marketing and distribution agreement.

The arrangement allows ABI to exclusively integrate Celera Discovery System data and other genomic and biological information into its product offerings, including TaqMan assays, SNPlex Genotyping Systems, and Expression Array System, in return for royalties based on revenues generated by sales of some products.

Disclosed in an SEC filing this week, the amended agreement increases the royalty rate to 4 percent from 3 percent. The deal also extends the agreement by five years, to the end of the company’s FY 2017.

Filed under

The Scan

Genetic Tests Lead to Potential Prognostic Variants in Dutch Children With Dilated Cardiomyopathy

Researchers in Circulation: Genomic and Precision Medicine found that the presence of pathogenic or likely pathogenic variants was linked to increased risk of death and poorer outcomes in children with pediatric dilated cardiomyopathy.

Fragile X Syndrome Mutations Found With Comprehensive Testing Method

Researchers in Clinical Chemistry found fragile X syndrome expansions and other FMR1 mutations with ties to the intellectual disability condition using a long-range PCR and long-read sequencing approach.

Team Presents Strategy for Speedy Species Detection in Metagenomic Sequence Data

A computational approach presented in PLOS Computational Biology produced fewer false-positive species identifications in simulated and authentic metagenomic sequences.

Genetic Risk Factors for Hypertension Can Help Identify Those at Risk for Cardiovascular Disease

Genetically predicted high blood pressure risk is also associated with increased cardiovascular disease risk, a new JAMA Cardiology study says.