Genetics News and Research

Latest Genetics News and Research

Raw fruits and veggies may offset genetic risk for heart disease: Study

In a new study a team of researchers looked at the genotypes of 27,243 people from two separate studies to see if they had a certain gene variant. Earlier studies including a 2010 meta-analysis in the Journal of the American Medical Assn. found that the 9p21 gene is associated with a higher risk of heart attack and cardiovascular disease.

13 Oct 2011

Roche launches LightCycler Nano real-time PCR system in the U.S.

Roche announced today the U.S. launch of the latest addition to the company's real-time PCR portfolio of LightCycler instruments for use in research, the LightCycler Nano real-time PCR system.

From Roche Sequencing and Life Science 13 Oct 2011

Genetic mystery of bacterium causing ‘Black Death’ revealed

Between 1347 and 1351 - a period of just five years, Europe's Black Death wiped out about 30 million people - 30 to 50% of the population on the continent. Now geneticists have reconstructed the genome of the bacterium that caused the plague. It is found to be an ancient strain of a bacterium called Yersinia pestis very similar to the strain the exists today.

13 Oct 2011

Skin cell to liver cell shows promise for genetic liver disease

In a new scientific breakthrough, researchers have taken skin cells from a patient with liver disease and turned them into replacement liver cells. Although the procedure is years before it can be used in humans, but if approved, it could launch a new era of personalized therapies for serious genetic disorders.

13 Oct 2011

NanoString introduces nCounter Analysis System

NanoString Technologies, Inc., a privately held provider of life science tools for translational research and developer of molecular diagnostics, today announced the launch of its second generation nCounter Analysis System.

From NanoString Technologies 13 Oct 2011

GeneDx launches new genetic test to accurately diagnose rare diseases

At the joint conference of the American Society of Human Genetics/International Congress on Human Genetics in Montreal on October 12, GeneDx, one of the foremost genetics laboratories in the world and a subsidiary of Bio-Reference Laboratories, Inc., is announcing a first-of-its-kind test that will enable physicians and patients to more accurately identify the genetic cause of rare diseases.

13 Oct 2011

Breakthrough in the study of chlamydia genetics

A breakthrough in the study of chlamydia genetics could open the way to new treatments and the development of a vaccine for this sexually transmitted disease.

13 Oct 2011

Pfizer, deCODE genetics collaborate to discover sequence variants linked with SLE

deCODE genetics today announced that it has entered into a research collaboration with Pfizer Inc., the objective of which is to discover sequence variants associated with specific clinical phenotypes related to Systemic Lupus Erythematosis by utilizing deCODE's expertise in gene discovery.

13 Oct 2011

Affymetrix launches Axiom Pan-African Array

Affymetrix, Inc. today announced at the ICHG/ASHG annual conference in Montreal, the worldwide launch of the Axiom Genome-Wide Pan-African Array, the first commercial product to maximize genomic coverage of both common and rare alleles in populations of African ancestry, including West African, East African, and African American.

13 Oct 2011

Vitamin D plays an essential role in the body's fight against TB

Not just important for building strong bones, an international team of scientists has found that vitamin D also plays an essential role in the body's fight against infections such as tuberculosis.

12 Oct 2011

Life Technologies launches Ion AmpliSeq Cancer Panel

Life Technologies Corporation today announced the launch of the Ion AmpliSeq Cancer Panel, enabling scientists to sequence dozens of genes in cancer research samples using a simple workflow.

12 Oct 2011

ASHG to honor U of U geneticist with William Allan Award

As a teenager just moved to Iowa from war-ravaged Germany in 1951, John M. Opitz, M.D., wanted to study developmental biology, but his "very Prussian" mother insisted he go to medical school instead.

12 Oct 2011

Chromosomal microarray can provide important information for patient treatment

Chromosomal microarray (CMA)—a powerful test for diagnosing the genetic abnormalities causing some types of developmental delay and birth defects—can be used in an evidence-based manner to provide important information for patient treatment, according to a pair of studies in the September issue of Genetics in Medicine, the official peer-reviewed journal of The American College of Medical Genetics.

12 Oct 2011

Journal of Alzheimer's Disease supplement explores neuroimaging

Alzheimer's disease (AD) is a common problem that is becoming progressively burdensome throughout the world. A new supplement to the Journal of Alzheimer's Disease, Imaging the Alzheimer Brain, clearly shows that multiple imaging systems are now available to help understand, diagnose, and treat the disease.

12 Oct 2011

New robust technique holds promise for identifying trace mutant DNA sequences

Molecular DNA testing methods offer clinicians powerful tools that serve to confirm or identify disease diagnoses. High sensitivity and high specificity, however, are frequently a challenge to achieve with these methods. In a study scheduled for publication in the November issue of The Journal of Molecular Diagnostics, researchers describe a new, robust technique that holds promise for identifying trace mutant DNA sequences in an overwhelming population of unmutated DNA.

12 Oct 2011

CHOP, Albert Einstein College of Medicine to study genetics of conotruncal defects

The Eunice Kennedy Shriver National Institute of Child Health & Human Development, part of the National Institutes of Health, has awarded researchers at Albert Einstein College of Medicine of Yeshiva University and collaborators at the Children's Hospital of Philadelphia (CHOP) a five-year, $6.7 million grant to study the genetics of both rare and common congenital heart abnormalities known as conotruncal defects.

12 Oct 2011

Roche NimbleGen launches pre-capture multiplex target enrichment protocol

With the decreasing cost and increasing throughput of sequencing, researchers require a high-performance, cost-effective sample preparation pipeline for targeted sequencing. To enable researchers to more readily match targeted sequencing sample preparation throughput to the ever increasing throughput of next-generation sequencing, Roche NimbleGen announces the imminent launch of a pre-capture multiplex target enrichment protocol.

11 Oct 2011

Brown signs Calif. measures to aid children with autism, ban kids younger than 18 from using tanning beds

In other state news, Wisconsin last month began scrutinizing health insurance rate increases, Los Angeles County steps in ahead of health law's mandated coverage expansions and a Georgia report notes the state's progress in providing services for people with mental illness and developmental disabilities.

11 Oct 2011

Genetics & IVF Institute now offers 24 Chromosome Microarray

The Genetics & IVF Institute is now offering 24 Chromosome Microarray, which is a new, comprehensive test used as part of an IVF cycle to evaluate the number of chromosomes present in an embryo before it is transferred to the mother.

11 Oct 2011

CXCL12 protein can inhibit metastasis of colon and melanoma cancers

Researchers at the Medical College of Wisconsin have shown that a protein can inhibit metastasis of colon and melanoma cancers. The findings are published in the October 10, 2011 issue of Proceedings of the National Academy of Sciences.

11 Oct 2011