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DNAstack receives NRC-IRAP funding to build cloud-based genomics software platform

DNAstack, a Toronto based company, today is announcing the investment into its cloud-based genomics software platform from the National Research Council of Canada Industrial Research Assistance Program.

16 Jan 2017

People with schizophrenia more likely to have diabetes than general population

People with early schizophrenia are at an increased risk of developing diabetes, even when the effects of antipsychotic drugs, diet and exercise are taken out of the equation, according to an analysis by researchers from King's College London.

12 Jan 2017

Endogenous retroviruses may have played significant role in development of the brain

Over millions of years retroviruses have been incorporated into our human DNA, where they today make up almost 10 per cent of the total genome.

12 Jan 2017

Diet and exercise can help lessen damage caused by malaria, UTA study suggests

The right amount of diet and exercise can help lessen damage to the heart and skeletal muscles brought on by malaria, according to a new UTA study.

12 Jan 2017

Concussions accelerate Alzheimer's disease-related brain atrophy and cognitive decline, research finds

New research has found concussions accelerate Alzheimer's disease-related brain atrophy and cognitive decline in people who are at genetic risk for the condition.

12 Jan 2017

Harvard scientists discuss promise and peril of emerging IVG technique

In vitro fertilization has transformed reproductive medicine and sparked a number of therapeutic and diagnostic breakthroughs.

12 Jan 2017

Could pathogen infection really lead to Alzheimer’s?

New concepts of infectious disease are evolving with the realization that pathogens are key players in the development of progressive chronic diseases that originally were not thought to be infectious. Infection is well-known to be associated with numerous neurological diseases for which...

12 Jan 2017

NovaSeq, the new sequencer by Illumina, said to transform the field of genomics

Illumina, Inc., the global leader in next-generation sequencing technology, today introduced the NovaSeqTM Series, a new and scalable sequencing architecture expected one day to enable a $100 genome. Unveiled at the J.P. Morgan Healthcare Conference, this platform redefines high throughput sequencing with unrivaled throughput, ease of use, low per sample costs, and unmatched flexibility.

From Illumina, Inc. 12 Jan 2017

Inhibition of EZH2 protein could be new strategy to treat multiple myeloma

In a study published in the scientific journal Oncotarget, researchers from Uppsala University show how the protein EZH2 affects the development of multiple myeloma, and that inhibition of EZH2 could be used as a new strategy to treat the disease.

12 Jan 2017

New Vanderbilt Center offers comprehensive care for patients with Marfan syndrome and aortic disease

With the recent opening of the Vanderbilt Marfan Syndrome and Aortic Disorders Center, the state's only comprehensive clinic serving entire families, hundreds of patients with connective tissue disorders now have a one-stop shop for health care.

12 Jan 2017

Ecologists reveal reasons for regional differences in Lyme disease prevalence

The ticks that transmit Lyme disease to people die of dehydration when exposed to a combination of high temperature and lowered humidity, a new USGS-led study has found.

12 Jan 2017

Epigenetic modification may be cause of adult throat cancers linked to alcohol, tobacco use

A team of researchers at the Research Institute of the McGill University Health Centre has found an epigenetic modification that might be the cause of 15% of adult cancers of the throat linked to alcohol and tobacco use.

12 Jan 2017

Genetic testing at UMMC helps doctors identify effective medication for heart stent patients

The University of Maryland Medical Center is now offering a simple genetic test to patients who receive heart stents to determine whether they have a genetic deficiency that affects how they respond to a common drug to prevent blood clots.

12 Jan 2017

Genes implicated in rare pediatric epilepsy contribute to common forms of disorder, study finds

An international study led by Columbia University Medical Center and NewYork-Presbyterian researchers has found that several genes previously implicated only in rare, severe forms of pediatric epilepsy also contribute to common forms of the disorder.

12 Jan 2017

Duke researchers use cancer-seeking salmonella to treat glioblastoma

Biomedical engineers at Duke University have recruited an unlikely ally in the fight against the deadliest form of brain cancer -- a strain of salmonella that usually causes food poisoning.

11 Jan 2017

Forensic experts need statistical models to give weight to DNA-evidence

How do forensic scientists deal with complex DNA-evidence found at crime scenes? Giulia Cereda developed new statistical models to analyse them.

11 Jan 2017

CSHL scientists create first model of genetically induced obesity in fruit flies

Why do people become obese? Poor dietary choices and overeating seem like clear causes, but what is at the root of these behaviors? Significantly overweight people may be genetically predisposed to be affected disproportionately when faced with the ready availability of calorie-laden treats.

11 Jan 2017

Illumina and IBM join forces to grow accessibility to genome data interpretation

IBM Watson Health and Illumina, Inc. today announced a groundbreaking partnership to expand access to genome data interpretation by integrating Watson for Genomics into Illumina’s BaseSpace Sequence Hub and tumor sequencing process. The collaboration is designed to help standardize and simplify genomic data interpretation.

From Illumina, Inc. 11 Jan 2017

Roswell Park study provides new insights into gene mutations that can lead to cancer

Predisposition to cancer and cancer progression can result from gene mutations that cause elevated rates of genetic damage.

11 Jan 2017

Protein aggregation may trigger inflammatory response linked to neurodegenerative diseases

A recent review article published online in The FASEB Journal points to the "trigger" for the inflammatory response, caused by the immune system, that precedes Alzheimer's disease and other neurological conditions.

11 Jan 2017

Genetic News and Research

DNAstack receives NRC-IRAP funding to build cloud-based genomics software platform

People with schizophrenia more likely to have diabetes than general population

Endogenous retroviruses may have played significant role in development of the brain

Diet and exercise can help lessen damage caused by malaria, UTA study suggests

Concussions accelerate Alzheimer's disease-related brain atrophy and cognitive decline, research finds

Harvard scientists discuss promise and peril of emerging IVG technique

Could pathogen infection really lead to Alzheimer’s?

NovaSeq, the new sequencer by Illumina, said to transform the field of genomics

Inhibition of EZH2 protein could be new strategy to treat multiple myeloma

New Vanderbilt Center offers comprehensive care for patients with Marfan syndrome and aortic disease

Ecologists reveal reasons for regional differences in Lyme disease prevalence

Epigenetic modification may be cause of adult throat cancers linked to alcohol, tobacco use

Genetic testing at UMMC helps doctors identify effective medication for heart stent patients

Genes implicated in rare pediatric epilepsy contribute to common forms of disorder, study finds

Duke researchers use cancer-seeking salmonella to treat glioblastoma

Forensic experts need statistical models to give weight to DNA-evidence

CSHL scientists create first model of genetically induced obesity in fruit flies

Illumina and IBM join forces to grow accessibility to genome data interpretation

Roswell Park study provides new insights into gene mutations that can lead to cancer

Protein aggregation may trigger inflammatory response linked to neurodegenerative diseases

Sequencing & Genomics: Elevating Science and Healthcare eBook

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

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