Whole Genome Sequencing News and Research

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Delivering more personalized care for breast cancer patients

By studying the genetic makeup of breast cancer patients, doctors are taking the next steps forward in delivering more personalized care to patients. Whole genome sequencing from cancers is not a new concept, but recently researchers have delved more deeply into the evolution of breast cancers identifying that it comes in four distinct types.

9 Oct 2013

New smartphone app puts genetic information in the hands of people

Until now, understanding and using genetic information has depended on the scientists and doctors who do the testing. No longer.

9 Oct 2013

UCLA investigates high rates of schizophrenia in people with 22q11.2 deletion syndrome

UCLA has joined an international consortium to investigate the high rates of schizophrenia and other neuropsychiatric disorders in those who are affected with Chromosome 22q11.2 deletion syndrome, a disorder caused by the deletion of a small piece of chromosome number 22.

9 Oct 2013

Study shows precision medicine provides better treatment options for mentally ill person

A multidisciplinary team led by a geneticist and psychiatrist from Cold Spring Harbor Laboratory's (CSHL) Stanley Institute for Cognitive Genomics today publish a paper providing a glimpse of both the tremendous power and the current limitations of what is sometimes called "precision medicine."

5 Oct 2013

CHOP’s 22q and You Center plays major role in brain and behavior consortium

Genetics experts from The Children's Hospital of Philadelphia (CHOP) are among the top leaders of a major international collaboration researching why patients with chromosome 22q11.2 deletion syndrome have an elevated risk of schizophrenia and other psychiatric illnesses.

4 Oct 2013

Pan-Cancer Initiative: Patterns Emerge Across Diverse Tumor Types

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27 Sep 2013

Global Genomics Group Enlists Illumina For Cardiovascular Disease Study

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From Illumina, Inc. 25 Sep 2013

Research team receives nearly $17M to focus on nanopore technology in DNA sequencing

The use of nanopore technology aimed at more accurate and efficient DNA sequencing is the main focus of grants awarded by the National Institutes of Health. The grants - nearly $17 million to eight research teams - are the latest awarded through the National Human Genome Research Institute (NHGRI)'s Advanced DNA Sequencing Technology program, which was launched in 2004. NHGRI is part of NIH.

7 Sep 2013

Researchers identify origin of human TB

Tuberculosis remains one of deadliest infectious diseases of humans, killing 50% of individuals when left untreated. Even today, TB causes 1-2 million deaths every year mainly in developing countries. Multidrug-resistance is a growing threat in the fight against the disease.

2 Sep 2013

'Quest to Cure MSA in Honor of Rex Griswold' drives in-depth genomic investigation of rare nerve disorder

Rex Griswold, Vice President of Sales for Nestl- Waters North America, was a driving force at the company for more than two decades until Multiple System Atrophy (MSA) suddenly struck him.

31 Aug 2013

Oxford Gene Technology releases next generation sequencing survey results

Oxford Gene Technology, provider of innovative genetics research and biomarker solutions to advance molecular medicine, has released the results from a recent survey of researchers using next generation sequencing.

From Oxford Gene Technology 21 Aug 2013

Study provides information that validates genetic basis of adaptation to high altitudes

Research led by scientists from the University of California, San Diego has decoded the genetic basis of chronic mountain sickness (CMS) or Monge's disease. Their study provides important information that validates the genetic basis of adaptation to high altitudes, and provides potential targets for CMS treatment.

16 Aug 2013

Four research teams receive NIH grants to explore use of genome sequencing in medical care

The National Institutes of Health has awarded four grants for up to four years to multidisciplinary research teams to explore the use of genome sequencing in medical care. The awards total approximately $6.7 million in the first year and, if funding remains available, approximately $27 million in total.

24 Jul 2013

OGT produces free-to-download whitepaper on targeted resequencing strategies

Oxford Gene Technology, provider of innovative genetics research and biomarker solutions to advance molecular medicine, has produced a new, free-to-download whitepaper titled ‘When to use targeted resequencing — Choosing the right NGS method.’

From Oxford Gene Technology 17 Jul 2013

Genome sequencing promises to identify rare mutations that give rise to autism

An international consortium, consisting of Autism Speaks, Duke University School of Medicine, The Hospital for Sick Children of Toronto, BGI and other institutes, has investigated the genetic variants in 32 families with Autism Spectrum Disorder (ASD).

12 Jul 2013

Study reveals strain of V. cholerae in Haiti cholera outbreak originated from single source

The strain of cholera that has sickened thousands in Haiti came from a single source and was not repeatedly introduced to the island over the past three years as some have thought, according to a new study published in mBio-, the online open-access journal of the American Society for Microbiology.

2 Jul 2013

IDC announces recipients of HPC Innovation Excellence Award at ISC'13

International Data Corporation today announced the fifth round of recipients of the HPC Innovation Excellence Award at the ISC'13 supercomputer industry conference in Leipzig, Germany. Prior winners were announced at the ISC'11, SC'11, ISC'12, and SC'12 supercomputing conferences.

18 Jun 2013

MGH researchers discover CNVs in members of 10 families with early-onset Alzheimer's

Although a family history of Alzheimer's disease is a primary risk factor for the devastating neurological disorder, mutations in only three genes - the amyloid precursor protein and presenilins 1 and 2 - have been established as causative for inherited, early-onset Alzheimer's, accounting for about half of such cases.

18 Jun 2013

New findings suggest development of pharmacological treatments for uterine leiomyomata

Uterine leiomyomata, or fibroids, are benign tumours that nevertheless affect the health of millions of women. They may cause, for instance, pain, bleeding and infertility. Fibroids are also the most common reason for a hysterectomy; for example, some 8,000 hysterectomies are made in Finland each year.

10 Jun 2013

Mayo Clinic, Cancer Genetics form joint venture to improve cancer care

Mayo Clinic and Cancer Genetics Inc. today launched OncoSpire Genomics, a joint venture with the singular goal of improving cancer care by discovering and commercializing diagnostic tests that leverage next-generation sequencing.

23 May 2013

Whole Genome Sequencing News and Research

Delivering more personalized care for breast cancer patients

New smartphone app puts genetic information in the hands of people

UCLA investigates high rates of schizophrenia in people with 22q11.2 deletion syndrome

Study shows precision medicine provides better treatment options for mentally ill person

CHOP’s 22q and You Center plays major role in brain and behavior consortium

Pan-Cancer Initiative: Patterns Emerge Across Diverse Tumor Types

Global Genomics Group Enlists Illumina For Cardiovascular Disease Study

Research team receives nearly $17M to focus on nanopore technology in DNA sequencing

Researchers identify origin of human TB

'Quest to Cure MSA in Honor of Rex Griswold' drives in-depth genomic investigation of rare nerve disorder

Oxford Gene Technology releases next generation sequencing survey results

Study provides information that validates genetic basis of adaptation to high altitudes

Four research teams receive NIH grants to explore use of genome sequencing in medical care

OGT produces free-to-download whitepaper on targeted resequencing strategies

Genome sequencing promises to identify rare mutations that give rise to autism

Study reveals strain of V. cholerae in Haiti cholera outbreak originated from single source

IDC announces recipients of HPC Innovation Excellence Award at ISC'13

MGH researchers discover CNVs in members of 10 families with early-onset Alzheimer's

New findings suggest development of pharmacological treatments for uterine leiomyomata

Mayo Clinic, Cancer Genetics form joint venture to improve cancer care

Sequencing & Genomics: Elevating Science and Healthcare eBook

Achieving and maintaining ISO 27001 and BS 10012 certifications

Expanding research and clinical options for children with cancer

Examining how pain could play a direct protective role in the gut

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