Genomics News and Research

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Genomics is the study of the complete genetic material, including genes and their functions, of an organism.

Porvair sciences introduce products for use in animal and plant genetics

Porvair Sciences will showcase two important technical breakthroughs at PAG XXV in San Diego (USA) from January 14-18, 2017.

From Chromatrap® - Porvair Sciences Ltd 15 Dec 2016

Research into common congenital brain defect identifies molecular basis

Scientists at Sanford Burnham Prebys Medical Discovery Institute (SBP) have discovered a molecular cause of hydrocephalus, a common, potentially life-threatening birth defect in which the head is enlarged due to excess fluid surrounding the brain.

14 Dec 2016

GWAS identifies genomic locations linked to personality traits and psychiatric disorders

A meta-analysis of genome-wide association studies has identified six loci or regions of the human genome that are significantly linked to personality traits, report researchers at University of California San Diego School of Medicine in this week's advance online publication of Nature Genetics.

9 Dec 2016

Synthetic sgRNA for CRISPR genome editing

Chemically synthesized single guide RNA is the best way to do CRISPR genome editing. It is more pure than biological methods of creating guide RNAs, like in vitro transcription or plasmids. As a result, sgRNA leads to more consistency and higher quality.

8 Dec 2016

Stem cell-based risk scoring tool could predict AML patient’s response to standard treatment

Leukemia researchers at Princess Margaret Cancer Centre have developed a 17-gene signature derived from leukemia stem cells that can predict at diagnosis if patients with acute myeloid leukemia (AML) will respond to standard treatment.

8 Dec 2016

Sophia Genetics introduces privacy-protecting technology for storage and access to patients’ genomic information

Sophia Genetics, global leader in Data-Driven Medicine, unveiled today a new privacy-protecting technology for the storage and access to patients’ genomic information worldwide, paving the way to a new industry standard.

7 Dec 2016

New study suggests how risk gene linked to ADHD may work

Genetics play a strong part in the development of attention-deficit/hyperactivity disorder (ADHD), but the path from a gene to risk for the disorder has remained a black box to researchers.

7 Dec 2016

Researchers identify critical paralog groups with indispensable role in cellular signalling pathways

Throughout evolutionary history, there have been genetic elements that have duplicated - giving rise to genes with different functions.

7 Dec 2016

Experts discuss ways to integrate whole genome analysis into clinical practice at Congenica webinar

Whole genome analysis – where all of a patient’s genes are screened for potential disease causing variants – offers the potential for a rapid, responsive NHS testing service.

6 Dec 2016

Cigarette smoking may lead to fibrosis in the heart and kidneys, study reveals

Smoking may lead to fibrosis in the heart and kidneys and can worsen existing kidney disease, according to a new study.

1 Dec 2016

TGen and City of Hope collaborate to accelerate precision medicine research

City of Hope, a world-renowned independent research and cancer and diabetes treatment center, and Translational Genomics Research Institute, a leading biomedical research institute, announced today that they have formed an alliance to make precision medicine a reality for patients.

30 Nov 2016

Allen Institute for Cell Science releases gene edited, fluorescently tagged human iPS cells

The Allen Institute for Cell Science has released the Allen Cell Collection: the first publicly available collection of gene edited, fluorescently tagged human induced pluripotent stem cells that target key cellular structures with unprecedented clarity.

30 Nov 2016

OmniPath provides gateway for literature-curated signalling pathways with unprecedented accuracy

Combining the power of 27 data resources, Omnipath helps researchers see biological signalling pathways with unprecedented accuracy.

29 Nov 2016

Scientists develop easy-to-use software tool to detect important genetic mutations

Scientists have developed an easy-to-use software tool that can detect important genetic mutations that previously needed to be identified by a separate test.

29 Nov 2016

Metabolomics research at the Phenome Centre Birmingham

An interview with Professor Mark Viant, University of Birmingham, UK, Executive Director of Phenome Centre Birmingham and Director of the NERC Biomolecular Analysis Facility.

From Bruker BioSpin Group 28 Nov 2016

Landmark study of virosphere uncovers 1445 viruses

A landmark study of the virosphere of the most populous animals – those without backbones such as insects, spiders and worms and that live around our houses – has uncovered 1445 viruses, revealing people have only scratched the surface of the world of viruses – but it is likely that only a few cause disease.

25 Nov 2016

Cancer gene mutations can predict response to less intensive treatment in AML patients

Patients with the most lethal form of acute myeloid leukemia (AML) - based on genetic profiles of their cancers - typically survive for only four to six months after diagnosis, even with aggressive chemotherapy.

23 Nov 2016

Study finds genomic regions with copy number variants linked to schizophrenia risk

Many of the genetic variations that increase risk for schizophrenia are rare, making it difficult to study their role in the disease.

22 Nov 2016

Wellcome Trust Sanger Institute open new biodata innovation centre and sequencing facility

The UK Prime Minister Rt Hon Theresa May today joined key stakeholders from across the life sciences sector to open the Wellcome Trust Sanger Institute’s new Bridget Ogilvie Building and the Biodata Innovation Centre at the Wellcome Genome Campus in Cambridge.

22 Nov 2016

Researchers propose zebrafish as model to predict effects of EDCs

Water is vital for our survival. However, water quality is always a concern for public health authorities as it may contain diverse environmental pollutants, including endocrine disrupting chemicals (EDCs).

18 Nov 2016

Genomics News and Research

Further Reading

Porvair sciences introduce products for use in animal and plant genetics

Research into common congenital brain defect identifies molecular basis

GWAS identifies genomic locations linked to personality traits and psychiatric disorders

Synthetic sgRNA for CRISPR genome editing

Stem cell-based risk scoring tool could predict AML patient’s response to standard treatment

Sophia Genetics introduces privacy-protecting technology for storage and access to patients’ genomic information

New study suggests how risk gene linked to ADHD may work

Researchers identify critical paralog groups with indispensable role in cellular signalling pathways

Experts discuss ways to integrate whole genome analysis into clinical practice at Congenica webinar

Cigarette smoking may lead to fibrosis in the heart and kidneys, study reveals

TGen and City of Hope collaborate to accelerate precision medicine research

Allen Institute for Cell Science releases gene edited, fluorescently tagged human iPS cells

OmniPath provides gateway for literature-curated signalling pathways with unprecedented accuracy

Scientists develop easy-to-use software tool to detect important genetic mutations

Metabolomics research at the Phenome Centre Birmingham

Landmark study of virosphere uncovers 1445 viruses

Cancer gene mutations can predict response to less intensive treatment in AML patients

Study finds genomic regions with copy number variants linked to schizophrenia risk

Wellcome Trust Sanger Institute open new biodata innovation centre and sequencing facility

Researchers propose zebrafish as model to predict effects of EDCs

Industry focus eBook: Genomics (4th edition) eBook

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Industry Focus eBook - Analytical Chemistry (3rd edition)

Industry Focus eBook - Microbiome (1st edition)

Industry Focus eBook - Cell biology (5th edition)

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