Genomics

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A newly-emerging species of C. difficile highly adapted to spread in hospitals

Scientists have discovered that the gut-infecting bacterium Clostridium difficile is evolving into two separate species, with one group highly adapted to spread in hospitals.

12 Aug 2019

Neuronal gene malfunction is behind seizures associated with long QT syndrome, study suggests

Most people with a medical condition called long QT syndrome have a mutation in a gene that causes bouts of fast, chaotic heartbeats.

9 Aug 2019

New genomic module facilitates more personalized forms of medicine

Researchers from the HSE Epilepsy Lighthouse Project and FutureNeuro, the SFI Research Centre for Chronic and Rare Neurological Diseases hosted by RCSI, have developed a new genomics module in the Irish National Epilepsy Electronic Patient Record system.

9 Aug 2019

New technique finds medically and ecologically relevant bacteria groups

Identifying species among plants and animals has been a full-time occupation for some biologists, but the task is even more daunting for the myriad microbes that inhabit the planet.

9 Aug 2019

Whole genome sequencing could give officials a powerful weapon to track disease outbreaks

Whole genome sequencing technology may give epidemiologists and healthcare workers a powerful weapon in tracking and, possibly, controlling outbreaks of serious diseases, according to a team of researchers.

8 Aug 2019

Researchers identify gene mutation combo linked to endometrial cancer

Michigan State University researchers, in collaboration with the Van Andel Institute, have identified a combination of two gene mutations that is linked to endometrial cancer.

7 Aug 2019

Genome editing strategy opens new perspectives in the treatment of cystic fibrosis

The approach adopted by the team of the University of Trento, led by Anna Cereseto, opens new perspectives in the treatment of cystic fibrosis, a genetic disease for which no cure is currently available.

7 Aug 2019

APOE gene variant may be protective and prolong life, finds study

A new study of 38,537 persons of European ancestry suggests that a rare variation of a gene called APOE may be protective and prolong life, in sharp contrast to a more widely studied APOE variant that increases risk of death.

7 Aug 2019

Uncovering how cyanobacteria edit their genomes

Unique editing mechanisms in cyanobacteria, commonly known as blue-green algae, make them able to remove large sections of the genome to give cells the ability to fix nitrogen, when necessary.

7 Aug 2019

University of North Dakota receives $10 million to expand epigenetics research program

The National Institutes of Health has awarded the University of North Dakota School of Medicine & Health Sciences a $10 million, five-year grant to expand the School's epigenetics research program.

6 Aug 2019

New theory demystifies evolution of human imagination

A genetic mutation may have triggered a cascade of events that enabled the acquisition of recursive language and imagination in homo sapiens.

5 Aug 2019

New computational method reveals genetic patterns in massive jumble of cells

Scientists have devised a new computational method that reveals genetic patterns in the massive jumble of individual cells in the body.

5 Aug 2019

Fraunhofer scientists develop method for measuring a person’s biological age

Chemical reactions and molecular modifications change the genome of each and every human over the course of their lifetime.

3 Aug 2019

Understanding how positively charged peptides formed on pre-biotic earth

Earth didn't always harbor life. But around 4 billion years ago, something in the environment changed, and systems with biological properties began to emerge.

2 Aug 2019

Discovery of protective protein could open door to better treatment of fast-growing cancer cells

The discovery that an essential protein plays a protective role during cell division, could open the door to better targeted treatment of fast-growing cancer cells.

1 Aug 2019

Unique genetic history of Finnish people offers clues to disease

A new study harnessed the unique genetic history of the people of Finland to identify variations in DNA that might predispose certain individuals to disease, whether or not they are Finnish themselves.

1 Aug 2019

Understanding creation of antibiotic scaffolds could drive new class of antibiotics

Understanding how antibiotic scaffolds are constructed in nature can help scientists prospect for new classes of antibiotics through DNA sequencing and genome mining.

31 Jul 2019

New study helps better understand molecular basis of diseases affecting motor control

Neuroscientists at the University of Sussex have revealed that complex movements, such as those that maintain our posture, can be controlled by a simple genetic system, providing a framework to better understand the molecular basis of diseases that affect motor control, like Huntington's and Parkinson's.

31 Jul 2019

Researchers develop new method to accurately identify nontuberculous mycobacteria

The bacterial genus Mycobacterium has the dubious honor of including species responsible for two of the best-known chronic human infectious diseases: tuberculosis and leprosy.

30 Jul 2019

NemaMetrix raises $5 million USD funding to expand its Precisome platform

NemaMetrix, an Oregon-based company that provides phenotyping and functional analysis using C. elegans nematodes, today announced it has closed a $5 million USD funding round to expand its Precisome platform: a tool for in vivo testing for early drug discovery, agribio, and precision medicine.

From InVivo Biosystems 30 Jul 2019

Genomics

A newly-emerging species of C. difficile highly adapted to spread in hospitals

Neuronal gene malfunction is behind seizures associated with long QT syndrome, study suggests

New genomic module facilitates more personalized forms of medicine

New technique finds medically and ecologically relevant bacteria groups

Whole genome sequencing could give officials a powerful weapon to track disease outbreaks

Researchers identify gene mutation combo linked to endometrial cancer

Genome editing strategy opens new perspectives in the treatment of cystic fibrosis

APOE gene variant may be protective and prolong life, finds study

Uncovering how cyanobacteria edit their genomes

University of North Dakota receives $10 million to expand epigenetics research program

New theory demystifies evolution of human imagination

New computational method reveals genetic patterns in massive jumble of cells

Fraunhofer scientists develop method for measuring a person’s biological age

Understanding how positively charged peptides formed on pre-biotic earth

Discovery of protective protein could open door to better treatment of fast-growing cancer cells

Unique genetic history of Finnish people offers clues to disease

Understanding creation of antibiotic scaffolds could drive new class of antibiotics

New study helps better understand molecular basis of diseases affecting motor control

Researchers develop new method to accurately identify nontuberculous mycobacteria

NemaMetrix raises $5 million USD funding to expand its Precisome platform

Achieving and maintaining ISO/IEC 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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