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Next-generation sequencing expands possibilities for newborn screening

Every year, millions of newborns undergo routine screening as a preventive strategy to detect inherited disorders before symptoms emerge.

4 Feb 2026

New liquid biopsy detects early cancers through epigenetic instability

Researchers at the Johns Hopkins Kimmel Cancer Center have developed a novel liquid biopsy approach to identify early-stage cancers by measuring the random variation in DNA methylation patterns, rather than the absolute level of those patterns as in other liquid biopsies.

2 Feb 2026

Bat viruses in Indochina Peninsula reveal viral diversity, PEDV origins, and spillover risks

Bats, critical reservoirs of viruses with significant cross-species spillover risks, have long been understudied in the Indochina Peninsula.

2 Feb 2026

Scientists create new map showing how cancer gene mutations influence tumor growth

Scientists have created a complete map showing how hundreds of possible mutations in a key cancer gene influence tumor growth.

2 Feb 2026

Genetic ancestry influences tumor biology and survival in head and neck cancers

Genetic ancestry plays a key role in determining the behavior of head and neck tumors and may help explain why African-American patients survive for half as long as their counterparts of European ancestry, according to a new review study led by researchers from the University of Maryland School of Medicine's (UMSOM) Institute for Genome Sciences (IGS) and the University of Maryland Greenebaum Comprehensive Cancer Center (UMGCCC).

31 Jan 2026

Research reveals a link between defective DNA repair and immune-driven inflammatory disease

Unrepaired DNA-protein crosslinks (DPCs) – highly toxic tangles of protein and DNA – cause a process that leads to premature aging and embryonic lethality in mice.

31 Jan 2026

King’s researchers help transform UK mental health research infrastructure

King’s researchers will help transform mental health data, clinical trials and industry partnerships as part of the UK Government’s Mental Health Goals programme.

30 Jan 2026

New diagnostic framework addresses challenges of rapidly-mutating RNA viruses

The rapid evolutionary dynamics of RNA viruses, driven by high mutation rates and the consequent formation of complex quasispecies populations, present a formidable obstacle to conventional molecular diagnostic approaches.

30 Jan 2026

New mode of communication inside cells helps bacterial pathogens to evade drugs

Biologists have uncovered a new mode of communication inside cells that helps bacterial pathogens learn how to evade drugs.

30 Jan 2026

DNA repair enzyme failure triggers inflammation and accelerates aging in cells

If severe DNA damage is not repaired, the consequences for the health of cells and tissues are dramatic.

30 Jan 2026

Research uncovers why certain brain cells are more resilient to tau protein buildup

New research by UCLA Health and UC San Francisco has uncovered why certain brain cells are more resilient than others to the buildup of a toxic protein that is a hallmark of Alzheimer's disease and related dementias, potentially leading to new targets for therapies or treatments.

30 Jan 2026

Navigating the multi-dimensional world of modern cancer research

An enduring challenge for the study of human cancer is just how complex it is: how many different ways there are for cancers to originate, progress, and spread in the people who are diagnosed with them.

30 Jan 2026

Data-driven modeling uncovers dynamic genome folding in three dimensions

Chromosomes are masters of organization. These long strings of DNA fold down into an ensemble of compact structures that keep needed parts of the genome accessible while tucking away those that aren't used as often.

29 Jan 2026

Genetic inheritance and life experience leave distinct epigenetic marks in immune cells

The COVID-19 pandemic gave us tremendous perspective on how wildly symptoms and outcomes can vary between patients experiencing the same infection.

29 Jan 2026

Study uncovers genes and proteins likely to play a causal role in Type 2 diabetes

An international study co-led by researchers from the University of Massachusetts Amherst and Helmholtz Munich in Germany has uncovered hundreds of genes and proteins likely to play a causal role in Type 2 diabetes, many of which would have been missed by studies relying on blood samples alone.

29 Jan 2026

Neighborhood disadvantage accelerates biological aging through emotional distress

While scientists have long known that living in a disadvantaged neighborhood is associated with biological symptoms of accelerated aging, emotional distress accounts for a significant portion of these effects, researchers found in a recent study.

29 Jan 2026

How DNA and life experiences leave distinct marks on the human immune system

Using single-cell epigenomic profiling of immune cells from 110 individuals, researchers show that genetic variation and environmental exposures shape the human immune system through distinct DNA methylation mechanisms. Genetic effects concentrate within gene bodies of memory cells, while environmental exposures primarily remodel regulatory regions in naive immune cells.

28 Jan 2026

Tracking antibiotic resistance across environmental systems using advanced metagenomic tools

Antibiotic resistance is often framed as a hospital problem, but a growing body of evidence shows that the environment plays an equally critical role in the global spread of drug resistant bacteria.

27 Jan 2026

NIH grant advances Indigenous-driven genomic research in Alaska and Oklahoma

A transdisciplinary team led by Southcentral Foundation, a Tribal healthcare organization in Anchorage, Alaska, has been awarded a competitive grant from the National Institutes of Health. Jessica Blanchard, Ph.D., senior research scientist at the University of Oklahoma's Center for Applied Social Research, is a key collaborator on the project, representing the continuation of a longstanding partnership between OU and Southcentral Foundation.

27 Jan 2026

Large multi-ancestry study expands understanding of schizophrenia genetics

A landmark study led by researchers with the Department of Veterans Affairs has uncovered new genetic insights into schizophrenia by analyzing data from ancestrally diverse populations, including African Americans, through the Million Veteran Program (MVP) and Cooperative Studies Program (CSP).

24 Jan 2026

Genome News and Research

Next-generation sequencing expands possibilities for newborn screening

New liquid biopsy detects early cancers through epigenetic instability

Bat viruses in Indochina Peninsula reveal viral diversity, PEDV origins, and spillover risks

Scientists create new map showing how cancer gene mutations influence tumor growth

Genetic ancestry influences tumor biology and survival in head and neck cancers

Research reveals a link between defective DNA repair and immune-driven inflammatory disease

King’s researchers help transform UK mental health research infrastructure

New diagnostic framework addresses challenges of rapidly-mutating RNA viruses

New mode of communication inside cells helps bacterial pathogens to evade drugs

DNA repair enzyme failure triggers inflammation and accelerates aging in cells

Research uncovers why certain brain cells are more resilient to tau protein buildup

Navigating the multi-dimensional world of modern cancer research

Data-driven modeling uncovers dynamic genome folding in three dimensions

Genetic inheritance and life experience leave distinct epigenetic marks in immune cells

Study uncovers genes and proteins likely to play a causal role in Type 2 diabetes

Neighborhood disadvantage accelerates biological aging through emotional distress

How DNA and life experiences leave distinct marks on the human immune system

Tracking antibiotic resistance across environmental systems using advanced metagenomic tools

NIH grant advances Indigenous-driven genomic research in Alaska and Oklahoma

Large multi-ancestry study expands understanding of schizophrenia genetics

Genetics & Genomics - Second Edition eBook

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

Expanding access to NMR with the Fourier 80 Duo

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