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Cell-free DNA employed to identify measurable residual disease

Researchers demonstrated that cell-free DNA from CSF could be employed to examine MRD in children treated for the brain tumor medulloblastoma.

25 Oct 2021

Study uncovers new gene variants that may cause inherited retinal dystrophies

An international team of researchers, led by scientists at University of California San Diego and Shiley Eye Institute at UC San Diego Health, has broadened and deepened understanding of how inherited retinal dystrophies (IRDs) affect different populations of people and, in the process, have identified new gene variants that may cause the diseases.

20 Oct 2021

Researchers map proteo-genomic connections between different human diseases

Hundreds of connections between different human diseases have been uncovered through their shared origin in our genome by an international research team led by scientists from the Medical Research Council (MRC) Epidemiology Unit at the University of Cambridge, challenging the categorisation of diseases by organ, symptoms, or clinical speciality.

18 Oct 2021

AI-powered tool rapidly identifies genetic causes of rare disorders with high accuracy

An artificial intelligence (AI)-based technology rapidly diagnoses rare disorders in critically ill children with high accuracy, according to a report by scientists from University of Utah Health and Fabric Genomics, collaborators on a study led by Rady Children's Hospital in San Diego. The benchmark finding, published in Genomic Medicine, foreshadows the next phase of medicine, where technology helps clinicians quickly determine the root cause of disease so they can give patients the right treatment sooner.

From The University of Utah 18 Oct 2021

New research center brings advancements in genomic medicine to admixed individuals

One way to make health care more personalized is to use a person's DNA sequence -; or genome -; to predict their risk of disease. But as the field of precision medicine grows, so have concerns that we may be leaving a large fraction of Americans out.

From UC San Diego 13 Oct 2021

Experts come up with a powerful tool for illustrating genome folding

The intricate folds and arrangements of protein and DNA bundles inside the microscopic boundaries of a single human cell instruct the fate of an individual

13 Oct 2021

Experts create “living medicine” to combat biofilms on medical implants

Scientists have developed the first “living medicine” to treat antibiotic-resistant bacteria thriving on medical implants’ surfaces.

8 Oct 2021

Genome Research' special issue covers advanced developments in single-cell genomics

Genome Research (https://genome.org) publishes a special issue highlighting novel advances and insights in Single-cell Genomics.

5 Oct 2021

Supercomputer-driven dynamic model reveals hidden process in X chromosome inactivation

Using supercomputer-driven dynamic modeling based on experimental data, researchers can now probe the process that turns off one X chromosome in female mammal embryos.

5 Oct 2021

Researchers uncover previously unknown interactions between proteins that drive cancers

In three studies from the Cancer Cell Map Initiative, researchers uncovered previously unknown interactions between proteins that drive cancer and combined this new data to generate a map of protein pathways informing cancer outcomes.

1 Oct 2021

Study employs machine learning to predict outcomes in agriculture

Recent research emphasizes that machine learning can identify “genes of importance” that support crops to grow with reduced fertilizer.

From New York University (NYU) 28 Sep 2021

Researchers examine the deep past of human population dynamics

The current year marks the 20th anniversary of human genome sequencing. To mark this event, scientists headed by Professor Qiaomei Fu from the Institute of Vertebrate Paleontology and Paleoanthropology (IVPP) of the Chinese Academy of Sciences reviewed the current progress in the area of ancient DNA (aDNA)—DNA acquired from the remains of past organisms.

28 Sep 2021

Research provides new insights into growth hormone receptor gene's evolutionary history

A new study delves into the evolution and function of the human growth hormone receptor gene, and asks what forces in humanity's past may have driven changes to this vital piece of DNA.

27 Sep 2021

Tumor suppressor protein binding to RNA also binds DNA, says study

Scientists from the Medical University of South Carolina earlier displayed how hnRNP E1 attaches to metastatic-linked RNAs to prevent their translation.

27 Sep 2021

Master regulator behind the development of antibody-producing cells identified

Scientists from Weill Cornell Medicine recently found the master regulator behind the development of antibody-creating cells.

27 Sep 2021

Structural parameters of phosphatidylglycerol-DNA complex revealed

An interaction of DNA with lipids is of great interest because of their functions. As fatty acids and lipids can specifically bind to nucleic acids forming a code sequence of the genomic DNA, it is important to study the interaction of the oligonucleotide DNA (dA)20-(dT)20 with phosphatidylglycerol by the molecular dynamics method.

24 Sep 2021

NIH to renew grants to continue building the ClinGen resource

In an effort to continue building the Clinical Genome Resource, the National Institutes of Health will be renewing three awards amounting to $73.2 million over five years.

From National Human Genome Research Institute (NHGRI) 24 Sep 2021

Naturally occurring protein that blocks inflammatory response linked to better stroke recovery in mice

A naturally occurring protein that blocks an inflammatory immune response was associated with better stroke recovery in a study conducted in mice, according to preliminary research to be presented at the American Heart Association's Vascular Discovery: From Genes to Medicine Scientific Sessions 2021.

23 Sep 2021

Potential biomarkers help diagnose progressive stages of liver disease

Results of national research pinpointed potential biomarkers that could ultimately be employed for the diagnosis of progressive stages of liver disease.

23 Sep 2021

Genetic and epigenetic origin of pediatric liver cancer uncovered

Researchers at Hiroshima University have analyzed the molecular findings of almost 160 pediatric liver cancer cases and discovered molecular markers that should help to understand and treat the considerable variation in prognoses.

22 Sep 2021

Genomic News and Research

Cell-free DNA employed to identify measurable residual disease

Study uncovers new gene variants that may cause inherited retinal dystrophies

Researchers map proteo-genomic connections between different human diseases

AI-powered tool rapidly identifies genetic causes of rare disorders with high accuracy

New research center brings advancements in genomic medicine to admixed individuals

Experts come up with a powerful tool for illustrating genome folding

Experts create “living medicine” to combat biofilms on medical implants

Genome Research' special issue covers advanced developments in single-cell genomics

Supercomputer-driven dynamic model reveals hidden process in X chromosome inactivation

Researchers uncover previously unknown interactions between proteins that drive cancers

Study employs machine learning to predict outcomes in agriculture

Researchers examine the deep past of human population dynamics

Research provides new insights into growth hormone receptor gene's evolutionary history

Tumor suppressor protein binding to RNA also binds DNA, says study

Master regulator behind the development of antibody-producing cells identified

Structural parameters of phosphatidylglycerol-DNA complex revealed

NIH to renew grants to continue building the ClinGen resource

Naturally occurring protein that blocks inflammatory response linked to better stroke recovery in mice

Potential biomarkers help diagnose progressive stages of liver disease

Genetic and epigenetic origin of pediatric liver cancer uncovered

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