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.

Researchers develop an advanced tool for accurate assembly of organelle genomes

The mitochondrial genome and plastid genome denote the parts of endosymbiotic organelle inheritance in eukaryotes that have persisted in organelles.

16 Sep 2020

Study may lead to future treatments for hearing loss

Scientists have performed a study that has successfully established the role played by a crucial protein in the development of hair cells.

14 Sep 2020

Scientists visualize the exact timepoint when tumor initiating cells became immortal

Worldwide, cancer is the second leading cause of death - in 2018 alone, it claimed approximately 9.6 million lives, or one in six deaths.

14 Sep 2020

Study shows how genetic variants affect gene regulation and contribute to disease risk

The multi-institutional Genotype-Tissue Expression (GTEx) Consortium has published its final series of studies, as part of a final-phase initiative.

14 Sep 2020

CRISPR in a Box: New educational gene editing tool kit

Introducing CRISPR in a Box™ - it's not a new crunchy cereal or the latest snack - it's an educational tool kit consisting of state-of-the-science gene editing technology that could be coming to a school near you.

10 Sep 2020

Researchers develop statistical model that predicts risk of developing esophageal cancer

Globally, esophageal cancer is said to be the eighth most common cancer and it usually develops from a condition known as Barrett’s esophagus.

9 Sep 2020

Zika virus infection during pregnancy can cause severe abnormalities in the fetus

Zika virus infection during pregnancy can cause severe abnormalities in the fetus, including malformations such as microcephaly. In a small proportion of cases, the disease may lead to miscarriage and perinatal death.

4 Sep 2020

New technique tracks human milk nutrients in infant gut microbiome

A new study in mice helps explain why gut microbiomes of breastfed infants can differ greatly from those of formula-fed infants.

2 Sep 2020

Scientists publish most comprehensive genome information for major agricultural weeds

Representing some of the most troublesome agricultural weeds, waterhemp, smooth pigweed, and Palmer amaranth impact crop production systems across the U.S. and elsewhere with ripple effects felt by economies worldwide.

28 Aug 2020

Novel computational approach helps find genetic causes of severe childhood brain disorders

A team of researchers at Children's Hospital of Philadelphia affiliated with the CHOP Epilepsy Neurogenetics Initiative (ENGIN) have combined clinical information with large-scale genomic data to successfully link characteristic presentations of childhood epilepsies with specific genetic variants.

27 Aug 2020

Study reveals key biomolecule that can heal damaged heart tissues

When a person suffers a heart attack, parts of the heart can become stiff and scarred, leading to disability and possible progression toward heart failure.

26 Aug 2020

Genetic background influences cancer risk in individuals with single-gene variants

Life can change dramatically when someone learns they are genetically predisposed to a disease, such as a condition called familial hypercholesterolemia, where a mutated gene can lead to elevated cholesterol and increased risk for a premature heart attack.

21 Aug 2020

Study sheds light on inner workings of the human heart

Researchers have investigated the function of a complex mesh of muscle fibers that line the inner surface of the heart.

20 Aug 2020

Greater gut microbial diversity in kidney cancer patients linked to better treatment outcomes

Physicians at City of Hope, working in collaboration with scientists at Translational Genomics Research Institute (TGen), have found that greater gut microbial diversity in patients with metastatic kidney cancer is associated with better treatment outcomes on Food and Drug Administration-approved immunotherapy regimens.

20 Aug 2020

Extrachromosomal DNA with potential to cause cancer drives poor patient outcomes

The multiplication of genes located in extrachromosomal DNA that have the potential to cause cancer drives poor patient outcomes across many cancer types, according to a Nature Genetics study published Aug. 17, 2020 by a team of researchers including Professors Vineet Bafna and Dr.Paul Mischel of the University of California San Diego and Professor Roel Verhaak of Jackson Laboratories.

From UC San Diego 18 Aug 2020

Switching off 'master regulator' may offer neuroprotection from Parkinson's-related damage

Switching off a molecular "master regulator" may protect the brain from inflammatory damage and neurodegeneration in Parkinson's disease, reports a study published today in Nature Neuroscience.

18 Aug 2020

Genome analysis helps identify 568 cancer driver genes

Analysis of the genomes of 28,000 tumors from 66 types of cancer has led to the identification of 568 cancer driver gene.

18 Aug 2020

Novel technique of biofortification converts leaves into nutrient stores

A new collaborative study led by researchers from the Spanish National Research Council (CSIC) at the Centre for Research in Agricultural Genomics (CRAG) in Barcelona and the Institute for Plant Molecular and Cellular Biology (IBMCP) in Valencia describes a promising strategy to improve the nutritional benefits of crops.

18 Aug 2020

Single-cell analysis uncovers new details concerning mitochondrial diseases

Investigators led by a team at Massachusetts General Hospital (MGH) have made discoveries at the single cell level to uncover new details concerning mitochondrial diseases-- inherited disorders that interfere with energy production in the body and currently have no cure.

14 Aug 2020

New study shows how mitochondrial calcium transporter evolved over the years

According to a study performed by IRB Barcelona, the system that controls calcium levels in cells duplicated, giving rise to a pair of non-equivalent systems.

13 Aug 2020

Genomics News and Research

Further Reading

Researchers develop an advanced tool for accurate assembly of organelle genomes

Study may lead to future treatments for hearing loss

Scientists visualize the exact timepoint when tumor initiating cells became immortal

Study shows how genetic variants affect gene regulation and contribute to disease risk

CRISPR in a Box: New educational gene editing tool kit

Researchers develop statistical model that predicts risk of developing esophageal cancer

Zika virus infection during pregnancy can cause severe abnormalities in the fetus

New technique tracks human milk nutrients in infant gut microbiome

Scientists publish most comprehensive genome information for major agricultural weeds

Novel computational approach helps find genetic causes of severe childhood brain disorders

Study reveals key biomolecule that can heal damaged heart tissues

Genetic background influences cancer risk in individuals with single-gene variants

Study sheds light on inner workings of the human heart

Greater gut microbial diversity in kidney cancer patients linked to better treatment outcomes

Extrachromosomal DNA with potential to cause cancer drives poor patient outcomes

Switching off 'master regulator' may offer neuroprotection from Parkinson's-related damage

Genome analysis helps identify 568 cancer driver genes

Novel technique of biofortification converts leaves into nutrient stores

Single-cell analysis uncovers new details concerning mitochondrial diseases

New study shows how mitochondrial calcium transporter evolved over the years

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