Nucleotide News and Research

RSS

Study Links MICOS10 Gene Defect to Mitochondrial DNA Depletion Syndrome

Mitochondrial DNA depletion syndrome (MTDPS) is a rare genetic disorder characterized by a marked decrease in mitochondrial DNA (mtDNA).

27 Nov 2024

Novel Genetic Variant Associated with Severe Mitochondrial Dysfunction

The rare hereditary condition known as mitochondrial DNA depletion syndrome (MTDPS) is typified by a significant reduction in mitochondrial DNA (mtDNA).

26 Nov 2024

Discovery of Large Tandem Duplications Opens New Avenues for Cancer Treatment

Cancer researchers at the University of Chicago and the University of California, San Francisco (UCSF) have discovered that mutations in certain genes can lead to the accumulation of DNA errors, resulting in a specific type of genetic change known as large tandem duplications (TDs) that can arise from the collision of two critical cellular processes: transcription and DNA replication.

21 Nov 2024

Sylph: A Fast and Accurate Tool for Species-Level Metagenome Profiling

Sylph's innovative approach to metagenome profiling delivers high accuracy and efficiency, advancing research in microbial diversity and disease associations.

21 Nov 2024

How CRISPRi is Helping Combat Drug-Resistant Tuberculosis

Findings on isoniazid-resistant M. tuberculosis reveal key vulnerabilities, suggesting new avenues for treatment strategies against drug-resistant tuberculosis.

20 Nov 2024

Advanced Sequencing Uncovers Cause of Rare Mitochondrial Encephalopathy

Mitochondrial diseases are among the most prevalent hereditary metabolic disorders, known to occur in one out every 5000 births.

19 Nov 2024

New GIFT Method Outshines GWAS in Genetic Breakthrough

Genomic Informational Field Theory (GIFT) enhances genetic association detection, outperforming GWAS in mapping complex traits and subtle genetic interactions.

8 Nov 2024

Fabric Genomics partners with Intermountain Children’s Health to enhance precision diagnosis of infants and children using whole genome sequencing from Broad Clinical Labs

Fabric Genomics, the leader in artificial intelligence (AI)-powered next generation sequencing interpretation, is announcing a new partnership with Intermountain Children’s Health to analyze the whole genomes of children sequenced by the Broad Clinical Labs to help speed diagnosis of kids who may have genetic diseases.

From Fabric Genomics 30 Oct 2024

Unveiling the Molecular Mechanisms of CRISPR-Cas10's Cellular Shutdown

CRISPR-Cas9 can elegantly and precisely cut away any desired region of DNA and has long been compared to a type of genetic scissors.

29 Oct 2024

Unlocking the Secrets of Life Through Synthetic Biology

It is one of the most fundamental questions in science: how can lifeless molecules come together to form a living cell? Bert Poolman, Professor of Biochemistry at the University of Groningen, has been working on this problem for over twenty years.

22 Oct 2024

Study Unlocks Mechanisms Behind Nucleosome Arrays Using Signal Theory and Machine Learning

Findings show that machine learning can accurately predict nucleosome positions, emphasizing the relationship between nucleosome architecture and gene activity.

17 Oct 2024

Comprehensive multi-omics approach reveals detailed insights into diabetes mechanisms

In a recent study published in Nature Communications, researchers utilized a comprehensive multi-omics approach, integrating genomic, proteomic, and metabolomic data from a diverse cohort, to uncover detailed molecular interactions and identify distinct diabetes subgroups.

20 Sep 2024

Nucleotide News and Research

Study Links MICOS10 Gene Defect to Mitochondrial DNA Depletion Syndrome

Novel Genetic Variant Associated with Severe Mitochondrial Dysfunction

Discovery of Large Tandem Duplications Opens New Avenues for Cancer Treatment

Sylph: A Fast and Accurate Tool for Species-Level Metagenome Profiling

How CRISPRi is Helping Combat Drug-Resistant Tuberculosis

Advanced Sequencing Uncovers Cause of Rare Mitochondrial Encephalopathy

New GIFT Method Outshines GWAS in Genetic Breakthrough

Fabric Genomics partners with Intermountain Children’s Health to enhance precision diagnosis of infants and children using whole genome sequencing from Broad Clinical Labs

Unveiling the Molecular Mechanisms of CRISPR-Cas10's Cellular Shutdown

Unlocking the Secrets of Life Through Synthetic Biology

Study Unlocks Mechanisms Behind Nucleosome Arrays Using Signal Theory and Machine Learning

Comprehensive multi-omics approach reveals detailed insights into diabetes mechanisms

Modified Nucleotides Boost saRNA Vaccine Efficacy and Protection Against SARS-CoV-2

A Novel Method for Incorporating Non-Canonical Amino Acids into Proteins

CRISPR/Cas System Revolutionizes Tumor Variant and Biomarker Detection

Pan-Pathogen Deep Sequencing: A New Strategy in Combating Nosocomial Antimicrobial Resistant Bacterial Infections

High-Speed Atomic Force Microscopy Reveals Cofilin Binding Patterns in Actin Filaments

The Influence of 'Silent' Mutations on Genetic Disorders

Chloroplast Genome Research Enhances Identification and Breeding of Tea-Oil Camellia Species

CRISPR-Cas: A Promising Tool For Combatting Antibiotic-Resistant Staphylococcus aureus

Driving Support for Pharmaceutical Testing Through Continuous Innovation

From Memory to Metaplasticity: Unraveling the Brain's Secrets

Revolutionizing Mass Spectrometry: A Deep Dive into Plasmion’s SICRIT® Technology

Latest in Genomics