Top-Down Proteomics: Bridging the Genotype-to-Phenotype Gap

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	Genomics
	The latest genomics news from News Medical

Top-Down Proteomics: Bridging the Genotype-to-Phenotype Gap

In an enlightening interview with Neil Kelleher conducted at Pittcon 2023, Neil explores bridging the gap between genotypes and phenotypes.

Expect more insights within the field of Bioanalytics & Life Sciences at Pittcon 2024 in San Deigo!

Read the Full Interview Here

Discover important aspects of the genomic analysis of inherited cancer

Join Samantha Butler, Senior Principal Clinical Scientist in the NHS, and Sam Clokie, Director of Bioinformatics at Nonacus, as they discuss the important aspects of genomic testing for inherited cancers, including guidelines, challenges, and solutions within a clinical setting.

Join Clinical Experts

New study investigates role of rare gene variants in IBD risk for African Americans

The advent of whole genome sequencing technology has prompted an explosion in research into how genetics are associated with disease risk.

	New study identifies 4,749 key gene clusters that influence progression of 32 cancer types Researchers at the Mount Sinai Center for Transformative Disease Modeling have released a groundbreaking study identifying 4,749 key gene clusters, termed "prognostic modules," that significantly influence the progression of 32 different types of cancer.

	Gene therapy for rare diseases: A decade of progress and remaining challenges A new review article in the peer-reviewed journal Human Gene Therapy summarizes the significant milestones in the development of gene therapy medicinal products that have facilitated the treatment of a significant number of rare diseases.

	Long-term monitoring of gene therapy patients crucial for safety, study says Medical research has shown promising results regarding the potential of gene therapy to cure genetic conditions such as sickle cell disease and the findings of this study, published in Nature Medicine, offer important new insights into processes happening in the body after treatment.

	Experts recommend genomics for tackling antimicrobial resistance, outline key strategies for effective surveillance The Lancet Microbe article summarizes discussions by the Surveillance and Epidemiology of Drug-resistant Infections Consortium on using genomics for antimicrobial resistance surveillance, highlighting its benefits and challenges and providing key recommendations for effective implementation.

	Non-invasive genetic test for fetal DNA sequencing developed A team of investigators from Massachusetts General Hospital (MGH), Brigham and Women's Hospital (BWH), and the Broad Institute of MIT and Harvard have developed a non-invasive genetic test that can screen the blood of pregnant individuals to survey all genes for fetal DNA sequence variants.

	Epimutations in BRCA1 Gene Linked to Triple-Negative Breast Cancer Research reveals that around 20 per cent of all cases of the most severe form of breast cancer may arise from the small group of normal tissue cells carrying an epimutation of a specific gene.

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