Genomics - Enhanced Genomics and The ALBORADA Drug Discovery Institute partner to accelerate Alzheimer's drug discovery
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Your Ultimate Guide to NGS Library PrepYour Ultimate Guide to NGS Library Prep

Discover how automation is transforming next-generation sequencing (NGS) workflows. Opentrons' resource hub explores key applications, from library prep to normalization, and highlights strategies for increasing throughput, consistency, and reproducibility in genomic research. Learn how streamlined NGS processes can accelerate discoveries across clinical, pharmaceutical, and academic settings.

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   Enhanced Genomics and The ALBORADA Drug Discovery Institute partner to accelerate Alzheimer's drug discoveryEnhanced Genomics and The ALBORADA Drug Discovery Institute partner to accelerate Alzheimer's drug discovery
 
Enhanced Genomics ('Enhanced'), the biotechnology company pioneering 3D multi-omics to rapidly identify high-confidence, genetically validated drug targets for common diseases, today announced a strategic partnership with The ALBORADA Drug Discovery Institute at the University of Cambridge.
 
   New DNA test predicts chemotherapy resistance in cancer patientsNew DNA test predicts chemotherapy resistance in cancer patients
 
Cancer Research UK-funded scientists at the University of Cambridge, in collaboration with the Spanish National Cancer Research Centre (CNIO) and Cambridge-based startup Tailor Bio, have created a test which can successfully predict whether cancer will resist common forms of chemotherapy treatment.
 
 Stress-activated gene damages insulin-producing cells in type 2 diabetes
 
Stress-activated gene damages insulin-producing cells in type 2 diabetesStress does no one - not even your insulin-producing cells - any good.
 
 
 UNIGE scientists uncover two key proteins that regulate chromatin remodelling
 
UNIGE scientists uncover two key proteins that regulate chromatin remodellingCells depend on the precise reading of DNA sequences to function correctly. This process, known as gene expression, determines which genetic instructions are activated.
 
 
 New technology unlocks cellular ancestry with DNA barcodes
 
New technology unlocks cellular ancestry with DNA barcodesA landmark study by WEHI scientists has shed new light on one of the most fundamental mysteries of biology: how cells divide and grow into the complex structures that make up our bodies.
 
 
 Single-cell sequencing maps immune changes in chronic myeloid leukemia
 
Single-cell sequencing maps immune changes in chronic myeloid leukemiaChronic myeloid leukemia (CML) is a hematopoietic malignancy characterized by BCR-ABL1 gene fusion.
 
 
 Innovative genome editing approach could be the key to lifelong effective weight management
 
Innovative genome editing approach could be the key to lifelong effective weight managementWeight-loss drugs have surged in popularity, promising rapid results with regular injections. Now, researchers from Japan report a way for the body to make its own weight-loss drugs, doing away with injections in favor of a one-time treatment.
 
 
 CRISPR-mediated DNA methylation editing regulates inflammation and tumor growth
 
CRISPR-mediated DNA methylation editing regulates inflammation and tumor growthGenes, fragments of DNA located on our chromosomes, control much of what happens in cells.
 
 
 Urine-based DNA test predicts bladder cancer recurrence after immunotherapy
 
Urine-based DNA test predicts bladder cancer recurrence after immunotherapyIn a multi-institutional study published in Science Direct, researchers revealed that testing urine-based tumor DNA (utDNA) can help predict which bladder cancer patients are at higher risk for recurrence after treatment.
 
 
 Gene therapy brings back hearing in young and adult deaf patients
 
Gene therapy brings back hearing in young and adult deaf patientsGene therapy can improve hearing in children and adults with congenital deafness or severe hearing impairment, a new study involving researchers at Karolinska Institutet reports.
 
 
 New gene editing approach targets mutation behind common genetic heart disease
 
New gene editing approach targets mutation behind common genetic heart diseaseFourteen million people worldwide suffer from enlarged hearts, or hypertrophic cardiomyopathy (HCM), a genetic disease that thickens the heart's walls, making it harder for the organ to pump blood - but many of them don't know it.
 
 
 Scientists use base editing to repair mitochondrial DNA mutations
 
Scientists use base editing to repair mitochondrial DNA mutationsIn a step toward treating mitochondrial diseases, researchers in the Netherlands have successfully edited harmful mutations in mitochondrial DNA using a genetic tool known as a base editor.
 
 
 Largest Indian genome study reveals 50,000 years of genetic history
 
Largest Indian genome study reveals 50,000 years of genetic historyWith around 5,000 different ethno-linguistic and religious groups, India is one of the most culturally and genetically diverse countries in the world.
 
 
 FAU researchers secure key grants to target new gene in the fight against glioblastoma
 
FAU researchers secure key grants to target new gene in the fight against glioblastomaFlorida Atlantic University researchers have secured two key grants to investigate targeting a gene for the first time as a new approach to treat glioblastoma, a very aggressive and fast-growing type of brain cancer.
 
 
 Gene Editing Halts Symptoms of Rare Smooth Muscle Disease in Preclinical Study
 
Gene Editing Halts Symptoms of Rare Smooth Muscle Disease in Preclinical StudyUsing gene editing in a preclinical model, researchers at UT Southwestern Medical Center blocked the symptoms of a rare smooth muscle disease before they developed.
 
 
 Study elucidates relationship between Type 2 diabetes and salivary enzyme gene
 
Study elucidates relationship between Type 2 diabetes and salivary enzyme geneA new Cornell University study brings additional clarity to the relationship between Type 2 diabetes and genes that express a salivary enzyme that breaks down starch.
 
 
 Understanding the human brain architecture through gene coexpression analysis
 
Understanding the human brain architecture through gene coexpression analysisIn a comprehensive Genomic Press Interview published in Brain Medicine, Dr. Michael C. Oldham shares his unconventional journey from advertising executive to computational neuroscientist and his groundbreaking contributions to understanding the human brain's cellular and molecular architecture through gene coexpression analysis.
 
 

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