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Exome-Enriched Single-Nuclei Isoform Sequencing | Ebooks
2+ day, 6+ hour ago (221+ words) Get a More Complete View of RNA in Individual Cells Measuring gene expression can reveal which genes are active, but it does not always show the full picture. Different versions of the same gene, known as transcript isoforms, can play…...
BenchHub Turns Computational Biology Benchmarking Into a Living,
12+ hour, 2+ min ago (618+ words) Every day, computational biologists release new methods for analyzing genomes, single cells, microbiomes and molecular signatures, and every day researchers struggle with the same question: which method actually works best for their data? The answer usually depends on benchmarks—structured…...
Scientists Combine Genome and Gene Expression Data to Pinpoint Genes That
14+ hour, 50+ min ago (580+ words) Plant height may seem like a simple trait, but in soybean it sits at the heart of one of agriculture’s most consequential trade-offs. Tall plants can shade weeds and capture light, yet they topple in wind and rain, complicate harvest,…...
Prime Editing Gets a Size Upgrade: Researchers Insert Large DNA Fragments
21+ hour, 1+ min ago (653+ words) The gene-editing field has long faced a stubborn trade-off. Tools such as CRISPR-Cas9 excel at cutting DNA and at making small, targeted changes, but installing large pieces of genetic material into a genome at a precise location — without causing collateral…...
AlphaGenome Atlas maps more than 9 billion possible DNA changes
3+ day, 40+ min ago (883+ words) AlphaGenome Atlas predicts the effects of more than 9 billion possible DNA changes. Learn what AVI does—and why this is not a diagnostic tool. That distinction matters. The Atlas is a map of predictions about DNA function, not a catalog…...
Rising Sparks: Neha Talluri, computational biology - Morgridge Institute for Research
3+ day, 47+ min ago (705+ words) by Dennis Chaptman | September 10, 2026 Neha Talluri’s childhood ambitions were shaped by her grandparents, who ran a free clinic in India. Their example drew her to medicine as a form of service, and medical school was always Talluri’s goal — until her…...
New AI Model for DNA Learns from Evolution to Study the Human Genome - University of California, Berkeley
3+ day, 9+ hour ago (656+ words) UC Berkeley researchers have created a new genomic language model, called GPN-Star, that excels at spotting genetic variants that impact human health. More than two decades after scientists first sequenced the entire human genome — all 3 billion “letters,” or base pairs,…...
Advancing whole-genome sequencing with long-range data
3+ day, 8+ hour ago (162+ words) The system is able to unlock challenging genomic regions, structural variants, and phased variant calls across the human genome, resulting in an extensive, high-accuracy human genome made simple. The workflow delivers powerful genomic insights and only needs simple library preparation....
AI Identifies Disease-Relevant Genetic Variants
3+ day, 8+ hour ago (596+ words) More than two decades after scientists first sequenced the entire human genome — all 3 billion “letters,” or base pairs, of DNA code — the meaning of much of this code remains a mystery. Researchers at UC Berkeley have created a new genomic language…...
Exeter researcher pioneers AlphaGenome Atlas, identifying genetic regions that could link to disease
3+ day, 8+ hour ago (281+ words) University of Exeter News The University of Exeter has collaborated with Google DeepMind, becoming among the first researchers in the world to test a new platform which contain predictions for the effects of 9 billion genetic variants – every single letter change…...