The team profiled more than 600,000 cells from across the fish to build the whole-body single-cell transcriptome atlas of which genes are active in which cell. A cell’s transcriptome is the full set of RNA molecules it has made from its…
Complexity of pancreatic cancer reproduced in the laboratory The team used machine learning to categorize the newly grown organoids based on their morphologies in defined groups for further systematic analyses. "We identified different phenotypes within the two subtypes epithelial and…
Dublin, Oct. 29, 2026 (GLOBE NEWSWIRE) -- "Slide-Deoxyribonucleic Acid (DNA)-Sequencing for Copy Number Mapping Global Market Report 2026" has been added to ResearchAndMarkets.com's offering. The global slide-deoxyribonucleic acid (DNA) sequencing for copy number mapping market is experiencing rapid growth, supported by advances…
Adapting to serine and glycine scarcity rewires mitochondrial metabolism in pancreatic cancer cells and increases their cancer stem cell frequency, invasion and tumorigenicity.
Researchers have rebuilt the whitening transformation on a probabilistic footing, making correlation removal in ultra-high-dimensional genetic data faster and more accurate. New Whitening Method Speeds Up Giant Genetic Data Analysis News Source: Juliet Wilcox. (October 28, 2026). New Whitening Method Speeds Up…
This is why understanding the interactions surrounding G4 is so important. Biochemical assays give us more information about the intricacies of these interactions. These assays assess the way DNA and proteins interact, which occurs in processes such as DNA replication, transcription,…
An open-access study combined label-free brightfield microscopy, machine learning, and SHAP-based explainability to classify 17,781 red blood cells across ten morphology classes with an F1 score of 0.89.
An open-source pipeline called WEAP automates whole-exome sequencing analysis from raw reads to annotated variants, running key steps up to 7.7-fold faster than serial processing.
The work is the first major output of the TenK10K project, which seeks to map genetic variation and gene activity in immune cells from 10,000 people. With our findings, we've gone from understanding very few to thousands of the potential causal mechanisms…
Researchers have introduced HALE, an NP-hard optimization-based algorithm that corrects long-read sequencing errors while preserving haplotype-specific variation, matching the accuracy of state-of-the-art tools on human and plant genomes.
Software and methods for biological data: sequence analysis, genome assembly, variant calling, analysis pipelines and new algorithms.
An article joins this feed when it matches these terms. Each one is also a search of its own.