A new open-source web platform called CoMeDA unifies compositional data analysis and automated batch effect correction for ...
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Ambry Genetics launches whole genome sequencing tests to improve rare disease diagnosis
Ambry Genetics, a wholly owned subsidiary of Tempus AI (NASDAQ:TEM), has introduced GenomeNext and GenomeReveal, a new whole ...
A systematic subsampling analysis of twelve Hi-C libraries reveals that different chromatin metrics need vastly different ...
Prioritize recurring consumables, AI analytics, FFPE-compatible automation and end-to-end workflows; target oncology, research institutes and CRO partnerships.Dublin, Oct. 08, 2026 (GLOBE NEWSWIRE) -- ...
In a single experiment, scientists can decipher the entire genomes of many patient samples, animal models, or cultured cells. To fully realize the potential to study biology at this unprecedented ...
Long-read sequencing technologies analyze long, continuous stretches of DNA. These methods have the potential to improve researchers' ability to detect complex genetic alterations in cancer genomes.
Understand the stages of a standard RNA-seq bioinformatics workflow, including the role of QC, alignment, gene expression quantification, and specialized application analyses Identify key QC metrics ...
Ambry Genetics launches GenomeNext and GenomeReveal, whole genome sequencing solutions for diagnosing patients with rare ...
Modern sequencing technologies produce an intense amount of data, but raw reads alone can’t lead to novel biological insights. Well-designed bioinformatics workflows are now essential for rapidly ...
Understanding gene expression is a cornerstone of modern molecular biology and biomedical research. Whether studying disease mechanisms, drug responses, or developmental biology, accurate gene ...
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