Scientists at USC have definitively demonstrated that large sets of variations in the genetic code that do not individually appear to have much effect can collectively produce significant changes in ...
Researchers still do not have a comprehensive picture of the factors that influence gene expression in human cancers. Understanding gene expression in cancer is important because it can reveal how the ...
Since the first sequencing of a human genome more than 20 years ago, the study of human genomes has relied almost exclusively on a single reference genome to which others are compared to identify ...
EMBL researchers created SDR-seq, a next-generation tool that decodes both DNA and RNA from the same cell. It finally opens ...
Researchers have constructed a rough draft of a human pangenome, a collection of DNA that represents the genetic information from 47 individuals. The development — a landmark in genomics — magnifies ...
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Cracking India's genetic code
(NOTE: This article was originally published in the India Today issue dated April 28, 2025) India's largest-ever genomic study has identified genetic variants unique to the country, marking a crucial ...
The study of the genomes of our closest relatives, the Neanderthals and Denisovans, has opened up new research paths that can broaden our understanding of the evolutionary history of Homo sapiens. A ...
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Web-based tool improves CRISPR accuracy by identifying off-target effects across genetic variations
Genome editing technologies like CRISPR-Cas9 have transformed biology, medicine, and agriculture, but concerns remain about unintended edits at off-target DNA sites. These off-target effects can cause ...
Since the first sequencing of the human genome more than 20 years ago, the study of human genomes has relied almost exclusively on a single reference genome to which others are compared to identify ...
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