The global next generation sequencing (NGS) market is expected to register a robust CAGR of around 15% over the next five years. This growth is primarily driven by the rising adoption of precision ...
Scientists using TwinsUK data and ultra‑precise DNA sequencing have uncovered rare DNA mutations in healthy tissue that could ...
Roche’s SBX sequencing achieved a world record for the fastest human genome analysis and is driving breakthroughs in ...
Researchers at UW’s School of Medicine and the Institute for Research in Biomedicine Barcelona may have found an additional explanation as to why men and smokers are more likely to develop bladder ...
News-Medical.Net on MSN
New genomic method enables multiple people with rare conditions to receive diagnoses
A new genomic method has enabled multiple people with rare conditions to receive diagnoses that were previously unattainable ...
This insightful review explores key areas of cancer genetic research, focusing on genes that may benefit from ...
Experts have developed a new method for identifying structural changes in DNA, providing insights for ~145 families and highlighting the importance of incorporating these changes into clinical ...
New research using data from the TwinsUK cohort has helped reveal how naturally occurring DNA mutations in healthy tissue may ...
“We hope that this new ability to study somatic mutations in non-invasive tissue biopsies from healthy individuals becomes a useful tool for cancer prevention, by improving our ability to identify ...
AZoLifeSciences on MSN
New Genomic Method Unlocks Diagnoses for Rare Conditions
A new genomic method has enabled multiple people with rare conditions to receive diagnoses that were previously unattainable ...
The findings show that disease-causing mutations were found in around 2% of the sperm from men in their early 30s, increasing ...
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