Discover the top genomics startups revolutionizing genome sequencing technologies to enhance disease prevention and treatment ...

Long-read sequencing may be a better option for rare disease diagnosis than short-read sequencing, according to a recent ...

The innovation, he says, could transform the way scientists measure and address genomic breaks in gene-editing systems.

The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more ...

Comment from Associate Professor Jun Takayama, Tohoku University School of Medicine "The accuracy validation using the RASEN ...

AlleyWatch sat down with Nucleus CEO and Founder Kian Sadeghi to learn more about the business, its future plans, and recent ...

MyOme, a leading clinical innovation whole genomic analysis and polygenic risk modelling (PRS) company announced a strategic partnership with Novi Health, a company focused on delivering personalized ...

The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more ...

The SOLiD System's ability to generate over 400 million sequence tags (35−50-bp sequence reads) in a single run enables whole-genome ... third-party tools compatible with SOLiD sequencing ...