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 impetus for this study was to quantify the extent of genetic variation and inbreeding in Thoroughbreds,” said Ernest ...

The next-generation sequencing market valued at US$ 13.92 billion in 2023, is forecasted to grow at a robust CAGR of 11.0%, ...

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

Long read sequencing revealed more genetic information in cases of 42 patients with rare diseases while cutting time and cost of diagnoses.

The Genome India project was launched in 2020 to collect genome samples across diverse sections of the Indian society and conduct whole genome sequencing of 10,000 such samples. Genome sequencing of ...

Methods We performed whole-genome sequencing on six pathologically confirmed patients with OCCC ... Statistical analysis was performed with the R system version 3.5.0 or GraphPad Prism version 6.00.

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