You can create a release to package software, along with release notes and links to binary files, for other people to use. Learn more about releases in our docs.

Install vg following its README. Version 1.63.0 or later is required for long-read mapping. Also install rpvg following its README. If you don't want to follow the ...

In recent years, scientific advancements have transformed our understanding of diseases, particularly at the cellular level.

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

This is thanks to advances in bulk and single-cell RNA-sequencing (RNA-seq) technologies that can capture every RNA molecule expressed in a cell: its transcriptome. The computational methods ...

Long-read sequencing is being harnessed to improve the rate of rare disease diagnosis. Researchers at the University of California Santa Cruz (CA, USA) have demonstrated that long-read sequencing (LRS ...

I don’t think proteomics will win over genomics," Sanghera said. "They go hand-in-glove. We’ve been overly focused [on genomics], and now we’re going to see an emergence of proteomics. And when the ...

Dr. Aaron Wenger tells us about SPRQ chemistry, highlighting its unique benefits and role in expanding our understanding of rare diseases.