A streamlined, automated process helps scientists coordinate site-ready production-level whole genome sequencing results.

SAVANA uses a machine learning algorithm to identify cancer-specific structural variations and copy number aberrations in long-read DNA sequencing data. The complex structure of cancer genomes means ...

Advances in next-generation sequencing (NGS) have propelled genomics research to new heights. With the introduction of new sequencing platforms such as Element Biosciences’ AVITI and Ultima Genomics’ ...

Although machine learning (ML) and other artificial intelligence tools are useful to analyze the massive amounts of data being generated by sequencing technologies, most ML tools are difficult for non ...

BOSTON, Oct. 30, 2024 /PRNewswire/ -- Volta Labs™, a genomics applications company, announced today that it has joined the PacBio Compatible program, further expanding the partnership between Volta ...

Automated library preparation is critical for reducing errors, increasing repeatability, and reducing hands-on time, allowing researchers to generate sequence data from DNA more quickly. The CyBio ...

The study finds that AI can reduce certain burdens by managing intrinsic load more efficiently than traditional classroom ...