Researchers at a Harvard Medical School laboratory are uncertain how they will continue supporting a large public genetic database after its primary source of funding expired last month.

Working with his former doctoral student Pedro Feijão in 2009, he formulated the theoretical basis for a method of comparing entire genomes, known as the Single-Cut-or-Join (SCJ) operation, and last ...

A new bioinformatics tool, MHcut reveals that a natural repair system for DNA damage, microhomology-mediated end joining, is probably far more common in humans than originally assumed. Using MHcut and ...

"Fueled by advances in NGS and precision medicine, China’s DNA sequencing market sees rapid growth amid strong government support, rising clinical applications, and innovation hubs in Guangdong, ...

When Craig Venter's startup Celera beat the US government's Human Genome Project to sequencing human DNA, pundits heralded a new era in medicine. New drugs would target precise molecular processes, ...

Through cutting-edge methods and advanced artificial intelligence analysis, UNC Charlotte researchers leading a ...

A computer science lab challenges -- and beats -- deep learning in a test to see if a new bioinformatics approach effectively tracks the lab of origin of a synthetic genetic sequence. Tracking the ...

Using a computational platform and your DNA, bioinformatics startup InsideDNA aims to determine the right drug interaction for your body. The startup began three years ago as a cloud-based platform ...

Analysis of Roche KAPA Target Enrichment kit experimental data obtained on an Illumina sequencing system is most frequently performed using a variety of publicly available, open-source analysis tools.