Article
myVCF: a desktop application for high-throughput mutations data management.
Bioinformatics (Oxford, England) - 15 Nov 2017
Pietrelli Alessandro, Valenti Luca
Abstract excerpt
SUMMARY: Next-generation sequencing technologies have become the most powerful tool to discover genetic variants associated with human diseases. Although the dramatic reductions in the costs facilitate the use in the wet-lab and clinics, the huge amount of data generated renders their management by non-expert researchers and physicians extremely difficult. Therefore, there is an urgent need of novel approaches...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
