ISMB
In a keynote address at ISMB-ECCB, Dana Pe'er reviewed the development of single-cell analysis techniques that have been 20 years in the making.
EHR vendors have a new standard for sharing disease and phenotype data to aid clinical decision support, particularly in rare and hereditary conditions.
Software being built or updated for COVID-19 in India and Texas should be adaptable to future biosurveillance needs, developers say.
PyxisMap, unveiled at the recent ISMB conference, might soon be able to remove the human element from finding causal variants for rare diseases.
Research presented at the Intelligent Systems for Molecular Biology conference shows promise in uncovering more SNP-phenotype links in GWAS.
Jul 24, 2017
Jul 23, 2011