TY - JOUR
AU - Willighagen, Egon
AB -  Doi:10.1145/ 2366316. 2 3 6 6 3 3 4 Open-source chemistry software and molecular databases broaden the research horizons of drug discovery. BY JoeRG KuRt WeGneR, aaRon steRLinG, RaJaRshi Guha, anDReas BenDeR, Jean-LouP fauLon, Janna hastinGs, noeL o'BoYLe, John oVeRinGton, heRman Van VLiJmen, anD eGon WiLLiGhaGen cheminformatics the life sciences produce information at an accelerating rate, with public data stores (such as the one managed by the European Bioinformatics Institute http://www.ebi. ac.uk) containing on the order of 10PB of biological information. For nearly 40 years, the same was not so nov e l te C h n ol oG ie s in for chemical information, but in 2004 a large public small-molecule structure repository (PubChem http://pubchem. ncbi.nlm.nih.gov) was made freely available by the National Library of Medicine (part of the U.S. National Institutes of Health) and soon followed by other databases. Likewise, while many of the foundational algorithms of cheminformatics have been described since the 1950s, open-source software implementing many of them have become accessible only since the mid-1990s.10 Why is chemical information important? Why should chemists and computer scientists care about its public availability? And how does chemical information relate to the field of computer science? Though 
TI - Cheminformatics
JF - Communications of the ACM
DO - 10.1145/2366316.2366334
DA - 2012-11-01
UR - https://www.deepdyve.com/lp/association-for-computing-machinery/cheminformatics-PoNHva5jW0
SP - 65
VL - 55
IS - 11
DP - DeepDyve
ER -