Automated Image-Based Phenotypic Screening for High-Throughput Drug Discovery

被引:0
|
作者
Singh, Rahul [1 ,3 ]
Pittas, Michalis [1 ]
Heskia, Ido [2 ]
Xu, Fengyun [3 ]
McKerrow, James [3 ]
Caffrey, Conor R.
机构
[1] San Francisco State Univ, Dept Comp Sci, San Francisco, CA 94132 USA
[2] San Francisco State Univ, Dept Math, San Francisco, CA 94132 USA
[3] Univ California, Sndler Ctr Basic Res Parasit Dis, San Francisco, CA 94158 USA
关键词
MEAN-SHIFT; TRACKING;
D O I
暂无
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
At the state-of-the-art in drug discovery, one of the key challenges is to develop high-throughput screening (HTS) techniques that can measure changes as a continuum of complex phenotypes induced in a target pathogen. Such measurements are crucial in developing therapeutics against diseases like schistosomiasis, trypanosomiasis, and leishmaniasis, which impact millions worldwide. These diseases are caused by parasites that can manifest a variety of phenotypes at any given point in time in response to drugs. Consequently, a single end-point measurement of 'live or death' (e.g., ED50 value) commonly used for lead identification is over-simplistic. In our method to address this problem, the parasites are tracked during the entire course of (video) recorded observations and changes in their appearance-based and behavioral characteristics quantified using geometric, texture-based, color-based, and motion-based descriptors. Subsequently, within the on-line setting, machine learning techniques are used classify the exhibited phenotypes into well defined categories. Important advancements introduced as a consequence of the proposed approach include: (1) ability to assess the interactions between putative drugs and parasites in terms of multiple appearance and behavior-based phenotypes, (2) automatic classification and quantification of pathogen phenotypes. Experimental data from lead identification studies against the disease Schistosomiasis validate the proposed methodology.
引用
收藏
页码:198 / +
页数:2
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