Protein function in precision medicine: deep understanding with machine learning

被引:34
|
作者
Rost, Burkhard [1 ]
Radivojac, Predrag [2 ]
Bromberg, Yana [3 ]
机构
[1] Tech Univ Munich, Inst Adv Studies, Dept Informat & Bioinformat, Garching, Germany
[2] Indiana Univ, Sch Informat & Comp, Bloomington, IN USA
[3] Rutgers State Univ, Dept Biochem & Microbiol, New Brunswick, NJ USA
基金
美国国家科学基金会;
关键词
computational prediction; molecular mechanism of disease; protein function; variant effect; ONLINE MENDELIAN INHERITANCE; SECONDARY STRUCTURE; SEQUENCE VARIANTS; CRYSTAL-STRUCTURE; PATHWAY ANALYSIS; CANDIDATE GENES; PREDICTION; DISEASE; BIOINFORMATICS; MUTATIONS;
D O I
10.1002/1873-3468.12307
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Precision medicine and personalized health efforts propose leveraging complex molecular, medical and family history, along with other types of personal data toward better life. We argue that this ambitious objective will require advanced and specialized machine learning solutions. Simply skimming some low-hanging results off the data wealth might have limited potential. Instead, we need to better understand all parts of the system to define medically relevant causes and effects: how do particular sequence variants affect particular proteins and pathways? How do these effects, in turn, cause the health or disease-related phenotype? Toward this end, deeper understanding will not simply diffuse from deeper machine learning, but from more explicit focus on understanding protein function, context-specific protein interaction networks, and impact of variation on both.
引用
收藏
页码:2327 / 2341
页数:15
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