Advances in Genomics for Drug Development

被引:16
|
作者
Spreafico, Roberto [1 ]
Soriaga, Leah B. [1 ]
Grosse, Johannes [1 ]
Virgin, Herbert W. [1 ]
Telenti, Amalio [1 ]
机构
[1] Vir Biotechnol Inc, San Francisco, CA 94158 USA
关键词
druggability; loss-of-function; CRISPR; WIDE CRISPR SCREEN; OF-FUNCTION MUTATIONS; GENETIC SCREENS; IDENTIFIES GENES; CELL ATLAS; ZIKA VIRUS; TARGET; DISCOVERY; PLATFORM; SCALE;
D O I
10.3390/genes11080942
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Drug development (target identification, advancing drug leads to candidates for preclinical and clinical studies) can be facilitated by genetic and genomic knowledge. Here, we review the contribution of population genomics to target identification, the value of bulk and single cell gene expression analysis for understanding the biological relevance of a drug target, and genome-wide CRISPR editing for the prioritization of drug targets. In genomics, we discuss the different scope of genome-wide association studies using genotyping arrays, versus exome and whole genome sequencing. In transcriptomics, we discuss the information from drug perturbation and the selection of biomarkers. For CRISPR screens, we discuss target discovery, mechanism of action and the concept of gene to drug mapping. Harnessing genetic support increases the probability of drug developability and approval.
引用
收藏
页码:1 / 19
页数:19
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