A practical guide to linking brain-wide gene expression and neuroimaging data

被引:446
作者
Arnatkeviciute, Aurina [1 ]
Fulcher, Ben D. [1 ,2 ]
Fornito, Alex [1 ]
机构
[1] Monash Univ, Sch Psychol Sci, Monash Inst Cognit & Clin Neurosci, Brain & Mental Hlth Res Hub, 770 Blackburn Rd, Clayton, Vic 3168, Australia
[2] Univ Sydney, Sch Phys, Sydney, NSW 2006, Australia
基金
澳大利亚研究理事会; 澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Gene expression; Transcriptome; Allen human brain atlas; MRI; Connectome; Genome; Genetics; CORTICOBASAL DEGENERATION; MICROARRAY EXPERIMENTS; MOTION CORRECTION; IMAGING GENETICS; COMMON VARIANTS; RNA-SEQ; ASSOCIATION; RISK; TRANSCRIPTOME; NETWORKS;
D O I
10.1016/j.neuroimage.2019.01.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The recent availability of comprehensive, brain-wide gene expression atlases such as the Allen Human Brain Atlas (AHBA) has opened new opportunities for understanding how spatial variations on molecular scale relate to the macroscopic neuroimaging phenotypes. A rapidly growing body of literature is demonstrating relationships between gene expression and diverse properties of brain structure and function, but approaches for combining expression atlas data with neuroimaging are highly inconsistent, with substantial variations in how the expression data are processed. The degree to which these methodological variations affect findings is unclear. Here, we outline a seven-step analysis pipeline for relating brain-wide transcriptomic and neuroimaging data and compare how different processing choices influence the resulting data. We suggest that studies using the AHBA should work towards a unified data processing pipeline to ensure consistent and reproducible results in this burgeoning field.
引用
收藏
页码:353 / 367
页数:15
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