TY - JOUR
T1 - Evaluating performance and applications of sample-wise cell deconvolution methods on human brain transcriptomic data
AU - PsychENCODE Consortium
AU - Dai, Rujia
AU - Chu, Tianyao
AU - Zhang, Ming
AU - Wang, Xuan
AU - Jourdon, Alexandre
AU - Wu, Feinan
AU - Mariani, Jessica
AU - Vaccarino, Flora M.
AU - Lee, Donghoon
AU - Fullard, John F.
AU - Hoffman, Gabriel E.
AU - Roussos, Panos
AU - Wang, Yue
AU - Wang, Xusheng
AU - Pinto, Dalila
AU - Wang, Sidney H.
AU - Zhang, Chunling
AU - Chen, Chao
AU - Liu, Chunyu
N1 - Publisher Copyright:
Copyright © 2024 The.
PY - 2024/5/24
Y1 - 2024/5/24
N2 - Sample-wise deconvolution methods estimate cell-type proportions and gene expressions in bulk tissue samples, yet their performance and biological applications remain unexplored, particularly in human brain transcriptomic data. Here, nine deconvolution methods were evaluated with sample-matched data from bulk tissue RNA sequencing (RNA-seq), single-cell/nuclei (sc/sn) RNA-seq, and immunohistochemistry. A total of 1,130,767 nuclei per cells from 149 adult postmortem brains and 72 organoid samples were used. The results showed the best performance of dtangle for estimating cell proportions and bMIND for estimating sample-wise cell-type gene expressions. For eight brain cell types, 25,273 cell-type eQTLs were identified with deconvoluted expressions (decon-eQTLs). The results showed that decon-eQTLs explained more schizophrenia GWAS heritability than bulk tissue or single-cell eQTLs did alone. Differential gene expressions associated with Alzheimer’s disease, schizophrenia, and brain development were also examined using the deconvoluted data. Our findings, which were replicated in bulk tissue and single-cell data, provided insights into the biological applications of deconvoluted data in multiple brain disorders.
AB - Sample-wise deconvolution methods estimate cell-type proportions and gene expressions in bulk tissue samples, yet their performance and biological applications remain unexplored, particularly in human brain transcriptomic data. Here, nine deconvolution methods were evaluated with sample-matched data from bulk tissue RNA sequencing (RNA-seq), single-cell/nuclei (sc/sn) RNA-seq, and immunohistochemistry. A total of 1,130,767 nuclei per cells from 149 adult postmortem brains and 72 organoid samples were used. The results showed the best performance of dtangle for estimating cell proportions and bMIND for estimating sample-wise cell-type gene expressions. For eight brain cell types, 25,273 cell-type eQTLs were identified with deconvoluted expressions (decon-eQTLs). The results showed that decon-eQTLs explained more schizophrenia GWAS heritability than bulk tissue or single-cell eQTLs did alone. Differential gene expressions associated with Alzheimer’s disease, schizophrenia, and brain development were also examined using the deconvoluted data. Our findings, which were replicated in bulk tissue and single-cell data, provided insights into the biological applications of deconvoluted data in multiple brain disorders.
UR - http://www.scopus.com/inward/record.url?scp=85194127882&partnerID=8YFLogxK
U2 - 10.1126/sciadv.adh2588
DO - 10.1126/sciadv.adh2588
M3 - Article
C2 - 38781336
AN - SCOPUS:85194127882
SN - 2375-2548
VL - 10
JO - Science advances
JF - Science advances
IS - 21
M1 - 2588
ER -