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Gene-set Enrichment with Mathematical Biology (GEMB)

BACKGROUND: Gene-set analyses measure the association between a disease of interest and a “set" of genes related to a biological pathway. These analyses often incorporate gene network properties to account for differential contributions of each gene. We extend this concept further—defining gene...

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Autores principales: Cochran, Amy L, Nieser, Kenneth J, Forger, Daniel B, Zöllner, Sebastian, McInnis, Melvin G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546080/
https://www.ncbi.nlm.nih.gov/pubmed/33034635
http://dx.doi.org/10.1093/gigascience/giaa091
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author Cochran, Amy L
Nieser, Kenneth J
Forger, Daniel B
Zöllner, Sebastian
McInnis, Melvin G
author_facet Cochran, Amy L
Nieser, Kenneth J
Forger, Daniel B
Zöllner, Sebastian
McInnis, Melvin G
author_sort Cochran, Amy L
collection PubMed
description BACKGROUND: Gene-set analyses measure the association between a disease of interest and a “set" of genes related to a biological pathway. These analyses often incorporate gene network properties to account for differential contributions of each gene. We extend this concept further—defining gene contributions based on biophysical properties—by leveraging mathematical models of biology to predict the effects of genetic perturbations on a particular downstream function. RESULTS: We present a method that combines gene weights from model predictions and gene ranks from genome-wide association studies into a weighted gene-set test. We demonstrate in simulation how such a method can improve statistical power. To this effect, we identify a gene set, weighted by model-predicted contributions to intracellular calcium ion concentration, that is significantly related to bipolar disorder in a small dataset (P = 0.04; n = 544). We reproduce this finding using publicly available summary data from the Psychiatric Genomics Consortium (P = 1.7 × 10(−4); n = 41,653). By contrast, an approach using a general calcium signaling pathway did not detect a significant association with bipolar disorder (P = 0.08). The weighted gene-set approach based on intracellular calcium ion concentration did not detect a significant relationship with schizophrenia (P = 0.09; n = 65,967) or major depression disorder (P = 0.30; n = 500,199). CONCLUSIONS: Together, these findings show how incorporating math biology into gene-set analyses might help to identify biological functions that underlie certain polygenic disorders.
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spelling pubmed-75460802020-10-15 Gene-set Enrichment with Mathematical Biology (GEMB) Cochran, Amy L Nieser, Kenneth J Forger, Daniel B Zöllner, Sebastian McInnis, Melvin G Gigascience Technical Note BACKGROUND: Gene-set analyses measure the association between a disease of interest and a “set" of genes related to a biological pathway. These analyses often incorporate gene network properties to account for differential contributions of each gene. We extend this concept further—defining gene contributions based on biophysical properties—by leveraging mathematical models of biology to predict the effects of genetic perturbations on a particular downstream function. RESULTS: We present a method that combines gene weights from model predictions and gene ranks from genome-wide association studies into a weighted gene-set test. We demonstrate in simulation how such a method can improve statistical power. To this effect, we identify a gene set, weighted by model-predicted contributions to intracellular calcium ion concentration, that is significantly related to bipolar disorder in a small dataset (P = 0.04; n = 544). We reproduce this finding using publicly available summary data from the Psychiatric Genomics Consortium (P = 1.7 × 10(−4); n = 41,653). By contrast, an approach using a general calcium signaling pathway did not detect a significant association with bipolar disorder (P = 0.08). The weighted gene-set approach based on intracellular calcium ion concentration did not detect a significant relationship with schizophrenia (P = 0.09; n = 65,967) or major depression disorder (P = 0.30; n = 500,199). CONCLUSIONS: Together, these findings show how incorporating math biology into gene-set analyses might help to identify biological functions that underlie certain polygenic disorders. Oxford University Press 2020-10-09 /pmc/articles/PMC7546080/ /pubmed/33034635 http://dx.doi.org/10.1093/gigascience/giaa091 Text en © The Author(s) 2020. Published by Oxford University Press GigaScience. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Note
Cochran, Amy L
Nieser, Kenneth J
Forger, Daniel B
Zöllner, Sebastian
McInnis, Melvin G
Gene-set Enrichment with Mathematical Biology (GEMB)
title Gene-set Enrichment with Mathematical Biology (GEMB)
title_full Gene-set Enrichment with Mathematical Biology (GEMB)
title_fullStr Gene-set Enrichment with Mathematical Biology (GEMB)
title_full_unstemmed Gene-set Enrichment with Mathematical Biology (GEMB)
title_short Gene-set Enrichment with Mathematical Biology (GEMB)
title_sort gene-set enrichment with mathematical biology (gemb)
topic Technical Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546080/
https://www.ncbi.nlm.nih.gov/pubmed/33034635
http://dx.doi.org/10.1093/gigascience/giaa091
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