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Automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns

BACKGROUND: Differential gene expression patterns in cells of the mammalian brain result in the morphological, connectional, and functional diversity of cells. A wide variety of studies have shown that certain genes are expressed only in specific cell-types. Analysis of cell-type-specific gene expre...

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Detalles Bibliográficos
Autores principales: Li, Rongjian, Zhang, Wenlu, Ji, Shuiwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078975/
https://www.ncbi.nlm.nih.gov/pubmed/24947138
http://dx.doi.org/10.1186/1471-2105-15-209
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author Li, Rongjian
Zhang, Wenlu
Ji, Shuiwang
author_facet Li, Rongjian
Zhang, Wenlu
Ji, Shuiwang
author_sort Li, Rongjian
collection PubMed
description BACKGROUND: Differential gene expression patterns in cells of the mammalian brain result in the morphological, connectional, and functional diversity of cells. A wide variety of studies have shown that certain genes are expressed only in specific cell-types. Analysis of cell-type-specific gene expression patterns can provide insights into the relationship between genes, connectivity, brain regions, and cell-types. However, automated methods for identifying cell-type-specific genes are lacking to date. RESULTS: Here, we describe a set of computational methods for identifying cell-type-specific genes in the mouse brain by automated image computing of in situ hybridization (ISH) expression patterns. We applied invariant image feature descriptors to capture local gene expression information from cellular-resolution ISH images. We then built image-level representations by applying vector quantization on the image descriptors. We employed regularized learning methods for classifying genes specifically expressed in different brain cell-types. These methods can also rank image features based on their discriminative power. We used a data set of 2,872 genes from the Allen Brain Atlas in the experiments. Results showed that our methods are predictive of cell-type-specificity of genes. Our classifiers achieved AUC values of approximately 87% when the enrichment level is set to 20. In addition, we showed that the highly-ranked image features captured the relationship between cell-types. CONCLUSIONS: Overall, our results showed that automated image computing methods could potentially be used to identify cell-type-specific genes in the mouse brain.
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spelling pubmed-40789752014-07-07 Automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns Li, Rongjian Zhang, Wenlu Ji, Shuiwang BMC Bioinformatics Methodology Article BACKGROUND: Differential gene expression patterns in cells of the mammalian brain result in the morphological, connectional, and functional diversity of cells. A wide variety of studies have shown that certain genes are expressed only in specific cell-types. Analysis of cell-type-specific gene expression patterns can provide insights into the relationship between genes, connectivity, brain regions, and cell-types. However, automated methods for identifying cell-type-specific genes are lacking to date. RESULTS: Here, we describe a set of computational methods for identifying cell-type-specific genes in the mouse brain by automated image computing of in situ hybridization (ISH) expression patterns. We applied invariant image feature descriptors to capture local gene expression information from cellular-resolution ISH images. We then built image-level representations by applying vector quantization on the image descriptors. We employed regularized learning methods for classifying genes specifically expressed in different brain cell-types. These methods can also rank image features based on their discriminative power. We used a data set of 2,872 genes from the Allen Brain Atlas in the experiments. Results showed that our methods are predictive of cell-type-specificity of genes. Our classifiers achieved AUC values of approximately 87% when the enrichment level is set to 20. In addition, we showed that the highly-ranked image features captured the relationship between cell-types. CONCLUSIONS: Overall, our results showed that automated image computing methods could potentially be used to identify cell-type-specific genes in the mouse brain. BioMed Central 2014-06-20 /pmc/articles/PMC4078975/ /pubmed/24947138 http://dx.doi.org/10.1186/1471-2105-15-209 Text en Copyright © 2014 Li et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Li, Rongjian
Zhang, Wenlu
Ji, Shuiwang
Automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns
title Automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns
title_full Automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns
title_fullStr Automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns
title_full_unstemmed Automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns
title_short Automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns
title_sort automated identification of cell-type-specific genes in the mouse brain by image computing of expression patterns
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078975/
https://www.ncbi.nlm.nih.gov/pubmed/24947138
http://dx.doi.org/10.1186/1471-2105-15-209
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