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InferLoop: leveraging single-cell chromatin accessibility for the signal of chromatin loop
Deciphering cell-type-specific 3D structures of chromatin is challenging. Here, we present InferLoop, a novel method for inferring the strength of chromatin interaction using single-cell chromatin accessibility data. The workflow of InferLoop is, first, to conduct signal enhancement by grouping near...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199765/ https://www.ncbi.nlm.nih.gov/pubmed/37139553 http://dx.doi.org/10.1093/bib/bbad166 |
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author | Zhang, Feng Jiao, Huiyuan Wang, Yihao Yang, Chen Li, Linying Wang, Zhiming Tong, Ran Zhou, Junmei Shen, Jianfeng Li, Lingjie |
author_facet | Zhang, Feng Jiao, Huiyuan Wang, Yihao Yang, Chen Li, Linying Wang, Zhiming Tong, Ran Zhou, Junmei Shen, Jianfeng Li, Lingjie |
author_sort | Zhang, Feng |
collection | PubMed |
description | Deciphering cell-type-specific 3D structures of chromatin is challenging. Here, we present InferLoop, a novel method for inferring the strength of chromatin interaction using single-cell chromatin accessibility data. The workflow of InferLoop is, first, to conduct signal enhancement by grouping nearby cells into bins, and then, for each bin, leverage accessibility signals for loop signals using a newly constructed metric that is similar to the perturbation of the Pearson correlation coefficient. In this study, we have described three application scenarios of InferLoop, including the inference of cell-type-specific loop signals, the prediction of gene expression levels and the interpretation of intergenic loci. The effectiveness and superiority of InferLoop over other methods in those three scenarios are rigorously validated by using the single-cell 3D genome structure data of human brain cortex and human blood, the single-cell multi-omics data of human blood and mouse brain cortex, and the intergenic loci in the GWAS Catalog database as well as the GTEx database, respectively. In addition, InferLoop can be applied to predict loop signals of individual spots using the spatial chromatin accessibility data of mouse embryo. InferLoop is available at https://github.com/jumphone/inferloop. |
format | Online Article Text |
id | pubmed-10199765 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101997652023-05-21 InferLoop: leveraging single-cell chromatin accessibility for the signal of chromatin loop Zhang, Feng Jiao, Huiyuan Wang, Yihao Yang, Chen Li, Linying Wang, Zhiming Tong, Ran Zhou, Junmei Shen, Jianfeng Li, Lingjie Brief Bioinform Problem Solving Protocol Deciphering cell-type-specific 3D structures of chromatin is challenging. Here, we present InferLoop, a novel method for inferring the strength of chromatin interaction using single-cell chromatin accessibility data. The workflow of InferLoop is, first, to conduct signal enhancement by grouping nearby cells into bins, and then, for each bin, leverage accessibility signals for loop signals using a newly constructed metric that is similar to the perturbation of the Pearson correlation coefficient. In this study, we have described three application scenarios of InferLoop, including the inference of cell-type-specific loop signals, the prediction of gene expression levels and the interpretation of intergenic loci. The effectiveness and superiority of InferLoop over other methods in those three scenarios are rigorously validated by using the single-cell 3D genome structure data of human brain cortex and human blood, the single-cell multi-omics data of human blood and mouse brain cortex, and the intergenic loci in the GWAS Catalog database as well as the GTEx database, respectively. In addition, InferLoop can be applied to predict loop signals of individual spots using the spatial chromatin accessibility data of mouse embryo. InferLoop is available at https://github.com/jumphone/inferloop. Oxford University Press 2023-05-03 /pmc/articles/PMC10199765/ /pubmed/37139553 http://dx.doi.org/10.1093/bib/bbad166 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Problem Solving Protocol Zhang, Feng Jiao, Huiyuan Wang, Yihao Yang, Chen Li, Linying Wang, Zhiming Tong, Ran Zhou, Junmei Shen, Jianfeng Li, Lingjie InferLoop: leveraging single-cell chromatin accessibility for the signal of chromatin loop |
title | InferLoop: leveraging single-cell chromatin accessibility for the signal of chromatin loop |
title_full | InferLoop: leveraging single-cell chromatin accessibility for the signal of chromatin loop |
title_fullStr | InferLoop: leveraging single-cell chromatin accessibility for the signal of chromatin loop |
title_full_unstemmed | InferLoop: leveraging single-cell chromatin accessibility for the signal of chromatin loop |
title_short | InferLoop: leveraging single-cell chromatin accessibility for the signal of chromatin loop |
title_sort | inferloop: leveraging single-cell chromatin accessibility for the signal of chromatin loop |
topic | Problem Solving Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199765/ https://www.ncbi.nlm.nih.gov/pubmed/37139553 http://dx.doi.org/10.1093/bib/bbad166 |
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