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A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data
BACKGROUND: The development of chromosomal conformation capture techniques, particularly, the Hi-C technique, has made the analysis and study of the spatial conformation of a genome an important topic in bioinformatics and computational biology. Aided by high-throughput next generation sequencing te...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824572/ https://www.ncbi.nlm.nih.gov/pubmed/29471801 http://dx.doi.org/10.1186/s12864-018-4546-8 |
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author | Oluwadare, Oluwatosin Zhang, Yuxiang Cheng, Jianlin |
author_facet | Oluwadare, Oluwatosin Zhang, Yuxiang Cheng, Jianlin |
author_sort | Oluwadare, Oluwatosin |
collection | PubMed |
description | BACKGROUND: The development of chromosomal conformation capture techniques, particularly, the Hi-C technique, has made the analysis and study of the spatial conformation of a genome an important topic in bioinformatics and computational biology. Aided by high-throughput next generation sequencing techniques, the Hi-C technique can generate genome-wide, large-scale intra- and inter-chromosomal interaction data capable of describing in details the spatial interactions within a genome. These data can be used to reconstruct 3D structures of chromosomes that can be used to study DNA replication, gene regulation, genome interaction, genome folding, and genome function. RESULTS: Here, we introduce a maximum likelihood algorithm called 3DMax to construct the 3D structure of a chromosome from Hi-C data. 3DMax employs a maximum likelihood approach to infer the 3D structures of a chromosome, while automatically re-estimating the conversion factor (α) for converting Interaction Frequency (IF) to distance. Our results show that the models generated by 3DMax from a simulated Hi-C dataset match the true models better than most of the existing methods. 3DMax is more robust to structural variability and noise. Compared on a real Hi-C dataset, 3DMax constructs chromosomal models that fit the data better than most methods, and it is faster than all other methods. The models reconstructed by 3DMax were consistent with fluorescent in situ hybridization (FISH) experiments and existing knowledge about the organization of human chromosomes, such as chromosome compartmentalization. CONCLUSIONS: 3DMax is an effective approach to reconstructing 3D chromosomal models. The results, and the models generated for the simulated and real Hi-C datasets are available here: http://sysbio.rnet.missouri.edu/bdm_download/3DMax/. The source code is available here: https://github.com/BDM-Lab/3DMax. A short video demonstrating how to use 3DMax can be found here: https://youtu.be/ehQUFWoHwfo. |
format | Online Article Text |
id | pubmed-5824572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58245722018-02-26 A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data Oluwadare, Oluwatosin Zhang, Yuxiang Cheng, Jianlin BMC Genomics Methodology Article BACKGROUND: The development of chromosomal conformation capture techniques, particularly, the Hi-C technique, has made the analysis and study of the spatial conformation of a genome an important topic in bioinformatics and computational biology. Aided by high-throughput next generation sequencing techniques, the Hi-C technique can generate genome-wide, large-scale intra- and inter-chromosomal interaction data capable of describing in details the spatial interactions within a genome. These data can be used to reconstruct 3D structures of chromosomes that can be used to study DNA replication, gene regulation, genome interaction, genome folding, and genome function. RESULTS: Here, we introduce a maximum likelihood algorithm called 3DMax to construct the 3D structure of a chromosome from Hi-C data. 3DMax employs a maximum likelihood approach to infer the 3D structures of a chromosome, while automatically re-estimating the conversion factor (α) for converting Interaction Frequency (IF) to distance. Our results show that the models generated by 3DMax from a simulated Hi-C dataset match the true models better than most of the existing methods. 3DMax is more robust to structural variability and noise. Compared on a real Hi-C dataset, 3DMax constructs chromosomal models that fit the data better than most methods, and it is faster than all other methods. The models reconstructed by 3DMax were consistent with fluorescent in situ hybridization (FISH) experiments and existing knowledge about the organization of human chromosomes, such as chromosome compartmentalization. CONCLUSIONS: 3DMax is an effective approach to reconstructing 3D chromosomal models. The results, and the models generated for the simulated and real Hi-C datasets are available here: http://sysbio.rnet.missouri.edu/bdm_download/3DMax/. The source code is available here: https://github.com/BDM-Lab/3DMax. A short video demonstrating how to use 3DMax can be found here: https://youtu.be/ehQUFWoHwfo. BioMed Central 2018-02-23 /pmc/articles/PMC5824572/ /pubmed/29471801 http://dx.doi.org/10.1186/s12864-018-4546-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Oluwadare, Oluwatosin Zhang, Yuxiang Cheng, Jianlin A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data |
title | A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data |
title_full | A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data |
title_fullStr | A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data |
title_full_unstemmed | A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data |
title_short | A maximum likelihood algorithm for reconstructing 3D structures of human chromosomes from chromosomal contact data |
title_sort | maximum likelihood algorithm for reconstructing 3d structures of human chromosomes from chromosomal contact data |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824572/ https://www.ncbi.nlm.nih.gov/pubmed/29471801 http://dx.doi.org/10.1186/s12864-018-4546-8 |
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