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A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns
Variations in DNA copy number carry important information on genome evolution and regulation of DNA replication in cancer cells. The rapid development of single-cell sequencing technology enables exploration of gene-expression heterogeneity among single cells, providing important information on cell...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575355/ https://www.ncbi.nlm.nih.gov/pubmed/28851906 http://dx.doi.org/10.1038/s41598-017-09139-8 |
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author | Zhang, Yue Cheung, Yiu-ming Su, Weifeng |
author_facet | Zhang, Yue Cheung, Yiu-ming Su, Weifeng |
author_sort | Zhang, Yue |
collection | PubMed |
description | Variations in DNA copy number carry important information on genome evolution and regulation of DNA replication in cancer cells. The rapid development of single-cell sequencing technology enables exploration of gene-expression heterogeneity among single cells, providing important information on cell evolution. Evolutionary relationships in accumulated sequence data can be visualized by adjacent positioning of similar cells so that similar copy-number profiles are shown by block patterns. However, single-cell DNA sequencing data usually have low amount of starting genome, which requires an extra step of amplification to accumulate sufficient samples, introducing noise and making regular pattern-finding challenging. In this paper, we will propose to tackle this issue of recovering the hidden blocks within single-cell DNA-sequencing data through continuous sample permutations such that similar samples are positioned adjacently. The permutation is guided by the total variational norm of the recovered copy number profiles, and is continued until the total variational norm is minimized when similar samples are stacked together to reveal block patterns. An efficient numerical scheme for finding this permutation is designed, tailored from the alternating direction method of multipliers. Application of this method to both simulated and real data demonstrates its ability to recover the hidden structures of single-cell DNA sequences. |
format | Online Article Text |
id | pubmed-5575355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55753552017-09-01 A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns Zhang, Yue Cheung, Yiu-ming Su, Weifeng Sci Rep Article Variations in DNA copy number carry important information on genome evolution and regulation of DNA replication in cancer cells. The rapid development of single-cell sequencing technology enables exploration of gene-expression heterogeneity among single cells, providing important information on cell evolution. Evolutionary relationships in accumulated sequence data can be visualized by adjacent positioning of similar cells so that similar copy-number profiles are shown by block patterns. However, single-cell DNA sequencing data usually have low amount of starting genome, which requires an extra step of amplification to accumulate sufficient samples, introducing noise and making regular pattern-finding challenging. In this paper, we will propose to tackle this issue of recovering the hidden blocks within single-cell DNA-sequencing data through continuous sample permutations such that similar samples are positioned adjacently. The permutation is guided by the total variational norm of the recovered copy number profiles, and is continued until the total variational norm is minimized when similar samples are stacked together to reveal block patterns. An efficient numerical scheme for finding this permutation is designed, tailored from the alternating direction method of multipliers. Application of this method to both simulated and real data demonstrates its ability to recover the hidden structures of single-cell DNA sequences. Nature Publishing Group UK 2017-08-29 /pmc/articles/PMC5575355/ /pubmed/28851906 http://dx.doi.org/10.1038/s41598-017-09139-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Yue Cheung, Yiu-ming Su, Weifeng A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns |
title | A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns |
title_full | A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns |
title_fullStr | A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns |
title_full_unstemmed | A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns |
title_short | A Total-variation Constrained Permutation Model for Revealing Common Copy Number Patterns |
title_sort | total-variation constrained permutation model for revealing common copy number patterns |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575355/ https://www.ncbi.nlm.nih.gov/pubmed/28851906 http://dx.doi.org/10.1038/s41598-017-09139-8 |
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