SECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification.

With rapid advances in the development of DNA sequencing technologies, a plethora of high-throughput genome and proteome data from a diverse spectrum of organisms have been generated. The functional annotation and evolutionary history of proteins are usually inferred from domains predicted from the...

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Autores principales: Ming Fan, Ka-Chun Wong, Taewoo Ryu, Timothy Ravasi, Xin Gao
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Publicado: Public Library of Science (PLoS) 2012
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Acceso en línea:https://doaj.org/article/c665281c5d40454c9c64b3d7f684391a
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spelling oai:doaj.org-article:c665281c5d40454c9c64b3d7f684391a2021-11-18T07:14:08ZSECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification.1932-620310.1371/journal.pone.0039475https://doaj.org/article/c665281c5d40454c9c64b3d7f684391a2012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22761802/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203With rapid advances in the development of DNA sequencing technologies, a plethora of high-throughput genome and proteome data from a diverse spectrum of organisms have been generated. The functional annotation and evolutionary history of proteins are usually inferred from domains predicted from the genome sequences. Traditional database-based domain prediction methods cannot identify novel domains, however, and alignment-based methods, which look for recurring segments in the proteome, are computationally demanding. Here, we propose a novel genome-wide domain prediction method, SECOM. Instead of conducting all-against-all sequence alignment, SECOM first indexes all the proteins in the genome by using a hash seed function. Local similarity can thus be detected and encoded into a graph structure, in which each node represents a protein sequence and each edge weight represents the shared hash seeds between the two nodes. SECOM then formulates the domain prediction problem as an overlapping community-finding problem in this graph. A backward graph percolation algorithm that efficiently identifies the domains is proposed. We tested SECOM on five recently sequenced genomes of aquatic animals. Our tests demonstrated that SECOM was able to identify most of the known domains identified by InterProScan. When compared with the alignment-based method, SECOM showed higher sensitivity in detecting putative novel domains, while it was also three orders of magnitude faster. For example, SECOM was able to predict a novel sponge-specific domain in nucleoside-triphosphatase (NTPases). Furthermore, SECOM discovered two novel domains, likely of bacterial origin, that are taxonomically restricted to sea anemone and hydra. SECOM is an open-source program and available at http://sfb.kaust.edu.sa/Pages/Software.aspx.Ming FanKa-Chun WongTaewoo RyuTimothy RavasiXin GaoPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 6, p e39475 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Ming Fan
Ka-Chun Wong
Taewoo Ryu
Timothy Ravasi
Xin Gao
SECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification.
description With rapid advances in the development of DNA sequencing technologies, a plethora of high-throughput genome and proteome data from a diverse spectrum of organisms have been generated. The functional annotation and evolutionary history of proteins are usually inferred from domains predicted from the genome sequences. Traditional database-based domain prediction methods cannot identify novel domains, however, and alignment-based methods, which look for recurring segments in the proteome, are computationally demanding. Here, we propose a novel genome-wide domain prediction method, SECOM. Instead of conducting all-against-all sequence alignment, SECOM first indexes all the proteins in the genome by using a hash seed function. Local similarity can thus be detected and encoded into a graph structure, in which each node represents a protein sequence and each edge weight represents the shared hash seeds between the two nodes. SECOM then formulates the domain prediction problem as an overlapping community-finding problem in this graph. A backward graph percolation algorithm that efficiently identifies the domains is proposed. We tested SECOM on five recently sequenced genomes of aquatic animals. Our tests demonstrated that SECOM was able to identify most of the known domains identified by InterProScan. When compared with the alignment-based method, SECOM showed higher sensitivity in detecting putative novel domains, while it was also three orders of magnitude faster. For example, SECOM was able to predict a novel sponge-specific domain in nucleoside-triphosphatase (NTPases). Furthermore, SECOM discovered two novel domains, likely of bacterial origin, that are taxonomically restricted to sea anemone and hydra. SECOM is an open-source program and available at http://sfb.kaust.edu.sa/Pages/Software.aspx.
format article
author Ming Fan
Ka-Chun Wong
Taewoo Ryu
Timothy Ravasi
Xin Gao
author_facet Ming Fan
Ka-Chun Wong
Taewoo Ryu
Timothy Ravasi
Xin Gao
author_sort Ming Fan
title SECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification.
title_short SECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification.
title_full SECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification.
title_fullStr SECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification.
title_full_unstemmed SECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification.
title_sort secom: a novel hash seed and community detection based-approach for genome-scale protein domain identification.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/c665281c5d40454c9c64b3d7f684391a
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