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Identification of representative species-specific genes for abundance measurements
MOTIVATION: Metagenomic binning facilitates the reconstruction of genomes and identification of Metagenomic Species Pan-genomes or Metagenomic Assembled Genomes. We propose a method for identifying a set of de novo representative genes, termed signature genes, which can be used to measure the relati...
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/PMC10199311/ https://www.ncbi.nlm.nih.gov/pubmed/37213867 http://dx.doi.org/10.1093/bioadv/vbad060 |
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author | Zachariasen, Trine Petersen, Anders Østergaard Brejnrod, Asker Vestergaard, Gisle Alberg Eklund, Aron Nielsen, Henrik Bjørn |
author_facet | Zachariasen, Trine Petersen, Anders Østergaard Brejnrod, Asker Vestergaard, Gisle Alberg Eklund, Aron Nielsen, Henrik Bjørn |
author_sort | Zachariasen, Trine |
collection | PubMed |
description | MOTIVATION: Metagenomic binning facilitates the reconstruction of genomes and identification of Metagenomic Species Pan-genomes or Metagenomic Assembled Genomes. We propose a method for identifying a set of de novo representative genes, termed signature genes, which can be used to measure the relative abundance and used as markers of each metagenomic species with high accuracy. RESULTS: An initial set of the 100 genes that correlate with the median gene abundance profile of the entity is selected. A variant of the coupon collector’s problem was utilized to evaluate the probability of identifying a certain number of unique genes in a sample. This allows us to reject the abundance measurements of strains exhibiting a significantly skewed gene representation. A rank-based negative binomial model is employed to assess the performance of different gene sets across a large set of samples, facilitating identification of an optimal signature gene set for the entity. When benchmarked the method on a synthetic gene catalog, our optimized signature gene sets estimate relative abundance significantly closer to the true relative abundance compared to the starting gene sets extracted from the metagenomic species. The method was able to replicate results from a study with real data and identify around three times as many metagenomic entities. AVAILABILITY AND IMPLEMENTATION: The code used for the analysis is available on GitHub: https://github.com/trinezac/SG_optimization. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics Advances online. |
format | Online Article Text |
id | pubmed-10199311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101993112023-05-21 Identification of representative species-specific genes for abundance measurements Zachariasen, Trine Petersen, Anders Østergaard Brejnrod, Asker Vestergaard, Gisle Alberg Eklund, Aron Nielsen, Henrik Bjørn Bioinform Adv Original Paper MOTIVATION: Metagenomic binning facilitates the reconstruction of genomes and identification of Metagenomic Species Pan-genomes or Metagenomic Assembled Genomes. We propose a method for identifying a set of de novo representative genes, termed signature genes, which can be used to measure the relative abundance and used as markers of each metagenomic species with high accuracy. RESULTS: An initial set of the 100 genes that correlate with the median gene abundance profile of the entity is selected. A variant of the coupon collector’s problem was utilized to evaluate the probability of identifying a certain number of unique genes in a sample. This allows us to reject the abundance measurements of strains exhibiting a significantly skewed gene representation. A rank-based negative binomial model is employed to assess the performance of different gene sets across a large set of samples, facilitating identification of an optimal signature gene set for the entity. When benchmarked the method on a synthetic gene catalog, our optimized signature gene sets estimate relative abundance significantly closer to the true relative abundance compared to the starting gene sets extracted from the metagenomic species. The method was able to replicate results from a study with real data and identify around three times as many metagenomic entities. AVAILABILITY AND IMPLEMENTATION: The code used for the analysis is available on GitHub: https://github.com/trinezac/SG_optimization. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics Advances online. Oxford University Press 2023-05-08 /pmc/articles/PMC10199311/ /pubmed/37213867 http://dx.doi.org/10.1093/bioadv/vbad060 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Zachariasen, Trine Petersen, Anders Østergaard Brejnrod, Asker Vestergaard, Gisle Alberg Eklund, Aron Nielsen, Henrik Bjørn Identification of representative species-specific genes for abundance measurements |
title | Identification of representative species-specific genes for abundance measurements |
title_full | Identification of representative species-specific genes for abundance measurements |
title_fullStr | Identification of representative species-specific genes for abundance measurements |
title_full_unstemmed | Identification of representative species-specific genes for abundance measurements |
title_short | Identification of representative species-specific genes for abundance measurements |
title_sort | identification of representative species-specific genes for abundance measurements |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199311/ https://www.ncbi.nlm.nih.gov/pubmed/37213867 http://dx.doi.org/10.1093/bioadv/vbad060 |
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