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The effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance

MOTIVATION: Intra-sample heterogeneity describes the phenomenon where a genomic sample contains a diverse set of genomic sequences. In practice, the true string sets in a sample are often unknown due to limitations in sequencing technology. In order to compare heterogeneous samples, genome graphs ca...

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Autores principales: Qiu, Yutong, Kingsford, Carl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235494/
https://www.ncbi.nlm.nih.gov/pubmed/35758819
http://dx.doi.org/10.1093/bioinformatics/btac264
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author Qiu, Yutong
Kingsford, Carl
author_facet Qiu, Yutong
Kingsford, Carl
author_sort Qiu, Yutong
collection PubMed
description MOTIVATION: Intra-sample heterogeneity describes the phenomenon where a genomic sample contains a diverse set of genomic sequences. In practice, the true string sets in a sample are often unknown due to limitations in sequencing technology. In order to compare heterogeneous samples, genome graphs can be used to represent such sets of strings. However, a genome graph is generally able to represent a string set universe that contains multiple sets of strings in addition to the true string set. This difference between genome graphs and string sets is not well characterized. As a result, a distance metric between genome graphs may not match the distance between true string sets. RESULTS: We extend a genome graph distance metric, Graph Traversal Edit Distance (GTED) proposed by Ebrahimpour Boroojeny et al., to FGTED to model the distance between heterogeneous string sets and show that GTED and FGTED always underestimate the Earth Mover’s Edit Distance (EMED) between string sets. We introduce the notion of string set universe diameter of a genome graph. Using the diameter, we are able to upper-bound the deviation of FGTED from EMED and to improve FGTED so that it reduces the average error in empirically estimating the similarity between true string sets. On simulated T-cell receptor sequences and actual Hepatitis B virus genomes, we show that the diameter-corrected FGTED reduces the average deviation of the estimated distance from the true string set distances by more than 250%. AVAILABILITY AND IMPLEMENTATION: Data and source code for reproducing the experiments are available at: https://github.com/Kingsford-Group/gtedemedtest/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-92354942022-06-29 The effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance Qiu, Yutong Kingsford, Carl Bioinformatics ISCB/Ismb 2022 MOTIVATION: Intra-sample heterogeneity describes the phenomenon where a genomic sample contains a diverse set of genomic sequences. In practice, the true string sets in a sample are often unknown due to limitations in sequencing technology. In order to compare heterogeneous samples, genome graphs can be used to represent such sets of strings. However, a genome graph is generally able to represent a string set universe that contains multiple sets of strings in addition to the true string set. This difference between genome graphs and string sets is not well characterized. As a result, a distance metric between genome graphs may not match the distance between true string sets. RESULTS: We extend a genome graph distance metric, Graph Traversal Edit Distance (GTED) proposed by Ebrahimpour Boroojeny et al., to FGTED to model the distance between heterogeneous string sets and show that GTED and FGTED always underestimate the Earth Mover’s Edit Distance (EMED) between string sets. We introduce the notion of string set universe diameter of a genome graph. Using the diameter, we are able to upper-bound the deviation of FGTED from EMED and to improve FGTED so that it reduces the average error in empirically estimating the similarity between true string sets. On simulated T-cell receptor sequences and actual Hepatitis B virus genomes, we show that the diameter-corrected FGTED reduces the average deviation of the estimated distance from the true string set distances by more than 250%. AVAILABILITY AND IMPLEMENTATION: Data and source code for reproducing the experiments are available at: https://github.com/Kingsford-Group/gtedemedtest/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2022-06-27 /pmc/articles/PMC9235494/ /pubmed/35758819 http://dx.doi.org/10.1093/bioinformatics/btac264 Text en © The Author(s) 2022. 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 ISCB/Ismb 2022
Qiu, Yutong
Kingsford, Carl
The effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance
title The effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance
title_full The effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance
title_fullStr The effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance
title_full_unstemmed The effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance
title_short The effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance
title_sort effect of genome graph expressiveness on the discrepancy between genome graph distance and string set distance
topic ISCB/Ismb 2022
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9235494/
https://www.ncbi.nlm.nih.gov/pubmed/35758819
http://dx.doi.org/10.1093/bioinformatics/btac264
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