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Towards a theoretical understanding of false positives in DNA motif finding
BACKGROUND: Detection of false-positive motifs is one of the main causes of low performance in de novo DNA motif-finding methods. Despite the substantial algorithm development effort in this area, recent comprehensive benchmark studies revealed that the performance of DNA motif-finders leaves room f...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436861/ https://www.ncbi.nlm.nih.gov/pubmed/22738169 http://dx.doi.org/10.1186/1471-2105-13-151 |
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author | Zia, Amin Moses, Alan M |
author_facet | Zia, Amin Moses, Alan M |
author_sort | Zia, Amin |
collection | PubMed |
description | BACKGROUND: Detection of false-positive motifs is one of the main causes of low performance in de novo DNA motif-finding methods. Despite the substantial algorithm development effort in this area, recent comprehensive benchmark studies revealed that the performance of DNA motif-finders leaves room for improvement in realistic scenarios. RESULTS: Using large-deviations theory, we derive a remarkably simple relationship that describes the dependence of false positives on dataset size for the one-occurrence per sequence motif-finding problem. As expected, we predict that false-positives can be reduced by decreasing the sequence length or by adding more sequences to the dataset. Interestingly, we find that the false-positive strength depends more strongly on the number of sequences in the dataset than it does on the sequence length, but that the dependence on the number of sequences diminishes, after which adding more sequences does not reduce the false-positive rate significantly. We compare our theoretical predictions by applying four popular motif-finding algorithms that solve the one-occurrence-per-sequence problem (MEME, the Gibbs Sampler, Weeder, and GIMSAN) to simulated data that contain no motifs. We find that the dependence of false positives detected by these softwares on the motif-finding parameters is similar to that predicted by our formula. CONCLUSIONS: We quantify the relationship between the sequence search space and motif-finding false-positives. Based on the simple formula we derive, we provide a number of intuitive rules of thumb that may be used to enhance motif-finding results in practice. Our results provide a theoretical advance in an important problem in computational biology. |
format | Online Article Text |
id | pubmed-3436861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34368612012-09-11 Towards a theoretical understanding of false positives in DNA motif finding Zia, Amin Moses, Alan M BMC Bioinformatics Research Article BACKGROUND: Detection of false-positive motifs is one of the main causes of low performance in de novo DNA motif-finding methods. Despite the substantial algorithm development effort in this area, recent comprehensive benchmark studies revealed that the performance of DNA motif-finders leaves room for improvement in realistic scenarios. RESULTS: Using large-deviations theory, we derive a remarkably simple relationship that describes the dependence of false positives on dataset size for the one-occurrence per sequence motif-finding problem. As expected, we predict that false-positives can be reduced by decreasing the sequence length or by adding more sequences to the dataset. Interestingly, we find that the false-positive strength depends more strongly on the number of sequences in the dataset than it does on the sequence length, but that the dependence on the number of sequences diminishes, after which adding more sequences does not reduce the false-positive rate significantly. We compare our theoretical predictions by applying four popular motif-finding algorithms that solve the one-occurrence-per-sequence problem (MEME, the Gibbs Sampler, Weeder, and GIMSAN) to simulated data that contain no motifs. We find that the dependence of false positives detected by these softwares on the motif-finding parameters is similar to that predicted by our formula. CONCLUSIONS: We quantify the relationship between the sequence search space and motif-finding false-positives. Based on the simple formula we derive, we provide a number of intuitive rules of thumb that may be used to enhance motif-finding results in practice. Our results provide a theoretical advance in an important problem in computational biology. BioMed Central 2012-06-27 /pmc/articles/PMC3436861/ /pubmed/22738169 http://dx.doi.org/10.1186/1471-2105-13-151 Text en Copyright ©2012 Zia and Moses; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zia, Amin Moses, Alan M Towards a theoretical understanding of false positives in DNA motif finding |
title | Towards a theoretical understanding of false positives in DNA motif finding |
title_full | Towards a theoretical understanding of false positives in DNA motif finding |
title_fullStr | Towards a theoretical understanding of false positives in DNA motif finding |
title_full_unstemmed | Towards a theoretical understanding of false positives in DNA motif finding |
title_short | Towards a theoretical understanding of false positives in DNA motif finding |
title_sort | towards a theoretical understanding of false positives in dna motif finding |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436861/ https://www.ncbi.nlm.nih.gov/pubmed/22738169 http://dx.doi.org/10.1186/1471-2105-13-151 |
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