Evidence map›Paper›PMID 23281969›Full record

ArticleBMC bioinformatics2012

A hybrid method for the exact planted (l, d) motif finding problem and its parallelization.

Mostafa M Abbas, Mohamed Abouelhoda, Hazem M Bahig

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Article in BMC bioinformatics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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4 citing papers in PubMed.

  1. ChIP-seq predicted estrogen receptor biding sites in human breast cancer cell line MCF7.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
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5 · Who and what money

Authors and funding

3 authors.

Mostafa M AbbasDepartment of Basic Sciences, Faculty of Engineering, Sinai University, El-Arish, Egypt. mabbas@su.edu.eg
Mohamed Abouelhoda
Hazem M Bahig

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGiven a set of DNA sequences s1, ..., st, the (l, d) motif problem is to find an l-length motif sequence M , not necessary existing in any of the input sequences, such that for each sequence si, 1 ≤ i ≤ t, there is at least one subsequence differing with at most d mismatches from M. Many exact algorithms have been developed to solve the motif finding problem in the last three decades. However, the problem is still challenging and its solution is limited to small values of l and d.

resultsIn this paper we present a new efficient method to improve the performance of the exact algorithms for the motif finding problem. Our method is composed of two main steps: First, we process q ≤ t sequences to find candidate motifs. Second, the candidate motifs are searched in the remaining sequences. For both steps, we use the best available algorithms. Our method is a hybrid one, because it integrates currently existing algorithms to achieve the best running time. In this paper, we show how the optimal value of q is determined to achieve the best running time. Our experimental results show that there is about 24% speed-up achieved by our method compared to the best existing algorithm. Furthermore, we also present a parallel version of our method running on shared memory architecture. Our experiments show that the performance of our algorithm scales linearly with the number of processors. Using the parallel version, we were able to solve the (21, 8) challenging instance using 8 processors in 20.42 hours instead of 6.68 days of the serial version.

conclusionsOur method speeds up the solution of the exact motif problem. Our method is generic, because it can accommodate any new faster algorithm based on traditional methods. We expect that our method will help to discover longer motifs. The software we developed is available for free for academic research at http://www.nubios.nileu.edu.eg/tools/hymotif.

Indexed as

Nucleotide MotifsComputational BiologySequence Analysis, DNASoftware

Identifiers

PMID23281969
PMCPMC3521218

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.