Literature DB >> 24109755

Nucleotide sequence alignment using sparse coding and belief propagation.

Aminmohammad Roozgard, Nafise Barzigar, Shuang Wang, Xiaoqian Jiang, Lucila Ohno-Machado, Samuel Cheng.   

Abstract

Advances in DNA information extraction techniques have led to huge sequenced genomes from organisms spanning the tree of life. This increasing amount of genomic information requires tools for comparison of the nucleotide sequences. In this paper, we propose a novel nucleotide sequence alignment method based on sparse coding and belief propagation to compare the similarity of the nucleotide sequences. We used the neighbors of each nucleotide as features, and then we employed sparse coding to find a set of candidate nucleotides. To select optimum matches, belief propagation was subsequently applied to these candidate nucleotides. Experimental results show that the proposed approach is able to robustly align nucleotide sequences and is competitive to SOAPaligner [1] and BWA [2].

Entities:  

Mesh:

Year:  2013        PMID: 24109755      PMCID: PMC3909563          DOI: 10.1109/EMBC.2013.6609568

Source DB:  PubMed          Journal:  Conf Proc IEEE Eng Med Biol Soc        ISSN: 1557-170X


  15 in total

1.  Efficient multiple genome alignment.

Authors:  Michael Höhl; Stefan Kurtz; Enno Ohlebusch
Journal:  Bioinformatics       Date:  2002       Impact factor: 6.937

2.  Mauve: multiple alignment of conserved genomic sequence with rearrangements.

Authors:  Aaron C E Darling; Bob Mau; Frederick R Blattner; Nicole T Perna
Journal:  Genome Res       Date:  2004-07       Impact factor: 9.043

3.  Aligning multiple genomic sequences with the threaded blockset aligner.

Authors:  Mathieu Blanchette; W James Kent; Cathy Riemer; Laura Elnitski; Arian F A Smit; Krishna M Roskin; Robert Baertsch; Kate Rosenbloom; Hiram Clawson; Eric D Green; David Haussler; Webb Miller
Journal:  Genome Res       Date:  2004-04       Impact factor: 9.043

4.  MUSCLE: multiple sequence alignment with high accuracy and high throughput.

Authors:  Robert C Edgar
Journal:  Nucleic Acids Res       Date:  2004-03-19       Impact factor: 16.971

Review 5.  The many faces of sequence alignment.

Authors:  Serafim Batzoglou
Journal:  Brief Bioinform       Date:  2005-03       Impact factor: 11.622

6.  SOAP2: an improved ultrafast tool for short read alignment.

Authors:  Ruiqiang Li; Chang Yu; Yingrui Li; Tak-Wah Lam; Siu-Ming Yiu; Karsten Kristiansen; Jun Wang
Journal:  Bioinformatics       Date:  2009-06-03       Impact factor: 6.937

7.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.

Authors:  J D Thompson; D G Higgins; T J Gibson
Journal:  Nucleic Acids Res       Date:  1994-11-11       Impact factor: 16.971

8.  Gene expression of a gene family in maize based on noncollinear haplotypes.

Authors:  Rentao Song; Joachim Messing
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-09       Impact factor: 11.205

9.  Intraspecific sequence comparisons reveal similar rates of non-collinear gene insertion in the B and D genomes of bread wheat.

Authors:  Jan Bartoš; Cestmír Vlček; Frédéric Choulet; Mária Džunková; Kateřina Cviková; Jan Safář; Hana Simková; Jan Pačes; Hynek Strnad; Pierre Sourdille; Hélène Bergès; Federica Cattonaro; Catherine Feuillet; Jaroslav Doležel
Journal:  BMC Plant Biol       Date:  2012-08-30       Impact factor: 4.215

10.  Fast and accurate short read alignment with Burrows-Wheeler transform.

Authors:  Heng Li; Richard Durbin
Journal:  Bioinformatics       Date:  2009-05-18       Impact factor: 6.937

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  1 in total

1.  Empirical Transition Probability Indexing Sparse-Coding Belief Propagation (ETPI-SCoBeP) Genome Sequence Alignment.

Authors:  Aminmohammad Roozgard; Nafise Barzigar; Shuang Wang; Xiaoqian Jiang; Samuel Cheng
Journal:  Cancer Inform       Date:  2015-02-01
  1 in total

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