Literature DB >> 12169561

Efficient multiple genome alignment.

Michael Höhl1, Stefan Kurtz, Enno Ohlebusch.   

Abstract

MOTIVATION: To allow a direct comparison of the genomic DNA sequences of sufficiently similar organisms, there is an urgent need for software tools that can align more than two genomic sequences.
RESULTS: We developed new algorithms and a software tool 'Multiple Genome Aligner' (MGA for short) that efficiently computes multiple genome alignments of large, closely related DNA sequences. For example, it can align 85% percent of the complete genomes of six human adenoviruses (average length 35305 bp.) in 159 seconds. An alignment of 74% of the complete genomes of three of strains of E. coli (lengths: 5528445; 5498450; 4639221 approximately bp.) is produced in 30 minutes.

Entities:  

Mesh:

Year:  2002        PMID: 12169561     DOI: 10.1093/bioinformatics/18.suppl_1.s312

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  50 in total

1.  LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA.

Authors:  Michael Brudno; Chuong B Do; Gregory M Cooper; Michael F Kim; Eugene Davydov; Eric D Green; Arend Sidow; Serafim Batzoglou
Journal:  Genome Res       Date:  2003-03-12       Impact factor: 9.043

2.  Identification of patterns in biological sequences at the ALGGEN server: PROMO and MALGEN.

Authors:  Domènec Farré; Romà Roset; Mario Huerta; José E Adsuara; Llorenç Roselló; M Mar Albà; Xavier Messeguer
Journal:  Nucleic Acids Res       Date:  2003-07-01       Impact factor: 16.971

3.  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

4.  DIALIGN P: fast pair-wise and multiple sequence alignment using parallel processors.

Authors:  Martin Schmollinger; Kay Nieselt; Michael Kaufmann; Burkhard Morgenstern
Journal:  BMC Bioinformatics       Date:  2004-09-09       Impact factor: 3.169

5.  Separating significant matches from spurious matches in DNA sequences.

Authors:  Hugo Devillers; Sophie Schbath
Journal:  J Comput Biol       Date:  2011-12-09       Impact factor: 1.479

6.  Homology-dependent methylation in primate repetitive DNA.

Authors:  Julien Meunier; Adel Khelifi; Vincent Navratil; Laurent Duret
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-29       Impact factor: 11.205

7.  A practical algorithm for finding maximal exact matches in large sequence datasets using sparse suffix arrays.

Authors:  Zia Khan; Joshua S Bloom; Leonid Kruglyak; Mona Singh
Journal:  Bioinformatics       Date:  2009-04-23       Impact factor: 6.937

8.  A genomic distance based on MUM indicates discontinuity between most bacterial species and genera.

Authors:  Marc Deloger; Meriem El Karoui; Marie-Agnès Petit
Journal:  J Bacteriol       Date:  2008-10-31       Impact factor: 3.490

9.  An algorithm for identifying novel targets of transcription factor families: application to hypoxia-inducible factor 1 targets.

Authors:  Yue Jiang; Bojan Cukic; Donald A Adjeroh; Heath D Skinner; Jie Lin; Qingxi J Shen; Bing-Hua Jiang
Journal:  Cancer Inform       Date:  2009-03-04

10.  mkESA: enhanced suffix array construction tool.

Authors:  Robert Homann; David Fleer; Robert Giegerich; Marc Rehmsmeier
Journal:  Bioinformatics       Date:  2009-02-26       Impact factor: 6.937

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