Literature DB >> 18849524

Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs.

Benedict Paten1, Javier Herrero, Kathryn Beal, Stephen Fitzgerald, Ewan Birney.   

Abstract

Pairwise whole-genome alignment involves the creation of a homology map, capable of performing a near complete transformation of one genome into another. For multiple genomes this problem is generalized to finding a set of consistent homology maps for converting each genome in the set of aligned genomes into any of the others. The problem can be divided into two principal stages. First, the partitioning of the input genomes into a set of colinear segments, a process which essentially deals with the complex processes of rearrangement. Second, the generation of a base pair level alignment map for each colinear segment. We have developed a new genome-wide segmentation program, Enredo, which produces colinear segments from extant genomes handling rearrangements, including duplications. We have then applied the new alignment program Pecan, which makes the consistency alignment methodology practical at a large scale, to create a new set of genome-wide mammalian alignments. We test both Enredo and Pecan using novel and existing assessment analyses that incorporate both real biological data and simulations, and show that both independently and in combination they outperform existing programs. Alignments from our pipeline are publicly available within the Ensembl genome browser.

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Year:  2008        PMID: 18849524      PMCID: PMC2577869          DOI: 10.1101/gr.076554.108

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  42 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.  Glocal alignment: finding rearrangements during alignment.

Authors:  Michael Brudno; Sanket Malde; Alexander Poliakov; Chuong B Do; Olivier Couronne; Inna Dubchak; Serafim Batzoglou
Journal:  Bioinformatics       Date:  2003       Impact factor: 6.937

3.  Evolution's cauldron: duplication, deletion, and rearrangement in the mouse and human genomes.

Authors:  W James Kent; Robert Baertsch; Angie Hinrichs; Webb Miller; David Haussler
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-19       Impact factor: 11.205

4.  The CHAOS/DIALIGN WWW server for multiple alignment of genomic sequences.

Authors:  Michael Brudno; Rasmus Steinkamp; Burkhard Morgenstern
Journal:  Nucleic Acids Res       Date:  2004-07-01       Impact factor: 16.971

5.  De novo repeat classification and fragment assembly.

Authors:  Pavel A Pevzner; Paul A Pevzner; Haixu Tang; Glenn Tesler
Journal:  Genome Res       Date:  2004-09       Impact factor: 9.043

6.  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

7.  MAVID: constrained ancestral alignment of multiple sequences.

Authors:  Nicolas Bray; Lior Pachter
Journal:  Genome Res       Date:  2004-04       Impact factor: 9.043

8.  Fragment assembly with short reads.

Authors:  Mark Chaisson; Pavel Pevzner; Haixu Tang
Journal:  Bioinformatics       Date:  2004-04-01       Impact factor: 6.937

9.  Versatile and open software for comparing large genomes.

Authors:  Stefan Kurtz; Adam Phillippy; Arthur L Delcher; Michael Smoot; Martin Shumway; Corina Antonescu; Steven L Salzberg
Journal:  Genome Biol       Date:  2004-01-30       Impact factor: 13.583

10.  Human-mouse alignments with BLASTZ.

Authors:  Scott Schwartz; W James Kent; Arian Smit; Zheng Zhang; Robert Baertsch; Ross C Hardison; David Haussler; Webb Miller
Journal:  Genome Res       Date:  2003-01       Impact factor: 9.043

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  156 in total

1.  Ensembl variation resources.

Authors:  Yuan Chen; Fiona Cunningham; Daniel Rios; William M McLaren; James Smith; Bethan Pritchard; Giulietta M Spudich; Simon Brent; Eugene Kulesha; Pablo Marin-Garcia; Damian Smedley; Ewan Birney; Paul Flicek
Journal:  BMC Genomics       Date:  2010-05-11       Impact factor: 3.969

2.  Comparative assessment of methods for aligning multiple genome sequences.

Authors:  Xiaoyu Chen; Martin Tompa
Journal:  Nat Biotechnol       Date:  2010-05-23       Impact factor: 54.908

3.  Multiple whole-genome alignments without a reference organism.

Authors:  Inna Dubchak; Alexander Poliakov; Andrey Kislyuk; Michael Brudno
Journal:  Genome Res       Date:  2009-01-28       Impact factor: 9.043

4.  PSAR-align: improving multiple sequence alignment using probabilistic sampling.

Authors:  Jaebum Kim; Jian Ma
Journal:  Bioinformatics       Date:  2013-11-12       Impact factor: 6.937

5.  Genome-wide nucleotide-level mammalian ancestor reconstruction.

Authors:  Benedict Paten; Javier Herrero; Stephen Fitzgerald; Kathryn Beal; Paul Flicek; Ian Holmes; Ewan Birney
Journal:  Genome Res       Date:  2008-10-10       Impact factor: 9.043

6.  Cactus: Algorithms for genome multiple sequence alignment.

Authors:  Benedict Paten; Dent Earl; Ngan Nguyen; Mark Diekhans; Daniel Zerbino; David Haussler
Journal:  Genome Res       Date:  2011-06-10       Impact factor: 9.043

7.  Disease and phenotype data at Ensembl.

Authors:  Giulietta M Spudich; Xosé M Fernández-Suárez
Journal:  Curr Protoc Hum Genet       Date:  2011-04

8.  An effective model for natural selection in promoters.

Authors:  Michael M Hoffman; Ewan Birney
Journal:  Genome Res       Date:  2010-03-01       Impact factor: 9.043

9.  Evolutionary dynamics of gene and isoform regulation in Mammalian tissues.

Authors:  Jason Merkin; Caitlin Russell; Ping Chen; Christopher B Burge
Journal:  Science       Date:  2012-12-21       Impact factor: 47.728

10.  A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.

Authors:  Damian Smedley; Max Schubach; Julius O B Jacobsen; Sebastian Köhler; Tomasz Zemojtel; Malte Spielmann; Marten Jäger; Harry Hochheiser; Nicole L Washington; Julie A McMurry; Melissa A Haendel; Christopher J Mungall; Suzanna E Lewis; Tudor Groza; Giorgio Valentini; Peter N Robinson
Journal:  Am J Hum Genet       Date:  2016-08-25       Impact factor: 11.025

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