Literature DB >> 17489682

Computation and analysis of genomic multi-sequence alignments.

Mathieu Blanchette1.   

Abstract

Multi-sequence alignments of large genomic regions are at the core of many computational genome-annotation approaches aimed at identifying coding regions, RNA genes, regulatory regions, and other functional features. Such alignments also underlie many genome-evolution studies. Here we review recent computational advances in the area of multi-sequence alignment, focusing on methods suitable for aligning whole vertebrate genomes. We introduce the key algorithmic ideas in use today, and identify publicly available resources for computing, accessing, and visualizing genomic alignments. Finally, we describe the latest alignment-based approaches to identify and characterize various types of functional sequences. Key areas of research are identified and directions for future improvements are suggested.

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Year:  2007        PMID: 17489682     DOI: 10.1146/annurev.genom.8.080706.092300

Source DB:  PubMed          Journal:  Annu Rev Genomics Hum Genet        ISSN: 1527-8204            Impact factor:   8.929


  13 in total

1.  PhyLAT: a phylogenetic local alignment tool.

Authors:  Hongtao Sun; Jeremy D Buhler
Journal:  Bioinformatics       Date:  2012-04-06       Impact factor: 6.937

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.  Principal components analysis of protein sequence clusters.

Authors:  Bo Wang; Michael A Kennedy
Journal:  J Struct Funct Genomics       Date:  2014-02-05

4.  PSAR: measuring multiple sequence alignment reliability by probabilistic sampling.

Authors:  Jaebum Kim; Jian Ma
Journal:  Nucleic Acids Res       Date:  2011-05-16       Impact factor: 16.971

Review 5.  Positional orthology: putting genomic evolutionary relationships into context.

Authors:  Colin N Dewey
Journal:  Brief Bioinform       Date:  2011-06-24       Impact factor: 11.622

6.  Phylo: a citizen science approach for improving multiple sequence alignment.

Authors:  Alexander Kawrykow; Gary Roumanis; Alfred Kam; Daniel Kwak; Clarence Leung; Chu Wu; Eleyine Zarour; Luis Sarmenta; Mathieu Blanchette; Jérôme Waldispühl
Journal:  PLoS One       Date:  2012-03-07       Impact factor: 3.240

7.  Exploiting ancestral mammalian genomes for the prediction of human transcription factor binding sites.

Authors:  Mathieu Blanchette
Journal:  BMC Bioinformatics       Date:  2012-12-19       Impact factor: 3.169

8.  Performance and scalability of discriminative metrics for comparative gene identification in 12 Drosophila genomes.

Authors:  Michael F Lin; Ameya N Deoras; Matthew D Rasmussen; Manolis Kellis
Journal:  PLoS Comput Biol       Date:  2008-04-18       Impact factor: 4.475

9.  Rapid detection and curation of conserved DNA via enhanced-BLAT and EvoPrinterHD analysis.

Authors:  Amarendra S Yavatkar; Yong Lin; Jermaine Ross; Yang Fann; Thomas Brody; Ward F Odenwald
Journal:  BMC Genomics       Date:  2008-02-28       Impact factor: 3.969

10.  Open-Phylo: a customizable crowd-computing platform for multiple sequence alignment.

Authors:  Daniel Kwak; Alfred Kam; David Becerra; Qikuan Zhou; Adam Hops; Eleyine Zarour; Arthur Kam; Luis Sarmenta; Mathieu Blanchette; Jérôme Waldispühl
Journal:  Genome Biol       Date:  2013       Impact factor: 13.583

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