BlastAlign: a program that uses blast to align problematic nucleotide sequences
Author(s) -
Robert Belshaw,
Aris Katzourakis
Publication year - 2004
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/bth459
Subject(s) - perl , unix , computer science , python (programming language) , indel , software , sequence alignment , multiple sequence alignment , programming language , sequence homology , sequence (biology) , nucleic acid sequence , base sequence , genetics , biology , peptide sequence , single nucleotide polymorphism , dna , genotype , gene
BlastAlign uses NCBI blastn to build a multiple nucleotide alignment and is intended for use with sequences that have large indels or are otherwise difficult to align globally. The program builds a matrix representing regions of homology along the sequences, from which it selects the 'most representative' sequence and then extracts the blastn query-anchored multiple alignment for this sequence. The matrix is printed and allows subgroups to be identified visually and an option allows other sequences to be used as the 'most representative'. The program contains elements of both Perl and Python and will run on UNIX (including Mac OSX) and DOS. An additional Perl program BlastAlignP uses tblastn to align nucleotide sequences to a single amino acid sequence, thus allowing an open reading frame to be maintained in the resulting multiple alignment.
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