Software tools for analyzing pairwise alignments of long sequences
Open Access
- 11 September 1991
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 19 (17) , 4663-4667
- https://doi.org/10.1093/nar/19.17.4663
Abstract
Pairwise comparison of long stretches of genomic DNA sequence can Identify regions conserved across species, which often indicate functional significance. However, the novel insights frequently must be winnowed from a flood of information; for instance, running an alignment program on two 50-kilobase sequences might yield over a hundred pages of alignments. Direct inspection of such a volume of printed output Is infeasible, or at best highly undesirable, and computer tools are needed to summarize the information, to assist in its analysis, and to report the findings. This paper describes two such software tools. One tool prepares publication-quality pictorial representations of alignments, while another facilitates interactive browsing of pairwise alignment data. Their effectiveness is illustrated by comparing the β-like globin gene clusters between humans and rabbits. A second example compares the chioroplast genomes of tobacco and liverwort.Keywords
This publication has 15 references indexed in Scilit:
- Amplification of an ancestral mammalian L1 family of long interspersed repeated DNA occurred just before the murine radiation.Proceedings of the National Academy of Sciences, 1990
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes.Proceedings of the National Academy of Sciences, 1990
- [5] Rapid and sensitive sequence comparison with FASTP and FASTAPublished by Elsevier ,1990
- Complete nucleotide sequence of the rabbit β-like globin gene clusterJournal of Molecular Biology, 1989
- Improved tools for biological sequence comparison.Proceedings of the National Academy of Sciences, 1988
- Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in manNature, 1988
- Origin of the human L1 elements: Proposed progenitor genes deduced from a consensus DNA sequenceGenomics, 1987
- NONVIRAL RETROPOSONS: GENES, PSEUDOGENES, AND TRANSPOSABLE ELEMENTS GENERATED BY THE REVERSE FLOW OF GENETIC INFORMATIONAnnual Review of Biochemistry, 1986
- Enhanced graphic matrix analysis of nucleic acid and protein sequences.Proceedings of the National Academy of Sciences, 1981