ABCC Advanced Biomedical Computing Center Advanced Biomedical Computing Center ABCC Home Jobs Search Sitemap
About ABCC Science Resources Communications Training Links Contact Us





Category Menu
Bioinformatics
Molecular Modeling(1)
Molecular Modeling(2)
Molecular Visualization(1)
Molecular Visualization(2)
Quantum Chemistry
XRay/NMR Structure Refinement
Other

   
ABCC Applications Web Page

Welcome to the ABCC Accessible Application Web Page.

From this page, you can get information about our scientific applications and databases. To get more information about any topic, or to run an application, click on any of the mouseover popup menu items on the left-hand side. Program with a tag "Run" is runnable. This site continues to grow, so come back often to check out the many accessible applications available here at the Advanced Biomedical Computing Center (ABCC).

If you have any comments or suggestions, please contact us Help link

Phylogenetic Analysis

LARD
LARD detects and characterizes recombination between DNA sequences using maximum likelihood. LARD is decscribed in detail in the following paper: Holmes, E.C., Worobey, M., and Rambaut, A., 1999 "Phylogenetic Evidence for Recombination in Dengue Virus" Molecular Biology and Evolution 16:405.
Website: Click Here

PHYLIP
PHYLIP (the PHYLogeny Inference Package) is a package of programs for inferring phylogenies (evolutionary trees). Methods that are available in the package include parsimony, distance matrix, and likelihood methods, including bootstrapping and consensus trees. Data types that can be handled include molecular sequences, gene frequencies, restriction sites, distance matrices, and 0/1 discrete characters. The programs are controlled through a menu, which asks the users which options they want to set, and allows them to start the computation. The data are read into the program from a text file, which the user can prepare using any word processor or text editor. Some sequence analysis programs such as alignment programs can write data files in the PHYLIP format. Output is written onto special files with names like "outfile" and "treefile". Trees written onto "treefile" are in the Newick format, an informal standard agreed to in 1986 by authors of a number of major phylogeny packages.
Website: Click Here

Topal
TOPAL checks for evidence of past recombination events, by looking for changes in the inferred phylogenetic tree topology between adjacent regions of a multiple sequence alignment. It detects recombinations by sliding a window along a sequence alignment, and measuring the discrepancy between the trees suggested by the first and second halves of the window, using distance matrix methods. Topal method is described in: - McGuire, G., F. Wright, and M. J. Prentice. 1997. A graphical method for detecting recombination in phylogenetic data sets. Molecular Biology and Evolution 14: 1125-1131. The TOPAL 2.0 program, and recent changes to the method, are described in: - McGuire, G. and F. Wright. 2000. TOPAL 2.0 : improved detection of mosaic sequences within multiple alignments. Bioinformatics 16: 130-134.
Website: Click Here



National Cancer Institute
National Cancer Institute at Frederick
Problems/Comments: Feedback & Issues
Site Coordinator: ABCC Site Coordinator Last Modified: July 28, 2004
Copyright © 2002, ABCC
National Institutes of Health
Advanced Biomedical Computing Center