Kangaroo – A pattern-matching program for biological sequences

<p>Abstract</p> <p>Background</p> <p>Biologists are often interested in performing a simple database search to identify proteins or genes that contain a well-defined sequence pattern. Many databases do not provide straightforward or readily available query tools to perf...

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Bibliographic Details
Main Authors: Betel Doron, Hogue Christopher WV
Format: Article
Language:English
Published: BMC 2002-07-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/3/20
Description
Summary:<p>Abstract</p> <p>Background</p> <p>Biologists are often interested in performing a simple database search to identify proteins or genes that contain a well-defined sequence pattern. Many databases do not provide straightforward or readily available query tools to perform simple searches, such as identifying transcription binding sites, protein motifs, or repetitive DNA sequences. However, in many cases simple pattern-matching searches can reveal a wealth of information. We present in this paper a regular expression pattern-matching tool that was used to identify short repetitive DNA sequences in human coding regions for the purpose of identifying potential mutation sites in mismatch repair deficient cells.</p> <p>Results</p> <p>Kangaroo is a web-based regular expression pattern-matching program that can search for patterns in DNA, protein, or coding region sequences in ten different organisms. The program is implemented to facilitate a wide range of queries with no restriction on the length or complexity of the query expression. The program is accessible on the web at <url>http://bioinfo.mshri.on.ca/kangaroo/</url> and the source code is freely distributed at <url>http://sourceforge.net/projects/slritools/</url>.</p> <p>Conclusion</p> <p>A low-level simple pattern-matching application can prove to be a useful tool in many research settings. For example, Kangaroo was used to identify potential genetic targets in a human colorectal cancer variant that is characterized by a high frequency of mutations in coding regions containing mononucleotide repeats.</p>
ISSN:1471-2105