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Massachusetts Institute of Technology

Development of gene-finding algorithms for fungal genomes : dealing with small datasets and leveraging comparative genomics

Abstract

dc:description.abstract

A computer program called FUNSCAN was developed which identifies protein coding regions in fungal genomes. Gene structural and compositional properties are modeled using a Hidden Markov Model. Separate training and testing sets for FUNSCAN were obtained by aligning cDNAs from an organism to their genomic loci, generating a 'gold standard' set of annotated genes. The performance of FUNSCAN is competitive with other computer programs design to identify protein coding regions in fungal genomes. A technique called 'Training Set Augmentation' is described which can be used to train FUNSCAN when only a small training set of genes is available. Techniques that combine alignment algorithms with FUNSCAN to identify novel genes are also discussed and explored.

Degree

thesis:*
Department dc:contributor.department
Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science.
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2003

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Lazarovici, Allan, 1979-
Advisor dc:contributor.advisor
  • Christopher Burge.

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/1721.1/29681
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/29681

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Lazarovici, Allan, 1979-. Development of gene-finding algorithms for fungal genomes : dealing with small datasets and leveraging comparative genomics. Massachusetts Institute of Technology, 2003. http://hdl.handle.net/1721.1/29681