Literature DB >> 18440999

MAMOT: hidden Markov modeling tool.

Frédéric Schütz1, Mauro Delorenzi.   

Abstract

UNLABELLED: Hidden Markov models (HMMs) are probabilistic models that are well adapted to many tasks in bioinformatics, for example, for predicting the occurrence of specific motifs in biological sequences. MAMOT is a command-line program for Unix-like operating systems, including MacOS X, that we developed to allow scientists to apply HMMs more easily in their research. One can define the architecture and initial parameters of the model in a text file and then use MAMOT for parameter optimization on example data, decoding (like predicting motif occurrence in sequences) and the production of stochastic sequences generated according to the probabilistic model. Two examples for which models are provided are coiled-coil domains in protein sequences and protein binding sites in DNA. A wealth of useful features include the use of pseudocounts, state tying and fixing of selected parameters in learning, and the inclusion of prior probabilities in decoding. AVAILABILITY: MAMOT is implemented in C++, and is distributed under the GNU General Public Licence (GPL). The software, documentation, and example model files can be found at http://bcf.isb-sib.ch/mamot

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Year:  2008        PMID: 18440999     DOI: 10.1093/bioinformatics/btn201

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  8 in total

1.  Construction of a rationally designed antibody platform for sequencing-assisted selection.

Authors:  H Benjamin Larman; George Jing Xu; Natalya N Pavlova; Stephen J Elledge
Journal:  Proc Natl Acad Sci U S A       Date:  2012-10-11       Impact factor: 11.205

2.  StochHMM: a flexible hidden Markov model tool and C++ library.

Authors:  Paul C Lott; Ian Korf
Journal:  Bioinformatics       Date:  2014-01-30       Impact factor: 6.937

3.  The Wnt inhibitory factor 1 (WIF1) is targeted in glioblastoma and has a tumor suppressing function potentially by induction of senescence.

Authors:  Wanyu L Lambiv; Irene Vassallo; Mauro Delorenzi; Tal Shay; Annie-Claire Diserens; Anjan Misra; Burt Feuerstein; Anastasia Murat; Eugenia Migliavacca; Marie-France Hamou; Davide Sciuscio; Raphael Burger; Eytan Domany; Roger Stupp; Monika E Hegi
Journal:  Neuro Oncol       Date:  2011-06-03       Impact factor: 12.300

4.  MER41 repeat sequences contain inducible STAT1 binding sites.

Authors:  Christoph D Schmid; Philipp Bucher
Journal:  PLoS One       Date:  2010-07-06       Impact factor: 3.240

5.  Genome-wide analysis of binding sites and direct target genes of the orphan nuclear receptor NR2F1/COUP-TFI.

Authors:  Celina Montemayor; Oscar A Montemayor; Alex Ridgeway; Feng Lin; David A Wheeler; Scott D Pletcher; Fred A Pereira
Journal:  PLoS One       Date:  2010-01-27       Impact factor: 3.240

6.  Evaluation of methods for modeling transcription factor sequence specificity.

Authors:  Matthew T Weirauch; Atina Cote; Raquel Norel; Matti Annala; Yue Zhao; Todd R Riley; Julio Saez-Rodriguez; Thomas Cokelaer; Anastasia Vedenko; Shaheynoor Talukder; Harmen J Bussemaker; Quaid D Morris; Martha L Bulyk; Gustavo Stolovitzky; Timothy R Hughes
Journal:  Nat Biotechnol       Date:  2013-01-27       Impact factor: 54.908

7.  HMMCONVERTER 1.0: a toolbox for hidden Markov models.

Authors:  Tin Yin Lam; Irmtraud M Meyer
Journal:  Nucleic Acids Res       Date:  2009-11       Impact factor: 16.971

8.  Nuclear Factor I genomic binding associates with chromatin boundaries.

Authors:  Milos Pjanic; Christoph D Schmid; Armelle Gaussin; Giovanna Ambrosini; Jozef Adamcik; Petar Pjanic; Genta Plasari; Jan Kerschgens; Giovani Dietler; Philipp Bucher; Nicolas Mermod
Journal:  BMC Genomics       Date:  2013-02-12       Impact factor: 3.969

  8 in total

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