trace2dbEST 3.0.1 – Turn Traces into Expressed Sequence Tags

trace2dbEST 3.0.1

:: DESCRIPTION

trace2dbEST process raw sequenceing chromatograph trace files from EST projects into quality-checked sequences, ready for submission to dbEST. trace2dbEST guides you through the creation of all the necessary files for submission of ESTs to dbEST.

::DEVELOPER

The Blaxter Lab at The Institute of Evolutionary Biology University of Edinburgh

:: SCREENSHOTS

N/A

:: REQUIREMENTS

:: DOWNLOAD

trace2dbEST

:: MORE INFORMATION

Citation:

J Parkinson, A Anthony, J Wasmuth, R Schmid, A Hedley, M Blaxter: PartiGene—constructing partial genomes, Bioinformatics 2004 20(9):1398-404).

 

Sybil 1.5.1 – Web-based software for Comparative Genomics

Sybil 1.5.1

:: DESCRIPTION

Sybil is a web-based software package for comparative genomics, whose primary goal is to facilitate the analysis and visualization of comparative genome data, with a particular emphasis on protein and gene cluster data. Herein, a two-phase protein clustering algorithm, used to generate protein clusters suitable for analysis through Sybil and a method for creating graphical displays of protein or gene clusters that span multiple genomes are described. When combined, these two relatively simple techniques provide the user of the Sybil software (The Institute for Genomic Research [TIGR] Bioinformatics Department) with a browsable graphical display of his or her “input” genomes, showing which genes are conserved based on the parameters supplied to the protein clustering algorithm. For any given protein cluster the graphical display consists of a local alignment of the genomes in which the clustered genes are located. The genomes are arranged in a vertical stack, as in a multiple alignment, and shaded areas are used to connect genes in the same cluster, thus displaying conservation at the protein level in the context of the underlying genomic sequences. The authors have found this display-and slight variants thereof-useful for a variety of annotation and comparison tasks, ranging from identifying “missed” gene models or single-exon discrepancies between orthologous genes, to finding large or small regions of conserved gene synteny, and investigating the properties of the breakpoints between such regions.

::DEVELOPER

J. Craig Venter Institute

:: SCREENSHOTS

:: REQUIREMENTS

:: DOWNLOAD

Sybil

:: MORE INFORMATION

Citation:

Crabtree J, Angiuoli SV, Wortman JR, White OR.
Sybil: methods and software for multiple genome comparison and visualization.
Methods Mol Biol. 2007;408:93-108.

VariantClassifier 20100603 – Hierarchical Variant Classifier for Annotated Genomes

VariantClassifier 20100603

:: DESCRIPTION

VariantClassifier is a software tool for hierarchically classifying variants based on the genome annotation that is provided.  Instead of looking at a region of the genome and seeing all the features relative to each other on the genomic axis, the VariantClassifier inverts the process so that novel variants can be tested for interest, based on the known features on the genomic axis.  Furthermore, our hierarchical classification provides a prioritization of the variants that should be considered for more intensive study.

::DEVELOPER

J. Craig Venter Institute

:: SCREENSHOTS

N/A

:: REQUIREMENTS

:: DOWNLOAD

VariantClassifier

:: MORE INFORMATION

Citation:

Kelvin Li and Timothy B Stockwell
VariantClassifier: A hierarchical variant classifier for annotated genomes
BMC Research Notes 2010, 3:191doi:10.1186/1756-0500-3-191

DIYA 1.0.1 – Microbial Genome Sequences Annotation

DIYA 1.0.1

:: DESCRIPTION

DIYA (Do-It-Yourself Annotator) is a modular and configurable open source pipeline framework, written in Perl, used for the rapid annotation of microbial genome sequences. The software is currently used to take nucleotide sequence contigs as input, either in the form of complete genomes or the result of shotgun sequencing, and produce an annotated sequence.

::DEVELOPER

Navy Medical Research Center

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux / Windows /Mac OsX
  • Perl

:: DOWNLOAD

DIYA

:: MORE INFORMATION

Citation:

Andrew C. Stewart, Brian Osborne and Timothy D. Read
DIYA: a bacterial annotation pipeline for any genomics lab
Bioinformatics (2009) 25 (7): 962-963.doi: 10.1093

GeneSplicer – Detecting Splice Sites in Eukaryotic Genomic DNA

GeneSplicer

:: DESCRIPTION

GeneSplicer is a fast, flexible system for detecting splice sites in the genomic DNA of various eukaryotes. The system has been trained and tested successfully on Plasmodium falciparum (malaria), Arabidopsis thaliana, human, Drosophila, and rice . Training data sets for human and Arabidopsis thaliana are included.

::DEVELOPER

the Center for Bioinformatics and Computational Biology

:: SCREENSHOTS

N/A

:: REQUIREMENTS

:: DOWNLOAD

GeneSplicer

:: MORE INFORMATION

The GeneSplicer software is OSI Certified Open Source Software.

Citation:

Pertea , X. Lin , S. L. Salzberg . GeneSplicer : a new computational method for splice site prediction . Nucleic Acids Res . 2001 Mar 1;29(5):1185-90 .

JIGSAW 3.2.10 – Automated Gene Annotation System

JIGSAW 3.2.10

:: DESCRIPTION

JIGSAW is a program designed to use the output from gene finders, splice site prediction programs and sequence alignments to predict gene models. The program provides an automated way to take advantage of the many succsessful methods for computational gene prediction and can provide substantial improvements in accuracy over an individual gene prediction program.

::DEVELOPER

Jonathan E. Allen at the Center for Bioinformatics and Computational Biology

:: SCREENSHOTS

N/A

:: REQUIREMENTS

:: DOWNLOAD

JIGSAW

:: MORE INFORMATION

The JIGSAW software is OSI Certified Open Source Software.

Citation:

J.E. Allen, W.H. Majoros, M. Pertea, and S.L. Salzberg.  JIGSAW, GeneZilla, and GlimmerHMM: puzzling out the features of human genes in the ENCODE regions.  Genome Biology 2007, 7(Suppl):S9.

ExAlt 1.0 – Alternative Exon Isoform Prediction

ExAlt 1.0

:: DESCRIPTION

ExAlt is a software program designed to predict alternatively spliced overlapping exons in genomic sequence. The program works in several ways depending on the available input. ExAlt can use information about existing gene structure as well as sequence conservation to improve the precision of its predictions. ExAlt can also make predictions when only a single genomic sequence is available.

::DEVELOPER

Jonathan E. Allen at the Center for Bioinformatics and Computational Biology

:: SCREENSHOTS

N/A

:: REQUIREMENTS

:: DOWNLOAD

ExAlt

:: MORE INFORMATION

The ExAlt software is OSI Certified Open Source Software.

Citation:

J. E. Allen and S. L. Salzberg. A phylogenetic generalized hidden Markov model for predicting alternatively spliced exons.Algorithms for Molecular Biology, 1:14, 2006.

 

TWAIN – Syntenic Gene Finder

TWAIN

:: DESCRIPTION

TWAIN is a software to predict genes simultaneously in two closely related eukaryotic organisms.TWAIN is a new syntenic genefinder which employs a Generalized Pair Hidden Markov Model (GPHMM) to predict genes in two closely related eukaryotic genomes simultaneously.It utilizes the MUMmer package to perform approximate alignment before applying a GPHMM based on an enhanced version of the TigrScan gene finder.

::DEVELOPER

Bill Majoros and Mihaela Pertea while at the J. Craig Venter Institute

:: SCREENSHOTS

N/A

:: REQUIREMENTS

:: DOWNLOAD

TWAIN

:: MORE INFORMATION

Citation

Majoros W.H., Pertea M., Salzberg S.L. (2005) Efficient implementation of a Generalized Pair Hidden Markov Model for comparative gene findingBioinformatics 21 1782-1788.

Refcomp 4.x – Compare Reference Sequence with Consensus Sequence

Refcomp 4.x

:: DESCRIPTION

Refcomp was designed to analyze sequencing traces which contains data from strictly homozygous samples (eg. cloned DNA, mitochondrial DNA, etc.).  This data represents a special case which can be analyzed for mismatches with a known reference sequence.  Refcomp will determine the high quality positions within an assembled DNA contig and produce a report listing sites which differ from a defined reference sequence.

Refcomp is designed as a member of an integrated suite of sequence analysis applications which includes Phred,Phrap and Consed, and is not a stand alone program.

::DEVELOPER

Dr. Deborah Nickerson’s lab at the University of Washington

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux/Mac OsX/Solaris/SGI IRIX/Compaq Tru64 Alpha/HP-UX

:: DOWNLOAD

Refcomp

:: MORE INFORMATION

RefComp is available for free to researchers at academic and non-profit institutions. To aquire RefComp, please Read the Academic License Agreement, and fill in and submit the request form.

Citation:

Rieder et al,Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome., Nucleic Acids Research, 26: 967-973, 1998.

 

PolyPhred 6.18 – SNP Detection

PolyPhred 6.18

:: DESCRIPTION

PolyPhred is a program that compares fluorescence-based sequences across traces obtained from different individuals to identify heterozygous sites for single nucleotide substitutions. PolyPhred is not a stand alone application. PolyPhred’s functions are integrated with the use of three other programs: Phred, Phrap, and Consed . PolyPhred identifies potential heterozygotes using the base calls and peak information provided by Phred and the sequence alignments provided by Phrap. Potential heterozygotes identified by PolyPhred are marked for rapid inspection using the Consed tool.

::DEVELOPER

Dr. Deborah Nickerson’s lab at the University of Washington

:: SCREENSHOTS

:: REQUIREMENTS

  • Linux/Mac OsX/Solaris/SGI IRIX/Compaq Tru64 Alpha/HP-UX

:: DOWNLOAD

PolyPhred ; Documation

:: MORE INFORMATION

PolyPhred is available for free to researchers at academic and non-profit institutions.

Commercial businesses wanting to acquire PolyPhred are required to purchase a commercial license agreement.