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http://cpfp.sourceforge.net/

Software providing a data analysis pipeline for shotgun mass-spectrometry proteomics.

Proper citation: CPFP (RRID:SCR_012043) Copy   

•   Source: SciCrunch Registry
  

http://open-ms.sourceforge.net/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 23rd,2023. Software that combines Lagrangian relaxation for solving an integer linear programming formulation with an adaptation of Yen''s k shortest paths algorithm.

Proper citation: Antilope (RRID:SCR_012046) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/swisspit/

Software for pipelined analysis of mass spectrometry data.

Proper citation: swissPIT (RRID:SCR_012045) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/icplquant/

A proteomics software tool for quantitatively analyzing large mass spectrometric datasets acquired from ICPL based proteomics experiments.

Proper citation: ICPL ESIQuant (RRID:SCR_012047) Copy   

•   Source: SciCrunch Registry
  

http://quantbio-tools.princeton.edu/cgi-bin/COALESCE

Software that can use large collections of genomic data and Bayesian integration to predict coregulated gene modules, the conditions of regulation, and the consensus binding motifs for regulation.

Proper citation: COALESCE (RRID:SCR_012005) Copy   

•   Source: SciCrunch Registry
  

http://www.bioinformatics.org/

Organization that serves the scientific and educational needs of bioinformatic practitioners and the general public. They develop and maintain computational resources to facilitate world-wide communications and collaborations between people of all educational and professional levels. They provide and promote open access to the materials and methods required for, and derived from, research, development and education.

Proper citation: Bioinformatics Organization (RRID:SCR_012008) Copy   

•   Source: SciCrunch Registry
  

http://bionotate.sourceforge.net/

An open source annotation tool for the distributed creation of a large corpus.

Proper citation: Bionotate (RRID:SCR_012098) Copy   

•   Source: SciCrunch Registry
  

http://bioinfo-out.curie.fr/projects/snp_gap/

Software for automatic detection of absolute segmental copy numbers and genotype status in complex cancer genome profiles measured by single-nucleotide polymorphism (SNP) arrays. The method is based on pattern recognition of segmented and smoothed copy number and allelic imbalance profiles. The method performs well even for poor-quality data, low tumor content, and highly rearranged tumor genomes.

Proper citation: Genome Alteration Print (RRID:SCR_012016) Copy   

•   Source: SciCrunch Registry
  

http://www.bioconductor.org/packages/2.11/bioc/html/easyRNASeq.html

Software that calculates the coverage of high-throughput short-reads against a genome of reference and summarizes it per feature of interest (e.g. exon, gene, transcript). The data can be normalized as ''RPKM'' or by the ''DESeq'' or ''edgeR'' package.

Proper citation: easyRNASeq (RRID:SCR_012020) Copy   

•   Source: SciCrunch Registry
  

http://srna-workbench.cmp.uea.ac.uk/tools/visualisation-tools/vissr/

Software to generate a visual representation of sRNAs and user-imported genomic features. The tool may be run on its own or from other tools, e.g. miRCat.

Proper citation: VisSR (RRID:SCR_012024) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/pegasus-fus/

Software that annotates biologically functional gene fusion candidates.

Proper citation: Pegasus-fus (RRID:SCR_012118) Copy   

•   Source: SciCrunch Registry
  

https://github.com/WaveCNV

Cancer specific CNV caller for Next Generation sequence.

Proper citation: WaveCNV (RRID:SCR_012244) Copy   

•   Source: SciCrunch Registry
  

https://github.com/BEETL/BEETL

Software tool as data transformation algorithm that restructures data in such a way that the transformed message is more compressible. Used for large scale compression of genomic sequence databases.

Proper citation: Burrows-Wheeler transform (RRID:SCR_012304) Copy   

•   Source: SciCrunch Registry
  

http://code.google.com/p/npstat/

Software that implements some population genetics tests and estimators that can be applied to pooled sequences from Next Generation Sequencing experiments.

Proper citation: npstat (RRID:SCR_012128) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/nailsystemsbiology/

A set of software tools to simplify the range of computational activities involved in regulatory network inference. It is technology-independent and includes an interface layer to allow easy integration of components into other applications. It is implemented in MATLAB and is available for all researchers to use.

Proper citation: NAIL (RRID:SCR_012134) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/imsat/

A python program that uses the polymorphism data obtained from mapping individual Illumina sequence reads onto a reference genome to identify polymorphic STRs.

Proper citation: iMSAT (RRID:SCR_012135) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/nesmapper/

A computational software tool to predict leucine-rich nuclear export signals (NESs) by using profiles that had been further optimized by training and combining the amino acid properties of the NES-flanking regions. It is a multiplatform command-line Perl application with activity-based NES profiles.

Proper citation: NESmapper (RRID:SCR_012138) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/dhacdist/

Software for clustering time-evolving networks.

Proper citation: DHAC (RRID:SCR_012139) Copy   

•   Source: SciCrunch Registry
  

https://code.google.com/p/mp-est/

Software that can consistently estimate the topology and branch lengths (in coalescent units) of the species tree. Although the pseudo-likelihood is derived from coalescent theory, and assumes no gene flow or horizontal gene transfer (HGT), the MP-EST method is robust to a small amount of HGT in the dataset. In addition, increasing the number of genes does not increase the computational time substantially. The MP-EST method is fast for analyzing datasets that involve a large number of genes but a moderate number of species.

Proper citation: MP-EST (RRID:SCR_012145) Copy   

•   Source: SciCrunch Registry
  

http://xmsanalyzer.sourceforge.net

A software package of utilities for data extraction, quality control assessment, detection of overlapping and unique metabolites in multiple datasets, and batch annotation of metabolites. xMSanalyzer comprises of utilities that can be classified into five main modules: 1) merging apLCMS or XCMS sample processing results from multiple sets of parameter settings, 2) evaluation of sample quality, feature consistency, and batch-effect, 3) feature matching, and 4) characterization of m/z using KEGG REST; 5) Batch-effect correction using ComBat.

Proper citation: xMSanalyzer (RRID:SCR_012144) Copy   

•   Source: SciCrunch Registry