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http://www.bioconductor.org/packages/release/bioc/html/TransView.html

Software package to generate, access and display read densities of sequencing based data sets such as from RNA-Seq and ChIP-Seq.

Proper citation: TransView (RRID:SCR_000358) Copy   

•   Source: SciCrunch Registry
  

http://www.bioconductor.org/packages/release/bioc/html/pvac.html

Software package that contains the function for filtering genes by the proportion of variation accounted for by the first principal component (PVAC).

Proper citation: pvac (RRID:SCR_000359) Copy   

•   Source: SciCrunch Registry
  

https://code.google.com/p/taps/

A bioinformatic tool for the identification of allele-specific copy numbers in tumor samples using data from Affymetrix SNP arrays.

Proper citation: TAPS (RRID:SCR_000356) Copy   

•   Source: SciCrunch Registry
  

https://code.google.com/p/pyrohmmsnp/

Software using a realignment-based SNP calling method for 454 and Ion Torrent sequencing data.

Proper citation: PyroHMMsnp (RRID:SCR_000357) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/cgap-align/

A time efficient read alignment tool built on the top of BWA.

Proper citation: CGAP-Align (RRID:SCR_000350) Copy   

•   Source: SciCrunch Registry
  

http://cutenmr.sourceforge.net/

A multi-platform NMR processing application.

Proper citation: cuteNMR (RRID:SCR_000347) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/jmoldraw/

2-D chemical structure drawing software program.

Proper citation: JMolDraw (RRID:SCR_000349) Copy   

•   Source: SciCrunch Registry
  

http://bioinformatics.research.nicta.com.au/software/is-rsnp/

Software tool that predicts whether a single nucleotide polymorphism (SNP) is a regulatory SNP (rSNP). For a given SNP, and using a statistical framework, it can successfully predict the set of transcription factors (TFs) for which binding is affected. The algorithm provides the statistical power to scan large numbers of SNPs, making it suitable to use to screen all associated SNPs output by a typical genome-wide association studies (GWAS).

Proper citation: is-rSNP (RRID:SCR_000387) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/as-peak/

A software that utilizes a peak detection algorithm to identify RNA-protein binding sites.

Proper citation: AS-Peak (RRID:SCR_000380) Copy   

•   Source: SciCrunch Registry
  

http://cellnet.cecad.uni-koeln.de/15763.html

R software package for transcription factor (TF) target gene prediction based on ChIP-seq data. Version 0.4 contains code to compute FDR-corrected q-values via permutations of the peak-to-gene assignments (ClosestGene only).

Proper citation: TargetCaller (RRID:SCR_000414) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/genseng/

Software for detecting copy number variations from next generation sequencing data. Used to identify regions of discrete copy number changes while simultaneously accounting for effects of multiple confounders.

Proper citation: GENSENG (RRID:SCR_000378) Copy   

•   Source: SciCrunch Registry
  

http://www.bzip.org/

A data compressor for files. This software is freely available, patent free, and is organized as a library with a programming interface.

Proper citation: bzip2 (RRID:SCR_000376) Copy   

•   Source: SciCrunch Registry
  

http://www.bioconductor.org/packages/release/bioc/html/flowFlowJo.html

A Bioconductor package that can import gates defined by the commercial package FlowJo and work with them in a manner consistent with the other flow packages in Bioconductor. FlowJo is a commercial GUI based software package from TreeStar Inc. for the visualization and analysis of flow cytometry data. One of the FlowJo standard export file types is the FlowJo Workspace. This is an XML document that describes files and manipulations that have been performed in the FlowJo GUI environment. This package can take apart the FlowJo workspace and deliver the data into R in the flowCore paradigm.

Proper citation: flowFlowJo (RRID:SCR_000410) Copy   

•   Source: SciCrunch Registry
  

http://www.bioconductor.org/packages/release/bioc/html/OLINgui.html

Software package providing a graphical user interface for the OLIN package.

Proper citation: OLINgui (RRID:SCR_000435) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/arrayplex/

Open source software that integrates various forms of microarray data from diverse annotation and primary data sources. This software provides a programmatic framework (API set) that will be used for collaborative development and deploys an easy to maintain client-server architecture.

Proper citation: ArrayPlex (RRID:SCR_000312) Copy   

•   Source: SciCrunch Registry
  

http://life.tongji.edu.cn/meqa/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 31, 2022. Software for pre-processing, quality assessment, read distribution and methylation estimation for MeDIP-sequence datasets. It has the ability to quickly analyze sequence data for DNA methylation. This software integrates customized scripting and existing utilities tools that work on both paired end and single end data.

Proper citation: MeQA (RRID:SCR_000317) Copy   

•   Source: SciCrunch Registry
  

http://sourceforge.net/projects/microanalyzer/

Java tool that performs the preprocessing of Expression and SNPs microarray Affymetrix. The software allows the automatic download and the use of the clustering and visualization software as the Mev 4.0. The tool is equipped by a graphical interface (Swing) that allows to the user to: Create the workspace (files .cel, preferred algorithms , output, libraries to use); Run/save analysis and workspace settings (xml); Efficient download of the libraries (http, ftp, MD5); Customize basic and graphical settings (objects serialization and deserialization). Type of SNPs: Mapping 500k or preceding chips, SNP 5.0, SNP 6.0. Available for 32 or 64 bit systems, and for Windows and Linux Systems.

Proper citation: Micro-Analyzer (RRID:SCR_000394) Copy   

•   Source: SciCrunch Registry
  

http://functsnp.sourceforge.net/

An R package for linking SNPs (Single Nucleotide Polymorphisms) to functional knowledge.

Proper citation: FunctSNP (RRID:SCR_000393) Copy   

•   Source: SciCrunch Registry
  

http://www.bioconductor.org/packages/release/bioc/html/flowStats.html

Software using statistical methods and functionality to analyze flow data that is beyond the basic infrastructure provided by the flowCore package.

Proper citation: flowStats (RRID:SCR_000399) Copy   

•   Source: SciCrunch Registry
  

http://code.google.com/p/d2-tools/

Software toolbox for counting the frequency of K-tuple from sequencing datasets and calculate the dissimilarity.

Proper citation: d2-tools (RRID:SCR_000425) Copy   

•   Source: SciCrunch Registry