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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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  • RRID:SCR_011880

    This resource has 1+ mentions.

http://www.windowsazure.com/en-us/

An open and flexible cloud platform that enables you to quickly build, deploy and manage applications across a global network of Microsoft-managed datacenters.

Proper citation: Windows Azure (RRID:SCR_011880) Copy   


  • RRID:SCR_011881

    This resource has 100+ mentions.

https://basespace.illumina.com/home/sequence

Cloud platform to be directly integrated in to the industry?s leading sequencing platforms, with no cumbersome and time consuming data transfer steps.

Proper citation: BaseSpace (RRID:SCR_011881) Copy   


  • RRID:SCR_011882

https://sites.google.com/site/biovlab/

Cloud Computing and a graphical workflow composer that uses distributed computing resources on demand.''''

Proper citation: BioVLAB (RRID:SCR_011882) Copy   


  • RRID:SCR_011883

    This resource has 1+ mentions.

http://cloudbiolinux.org/

Offers genome analysis resources for cloud computing platforms such as Amazon EC2.

Proper citation: CloudBioLinux (RRID:SCR_011883) Copy   


  • RRID:SCR_011927

    This resource has 1+ mentions.

http://weizhong-lab.ucsd.edu/rammcap/cgi-bin/rammcap.cgi

Metagenomic software pipeline for analysis and comparison of very large metagenomes with fast clustering and functional annotation.

Proper citation: RAMMCAP (RRID:SCR_011927) Copy   


  • RRID:SCR_011889

    This resource has 1+ mentions.

http://euler.bc.edu/marthlab/scotty/scotty.php/

A tool to assist in the designing of RNA Seq experiments that have adequate power to detect differential expression at the level required to achieve experimental aims.

Proper citation: Scotty (RRID:SCR_011889) Copy   


  • RRID:SCR_011892

http://www.cs.ucr.edu/~jianxing/IsoInfer.html

A C/C++ program to infer isoforms based on short RNA-Seq (single-end and paired-end) reads, exon-intron boundary and TSS/PAS information.

Proper citation: IsoInfer (RRID:SCR_011892) Copy   


  • RRID:SCR_011894

    This resource has 1+ mentions.

http://bioinformatics.childhealthresearch.org.au/software/fusionfinder/

A perl-based software package, which can be used to find fusion transcript candidates in RNA-Seq data.

Proper citation: FusionFinder (RRID:SCR_011894) Copy   


  • RRID:SCR_011903

    This resource has 50+ mentions.

http://guide.wehi.edu.au

A desktop application for the bench biologists to analyse RNA-Seq and microarray expression data. It performs gene-centric analyses such as differential expression and pathways using well-established R modules, integrates data from multiple sources, and enables editing of R commands., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: Guide (RRID:SCR_011903) Copy   


  • RRID:SCR_011904

    This resource has 10+ mentions.

http://www.unav.es/genetica/oncofuse.html

Software tool designed to predict the oncogenic potential of fusion genes found by Next-Generation Sequencing in cancer cells.

Proper citation: Oncofuse (RRID:SCR_011904) Copy   


  • RRID:SCR_011906

    This resource has 10+ mentions.

http://bioinformatics.mdanderson.org/main/PRADA:Overview

A pipeline to analyze paired end RNA-Seq data to generate gene expression values (RPKM) and gene-fusion candidates.

Proper citation: PRADA (RRID:SCR_011906) Copy   


  • RRID:SCR_011907

    This resource has 1+ mentions.

https://mcdonaldlab.biology.gatech.edu/r-sap/

An automated bioinformatics pipeline that analyzes and quantitates high-throughput RNA-Seq datasets.

Proper citation: R-SAP (RRID:SCR_011907) Copy   


  • RRID:SCR_011908

    This resource has 10+ mentions.

http://mapman.gabipd.org/web/guest/robin

Software package for RNA-Seq-based transcriptomics. Used to analyse Illumina/Solexa-based RNA-Seq data, Affymetrix data and generic tabular two color or single channel array data. Offers variety of quality control methods that can be used to gain overview of experimental data technical quality and structure.

Proper citation: RobiNA (RRID:SCR_011908) Copy   


  • RRID:SCR_011909

    This resource has 1+ mentions.

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

An RNA-Seq analysis pipeline which offers an express implementation of analysis steps for RNA sequencing datasets.

Proper citation: RseqFlow (RRID:SCR_011909) Copy   


  • RRID:SCR_011862

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

A command line-based pipeline framework for bioinformatics research.

Proper citation: SeqPipe (RRID:SCR_011862) Copy   


  • RRID:SCR_011863

    This resource has 100+ mentions.

http://1001genomes.org/software/shore.html

A mapping and analysis pipeline for short read data produced on the Illumina platform.

Proper citation: SHORE (RRID:SCR_011863) Copy   


  • RRID:SCR_011955

    This resource has 1+ mentions.

http://www.optimaldesign.com/ArrayMiner/ArrayMiner.htm

A set of analysis tools using advanced algorithms to reveal the true structure of your gene expression data.

Proper citation: ArrayMiner (RRID:SCR_011955) Copy   


  • RRID:SCR_012105

    This resource has 10+ mentions.

http://sourceforge.net/projects/mirplant/

A user-friendly plant miRNA prediction tool.

Proper citation: miRPlant (RRID:SCR_012105) Copy   


  • RRID:SCR_012104

    This resource has 1+ mentions.

http://pypedal.sourceforge.net/

A pedigree analysis software package that provides tools for error checking, mathematical analysis, report generation, pedigree simulation, and data visualization.

Proper citation: PyPedal (RRID:SCR_012104) Copy   


  • RRID:SCR_012106

http://sourceforge.net/projects/simulatepcr/

Software that can be run from the command line for high throughput applications which can calculate all products from large lists of primers and probes compared to a large sequence database such as nt.

Proper citation: Simulate PCR (RRID:SCR_012106) Copy   



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