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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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On page 2 showing 21 ~ 40 out of 436 results
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  • RRID:SCR_012060

    This resource has 10+ mentions.

http://matnmr.sourceforge.net/

A highly flexible software toolbox for processing 1D and 2D NMR and EPR spectra under MATLAB, creating high-quality 1D, 2D or 3D plots from the spectra and printing them in every type of format that is supported by MATLAB.

Proper citation: MatNMR (RRID:SCR_012060) Copy   


  • RRID:SCR_007935

    This resource has 1+ mentions.

http://genotan.sourceforge.net/

A free software tool to identify length variation of microsatellites from short sequence reads.

Proper citation: GenoTan (RRID:SCR_007935) Copy   


  • RRID:SCR_007802

    This resource has 100+ mentions.

http://brig.sourceforge.net/

A cross-platform (Windows/Mac/Unix) application that can display circular comparisons between a large number of genomes, with a focus on handling genome assembly data.

Proper citation: BRIG (RRID:SCR_007802) Copy   


  • RRID:SCR_008548

    This resource has 1+ mentions.

http://seqpig.sourceforge.net/

A software library for Apache Pig for the distributed analysis of large sequencing datasets on Hadoop clusters.

Proper citation: SeqPig (RRID:SCR_008548) Copy   


  • RRID:SCR_002739

    This resource has 1+ mentions.

http://sourceforge.net/projects/glprobs/

Software implementing a simple and effective approach to improve the accuracy of multiple sequence alignment.

Proper citation: GLProbs (RRID:SCR_002739) Copy   


  • RRID:SCR_002838

    This resource has 100+ mentions.

http://rdock.sourceforge.net/

A fast and versatile Open Source docking software program that can be used to dock small molecules against proteins and nucleic acids.

Proper citation: rDock (RRID:SCR_002838) Copy   


  • RRID:SCR_010814

    This resource has 100+ mentions.

http://contra-cnv.sourceforge.net/

A tool for copy number variation (CNV) detection for targeted resequencing data such as those from whole-exome capture data.

Proper citation: CONTRA (RRID:SCR_010814) Copy   


  • RRID:SCR_010812

    This resource has 10+ mentions.

http://svdetect.sourceforge.net/Site/Home.html

Software application for the isolation and the type prediction of intra- and inter-chromosomal rearrangements from paired-end/mate-pair sequencing data provided by the high-throughput sequencing technologies. This tool aims to identify structural variations with both clustering and sliding-window strategies, and helping in their visualization at the genome scale. It is compatible with SOLiD and Illumina (>=1.3) reads.

Proper citation: SVDetect (RRID:SCR_010812) Copy   


  • RRID:SCR_010750

    This resource has 50+ mentions.

http://sourceforge.net/apps/mediawiki/wgs-assembler/index.php?title=Main_Page

A de novo whole-genome shotgun (WGS) DNA sequence assembler.

Proper citation: Celera assembler (RRID:SCR_010750) Copy   


  • RRID:SCR_010857

    This resource has 100+ mentions.

http://sourceforge.net/apps/mediawiki/vancouvershortr/index.php?title=FindPeaks

Software application that can be used for converting Eland, Maq (.map), BED or other files into WIG files and identifying areas of enrichment (ChIP-Seq analysis).

Proper citation: FindPeaks (RRID:SCR_010857) Copy   


  • RRID:SCR_010930

    This resource has 1+ mentions.

http://genovar.sourceforge.net/

A Detection and Visualization software tool for Genomic Variants.

Proper citation: Genovar (RRID:SCR_010930) Copy   


  • RRID:SCR_010863

    This resource has 10+ mentions.

http://ranger.sourceforge.net/

Software for a multi-purpose ChIP Seq peak caller.

Proper citation: PeakRanger (RRID:SCR_010863) Copy   


  • RRID:SCR_010914

    This resource has 100+ mentions.

http://biodoop-seal.sourceforge.net/

A suite of distributed software applications for aligning short DNA reads, and manipulating and analyzing short read alignments.

Proper citation: SEAL (RRID:SCR_010914) Copy   


  • RRID:SCR_010911

http://sourceforge.net/apps/mediawiki/cloudburst-bio/index.php?title=CloudBurst

A new parallel read-mapping algorithm optimized for mapping next-generation sequence data to the human genome and other reference genomes, for use in a variety of biological analyses including SNP discovery, genotyping, and personal genomics.

Proper citation: CloudBurst (RRID:SCR_010911) Copy   


  • RRID:SCR_010912

    This resource has 10+ mentions.

http://erne.sourceforge.net/

A short string alignment package whose goal is to provide an all-inclusive set of tools to handle short (NGS-like) reads.

Proper citation: ERNE (RRID:SCR_010912) Copy   


  • RRID:SCR_010981

http://dnptrapper.sourceforge.net/

An assembly editing and visualization tool specifically designed for manual analysis and finishing of repeated regions.

Proper citation: DNPTrapper (RRID:SCR_010981) Copy   


  • RRID:SCR_010982

    This resource has 1+ mentions.

http://sourceforge.net/apps/mediawiki/amos/index.php?title=Hawkeye

A visual analytics tool for genome assembly analysis and validation, designed to aid in identifying and correcting assembly errors.

Proper citation: Hawkeye (RRID:SCR_010982) Copy   


  • RRID:SCR_012040

    This resource has 500+ mentions.

http://mzmine.sourceforge.net/

Software for mass-spectrometry data processing, with the main focus on LC-MS data.

Proper citation: MZmine (RRID:SCR_012040) Copy   


  • RRID:SCR_012097

    This resource has 1000+ mentions.

http://sourceforge.net/projects/exorca/

A Matlab package extending the scope of established COBRA metabolic modelling.

Proper citation: ORCA (RRID:SCR_012097) Copy   


  • RRID:SCR_012096

    This resource has 100+ mentions.

http://opencobra.sourceforge.net/openCOBRA/Welcome.html

Software Python package that provides support for basic COnstraint-Based Reconstruction and Analysis (COBRA) methods.

Proper citation: COBRApy (RRID:SCR_012096) Copy   



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