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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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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
SnpEff
 
Resource Report
Resource Website
5000+ mentions
SnpEff (RRID:SCR_005191) SnpEff software resource Genetic variant annotation and effect prediction software toolbox that annotates and predicts effects of variants on genes (such as amino acid changes). By using standards, such as VCF, SnpEff makes it easy to integrate with other programs. genome, genetic variant, annotation, effect, variant, gene, cancer variant, gatk, hgsv, single nucleotide polymorphisms, genome sequence, java, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Galaxy
is related to: GATK
has parent organization: SourceForge
has parent organization: Wayne State University; Michigan; USA
works with: SnpSift
Cancer PMID:22728672 Free, Freely available biotools:snpeff, OMICS_00186 https://bio.tools/snpeff, https://sources.debian.org/src/snpeff/ SCR_005191 SnpEff - Genetic variant annotation and effect prediction toolbox 2026-09-12 12:56:22 5640
inGAP
 
Resource Report
Resource Website
10+ mentions
inGAP (RRID:SCR_005261) inGAP software resource Software mining pipeline guided by a Bayesian principle to detect single nucleotide polymorphisms, insertion and deletions by comparing high-throughput pyrosequencing reads with a reference genome of related organisms. This pipeline is extended to identify and visualize large-size structural variations, including insertions, deletions, inversions and translocations. structural variation, genome, next-generation sequence, genome analysis, alignment, single nucleotide polymorphism, insertion, deletion, indel, inversion, translocation, windows, linux, macos/x, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
has parent organization: Fudan University; Shanghai; China
has parent organization: Chinese Academy of Sciences; Beijing; China
OMICS_00319, biotools:ingap https://bio.tools/ingap SCR_005261 inGAP-sv, inGAP-sv: structural variation detection and visualization, integrative next-generation genome analysis pipeline 2026-09-12 12:56:23 29
CoverageCalculator
 
Resource Report
Resource Website
1+ mentions
CoverageCalculator (RRID:SCR_005352) CoverageCalculator software resource Small and very fast utility to calculate X-coverage from Next-Generation-Sequencing data. next-generation sequencing is listed by: OMICtools
has parent organization: SourceForge
OMICS_01164 SCR_005352 2026-09-12 12:56:24 2
mrFAST
 
Resource Report
Resource Website
10+ mentions
mrFAST (RRID:SCR_005487) mrFAST software resource Software designed to map short reads generated with the Illumina platform to reference genome assemblies; in a fast and memory-efficient mannerl. Currently Supported Features: * Output in SAM format * Indels up to 8 bp (4 bp deletions and 4 bp insertions) * Paired-end mapping ** Discordant option to generate mapping file ready for VariationHunter to detect structural variants. * One end anchored (OEA) map locations for novel sequence insertion detection with NovelSeq * Matepair library mapping (long inserts with RF orientation). Planned Features: * Multithreading next-generation sequencing, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: SPLITREAD
has parent organization: SourceForge
PMID:19718026 biotools:mrfast, OMICS_00671 https://bio.tools/mrfast SCR_005487 mrFAST - Micro Read Fast Alignment Search Tool, Micro Read Fast Alignment Search Tool 2026-09-12 12:56:26 16
CUSHAW2-GPU
 
Resource Report
Resource Website
CUSHAW2-GPU (RRID:SCR_005480) CUSHAW2-GPU software resource Software program (based on CUSHAW2) designed and optimized for Kepler-based GPUs, but still workable on earlier-generation Fermi-based ones. c++, genome, alignment is listed by: OMICtools
is related to: CUSHAW
has parent organization: SourceForge
Apache License OMICS_00659 SCR_005480 2026-09-12 12:56:26 0
SolexaQA
 
Resource Report
Resource Website
100+ mentions
SolexaQA (RRID:SCR_005421) SolexaQA data analysis software, data processing software, data visualization software, sequence analysis software, software application, software resource Software package to calculate sequence quality statistics and create visual representations of data quality for Illumina's second-generation sequencing technology. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:20875133 Acknowledgement requested biotools:solexaqa, OMICS_01078 https://bio.tools/solexaqa SCR_005421 2026-09-12 12:56:25 297
CUSHAW
 
Resource Report
Resource Website
1+ mentions
CUSHAW (RRID:SCR_005479) CUSHAW software resource Software package for next-generation sequencing read alignment that is fast and parallel gapped read alignment to large genomes, such as the human genome. next-generation sequencing, read alignment, genome, alignment is listed by: OMICtools
is related to: CUSHAW2-GPU
has parent organization: Johannes Gutenberg University Mainz; Rhineland-Palatinate; Germany
has parent organization: SourceForge
PMID:22576173
PMID:24466273
OMICS_00658 SCR_005479 CUSHAW2, CUSHAW3 2026-09-12 12:56:26 2
NGSView
 
Resource Report
Resource Website
1+ mentions
NGSView (RRID:SCR_005637) NGSView software resource A generally applicable, flexible and extensible next-generation sequence alignment editor. The software allows for visualization and manipulation of millions of sequences simultaneously on a desktop computer, through a graphical interface. next-generation sequence, alignment, edit, visualization, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
Acknowledgement requested biotools:ngsview, OMICS_00891 https://bio.tools/ngsview SCR_005637 2026-09-12 12:56:29 2
SAMtools Text Alignment Viewer
 
Resource Report
Resource Website
1+ mentions
SAMtools Text Alignment Viewer (RRID:SCR_005611) SAMtools tview software resource Text alignment viewer software based on the GNU ncurses library that works with short indels and shows MAQ consensus. It uses different colors to display mapping quality or base quality, subjected to users' choice. text alignment, viewer, maq consensus, indel is listed by: OMICtools
has parent organization: SourceForge
OMICS_00893 SCR_005611 Text Alignment Viewer 2026-09-12 12:56:28 1
Manatee
 
Resource Report
Resource Website
50+ mentions
Manatee (RRID:SCR_005685) Manatee software resource Manatee is a web-based gene evaluation and genome annotation tool; Manatee can store and view annotation for prokaryotic and eukaryotic genomes. The Manatee interface allows biologists to quickly identify genes and make high quality functional assignments, such as GO classifications, using search data, paralogous families, and annotation suggestions generated from automated analysis. Manatee can be downloaded and installed to run under the CGI area of a web server, such as Apache. Platform: Online tool, Linux compatible, Solaris gene, genome, annotation, ontology or annotation browser, ontology or annotation editor is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: J. Craig Venter Institute
has parent organization: University of Maryland School of Medicine; Maryland; USA
has parent organization: SourceForge
Open unspecified license - Free for academic use nlx_149128 SCR_005685 2026-09-12 12:56:29 64
cancergrid-tma
 
Resource Report
Resource Website
cancergrid-tma (RRID:SCR_005595) cancergrid-tma software resource A web-based application for the management and storage of tissue microarray (TMA) images and the associated metadata. The application enables the user to navigate a grid of TMA core images within a slide, zoom and pan around an image, and enter a score constrained to a specific scoring system. The submitted scores are scored in the eXist open source database, in an XML format, which is compatible with existing TMA standards, and thus allow the data to be archived and re-used in future analysis. tissue microarray, image is listed by: OMICtools
has parent organization: SourceForge
OMICS_00816 SCR_005595 Cancergrid Image Scorer 2026-09-12 12:56:28 0
Sybil
 
Resource Report
Resource Website
10+ mentions
Sybil (RRID:SCR_005593) Sybil data or information resource, database, software resource A web-based software package for comparative genomics. comparative genomics, genome, synteny, protein cluster, protein, gene, genomic region, synteny gradient, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:22121156 OMICS_00945, biotools:sybil https://bio.tools/sybil SCR_005593 Sybil: Web-based software for comparative genomics 2026-09-12 12:56:28 37
dna-bison
 
Resource Report
Resource Website
1+ mentions
dna-bison (RRID:SCR_005913) dna-bison software resource Allows users with access to a computer cluster to rapidly align whole-genome bisulfite sequencing or RRBS reads. is listed by: OMICtools
has parent organization: SourceForge
OMICS_00582 SCR_005913 2026-09-12 12:56:33 1
Multiscale Object Orientation Simulation Environment
 
Resource Report
Resource Website
100+ mentions
Multiscale Object Orientation Simulation Environment (RRID:SCR_008031) simulation software, software application, software resource MOOSE is the Multiscale Object-Oriented Simulation Environment. It is the base and numerical core for large, detailed simulations including Computational Neuroscience and Systems Biology. MOOSE spans the range from single molecules to subcellular networks, from single cells to neuronal networks, and to still larger systems. it is backwards-compatible with GENESIS, and forward compatible with Python and XML-based model definition standards like SBML and MorphML. MOOSE is coordinating with the GENESIS-3 project towards the goals of developing educational resources for modeling. MOOSE is open source software, licensed under the LGPL (Lesser GNU Public License). It has absolutely no warranty. Sponsors: - National Center of Biological Sciences (NCBS) - National Institutes of Health (NIH) Collaboration - EU-India grid - Department of Atomic Energy Science Research Council (DAE/SRC) - Department of Biotechnology (DBT) cell, computational, molecule, network, neuronal, neuroscience, simulation, subcellular, systems biology is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: MUlti SImulation Coordinator
has parent organization: SourceForge
nif-0000-10307 http://www.nitrc.org/projects/moose SCR_008031 MOOSE 2026-09-12 12:56:59 313
GARM
 
Resource Report
Resource Website
10+ mentions
GARM (RRID:SCR_006731) GARM software resource A new software pipeline to merge and reconcile assemblies from different algorithms or sequencing technologies. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01420 SCR_006731 Genome Assembler Reconcilation and Merging 2026-09-12 12:56:44 12
Blox
 
Resource Report
Resource Website
1+ mentions
Blox (RRID:SCR_006667) Blox data processing software, data visualization software, image analysis software, software application, software resource A quantitative medical imaging and visualization program for use on brain MR, DTI, and MRS data. Programming Language: Java, JavaScript, Scheme magnetic resonance imaging, diffusion tensor imaging, magnetic resonance spectroscopy, 3d visualization, brain, 3d rendering, neuroimaging, registration, segmentation, visualization, volume is listed by: Biositemaps
has parent organization: SourceForge
has parent organization: Kennedy Krieger Institute
has parent organization: Johns Hopkins University; Maryland; USA
GNU General Public License nif-0000-00270 http://pni.med.jhu.edu/blox/ SCR_006667 2026-09-12 12:56:43 5
PowerMap
 
Resource Report
Resource Website
1+ mentions
PowerMap (RRID:SCR_006721) PowerMap software resource Software tool specifically designed for neuroimaging data that implements theoretical power calculation algorithms based on non-central random field theory. It can also calculate power for statistical analyses with FDR (false discovery rate) corrections. This GUI (graphical user interface)-based tool enables neuroimaging researchers without advanced knowledge in imaging statistics to calculate power and sample size in the form of 3D images. This tool is currently under limited release for beta testing. At this time, only users that have been directed to this site by the PowerMap developers will receive support. neuroimaging, statistical analyses, false discovery rate, 3d spatial image, power calculation, sample size has parent organization: Wake Forest School of Medicine; North Carolina; USA
has parent organization: SourceForge
NINDS NS059793 PMID:22644868 Free, Public nlx_152808 SCR_006721 2026-09-12 12:56:44 3
Samscope
 
Resource Report
Resource Website
Samscope (RRID:SCR_006715) Samscope software resource A lightweight SAM/BAM file viewer that makes visually exploring next generation sequencing data intuitive and maybe even fun! Quickly and easily generate aggregate statistics from SAM/BAM files like coverage, polarity, and minor allele frequencies, then scroll and explore freely with a simple mouse based interface. Multiple windows can be synchronized for careful comparison across multiple experiments. c++, visualization, opengl, next generation sequencing is listed by: OMICtools
has parent organization: SourceForge
GNU Affero General Public License OMICS_00892 SCR_006715 samscope - A lightweight OpenGL SAM/BAM viewer 2026-09-12 12:56:44 0
DMEAS
 
Resource Report
Resource Website
1+ mentions
DMEAS (RRID:SCR_006679) DMEAS software resource A user-friendly DNA methylation analysis tool for DNA methylation pattern extraction, DNA methylation level estimation, DNA methylation entropy analysis and multi-sample comparison. It was developed in order to assess the DNA methylation variations for a given genomic locus or genome-wide methylation data. c# is listed by: OMICtools
has parent organization: SourceForge
Creative Commons Attribution License OMICS_00598 SCR_006679 DNA Methylation Entropy Analysis Software, DMEAS - DNA Methylation Entropy Analysis Software 2026-09-12 12:56:43 2
HIA
 
Resource Report
Resource Website
HIA (RRID:SCR_006865) HIA software resource A sequence alignment tool to align both short and long reads to a reference genome. HIA has two indexes, a hash table index and a suffix array index. The hash table is capable of the direct lookup of a q-gram and the suffix array is very fast in the lookup of a variable length q-gram. Our experiments show that the hybrid of hash table and suffix array is useful at the perspective of speed to map NGS sequencing reads to a reference genome sequence. matlab, java, command-line is listed by: OMICtools
has parent organization: SourceForge
OMICS_00666 SCR_006865 Hybrid Index based sequence Alignment, HIA - Hybrid Index based sequence Alignment 2026-09-12 12:56:46 0

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