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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 Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
ASOoViR
 
Resource Report
Resource Website
ASOoViR (RRID:SCR_005161) ASOoViR software resource A set of Ruby modules to annotate consequence terms, defined by the Sequence Ontology, of variants (SNP/SNVs, INDELs, SVs, CNAs) using Ensembl gene sets. Prior to annotation of variants an Ensembl gene set and reference coding sequences are loaded into memory from a database file, which can be downloaded or generated by the user from reference files. This allows rapid annotation of variants, making it suitable for annotation of whole genome scale calls. Annotation is performed on a transcript level basis, identifying associated sequence ontology terms for affected and nearby transcripts. Default output can be obtained on a gene basis, summarising the consequences for each gene affected, or on a transcript level basis. Output information is also readily customisable using user-generated scripts. ruby, annotate is listed by: OMICtools
is related to: SO
has parent organization: SourceForge
OMICS_00167 SCR_005161 Annotating Sequence Ontology of Variants in Ruby, ASOoViR - Annotating Sequence Ontology of Variants in Ruby 2026-02-14 02:01:03 0
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 2026-02-14 02:01:05 5186
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 2026-02-14 02:00:51 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 2026-02-14 02:00:52 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 2026-02-14 02:00:54 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 2026-02-14 02:01:08 0
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 2026-02-14 02:00:56 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 2026-02-14 02:00:58 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 2026-02-14 02:00:56 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 2026-02-14 02:01:10 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 2026-02-14 02:01:08 0
EBARDenovo
 
Resource Report
Resource Website
1+ mentions
EBARDenovo (RRID:SCR_011890) EBARDenovo software resource Highly accurate de novo assembly of RNA-Seq with efficient chimera-detection. is listed by: OMICtools
has parent organization: SourceForge
OMICS_01317 SCR_011890 2026-02-14 02:02:06 2
SeqGene
 
Resource Report
Resource Website
1+ mentions
SeqGene (RRID:SCR_011861) SeqGene software resource An open-source software for mining next-gen sequencing datasets, focusing on post-alignment quality control, SNP and indel identification and annotation, RNA expression quantification, etc. is listed by: OMICtools
has parent organization: SourceForge
Open unspecified license OMICS_01134 SCR_011861 2026-02-14 02:02:29 2
naiveBayesCall
 
Resource Report
Resource Website
naiveBayesCall (RRID:SCR_011866) naiveBayesCall software resource An efficient model-based base-calling algorithm for high-throughput sequencing. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
OMICS_01152, biotools:bayescall https://bio.tools/bayescall SCR_011866 2026-02-14 02:02:06 0
Scalpel
 
Resource Report
Resource Website
50+ mentions
Scalpel (RRID:SCR_012107) software resource A software package for detecting INDELs (INsertions and DELetions) mutations in a reference genome which has been sequenced with next-generation sequencing technology (e.g., Illumina). software package, c++, perl, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:25128977 biotools:scalpel, OMICS_05395 https://bio.tools/scalpel SCR_012107 2026-02-14 02:02:35 57
SNP ratio test
 
Resource Report
Resource Website
1+ mentions
SNP ratio test (RRID:SCR_012070) software resource Software to calculate the number of significant SNPs in pathway divided by the number of SNPs in pathway. standalone software, perl, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:19620097 GNU General Public License biotools:snp_ratio_test, OMICS_04390 https://bio.tools/snp_ratio_test SCR_012070 2026-02-14 02:02:17 2
Toxtree
 
Resource Report
Resource Website
50+ mentions
Toxtree (RRID:SCR_012086) software resource A full-featured and flexible user-friendly open source software application, which is able to estimate toxic hazard by applying a decision tree approach. standalone software, web app is listed by: OMICtools
has parent organization: SourceForge
PMID:18853299 OMICS_05024 SCR_012086 2026-02-14 02:02:18 95
Viewmol
 
Resource Report
Resource Website
Viewmol (RRID:SCR_012088) software resource Software providing a graphical front end for computational chemistry programs. standalone software, windows, c, python is listed by: OMICtools
is listed by: Debian
has parent organization: SourceForge
GNU General Public License OMICS_05057 https://sources.debian.org/src/viewmol/ SCR_012088 2026-02-14 02:02:10 0
Toxmatch
 
Resource Report
Resource Website
1+ mentions
Toxmatch (RRID:SCR_012087) software resource A software tool to facilitate chemical similarity calculations. standalone software is listed by: OMICtools
has parent organization: SourceForge
PMID:18617309 OMICS_05025 SCR_012087 2026-02-14 02:02:35 2
QuteMol
 
Resource Report
Resource Website
10+ mentions
QuteMol (RRID:SCR_012089) software resource Open source (GPL) software providing an interactive, high quality molecular visualization system. standalone software, unix/linux, windows is listed by: OMICtools
is listed by: Debian
has parent organization: SourceForge
PMID:17080857
DOI:10.1109/TVCG.2006.115
Free, Freely available OMICS_05075 https://sources.debian.org/src/qutemol/ SCR_012089 2026-02-14 02:02:34 13

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