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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
MAGMA
 
Resource Report
Resource Website
100+ mentions
MAGMA (RRID:SCR_005757) MAGMA software resource Software that utilizes a multiobjective evolutionary algorithm for genetic mapping. It is based on a the ECJ evolutionary software package written by Sean Luke and includes the Strength Pareto Evoluationary Algorithm Version 2 changes for multiobjective analysis. The code runs on any platform with Java Version 2. A genetic mapping project, typically implemented during a search for genes responsible for a disease, requires the acquisition of a set of data from each of a large number of individuals. This data set includes the values of multiple genetic markers. These genetic markers occur at discrete positions along the genome, which is a collection of one or more linear chromosomes. Typing the value of a marker in an individual carries a cost; one seeks to minimize the number of markers typed without excessively jeopardizing the probability of detecting an association between a marker and a disease phenotype. MAGMA is a project which employ''s a multiobjective evolutionary algorithm to solve this problem. gene, genetic mapping, algorithm, genomics, single nucleotide polymorphism, population study, haplotype-block elucidation, java has parent organization: SourceForge Juvenile Diabetes Research Foundation PMID:12875658 Open unspecified license nlx_149220 SCR_005757 Multiobjective Analyzer for Genetic Marker Acquisition, MAGMA: Multiobjective Analyzer for Genetic Marker Acquisition 2026-08-01 12:02:58 456
SpliceGrapher
 
Resource Report
Resource Website
10+ mentions
SpliceGrapher (RRID:SCR_006657) SpliceGrapher software resource Software that predicts alternative splicing patterns and produces splice graphs that capture in a single structure the ways a gene''s exons may be assembled. It enhances gene models using evidence from next-generation sequencing and EST alignments. is listed by: OMICtools
has parent organization: SourceForge
PMID:22293517 OMICS_01266 SCR_006657 2026-08-01 12:03:14 22
GenoTan
 
Resource Report
Resource Website
1+ mentions
GenoTan (RRID:SCR_007935) GenoTan software resource A free software tool to identify length variation of microsatellites from short sequence reads. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:24135263 GNU General Public License, v3 biotools:genotan https://bio.tools/genotan SCR_007935 GenoTan - Genotyping of microsatellite loci 2026-08-01 12:03:25 1
BRIG
 
Resource Report
Resource Website
100+ mentions
BRIG (RRID:SCR_007802) BRIG software resource 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. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
DOI:10.1186/1471-2164-12-402 OMICS_00929, biotools:brig https://bio.tools/brig, https://sources.debian.org/src/brig/ SCR_007802 BLAST Ring Image Generator 2026-08-01 12:03:24 497
SeqPig
 
Resource Report
Resource Website
1+ mentions
SeqPig (RRID:SCR_008548) SeqPig software resource A software library for Apache Pig for the distributed analysis of large sequencing datasets on Hadoop clusters. mapreduce/hadoop is listed by: OMICtools
has parent organization: SourceForge
PMID:24149054 OMICS_01226 SCR_008548 2026-08-01 12:03:56 2
SeqExpress
 
Resource Report
Resource Website
SeqExpress (RRID:SCR_004013) software resource A cross-platform software that estimates gene/isoform expression level via mRNA-Seq data. SeqExpress exams the Sequencing bias in mRNA-Seq and correct it to get more accurate estimation. c++, mrna-seq, qt is listed by: OMICtools
has parent organization: SourceForge
PMID:15746290
PMID:14988116
GNU General Public License v2 OMICS_01289 SCR_004013 2026-08-01 12:02:29 0
HLASeq
 
Resource Report
Resource Website
HLASeq (RRID:SCR_004185) HLASeq software resource An open-source software tool for accurate genotyping the human HLA genes from Illumina GA high-throughput sequencing data. genotyping, hla, next generation sequencing, gene, command-line, python is listed by: OMICtools
has parent organization: SourceForge
GNU General Public License, v3 OMICS_01543 SCR_004185 2026-08-01 12:02:38 0
Vanator
 
Resource Report
Resource Website
1+ mentions
Vanator (RRID:SCR_004370) Vanator software resource A Perl pipeline utilising a large variety of common alignment, assembly and analysis tools to assess the metagenomic profiles of Illumina deep sequencing samples. The emphasis is on the discovery of novel viruses in clinical and environmental samples. perl, metagenomic, illumina, alignment, assembly, analysis, profile, virus, clinical, environment, next-generation sequencing, taxonomy, read is listed by: OMICtools
has parent organization: SourceForge
has parent organization: University of Glasgow; Glasgow; United Kingdom
PMID:23296970 OMICS_01505 SCR_004370 Vanator-CVR, Vanator-CVR - A metagenomics & virus discovery pipeline, Virus Alignment de Novo Assembly and Taxonomy On Reads, Vanator-CVR: A metagenomics and virus discovery pipeline 2026-08-01 12:02:36 2
SALT
 
Resource Report
Resource Website
1000+ mentions
SALT (RRID:SCR_003187) SALT software resource Software that can accurately and sensitivity classify short reads of next-generation sequencing (NGS) into protein domain families. It is based on profile HMM and a supervised graph contribution algorithm. Compared to existing tools, it has high sensitivity and specificity in classifying short reads into their native domain families. next-generation sequencing, protein, protein domain, short read, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:23782615 Free, Available for download, Freely available OMICS_01565, biotools:salt https://bio.tools/salt SCR_003187 SALT - Protein domain classifier 2026-08-01 12:02:17 1294
XORRO
 
Resource Report
Resource Website
1+ mentions
XORRO (RRID:SCR_003181) XORRO software resource Efficient paired-read overlap software program for use with Illumina sequencing. illumina, next-generation sequencing is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_01569 SCR_003181 XORRO: Rapid Paired-End Read Overlapper 2026-08-01 12:02:17 1
NovelSeq
 
Resource Report
Resource Website
NovelSeq (RRID:SCR_003136) NovelSeq software resource Software pipeline to detect novel sequence insertions using high throughput paired-end whole genome sequencing data. sequence, insertion, genome sequencing, genome, next-generation sequencing, illumina, unix, linux, c, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: SPLITREAD
has parent organization: Simon Fraser University; British Columbia; Canada
has parent organization: SourceForge
PMID:20385726 Free, Available for download, Freely available biotools:novelseq, nlx_156791, OMICS_02164 https://mybiosoftware.com/novelseq-1-0-2-sequence-insertions-detection.html#google_vignette SCR_003136 NovelSeq: Novel Sequence Insertion Detection 2026-08-01 12:02:03 0
mrCaNaVaR
 
Resource Report
Resource Website
10+ mentions
mrCaNaVaR (RRID:SCR_003135) mrCaNaVaR software resource Copy number caller that analyzes the whole-genome next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals. genome, next-generation sequence, duplication, deletion, copy number variant, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: SPLITREAD
has parent organization: SourceForge
Free, Freely available OMICS_02138, nlx_156790, biotools:mrcanavar https://bio.tools/mrcanavar SCR_003135 mrCaNaVaR - micro-read Copy Number Variant Regions, micro-read Copy Number Variant Regions 2026-08-01 12:02:27 14
SaskPrimerFS
 
Resource Report
Resource Website
SaskPrimerFS (RRID:SCR_003159) SaskPrimerFS software resource Software pipeline for designing gene family specific PCR primers. It infers intronic regions of a target species and design for them by utilizing DNA sequence information from a reference organism. gene family, pcr primer, pcr, primer, dna sequence, command-line, perl is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_02335 SCR_003159 2026-08-01 12:02:17 0
JCVI Primer Designer
 
Resource Report
Resource Website
1+ mentions
JCVI Primer Designer (RRID:SCR_003275) JCVI Primer Designer software resource High throughput PCR primer design software. Target regions defined through a rich set of descriptors, such as Ensembl accessions and arbitrary genomic coordinates, may be specified. Primer pairs are then selected computationally to produce a minimal amplicon set capable of tiling across the specified target regions. As part of the tiling process, primer pairs are computationally screened to meet the criteria for success with one of two PCR amplification protocols. perl, command-line, pcr primer design, pcr, primer, high throughput sequencing is listed by: OMICtools
has parent organization: SourceForge
PMID:18405373 Free, Available for download, Freely available OMICS_02330 SCR_003275 2026-08-01 12:02:07 1
PrimerSeq
 
Resource Report
Resource Website
1+ mentions
PrimerSeq (RRID:SCR_003295) PrimerSeq software resource Software that designs RT-PCR primers that evaluate alternative splicing events by incorporating RNA-Seq data. It is particularly advantageous for designing a large number of primers for validating alternative splicing events found in RNA-Seq data. It incorporates RNA-Seq data in the design process to weight exons by their read counts. Essentially, the RNA-Seq data allows primers to be placed using actually expressed transcripts. This could be for a particular cell line or experimental condition, rather than using annotations that incorporate transcripts that are not expressed for the data. Alternatively, you can design primers that are always on constitutive exons. PrimerSeq does not limit the use of gene annotations and can be used for a wide array of species. primer, rna-seq, rt-pcr, windows, mac os x, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:24747190 Free, Available for download, Freely available biotools:primerseq, OMICS_02328 https://bio.tools/primerseq SCR_003295 Primer Seek in RNA-Seq 2026-08-01 12:02:29 7
Mindtouch DekiWiki
 
Resource Report
Resource Website
1+ mentions
Mindtouch DekiWiki (RRID:SCR_003425) MindTouch source code, commercial organization, software resource A web based social authoring and publishing environment that adheres to open standards and RESTful design principals. It provides wiki-like ease of use with a sophisticated web services framework for rapid application development, creating flexible workflows and rapid integration. MindTouch creates a vibrant real-time information fabric by federating content from across enterprise silos, such as CRM, ERP, file servers, email, databases, web services and more. authoring, publishing, standard, web service, cloud is listed by: FORCE11
is listed by: Biositemaps
has parent organization: University of Wisconsin-Madison; Wisconsin; USA
has parent organization: SourceForge
Free, Freely available nif-0000-33097 http://sourceforge.net/projects/dekiwiki/, https://www.force11.org/node/4733 SCR_003425 MindTouch Core, DekiWiki, MindTouch Deki Wiki, Deki Wiki, MindTouch (frmly deki wiki) 2026-08-01 12:02:11 2
GLProbs
 
Resource Report
Resource Website
1+ mentions
GLProbs (RRID:SCR_002739) software resource Software implementing a simple and effective approach to improve the accuracy of multiple sequence alignment. standalone software is listed by: OMICtools
has parent organization: SourceForge
PMID:26357079 Free, Freely available, Available for download OMICS_03732 SCR_002739 2026-08-01 12:01:54 1
rDock
 
Resource Report
Resource Website
100+ mentions
rDock (RRID:SCR_002838) software resource A fast and versatile Open Source docking software program that can be used to dock small molecules against proteins and nucleic acids. standalone software is listed by: OMICtools
has parent organization: SourceForge
PMID:24722481 Free, Freely available, Available for download OMICS_03835 SCR_002838 2026-08-01 12:01:56 113
FAS-DPD
 
Resource Report
Resource Website
FAS-DPD (RRID:SCR_003068) FAS-DPD software resource Software program to design degenerate primers for PCR. command-line, java, primer, pcr, degenerate primer is listed by: OMICtools
has parent organization: SourceForge
PMID:23533783 Free, Available for download, Freely available OMICS_02340 SCR_003068 family-specific degenerate primer design 2026-08-01 12:02:25 0
PHACCS
 
Resource Report
Resource Website
1+ mentions
PHACCS (RRID:SCR_001232) software resource Software that gives estimates of the structure and diversity of uncultured viral communities using metagenomic information. matlab is listed by: OMICtools
has parent organization: SourceForge
PMID:15743531 Free, Available for download, Freely available OMICS_03529 SCR_001232 2026-08-01 12:01:35 1

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