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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
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 2026-02-14 02:01:26 497
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 2026-02-14 02:01:13 22
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 2026-02-14 02:00:19 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 2026-02-14 02:00:27 113
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 2026-02-14 02:00:38 0
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 2026-02-14 02:00:35 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 2026-02-14 02:00:38 0
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 2026-02-14 02:00:30 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 2026-02-14 02:00:41 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 2026-02-14 02:00:30 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 2026-02-14 02:00:40 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 2026-02-14 02:00:41 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 2026-02-14 02:00:44 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 2026-02-14 02:00:25 7
exomeSuite
 
Resource Report
Resource Website
exomeSuite (RRID:SCR_000129) software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. A software application designed to analyze variant call files from next generation sequencing data to identify variants causing disease. standalone software, c, matlab is listed by: OMICtools
has parent organization: SourceForge
PMID:24603341 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_04839 SCR_000129 2026-02-14 01:59:37 0
CG-Pipeline
 
Resource Report
Resource Website
CG-Pipeline (RRID:SCR_000047) software resource A software tool for assembling genome sequence data and running feature prediction and annotation tools on the assembly. perl has parent organization: SourceForge PMID:20519285 Free, Available for download, Freely available OMICS_04062 http://sourceforge.net/projects/cg-pipeline/ SCR_000047 2026-02-14 01:59:35 0
Batman-Seq
 
Resource Report
Resource Website
Batman-Seq (RRID:SCR_000048) Batman-Seq software resource A fast BWT-based short reads mapping tools which uses additional statistical method to model error profile of the sequencing experiment. c++ is hosted by: SourceForge Free, Available for download, Freely available OMICS_00651 SCR_000048 Basic Alignment Tool for MAny Nucleotides 2026-02-14 01:59:35 0
MS-Spectre
 
Resource Report
Resource Website
1+ mentions
MS-Spectre (RRID:SCR_000266) software resource Software that provides (Quantitiave) analysis of multiple ls-ms(ms) runs, using mzXML import of raw data coming from spectrometers. standalone software, java is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_02496 SCR_000266 Mass Spectrometry Analysis Software 2026-02-14 01:59:40 1
BLASTPLOT
 
Resource Report
Resource Website
BLASTPLOT (RRID:SCR_000162) BLASTPLOT software resource A PERL module that can quickly plot the BLAST results from short sequences (primers, probes, reads) against reference targets. This software generates PNG graphs for all of the reference sequences associated with a BLAST result set. perl, blast, short sequence, primer, png, png graph is listed by: OMICtools
has parent organization: SourceForge
PMID:24685334 Free, Available for download, Freely available OMICS_01433 SCR_000162 2026-02-14 01:59:38 0
GemSIM
 
Resource Report
Resource Website
GemSIM (RRID:SCR_000167) GemSIM software resource A software package for generating realistic simulated next-generation genome sequencing reads with quality score values. The software is written in Python with a command-line user interface. bioinformatics, simulation, sequencing, dna, rna, empirical models, Python, command-line, user interface, metagenomic, resequencing, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
is required by: Wessim
PMID:22336055
DOI:10.1186/1471-2164-13-74
Free, Available for download, Freely available OMICS_01507, biotools:GemSIM https://bio.tools/GemSIM SCR_000167 2026-02-14 01:59:38 0

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