Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

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.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Related Resources:sourceforge (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

435 Results - per page

Show More Columns | Download 435 Result(s)

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 Authority Synonyms Record Last Update Mentions Count
Mugsy
 
Resource Report
Resource Website
50+ mentions
Mugsy (RRID:SCR_001414) data analysis software, data processing software, sequence analysis software, software application, software resource Software resource for multiple whole genome alignment. It uses Nucmer, a custom graph-based segmentation procedure, for pairwise alignment, and the Seqan:TCoffee's multiple alignment strategy. software, genome, genome alignment, segmentation, pairwise alignment, sequence analysis software is listed by: OMICtools
is listed by: Debian
has parent organization: SourceForge
PMID:21148543
DOI:10.1093/bioinformatics/btq665
Free, Available for download, Freely available OMICS_03606 https://sources.debian.org/src/mugsy/ SCR_001414 SciCrunch Registry 2026-10-31 12:12:51 75
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 SciCrunch Registry Mass Spectrometry Analysis Software 2026-10-31 12:12:36 2
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 SciCrunch Registry 2026-10-31 12:12:34 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 SciCrunch Registry 2026-10-31 12:12:34 0
GMATo
 
Resource Report
Resource Website
1+ mentions
GMATo (RRID:SCR_000165) data analysis software, data processing software, sequence analysis software, software application, software resource A software tool used for simple sequence repeats (SSR) or microsatellite characterization. It also facilitates SSR marker design on a genomic scale, microsatellite mining at any length, and comprehensive statistical analysis for DNA sequences in any genome at any size. Analysis parameters are customizable. simple sequence repeat, ssr, microsatellite, genomic, marker design, sequence analysis software is listed by: OMICtools
has parent organization: SourceForge
PMID:23861572 Free, Available for download, Freely available OMICS_00106 SCR_000165 SciCrunch Registry Genome-wide Microsatellite Analyzing Tool, Genome Microsatellite Analyzing Tool, Genome-wide Microsatellite Analyzing Tool (GMATo) 2026-10-31 12:12:34 1
ProteinProphet
 
Resource Report
Resource Website
10+ mentions
ProteinProphet (RRID:SCR_000286) software resource Software that automatically validates protein identifications made on the basis of peptides assigned to MS/MS spectra by database search programs such as SEQUEST. standalone software, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
has parent organization: SourceForge
PMID:14632076 OMICS_02521, biotools:proteinprophet https://bio.tools/proteinprophet SCR_000286 SciCrunch Registry 2026-10-31 12:12:36 11
riboPicker
 
Resource Report
Resource Website
1+ mentions
riboPicker (RRID:SCR_000360) software resource Software to automatically identify and efficiently remove rRNA-like sequences from metatranscriptomic and metagenomic datasets. standalone software, perl, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:22155869 Free, Available for download, Freely available OMICS_02618, biotools:ribopicker https://bio.tools/ribopicker SCR_000360 SciCrunch Registry 2026-10-31 12:12:37 2
ParseCNV
 
Resource Report
Resource Website
1+ mentions
ParseCNV (RRID:SCR_000355) software resource Software that takes CNV calls as input and creates SNP based statistics for CNV occurrence in cases and controls then calls CNVRs based on neighboring SNPs of similar significance. standalone software is listed by: OMICtools
has parent organization: SourceForge
PMID:23293001 Free, Available for download, Freely available OMICS_02566 SCR_000355 SciCrunch Registry 2026-10-31 12:12:37 1
Kinannote
 
Resource Report
Resource Website
1+ mentions
Kinannote (RRID:SCR_000352) software resource Software that identifies and classifies protein kinases in a user-provided fasta file using an HMM derived from serine / threonine protein kinases, a position specific scoring matrix derived from the HMM, and comparison with a local version of the curated kinase database from kinase.com. standalone software, perl is listed by: OMICtools
has parent organization: SourceForge
PMID:23904509 Free, Available for download, Freely available OMICS_05965 SCR_000352 SciCrunch Registry 2026-10-31 12:12:37 2
Jnomics
 
Resource Report
Resource Website
Jnomics (RRID:SCR_000348) software resource A collection of cloud-scale DNA sequence analysis tools. mapreduce is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_04074 SCR_000348 SciCrunch Registry 2026-10-31 12:12:37 0
fqzcomp
 
Resource Report
Resource Website
1+ mentions
fqzcomp (RRID:SCR_000299) fqzcomp software resource A basic fastq compressor, designed primarily for high performance. c++ is listed by: OMICtools
has parent organization: SourceForge
PMID:23533605 Free, Available for download, Freely available OMICS_00957 SCR_000299 SciCrunch Registry 2026-10-31 12:12:36 1
BioLemmatizer
 
Resource Report
Resource Website
1+ mentions
BioLemmatizer (RRID:SCR_000117) software resource A domain-specific lemmatization software tool for the morphological analysis of biomedical literature. standalone software is listed by: OMICtools
has parent organization: SourceForge
PMID:22464129 Free, Available for download, Freely available OMICS_04827 https://sourceforge.net/projects/biolemmatizer/ SCR_000117 SciCrunch Registry 2026-10-31 12:12:34 2
SOAPfuse
 
Resource Report
Resource Website
1+ mentions
SOAPfuse (RRID:SCR_000078) SOAPfuse software resource THIS RESOURCE IS NO LONGER IN SERVICE.Documented on August 23,2022. An open source tool developed for genome-wide detection of fusion transcripts from human being paired-end RNA-Seq data. This tool is a part of a larger set of tools to efficiently align oligonucleotides onto reference sequences . software, resource, open license, DNA sequencing, genome, transcripts, RNA, oligonucleotide is listed by: OMICtools
is listed by: SourceForge
is listed by: SOAP
PMID:23409703 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01357 SCR_000078 SciCrunch Registry 2026-10-31 12:12:33 7
Sequence Read Format
 
Resource Report
Resource Website
1+ mentions
Sequence Read Format (RRID:SCR_000132) SRF data or information resource, interchange format, narrative resource, standard specification A generic format for DNA sequence data. The primary motivation for creating SRF has been to enable a single format capable of storing data generated by any DNA sequencing technology. dna sequence, dna sequencing, interchange format is listed by: OMICtools
has parent organization: SourceForge
Public, A C++ implementation of Sequence Read Format is available OMICS_05130 SCR_000132 SciCrunch Registry Sequence Read Format (SRF) 2026-10-31 12:12:34 1
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 SciCrunch Registry 2026-10-31 12:12:34 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 SciCrunch Registry 2026-10-31 12:12:32 0
BlackOPs
 
Resource Report
Resource Website
BlackOPs (RRID:SCR_000032) data analysis software, data processing software, sequence analysis software, software application, software resource Open source software tool that simulates experimental RNA-seq and DNA whole exome sequences derived from reference genome, aligns these sequences by custom parameters, detects variants and outputs blacklist of positions and alleles caused by mismapping. Used to characterize mappability of RNA-Seq reads and create blacklist of genomic positions of mismapped reads. This blacklist is used to filter potential false positives from variant or RNA editing calls. rna seq, false positive, genome editing, rna editing, mismapped reads has parent organization: SourceForge PMID:23935067 Free, Available for download, Freely available OMICS_01229 SCR_000032 SciCrunch Registry BlackOPs: RNA-Seq Variant Blacklist Tool 2026-10-31 12:12:32 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 SciCrunch Registry Basic Alignment Tool for MAny Nucleotides 2026-10-31 12:12:32 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 SciCrunch Registry 2026-10-31 12:13:48 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 SciCrunch Registry 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 2026-10-31 12:13:49 2

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. RRID Portal Resources

    Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that RRID has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.