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 Synonyms Record Last Update Mentions Count
Brain Networks
 
Resource Report
Resource Website
1+ mentions
Brain Networks (RRID:SCR_005841) Brain Networks data analysis software, software resource, source code, software application, data processing software Brain Networks: Code to perform network analysis on brain imaging data. brain, imaging, network analysis, brain imaging, neuroimaging has parent organization: SourceForge PMID:21031030 Open unspecified license - GNU General Public License (GPL) nlx_149364 SCR_005841 brainnetworks 2026-07-27 09:32:23 1
Maqview
 
Resource Report
Resource Website
Maqview (RRID:SCR_005632) MaqView software application, data visualization software, data processing software, software resource A graphical read alignment viewer specifically designed for the Maq alignment file and allows you to see the mismatches, base qualities and mapping qualities. It is highly efficient in speed, memory and disk usage. Maqview is based on OpenGL and is known to work on both Mac OS X and Linux. Porting to Windows is in principle easy. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
DOI:10.1101/gr.078212.108 GNU General Public License OMICS_00889, biotools:maqview https://bio.tools/maqview, https://sources.debian.org/src/maqview/ SCR_005632 Mapping and Assembly with Qualities Viewer, M.A.Q Viewer 2026-07-27 09:32:20 0
ESTScan
 
Resource Report
Resource Website
100+ mentions
ESTScan (RRID:SCR_005742) ESTScan software application, software resource, data processing software, data analysis software ESTScan is a program that can detect coding regions in DNA sequences, even if they are of low quality. ESTScan will also detect and correct sequencing errors that lead to frameshifts. ESTScan is not a gene prediction program , nor is it an open reading frame detector. In fact, its strength lies in the fact that it does not require an open reading frame to detect a coding region. As a result, the program may miss a few translated amino acids at either the N or the C terminus, but will detect coding regions with high selectivity and sensitivity. ESTScan takes advantages of the bias in hexanucleotide usage found in coding regions relative to non-coding regions. This bias is formalized as an inhomogeneous 3-periodic fifth-order Hidden Markov Model (HMM). Additionally, the HMM of ESTScan has been extended to allows insertions and deletions when these improve the coding region statistics. dna, dna sequence, coding region, perl module, c, btlib perl module is listed by: Debian
is listed by: OMICtools
has parent organization: SourceForge
PMID:10786296 OMICS_08423, nlx_149202 https://sources.debian.org/src/estscan/ SCR_005742 ESTScan project 2026-07-27 09:32:21 289
Predictive Networks
 
Resource Report
Resource Website
Predictive Networks (RRID:SCR_006110) PN service resource, data analysis service, database, analysis service resource, software resource, source code, production service resource, data or information resource A flexible, open-source, web-based application and data services framework that enables the integration, navigation, visualization and analysis of gene interaction networks. The primary goal of PN is to allow biomedical researchers to evaluate experimentally derived gene lists in the context of large-scale gene interaction networks. The PN analytical pipeline involves two key steps. The first is the collection of a comprehensive set of known gene interactions derived from a variety of publicly available sources. The second is to use these ''known'' interactions together with gene expression data to infer robust gene networks. The regression-based network inference algorithm creates a graph of gene interactions in which cycles may be present (but no self-loops). Based on information-theoretic techniques, a causal gene interaction network is inferred from both prior knowledge (interactions extracted from biomedical literature and structured biological databases) and gene expression data. A prediction model is fitted for each gene, given its parents, enabling assessment of the predictive ability of the network model. gene interaction network, gene, interaction, gene expression, graph, visualization, gene interaction, gene network, predictive network analysis, model, bio.tools is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
has parent organization: Dana-Farber Cancer Institute
has parent organization: SourceForge
NLM 1R01LM010129 PMID:22096235 Apache License, v2 nlx_151582, biotools:predictivenetworks https://bio.tools/predictivenetworks SCR_006110 2026-07-27 09:32:27 0
BLESS
 
Resource Report
Resource Website
10+ mentions
BLESS (RRID:SCR_005963) BLESS sequence analysis software, data analysis software, software resource, software application, algorithm resource, data processing software Software tool for Bloom-filter-based error correction for next-generation sequencing (NGS) reads. The algorithm produces accurate correction results with much less memory. c++, next-generation sequencing, bloom-filter, error correction, ngs, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:24451628 GNU General Public License v3 OMICS_02246, biotools:bless https://bio.tools/bless SCR_005963 BLoom-filter-based Error correction Solution for high-throughput Sequencing reads, BLESS - Bloom-filter-based Error Correction Tool for NGS reads 2026-07-27 09:32:25 45
Centroid Trajectory Analysis
 
Resource Report
Resource Website
10+ mentions
Centroid Trajectory Analysis (RRID:SCR_006331) CeTrAn software application, software resource, data processing software, data analysis software Open source software written in R that tracks a single animal walking in a homogenous environment (Buritrack) and analyzes its trajectory. It extracts eleven metrics and includes correlation analyses and a Principal Components Analysis (PCA). It was designed to be easily customized to personal requirements. In combination with inexpensive hardware, these tools can readily be used for teaching and research purposes. Buritrack is a program to track individual Drosophila fruit flies online with any camera as they walk in Buridan's paradigm. The program extracts the coordinate locations of the fly and stores them in a text file. trajectory, buridan, principal components analysis, correlation analysis, buridan's paradigm, locomotion, software, tracking, drosophila has parent organization: Free University of Berlin; Berlin; Germany
has parent organization: SourceForge
Swiss National Science Foundation PA00P3_124141;
EPSRC EP/F030673/1
PMID:22912692 Open source, Available for Mac and PC, Source code available for download nlx_152033 SCR_006331 CeTrAn: centroid trajectory analysis 2026-07-27 09:32:31 11
BMDExpress
 
Resource Report
Resource Website
10+ mentions
BMDExpress (RRID:SCR_006823) BMDExpress software application, software resource, data processing software, data analysis software Bioinformatics tool used to analyze microarray dose-response data. The analysis provides benchmark dose estimates at which different cellular processes are altered in toxicogenomic experiments. bioinformatics, microarray, software, toxicogenomics is related to: The Hamner Institute for Health Sciences: BMDExpress and The multiple-path particle dosimetry
has parent organization: SourceForge
MIT License nlx_152743 SCR_006823 2026-07-27 09:32:39 32
Adverse Event Ontology
 
Resource Report
Resource Website
Adverse Event Ontology (RRID:SCR_006807) AEO controlled vocabulary, ontology, data or information resource AEO represents the Adverse Event Ontology, a community-driven ontology developed to standardize and integrate data on biomedical adverse events (e.g., vaccine adverse events) and support computer-assisted reasoning. The AEO also can be found in BioPortal, http://bioportal.bioontology.org/ontologies/45534?p=terms has parent organization: SourceForge nlx_44108 SCR_006807 2026-07-27 09:32:39 0
FastSemSim
 
Resource Report
Resource Website
1+ mentions
FastSemSim (RRID:SCR_006919) FastSemSim software library, software resource, software toolkit A package that implements several semantic similarity measures. It is both a library and an end-user application, featuring an intuitive graphical user interface (GUI). It has been implemented with the aim of being fast, expandable, and easy to use. It allows the user to work with the most updated version of GO database and customizable annotation corpora. It provides a set of logically-organized classes that can be easily exploited to both integrate semantic similarity into different analysis pipelines and extend the library with new measures. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible software library, functional similarity, semantic similarity, graphical user interface, gene ontology, annotation, parse, gene, protein is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: University of Padua; Padua; Italy
has parent organization: SourceForge
Open unspecified license - Free for academic use. GNU GPL license. However, This software is currently unpublished work. You must contact us before using it or its results or any work/app. based on top of it in any published work. nlx_149309 SCR_006919 2026-07-27 09:32:41 6
Comparative Data Analysis Ontology
 
Resource Report
Resource Website
Comparative Data Analysis Ontology (RRID:SCR_010297) CDAO controlled vocabulary, ontology, data or information resource A formalization of concepts and relations relevant to evolutionary comparative analysis, such as phylogenetic trees, OTUs (operational taxonomic units) and compared characters (including molecular characters as well as other types). CDAO is being developed by scientists in biology, evolution, and computer science owl, biology, evolution, computer science, comparative analysis, phylogenetic tree, operational taxonomic unit, compared character, molecular is listed by: BioPortal
is listed by: OBO
is listed by: SourceForge
Public domain nlx_157371 http://purl.bioontology.org/ontology/CDAO, http://purl.obolibrary.org/obo/cdao.owl SCR_010297 2026-07-27 09:33:40 0
BWA
 
Resource Report
Resource Website
1000+ mentions
BWA (RRID:SCR_010910) BWA sequence analysis software, data analysis software, image analysis software, software resource, software application, data processing software, alignment software Software for aligning sequencing reads against large reference genome. Consists of three algorithms: BWA-backtrack, BWA-SW and BWA-MEM. First for sequence reads up to 100bp, and other two for longer sequences ranged from 70bp to 1Mbp. sequence, alignment, reference, genome, human, short, long, read, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
is related to: shovill
is related to: Proovread
is related to: BWA-MEM2
has parent organization: SourceForge
is required by: RelocaTE
PMID:19451168
PMID:20080505
DOI:10.1093/bioinformatics/btp324
Free, Available for download, Freely available SCR_015853, biotools:bwa-sw, OMICS_00654 https://sourceforge.net/projects/bio-bwa/files/, https://bio.tools/bwa-sw, https://sources.debian.org/src/bwa/ SCR_010910 Burrows-Wheeler Aligner (BWA), Burrows-Wheeler Aligner 2026-07-27 09:33:50 2291
ECHO
 
Resource Report
Resource Website
100+ mentions
ECHO (RRID:SCR_011851) ECHO sequence analysis software, data analysis software, software resource, software application, algorithm resource, data processing software Error correction algorithm designed for short-reads from next-generation sequencing platforms such as Illumina''s Genome Analyzer II. error correction, rnaseq, rna sequence, short-read, next-generation sequencing, ngs, illumina, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:21482625
DOI:10.1101/gr.111351.110
Free, Available for download biotools:echo, OMICS_01102 https://bio.tools/echo, https://sources.debian.org/src/uc-echo/ SCR_011851 ECHO: A reference-free short-read error correction algorithm 2026-07-27 09:33:58 310
TagCleaner
 
Resource Report
Resource Website
50+ mentions
TagCleaner (RRID:SCR_011846) software application, web application, software resource, standalone software A software tool which can automatically detect and efficiently remove tag sequences from genomic and metagenomic datasets. tag sequence, standalone software, web application, microbiome, genomic, metagenomic, datasets is listed by: OMICtools
is listed by: Human Microbiome Project
has parent organization: SourceForge
Available for download OMICS_01094 SCR_011846 2026-07-27 09:33:58 63
Multivariate Analysis of Transcript Splicing
 
Resource Report
Resource Website
100+ mentions
Multivariate Analysis of Transcript Splicing (RRID:SCR_013049) MATS software application, software resource, data processing software, data analysis software Software tool to detect differential alternative splicing events from RNA-Seq data. Calculates P value and false discovery rate that difference in isoform ratio of gene between two conditions exceeds given user defined threshold. Can automatically detect and analyze alternative splicing events corresponding to all major types of alternative splicing patterns. Handles replicate RNA-Seq data from both paired and unpaired study design. Differential alternative splicing events, splicing events calculation, RNA-Seq data, gene isoform ratio, alternative splicing patterns, patterns detection, patterns analysis, replicate RNA-Seq data is listed by: OMICtools
is listed by: SourceForge
has parent organization: Childrens Hospital of Philadelphia - Research Institute; Pennsylvania; USA
Free, Available for download, Freely available OMICS_01336, SCR_020941 SCR_013049 RNAseq MATS, RMATS, rMATS, MATS, RNA MATS 2026-07-27 09:34:19 192
Neuroimaging in Python
 
Resource Report
Resource Website
10+ mentions
Neuroimaging in Python (RRID:SCR_013141) NIPY, community building portal, software resource, software application, software development tool, software development environment, portal, data or information resource Community site to make brain imaging research easier that aims to build software that is clearly written, clearly explained, a good fit for the underlying ideas, and a natural home for collaboration. brain, imaging, neuroimaging, analysis, python, fmri, fmri analysis, magnetic resonance is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is related to: Python Programming Language
has parent organization: SourceForge
has parent organization: University of California at Berkeley; Berkeley; USA
has parent organization: Massachusetts Institute of Technology; Massachusetts; USA;
is parent organization of: Dipy
is parent organization of: NiLearn
is parent organization of: NIPY
is parent organization of: NiBabel
is parent organization of: Nipype
is parent organization of: Nitime
NIMH 5R01MH081909-02;
NIBIB 1R03EB008673-01
PMID:21897815 Revised BSD license nlx_149365 http://www.nitrc.org/projects/nipy-community http://www.nitrc.org/projects/nipype SCR_013141 NIPY Community 2026-07-27 09:34:20 24
(at)Note
 
Resource Report
Resource Website
1+ mentions
(at)Note (RRID:SCR_005342) (at)Note software application, text-mining software, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented September 18, 2017. Text Mining platform that copes with major Information Retrieval and Information Extraction tasks and promotes multi-disciplinary research. It aims to provide support to three different usage roles: biologists, text miners and application developers. The workbench supports the retrieval, processing and annotation of documents as well as their analysis at different levels. java, java swt, text, mining is listed by: OMICtools
has parent organization: SourceForge
has parent organization: University of Minho; Braga; Portugal
PMID:19393341 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01167 SCR_005342 (at)Note2 - A workbench for Biomedical Text Mining 2026-07-27 09:32:15 2
Dissect
 
Resource Report
Resource Website
Dissect (RRID:SCR_000058) Dissect image analysis software, software resource, software application, data processing software, alignment software THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. Software transcriptome-to-genome alignment tool, which can identify and characterize transcriptomic events such as duplications, inversions, rearrangements and fusions. Structural events containing transcripts, transcriptome-to-genome alignment, identify and characterize transcriptomic events, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
has parent organization: Simon Fraser University; British Columbia; Canada
PMID:22689759 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01346, biotools:dissect https://bio.tools/dissect SCR_000058 Dissect: DIScovery of Structural Events Containing Transcripts, DIScovery of Structural Events Containing Transcripts 2026-07-27 09:30:51 0
Biologic Stylus
 
Resource Report
Resource Website
Biologic Stylus (RRID:SCR_002991) Biologic Stylus software application, simulation software, software resource, source code Biologic Stylus is Biologic Institute's Stylus simulation software suite. Programming Language: C++, Python bioinformatics, simulation has parent organization: SourceForge Free, Available for download, Freely available nif-0000-30198 SCR_002991 biologicstylus 2026-07-27 09:31:39 0
Hadoop-BAM
 
Resource Report
Resource Website
1+ mentions
Hadoop-BAM (RRID:SCR_005516) Hadoop-BAM software library, software resource, software toolkit A Java library for the manipulation of files in common bioinformatics formats using the Hadoop MapReduce framework with the Picard SAM JDK, and command line tools similar to SAMtools. The file formats currently supported are BAM, SAM, FASTQ, FASTA, QSEQ, BCF, and VCF. mapreduce/hadoop, java, next generation sequencing data, cloud is listed by: OMICtools
has parent organization: SourceForge
PMID:22302568 MIT License OMICS_01051 SCR_005516 2026-07-27 09:32:18 7
SPInDel
 
Resource Report
Resource Website
1+ mentions
SPInDel (RRID:SCR_004509) SPInDel software resource, data or information resource, data set A multifunctional workbench for species identification using insertion/deletion variants. The SPInDel workbench provides a step-by-step environment for the alignment of target sequences, selection of informative hypervariable regions, design of PCR primers and the statistical validation of the species-identification process. It includes a large dataset comprising nearly 1,800 numeric profiles for the identification of eukaryotic, prokaryotic and viral species. virus, indel, dna barcoding, alignment, nucleotide sequence, visualization, conserved region, pcr primer, phylogenetic, variant is listed by: OMICtools
has parent organization: University of Porto; Porto; Portugal
has parent organization: SourceForge
PMID:22978681
PMID:20923781
Acknowledgement requested, Free, Public OMICS_01496 SCR_004509 SPecies Identification by Insertions/Deletions, SPInDel - Species identification by insertions/deletions 2026-07-27 09:32:03 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. NIDM Terminology Resources

    Welcome to the nidm-terms Resources search. From here you can search through a compilation of resources used by nidm-terms 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 nidm-terms 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 nidm-terms then you can log in from here to get additional features in nidm-terms 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 nidm-terms 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.