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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 Authority Synonyms Record Last Update Mentions Count
go-moose
 
Resource Report
Resource Website
go-moose (RRID:SCR_005666) go-moose data analysis software, data processing software, software application, software resource go-moose is intended as a replacement for the aging go-perl and go-db-perl Perl libraries. It is written using the object oriented Moose libraries. It can be used for performing a number of analyses on GO data, including the remapping of GO annotations to a selected subset of GO terms. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible software library, slimmer-type tool, analysis, gene ontology, other analysis is listed by: Gene Ontology Tools
is related to: Gene Ontology
is related to: go-perl
is related to: go-db-perl
has parent organization: SourceForge
has parent organization: Berkeley Bioinformatics Open-Source Projects
has parent organization: Lawrence Berkeley National Laboratory
Free for academic use nlx_149189 SCR_005666 SciCrunch Registry 2026-10-17 01:26:17 0
TMAJ
 
Resource Report
Resource Website
10+ mentions
TMAJ (RRID:SCR_005601) TMAJ software resource Open-source software to support information and images related to tissue micro-arrays. It contains support for multiple organ systems, multiple users, image analysis, and is designed to be compliant with HIPPA regulations. Patients, specimens, blocks, slides, cores, images, and scores can all be stored and viewed. Features include advanced security, custom dynamic fields, and an image analysis program. tissue microarray, java, java swing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Johns Hopkins University; Maryland; USA
has parent organization: SourceForge
GNU General Public License, v3 biotools:tmaj, OMICS_00823 https://bio.tools/tmaj SCR_005601 SciCrunch Registry TMAJ Software Project 2026-10-17 01:26:22 10
Maqview
 
Resource Report
Resource Website
Maqview (RRID:SCR_005632) MaqView data processing software, data visualization software, software application, 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 SciCrunch Registry Mapping and Assembly with Qualities Viewer, M.A.Q Viewer 2026-10-17 01:26:23 0
Staden Package
 
Resource Report
Resource Website
50+ mentions
Staden Package (RRID:SCR_005629) software resource A fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin) for Unix, Linux, MacOSX and MS Windows. c, unix/linux, sequence assembly, dna/protein analysis, spin, sequence alignment, genome, genome viewer, c++, fortran, tcl, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:20513662
DOI:10.1093/bioinformatics/btq268
BSD License OMICS_00894, biotools:staden https://bio.tools/staden, https://sources.debian.org/src/staden/ SCR_005629 SciCrunch Registry Staden Package 2026-10-17 01:26:21 87
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 SciCrunch Registry Multiobjective Analyzer for Genetic Marker Acquisition, MAGMA: Multiobjective Analyzer for Genetic Marker Acquisition 2026-10-17 01:26:27 495
Brain Networks
 
Resource Report
Resource Website
1+ mentions
Brain Networks (RRID:SCR_005841) Brain Networks data analysis software, data processing software, software application, software resource, source code 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 SciCrunch Registry brainnetworks 2026-10-17 01:26:24 1
ESTScan
 
Resource Report
Resource Website
100+ mentions
ESTScan (RRID:SCR_005742) ESTScan data analysis software, data processing software, software application, software resource 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 SciCrunch Registry ESTScan project 2026-10-17 01:26:19 291
BLESS
 
Resource Report
Resource Website
10+ mentions
BLESS (RRID:SCR_005963) BLESS algorithm resource, data analysis software, data processing software, sequence analysis software, software application, software resource 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 SciCrunch Registry BLoom-filter-based Error correction Solution for high-throughput Sequencing reads, BLESS - Bloom-filter-based Error Correction Tool for NGS reads 2026-10-17 01:26:29 46
Predictive Networks
 
Resource Report
Resource Website
Predictive Networks (RRID:SCR_006110) PN analysis service resource, data analysis service, data or information resource, database, production service resource, service resource, software resource, source code 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 SciCrunch Registry 2026-10-17 01:26:26 0
KAnalyze
 
Resource Report
Resource Website
1+ mentions
KAnalyze (RRID:SCR_001323) software resource A Java toolkit designed to convert DNA and RNA sequences into k-mers. standalone software, java, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:24642064 Free, Available for download, Freely available biotools:kanalyze, OMICS_03565 https://bio.tools/kanalyze SCR_001323 SciCrunch Registry 2026-10-17 01:24:52 2
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 2026-10-17 01:24:54 75
Drosophila anatomy and development ontologies
 
Resource Report
Resource Website
Drosophila anatomy and development ontologies (RRID:SCR_001607) FBbt controlled vocabulary, data or information resource, ontology A structured controlled vocabulary of the anatomy of Drosophila melanogaster. These ontologies are query-able reference sources for information on Drosophila anatomy and developmental stages. They also provide controlled vocabularies for use in annotation and classification of data related to Drosophila anatomy, such as gene expression, phenotype and images. They were originally developed by FlyBase, who continue to maintain them and have used them for over 200,000 annotations of phenotypes and expression. Extensive use of synonyms means that, given a suitably sophisticated autocomplete, users can find relevant content by searching with almost any anatomical term they find in the literature. These ontologies are developed in the web ontology language OWL2. Their extensive formalization in OWL can be used to drive sophisticated query systems. anatomy, development, developmental stage, gene expression, phenotype, owl is related to: OBO
is related to: Flannotator
is related to: REDfly Regulatory Element Database for Drosophilia
is related to: Bgee: dataBase for Gene Expression Evolution
has parent organization: FlyBase
has parent organization: SourceForge
NHGRI P41 HG000739 Free, Freely available nlx_153871 SCR_001607 SciCrunch Registry Drosophila anatomy & dev ontologies 2026-10-17 01:25:03 0
BACContigEditor
 
Resource Report
Resource Website
BACContigEditor (RRID:SCR_001617) BACContigEditor software resource A simple sequence alignment editing tool, written in Java. matlab is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_00875 SCR_001617 SciCrunch Registry 2026-10-17 01:24:57 0
DNACLUST
 
Resource Report
Resource Website
1+ mentions
DNACLUST (RRID:SCR_001771) software resource Software program for clustering large number of short similar DNA sequences. It was originally designed for clustering targeted 16S rRNA pyrosequencing reads. cluster, dna sequence, gene, 16s rrna pyrosequencing read, microbiome is listed by: OMICtools
is listed by: Human Microbiome Project
is listed by: Debian
has parent organization: SourceForge
PMID:21718538
DOI:10.1186/1471-2105-12-271
Free, Available for download, Freely available OMICS_01955 https://sources.debian.org/src/dnaclust/ SCR_001771 SciCrunch Registry DNAClust 2026-10-17 01:25:22 9
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 SciCrunch Registry SALT - Protein domain classifier 2026-10-17 01:25:47 1307
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 SciCrunch Registry XORRO: Rapid Paired-End Read Overlapper 2026-10-17 01:25:47 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 SciCrunch Registry NovelSeq: Novel Sequence Insertion Detection 2026-10-17 01:25:45 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 SciCrunch Registry mrCaNaVaR - micro-read Copy Number Variant Regions, micro-read Copy Number Variant Regions 2026-10-17 01:25:25 16
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 SciCrunch Registry 2026-10-17 01:25:48 1
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 SciCrunch Registry 2026-10-17 01:25:47 0

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