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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
JMolDraw
 
Resource Report
Resource Website
JMolDraw (RRID:SCR_000349) software resource 2-D chemical structure drawing software program. applet, mac os x, unix/linux, windows, java is listed by: OMICtools
has parent organization: SourceForge
Free, Available for download, Freely available OMICS_05000 SCR_000349 SciCrunch Registry 2026-10-24 12:44:12 0
AS-Peak
 
Resource Report
Resource Website
1+ mentions
AS-Peak (RRID:SCR_000380) ASPeak software resource A software that utilizes a peak detection algorithm to identify RNA-protein binding sites. rna, peak detection, protein, binding, site, algorithm, analysis is listed by: OMICtools
has parent organization: SourceForge
PMID:23929032 Free, Available for download, Freely available OMICS_00566 https://omictools.com/aspeak-tool SCR_000380 SciCrunch Registry 2026-10-24 12:44:13 2
GENSENG
 
Resource Report
Resource Website
1+ mentions
GENSENG (RRID:SCR_000378) data analysis software, data processing software, software application, software resource Software for detecting copy number variations from next generation sequencing data. Used to identify regions of discrete copy number changes while simultaneously accounting for effects of multiple confounders. next generation sequencing data, detecting copy number variations, discrete copy number changes, identify regions is listed by: OMICtools
has parent organization: SourceForge
PMID:23275535 Free, Available for download, Freely available OMICS_00345 SCR_000378 SciCrunch Registry 2026-10-24 12:44:14 1
ArrayPlex
 
Resource Report
Resource Website
ArrayPlex (RRID:SCR_000312) ArrayPlex software resource Open source software that integrates various forms of microarray data from diverse annotation and primary data sources. This software provides a programmatic framework (API set) that will be used for collaborative development and deploys an easy to maintain client-server architecture. microarray, programmatic framework, collaborative, client-server, is listed by: OMICtools
has parent organization: SourceForge
PMID:19014503 Free, Available for download, Freely available OMICS_00745 SCR_000312 SciCrunch Registry 2026-10-24 12:44:12 0
Micro-Analyzer
 
Resource Report
Resource Website
Micro-Analyzer (RRID:SCR_000394) Micro-Analyzer software resource Java tool that performs the preprocessing of Expression and SNPs microarray Affymetrix. The software allows the automatic download and the use of the clustering and visualization software as the Mev 4.0. The tool is equipped by a graphical interface (Swing) that allows to the user to: Create the workspace (files .cel, preferred algorithms , output, libraries to use); Run/save analysis and workspace settings (xml); Efficient download of the libraries (http, ftp, MD5); Customize basic and graphical settings (objects serialization and deserialization). Type of SNPs: Mapping 500k or preceding chips, SNP 5.0, SNP 6.0. Available for 32 or 64 bit systems, and for Windows and Linux Systems. windows, linux, java, java swing, gene expression, snp, microarray, affymetrix, preprocessing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:23731720 Free, Available for download, Freely available OMICS_01919, biotools:microanalyzer https://bio.tools/microanalyzer SCR_000394 SciCrunch Registry microAnalyzer 2026-10-24 12:44:15 0
FunctSNP
 
Resource Report
Resource Website
FunctSNP (RRID:SCR_000393) FunctSNP software resource An R package for linking SNPs (Single Nucleotide Polymorphisms) to functional knowledge. single nucleotide polymorphism is listed by: OMICtools
has parent organization: SourceForge
PMID:20534127 Free, Available for download, Freely available OMICS_01925 SCR_000393 SciCrunch Registry FunctSNP - Linking SNPs to functional knowledge 2026-10-24 12:44:15 0
LIPAGE
 
Resource Report
Resource Website
1+ mentions
LIPAGE (RRID:SCR_000290) data management software, software application, software resource Laboratory information management system for proteomics. The software works with 2DPAGE-based proteomics workflow. proteomics, laboratory, open source, 2dpage, management system is listed by: OMICtools
has parent organization: SourceForge
PMID:17018156 Free, Available for download, Freely available OMICS_02553 SCR_000290 SciCrunch Registry LIMS for proteomics 2026-10-24 12:44:11 1
fourSig
 
Resource Report
Resource Website
fourSig (RRID:SCR_000516) software resource A suite of software programs for analyzing and visualizing 4C-seq data. standalone software, perl, r is listed by: OMICtools
has parent organization: SourceForge
PMID:24561615 Free, Available for download, Freely available OMICS_02628 SCR_000516 SciCrunch Registry 2026-10-24 12:44:18 0
TOPPAS
 
Resource Report
Resource Website
1+ mentions
TOPPAS (RRID:SCR_000533) software resource A graphical user interface (GUI) for rapid composition of HPLC-MS analysis workflows. Workflow construction is reduced to drag-and-drop of analysis tools and adding connections in between. gui, graphical user interface, analysis, hplc-ms, workflow is listed by: OMICtools
has parent organization: SourceForge
PMID:22583024 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02640 http://open-ms.sourceforge.net/workflow-integration/toppasworkflows/ SCR_000533 SciCrunch Registry The OpenMS Proteomics Pipeline Assistant, TOPP Pipeline Assistant 2026-10-24 12:44:18 1
Ishtar
 
Resource Report
Resource Website
Ishtar (RRID:SCR_000538) software resource A program for designing primer pairs that amplify multiple target sequences using DNA thermodynamics and one class support vector machines. Written in Python. dna, thermodynamics, sequence, primer, pairs, loci, bioinformatics has parent organization: SourceForge Free, Available for download, Freely available, nlx_71525 SCR_000538 SciCrunch Registry 2026-10-24 12:44:18 0
Reprever
 
Resource Report
Resource Website
Reprever (RRID:SCR_000463) Reprever software resource Software that identifies (a) the insertion breakpoints where the extra duplicons inserted into the donor genome and (b) the actual sequence of the duplicon for any genomic regions that are increased in copy number. genomics, genomic region, insertion breakpoint, insertion, breakpoint, duplicon, genome is listed by: OMICtools
has parent organization: SourceForge
has parent organization: University of California at San Diego; California; USA
PMID:23658221 Free, Available for download, Freely available OMICS_01561 SCR_000463 SciCrunch Registry Reprever: resolving low-copy duplicated sequences using template drive 2026-10-24 12:44:17 0
ViReMa
 
Resource Report
Resource Website
1+ mentions
ViReMa (RRID:SCR_000566) ViReMa data analysis software, data processing software, software application, software resource, software toolkit Software Python package for detection, alignment and reporting of recombination events in Next-Generation Sequencing data. Detects and reports recombination or fusion events in virus genomes using deep sequencing datasets. virus genomes deep sequencing datasets, detection, alignment and reporting of recombination events, Next-Generation Sequencing data, is listed by: OMICtools
has parent organization: SourceForge
has parent organization: Scripps Research Institute
PMID:24137010 Free, Available for download, Freely available, OMICS_00225 SCR_000566 SciCrunch Registry Viral Recombination Mapper 2026-10-24 12:44:19 2
VariantMaster
 
Resource Report
Resource Website
VariantMaster (RRID:SCR_000569) VariantMaster software resource Software program that extracts causative variants in familial and sporadic genetic diseases. The algorithm takes into account predicted variants (SNPs and indels) in affected individuals or tumor samples and utilizes the row (BAM) data to robustly estimate the conditional probability of segregation in a family, as well as the probability of it being de novo or somatic. In familial cases, various modes of inheritance are considered: X-linked, autosomal dominant, and recessive (homozygosity or compound heterozygosity). Moreover, it integrates phenotypes and genotypes, and employs Annovar to produce additional information as allelic frequencies in general population and damaging scores. unix/linux, clinical, genetics, high throughput sequencing, monogenic disease, variant, snp, indel is listed by: OMICtools
has parent organization: SourceForge
Genetic disease, Tumor PMID:24389049 Free, Available for download, Freely available, OMICS_02261 SCR_000569 SciCrunch Registry VariantMaster - Extract causative variants for monogenic and sporadic genetic diseases 2026-10-24 12:44:19 0
DeNovoGear
 
Resource Report
Resource Website
1+ mentions
DeNovoGear (RRID:SCR_000670) software resource A software for detecting de novo mutations using sequencing data. It utilizes likelihood-based error modeling to reduce the false positive rate of mutative discovery in exome analysis. It also uses fragment information to identify the parental origin of germ-line mutations. de novo, mutation, sequence, dna, rna, error modeling, exome analysis is listed by: OMICtools
has parent organization: SourceForge
has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA
PMID:23975140 Free, Available for download, Freely available OMICS_00083 https://github.com/denovogear/denovogear SCR_000670 SciCrunch Registry 2026-10-24 12:44:21 3
SRMA
 
Resource Report
Resource Website
SRMA (RRID:SCR_000669) SRMA software resource A post-alignment micro re-aligner for next-generation high throughput sequencing data. matlab, sequence re-alignment, command-line, java, next generation sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:20932289 Free, Available for download, Freely available biotools:srma, OMICS_01079 https://bio.tools/srma SCR_000669 SciCrunch Registry Short Read Micro re-Aligner 2026-10-24 12:44:21 0
FineSplice
 
Resource Report
Resource Website
1+ mentions
FineSplice (RRID:SCR_000691) software resource A software pipeline based on TopHat2 combined with a splice junction detection algorithm. standalone software, python is listed by: OMICtools
has parent organization: SourceForge
PMID:24574529 Free, Available for download, Freely available OMICS_03274 SCR_000691 SciCrunch Registry 2026-10-24 12:44:22 1
D-Tailor
 
Resource Report
Resource Website
D-Tailor (RRID:SCR_000115) software resource A fully extendable software framework, for property-based design of synthetic DNA sequences. standalone software, python is listed by: OMICtools
has parent organization: SourceForge
PMID:24398007 Free, Available for download, Freely available OMICS_04768 SCR_000115 SciCrunch Registry DNA-Tailor 2026-10-24 12:44:08 0
siRNArules
 
Resource Report
Resource Website
siRNArules (RRID:SCR_000096) software resource An open-source JAVA program that is surprisingly efficient at predicting active siRNAs. standalone software, java is listed by: OMICtools
has parent organization: SourceForge
PMID:16870995 Free, Available for download, Freely available OMICS_04742 SCR_000096 SciCrunch Registry 2026-10-24 12:44:07 0
AbMining ToolBox
 
Resource Report
Resource Website
AbMining ToolBox (RRID:SCR_000090) software resource Python scripts to analyze antibody libraries sequenced by next generation sequencing methods (454, Ion Torrent, MiSeq). standalone software, illumina, roche, life technologies, python is listed by: OMICtools
has parent organization: SourceForge
PMID:24423623 Free, Available for download, Freely available OMICS_04063 SCR_000090 SciCrunch Registry 2026-10-24 12:44:07 0
SP-Designer
 
Resource Report
Resource Website
SP-Designer (RRID:SCR_000031) software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. An open source software program for the design of specific PCR primer pairs from a DNA sequence alignment containing sequences from various taxa. standalone software, windows is listed by: OMICtools
has parent organization: SourceForge
PMID:23634845 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_03932 SCR_000031 SciCrunch Registry 2026-10-24 12:44:05 0

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