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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
Benaroya Research Institute
 
Resource Report
Resource Website
1+ mentions
Benaroya Research Institute (RRID:SCR_001272) BRI institution Non-profit organization based out of Seattle, Washington that conducts medical research on autoimmune disease. research institute, nonprofit, medical, autoimmune disease is parent organization of: Immune Tolerance Network (ITN)
is parent organization of: Benaroya Research Institute: Neurological Diseases
is parent organization of: Benaroya Research Institute Cell and Tissue Analysis Group Core Facility
is parent organization of: Benaroya Research Institute Human Immunophenotyping Core Facility
is parent organization of: Benaroya Research Institute Genomics Core Facility
is parent organization of: Benaroya Research Institute BRI Biorepository Core Facility
, Wikidata Q4886865, nlx_152837, ISNI 0000 0004 0444 3749 https://ror.org/04j9rp686 SCR_001272 SciCrunch Registry Benaroya Research Institute at Virginia Mason, Benaroya 2026-10-24 12:44:28 1
mBPCR
 
Resource Report
Resource Website
mBPCR (RRID:SCR_001273) mBPCR software resource Software package that estimates the DNA copy number profile to detect regions with copy number changes. copy number variation, microarray, snp, acgh is listed by: OMICtools
has parent organization: Bioconductor
Free, Available for download, Freely available OMICS_02065 SCR_001273 SciCrunch Registry mBPCR - Bayesian Piecewise Constant Regression for DNA copy number estimation 2026-10-24 12:44:32 0
CGHregions
 
Resource Report
Resource Website
1+ mentions
CGHregions (RRID:SCR_001278) CGHregions software resource Software package for dimension Reduction for Array CGH Data with Minimal Information Loss. copy number variation, microarray, visualization is listed by: OMICtools
has parent organization: Bioconductor
PMID:19455235 Free, Available for download, Freely available OMICS_02058 SCR_001278 SciCrunch Registry CGHregions - Dimension Reduction for Array CGH Data with Minimal Information Loss 2026-10-24 12:44:32 4
CGHbase
 
Resource Report
Resource Website
1+ mentions
CGHbase (RRID:SCR_001279) CGHbase data analysis software, data processing software, software application, software resource Software package that contains functions and classes that are needed by arrayCGH packages. copy number variation, infrastructure, microarray is listed by: OMICtools
has parent organization: Bioconductor
Free, Available for download, Freely available OMICS_02057 SCR_001279 SciCrunch Registry CGHbase: Base functions and classes for arrayCGH data analysis 2026-10-24 12:44:28 1
quantsmooth
 
Resource Report
Resource Website
1+ mentions
quantsmooth (RRID:SCR_001271) quantsmooth software resource Software package for quantile smoothing and genomic visualization of array data. copy number variation, visualization, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
PMID:15572474 Free, Available for download, Freely available OMICS_02067, BioTools:quantsmooth, biotools:quantsmooth https://bio.tools/quantsmooth, https://bio.tools/quantsmooth, https://bio.tools/quantsmooth SCR_001271 SciCrunch Registry 2026-10-24 12:44:30 1
SNPchip
 
Resource Report
Resource Website
10+ mentions
SNPchip (RRID:SCR_001269) SNPchip software resource Software package that contains classes and methods useful for storing, visualizing and analyzing high density SNP data. Originally developed from the SNPscan web-tool, SNPchip utilizes S4 classes and extends other open source R tools available at Bioconductor, including the R packages Biobase and oligo. This has numerous advantages, including the ability to build statistical models for SNP-level data that operate on instances of the class, and to communicate with other R packages that add additional functionality. dna copy number, snp, genetic variability, visualization, high throughput, snp chip, microarray, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Bioconductor
has parent organization: Johns Hopkins Bloomberg School of Public Health; Maryland; USA
PMID:17204461 Free, Available for download, Freely available OMICS_02069, biotools:snpchip https://bio.tools/snpchip SCR_001269 SciCrunch Registry 2026-10-24 12:44:32 14
Simpleaffy
 
Resource Report
Resource Website
50+ mentions
Simpleaffy (RRID:SCR_001302) Simpleaffy data analysis software, data processing software, software application, software resource Software package that provides high level functions for reading Affy .CEL files, phenotypic data, and then computing simple things with it, such as t-tests, fold changes and the like. It makes heavy use of the affy library. It also has some basic scatter plot functions and mechanisms for generating high resolution journal figures. affymetrix, annotation, data import, differential expression, microarray, one channel, preprocessing, quality control, report writing, transcription, visualization is listed by: OMICtools
has parent organization: Bioconductor
PMID:16076888 GNU General Public License, v2 or newer OMICS_02034 SCR_001302 SciCrunch Registry Simpleaffy - Very simple high level analysis of Affymetrix data 2026-10-24 12:44:32 85
ADMIXTURE
 
Resource Report
Resource Website
1000+ mentions
ADMIXTURE (RRID:SCR_001263) ADMIXTURE software resource A software tool for maximum likelihood estimation of individual ancestries from multilocus SNP genotype datasets. It uses the same statistical model as STRUCTURE but calculates estimates much more rapidly using a fast numerical optimization algorithm. It uses a block relaxation approach to alternately update allele frequency and ancestry fraction parameters. Each block update is handled by solving a large number of independent convex optimization problems, which are tackled using a fast sequential quadratic programming algorithm. Convergence of the algorithm is accelerated using a novel quasi-Newton acceleration method., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. ancestry, macos x, linux, admixture, allele, genome, single nucleotide polymorphism, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of California at Los Angeles; California; USA
PMID:19648217 THIS RESOURCE IS NO LONGER IN SERVICE biotools:admixture, OMICS_02077 http://www.genetics.ucla.edu/software/admixture/ SCR_001263 SciCrunch Registry ADMIXTURE: fast ancestry estimation 2026-10-24 12:44:28 2699
frappe
 
Resource Report
Resource Website
50+ mentions
frappe (RRID:SCR_001264) frappe software resource Software using a f frequentist approach for estimating individual ancestry proportion. ancestry, admixture, genome, allele is listed by: OMICtools
has parent organization: Stanford University School of Medicine; California; USA
PMID:15712363 Free, Available for download, Freely available OMICS_02076 SCR_001264 SciCrunch Registry 2026-10-24 12:44:32 56
ipPCA
 
Resource Report
Resource Website
1+ mentions
ipPCA (RRID:SCR_001262) ipPCA, i2pPCA software resource Software implementing a population structure analysis algorithm which assigns individuals to subpopulations and infers the total number of subpopulations present. Additional functions have been included that result in improved population assignment accuracy. # Universal genotype data encoding scheme which allows the population analysis of all types of genetic markers; Single Nucleotide Polymorphism (SNP), Short Tandem Repeat (STR) and RFLP. # New termination criterion called ?EigenDev? which is more robust to population sampling, thus provides the better estimation of number of assigned subpopulations (K) and higher accuracy for the analysis of large complex population datasets. principal component analysis, population, genetic marker, single nucleotide polymorphism, short tandem repeat, rflp is listed by: OMICtools PMID:21699684
PMID:19930644
Free, Available for download, Freely available OMICS_02078 http://www4a.biotec.or.th/GI/tools/ippca SCR_001262 SciCrunch Registry i2pPCA, Iterative pruning Principal Component Analysis 2026-10-24 12:44:30 1
VegaMC
 
Resource Report
Resource Website
1+ mentions
VegaMC (RRID:SCR_001267) VegaMC software resource Software package that enables the detection of driver chromosomal imbalances including loss of heterozygosity (LOH) from array comparative genomic hybridization (aCGH) data. It performs a joint segmentation of a dataset and uses a statistical framework to distinguish between driver and passenger mutation. VegaMC has been implemented so that it can be immediately integrated with the output produced by PennCNV tool. In addition, it produces in output two web pages that allows a rapid navigation between both the detected regions and the altered genes. In the web page that summarizes the altered genes, the link to the respective Ensembl gene web page is reported. copy number variation, acgh, chromosomal imbalance is listed by: OMICtools
is related to: PennCNV
has parent organization: Bioconductor
Cancer PMID:22815357 Free, Available for download, Freely available OMICS_02071 SCR_001267 SciCrunch Registry VegaMC: A Package Implementing a Variational Piecewise Smooth Model for Identification of Driver Chromosomal Imbalances in Cancer 2026-10-24 12:44:30 1
VanillaICE
 
Resource Report
Resource Website
1+ mentions
VanillaICE (RRID:SCR_001268) VanillaICE software resource Software package using Hidden Markov Models for characterizing chromosomal alterations in high throughput SNP arrays. statistics, dna copy number, snp, genetic variability, visualization, high throughput, snp chip, microarray is listed by: OMICtools
has parent organization: Bioconductor
has parent organization: Johns Hopkins Bloomberg School of Public Health; Maryland; USA
PMID:19609370 GNU General Public License, v2 or newer OMICS_02070 http://www.biostat.jhsph.edu/~rscharpf/software/index.html SCR_001268 SciCrunch Registry vanilla-ice 2026-10-24 12:44:28 3
Mutascope
 
Resource Report
Resource Website
1+ mentions
Mutascope (RRID:SCR_001265) Mutascope data analysis software, data processing software, software application, software resource Software suite to analyze data from high throughput sequencing of PCR amplicons, with an emphasis on normal-tumor comparison for the accurate and sensitive identification of low prevalence mutations. high throughput sequencing, pcr amplicon, pcr, mutation, amplicon, sequencing, somatic variant is listed by: OMICtools
has parent organization: SourceForge
Tumor, Normal PMID:23712659 Free, Public OMICS_02074 SCR_001265 SciCrunch Registry Mutascope - Analysis software designed for PCR-amplicon sequencing data 2026-10-24 12:44:28 4
GemTools
 
Resource Report
Resource Website
10+ mentions
GemTools (RRID:SCR_001259) GemTools software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23,2022. Software tools for modeling genetic ancestry based on the single nucleotide polymorphism (SNP) information. This package of functions helps the user account for genetic ancestry of a large number of individuals using spectral graph theory and projections to break a large problem into smaller pieces and calculate genetic ancestry information efficiently, i.e., a divide and conquer (dac) strategy. It is completely written in R and runs on any platform that supports R. genetic, ancestry, single nucleotide polymorphism, r is listed by: OMICtools
has parent organization: University of Pittsburgh; Pennsylvania; USA
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02079 SCR_001259 SciCrunch Registry GemTools - A fast and efficient approach to estimating genetic ancestry 2026-10-24 12:44:28 45
SCAN.UPC
 
Resource Report
Resource Website
10+ mentions
SCAN.UPC (RRID:SCR_001334) SCAN.UPC software resource A microarray normalization software (SCAN) to facilitate personalized-medicine workflows with an extension (UPC) that estimates whether a given gene/transcript is active above background levels in a given sample. Rather than processing microarray samples as groups, which can introduce biases and present logistical challenges, SCAN normalizes each sample individually by modeling and removing probe- and array-specific background noise using only data from within each array. SCAN can be applied to one-channel (e.g., Affymetrix) or two-channel (e.g., Agilent) microarrays. The UPC method can be applied to one-channel or two-channel microarrays as well as to RNA-Seq read counts. Because UPC values are represented on the same scale and have an identical interpretation for each platform, they can be used for cross-platform data integration. A microarray, one channel, preprocessing, rna-seq, two channel is listed by: OMICtools
has parent organization: Bioconductor
Free, Available for download, Freely available OMICS_02006 SCR_001334 SciCrunch Registry Single-channel array normalization (SCAN) and Universal exPression Codes (UPC), Single-channel array normalization and Universal exPression Codes 2026-10-24 12:44:31 11
EEGbase
 
Resource Report
Resource Website
1+ mentions
EEGbase (RRID:SCR_001452) data or information resource, data repository, database, service resource, storage service resource EEG base is a system for storage and management of EEG/ERP resources - data, metadata, tools and materials related to EEG/ERP experiments. EEG base advances electrophysiology research by enabling access to public data, tools and results of research groups. The system essentially offers the following set of features (the set of accessible features depends on a specific user role): * User authentication * Storage, update, and download of EEG/ERP data and metadata * Storage, update and download of EEG/ERP experimental design (experimental scenarios) * Storage, update and download of data related to testing subjects * Fulltext search * Sharing of knowledge and working in groups The system is based on tree layer architecture (MVC pattern) consisting of persistent layer (relational database), application layer (object oriented code, object relational mapping from persistence layer) and presentation layer (JSP). The persistence layer uses Hibernate framework; Oracle 11g database server is used to ensure the processing of large data files. Application and presentation layers are designed and implemented using Spring technology. This framework supports MVC architecture, Dependency injection and Aspect Oriented Programming. There were no significant difficulties with integration of both frameworks, Hibernate and Spring MVC. Spring Security framework is used to ensure management of authentication and user roles. Since the system is thought to be finally open to the whole EEG/ERP community it is necessary to protect EEG/ERP data and metadata, and especially personal data of testing subjects stored in the database from an unauthorized access. Then a restricted user policy is applied and user roles are introduced. The complete overview of the system features and user roles (use case diagram) is available in (Pergler 2009). Concerning the architectural layers there is a question which layer is more feasible for mapping of its structure into ontology. Currently we have studied two possibilities: * Mapping from the persistence layer (relational database) * Mapping from the application layer (object oriented code) The mapping from the application layer to an ontology includes the precedent object relational mapping provided by Hibernate framework. eeg, erp, experiments, data storage and management, EEG/ERP data, EEG/ERP experiments, uses: NIX
uses: Open metadata mark up language
is used by: NIF Data Federation
has parent organization: University of West Bohemia; Pilsen; Czech Republic
Ministry of Education Czech Science Foundation Free, Freely Available nif-0000-08190 http://eegdatabase.kiv.zcu.cz/ SCR_001452 SciCrunch Registry 2026-10-24 12:44:34 7
betr
 
Resource Report
Resource Website
10+ mentions
betr (RRID:SCR_001332) betr software resource Software package that implements the Bayesian Estimation of Temporal Regulation algorithm to identify differentially expressed genes in microarray time-course data. differentially expression, gene, microarray, time-course is listed by: OMICtools
has parent organization: Bioconductor
PMID:20003283 Free, Available for download, Freely available OMICS_01997 http://www.bioconductor.org/packages/release/bioc/html/betr.html SCR_001332 SciCrunch Registry Bayesian Estimation of Temporal Regulation 2026-10-24 12:44:33 17
Wake Forest University School of Medicine: Department of Neurology
 
Resource Report
Resource Website
Wake Forest University School of Medicine: Department of Neurology (RRID:SCR_001453) data or information resource, department portal, organization portal, portal, university Department at the Wake Forest University's School of Medicine that hosts physicians who specialize in neurological topics such as neuromuscular disease, epilepsy, pediatric neurology, strokes, neuropsychology, neurosonology, and neurorehabilitaiton. neurology, medicine, wake forest, stroke, neuropsychology, physicain Free, Freely Available nif-0000-10549 http://www1.wfubmc.edu/neurology/ SCR_001453 SciCrunch Registry WFUBMC Neurology 2026-10-24 12:44:33 0
Roche
 
Resource Report
Resource Website
500+ mentions
Roche (RRID:SCR_001326) commercial organization A Swiss global health-care company that operates under two divisions: Pharmaceuticals and Diagnostics. pharmaceutical, diagnostic, drug, medicine, commercial is affiliated with: European Federation of Pharmaceutical Industries and Associations
is related to: EU-AIMS
is related to: eTRIKS
is related to: OncoTrack
is related to: GetReal
is related to: IMIDIA
is related to: Kinetics for Drug Discovery
is related to: NEWMEDS
is related to: PharmaCog
is related to: PREDECT
is related to: EMIF
is parent organization of: EU-AIMS
is parent organization of: Genentech
is parent organization of: Roche Diagnostics
is parent organization of: Roche: cobas�� e 601
ISNI: 0000 0004 1759 0967, grid.486917.5, nlx_152451, Wikidata: Q41568432 https://ror.org/02hv5e369 SCR_001326 SciCrunch Registry Hoffmann-La Roche AG, Hoffmann-La Roche, Roche Holding AG, F. Hoffmann-La Roche, F. Hoffmann-La Roche Ltd 2026-10-24 12:44:31 544
gprege
 
Resource Report
Resource Website
1+ mentions
gprege (RRID:SCR_001324) gprege software resource Software R package for Gaussian Process Ranking and Estimation of Gene Expression time-series. The software fits two Gaussian processes (GPs) with an radial basis function (RBF) (+ noise diagonal) kernel on each profile. One GP kernel is initialized wih a short lengthscale hyperparameter, signal variance as the observed variance and a zero noise variance. It is optimized via scaled conjugate gradients (netlab). A second GP has fixed hyperparameters: zero inverse-width, zero signal variance and noise variance as the observed variance. The log-ratio of marginal likelihoods of the two hypotheses acts as a score of differential expression for the profile. Comparison via receiver operating characteristic curves (ROC curves) is performed against Bayesian hierarchical model for the analysis of time-series (BATS) (Angelini et.al, 2007). differential expression, microarray, preprocessing, time course, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
PMID:21599902 Free, Available for download, Freely available OMICS_02011, biotools:gprege http://www.bioconductor.org/packages/release/bioc/html/gprege.html SCR_001324 SciCrunch Registry Gaussian Process Ranking and Estimation of Gene Expression time-series 2026-10-24 12:44:33 1

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