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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.
| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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POPGEN Resource Report Resource Website 100+ mentions |
POPGEN (RRID:SCR_007315) | software application, software resource | An R package that specifically focuses on statistical and population genetics methods. The motivation behind the package is to produce an easy to use interface to many of the commonly used methods and models used in statistical and population genetics and an alternative interface for some of the methodology produced by our group. (entry from Genetic Analysis Software) | gene, genetic, genomic, r | is listed by: Genetic Analysis Software | nlx_154543, SCR_009374, nlx_154596 | http://mathgen.stats.ox.ac.uk/software.html, https://cran.r-project.org/web/packages/popgen/index.html | SCR_007315 | R/POPGEN | 2026-08-05 10:44:40 | 198 | ||||||||
|
iOMICS Resource Report Resource Website |
iOMICS (RRID:SCR_000239) | iOMICS | service resource, software resource | A genomics data analysis platform which generates decision models for healthcare organizations and medical research. This service is meant to utilize data through machine learning methods. | genomic, decision model, machine learning, healthcare, machine learning, medical research | is listed by: OMICtools | Restricted | OMICS_02159 | http://www.iomics.in/overview | SCR_000239 | 2026-08-05 10:43:08 | 0 | |||||||
|
Short Course on the Genetics of Addiction Resource Report Resource Website |
Short Course on the Genetics of Addiction (RRID:SCR_005560) | Genetics of Addiction | short course, training resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented August 23, 2016. This course emphasizes genetic applications and approaches to drug addiction research through methodological instruction based on literature, data sets and informatics resources drawn from studies of addiction related phenotypes. The course includes plenary sessions on major progress in addiction genetics, and discussion sessions in which students present their work for discussion on applications of genetic methods. Students will leave the course able to design and interpret genetic and genomic studies of addiction as they relate to their specific research question, and will be able to make use of current bioinformatics resources to identify research resources and make use of public data sources in their own research. | addiction, gene, genetic, genomic, addiction, drug | has parent organization: Jackson Laboratory | Drug addiction | Howard Hughes Medical Institute ; NIDA R13 DA 032192 |
THIS RESOURCE IS NO LONGER IN SERVICE | nlx_146202 | SCR_005560 | 2026-08-05 10:44:16 | 0 | ||||||
|
GWAPOWER Resource Report Resource Website 1+ mentions |
GWAPOWER (RRID:SCR_009216) | software application, software resource | A R package for assessing the power of genome-wide association studies using commercially available genotyping chips. The package encapsulates extensive simulation results generated by our program HAPGEN. (entry from Genetic Analysis Software) | gene, genetic, genomic, r | is listed by: Genetic Analysis Software | nlx_154369, nlx_154586, SCR_000847 | SCR_009216 | R/GWAPOWER, Genome-Wide Association POWER | 2026-08-05 10:45:10 | 8 | |||||||||
|
FASTMAP (1) Resource Report Resource Website |
FASTMAP (1) (RRID:SCR_008346) | FASTMAP (1) | software toolkit, software application, software resource | Fluorescent allele-calling software toolkit: a computer software for fully automated microsatellite genotyping. (entry from Genetic Analysis Software) | gene, genetic, genomic, unix, macos, matlab, programming environment is required. | is listed by: Genetic Analysis Software | nlx_154310 | SCR_008346 | Fluorescent Allele-calling Software Toolkit: Microsatellite Automation Package | 2026-08-05 10:44:58 | 0 | ||||||||
|
University of North Carolina at Chapel Hill Translational Genomics Lab Core Facility Resource Report Resource Website 1+ mentions |
University of North Carolina at Chapel Hill Translational Genomics Lab Core Facility (RRID:SCR_025231) | TGL | access service resource, service resource, core facility | Core facility within Lineberger Comprehensive Cancer Center that performs sample processing for the molecular, pathologic, and genomic characterization of patient-derived specimens using high-end instrumentation and state-of-the-art methods. Service offerings include nucleic acid extraction, gene expression profiling, spatial genomics, next-generation sequencing library preparation, and high-throughput sequencing. Protocols leverage the reproducibility and reliability of automated instrumentation to minimize batch effects and processing errors (e.g. sample swaps). These workflows have been continuously optimized over the last decade, with a sample-to-answer historic success rate of ~90% for the >15,000 FFPE samples TGL has processed. | ABRF, sample processing, molecular, pathologic, genomic, patient derived specimens characterization, |
is listed by: ABRF CoreMarketplace has parent organization: University of North Carolina at Chapel Hill; North Carolina; USA |
ABRF_2716 | https://coremarketplace.org/?FacilityID=2716&citation=1 | SCR_025231 | , University of North Carolina at Chapel Hill UNC LCCC Translational Genomics Lab (TGL), UNC LCCC Translational Genomics Lab (TGL) | 2026-08-05 10:48:13 | 5 | |||||||
|
PathoMAN Resource Report Resource Website |
PathoMAN (RRID:SCR_026552) | PathoMAN | software resource, web application | Web application to automate germline genomic variant curation from clinical sequencing based on ACMG guidelines. Aggregates multiple tracks of genomic, protein and disease specific information from public sources. | Aggregates multiple tracks, automate germline genomic variant curation, clinical sequencing, genomic, protein, disease specific information, public sources, | NCI R21CA029533; NCI P50CA221745; NCI P30CA008748 |
PMID:30787465 | Free, Freely available, | SCR_026552 | Pathogenicity of Mutation Analyzer | 2026-08-05 10:48:32 | 0 | |||||||
|
University of Arkansas AIMRC Data Science Core Facility Resource Report Resource Website |
University of Arkansas AIMRC Data Science Core Facility (RRID:SCR_028681) | access service resource, service resource, core facility | Core specializes in artificial intelligence-based approaches to elucidate relationships between large imaging, bioenergetics, genomic, and proteomic data sets. Provided services include: 1) foundational training for those getting started with high-performance computing and Arkansas Research Platform (ARP), 2) training and support for the collaborative use of a 508 TB data storage server exclusively maintained for and catering to AIMRC researchers, 3) training for Python programming, basic data mining, and machine learning, 4) training and support for using open-source deep learning based biomedical imaging resources (e.g., ZeroCostDL4Mic and Bioimage Model Zoo), and 5) customized solutions for deep learning based and large foundational models based biomedical imaging analysis, multi-omics data integration and analysis, and quantitative analysis pipelines for large data sets. | ABRF, Center of Biomedical Research Excellence (COBRE), data science services, large imaging, bioenergetics, genomic, proteomic, data sets, |
is listed by: ABRF CoreMarketplace has parent organization: University of Arkansas; Arkansas; USA |
NIGMS P20GM139768 | ABRF_6033 | https://coremarketplace.org/RRID:SCR_028681/?citation=1 | SCR_028681 | , Arkansas Integrative Metabolic Center (AIMRC) Data Science Core | 2026-08-05 10:48:56 | 0 |
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