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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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On page 165 showing 3281 ~ 3300 out of 27,093 results
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  • RRID:SCR_000078

    This resource has 1+ mentions.

http://soap.genomics.org.cn/soapfuse.html

THIS RESOURCE IS NO LONGER IN SERVICE.Documented on August 23,2022. An open source tool developed for genome-wide detection of fusion transcripts from human being paired-end RNA-Seq data. This tool is a part of a larger set of tools to efficiently align oligonucleotides onto reference sequences .

Proper citation: SOAPfuse (RRID:SCR_000078) Copy   


  • RRID:SCR_000190

    This resource has 1+ mentions.

http://molegro-virtual-docker.software.informer.com/

An integrated platform for predicting protein-ligand interactions, the visualization of new ideas and analyzing protein targets.

Proper citation: Molegro Virtual Docker (RRID:SCR_000190) Copy   


  • RRID:SCR_000070

    This resource has 1+ mentions.

http://www.genemed.com/

A supplier of cancer and infectious disease diagnostic reagents. The company also provides services such as tissue-based and molecular diagnostics to their partners to accelerate their in vitro diagnostic device (IVD) product development and commercialization.

Proper citation: Genemed (RRID:SCR_000070) Copy   


  • RRID:SCR_000095

    This resource has 1+ mentions.

http://jchempaint.github.io/

Chemical 2D structure editor and viewer application/applet based on the Chemistry Development Kit (CDK).

Proper citation: JChemPaint (RRID:SCR_000095) Copy   


  • RRID:SCR_000093

    This resource has 10+ mentions.

http://www.epilepsygenetics.eu/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 16,2023. Group of clinical care and epilepsy research centers who are committed to improving the lives of people with epilepsy through an understanding of the genetics of epilepsy. The consoritum was in an effort to speed discovery to epilepsy genetics by pooling the resources of several research centres., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: EPIGEN (RRID:SCR_000093) Copy   


  • RRID:SCR_000101

http://www.bioconductor.org/packages/release/data/annotation/html/RmiR.Hs.miRNA.html

Software package for various databases of microRNA Targets.

Proper citation: RmiR.Hs.miRNA (RRID:SCR_000101) Copy   


http://acgt.cs.tau.ac.il/modent/

A computational tool that reconstructs gene regulatory networks from high throughput experimental data.

Proper citation: MODENT - A Tool For Reconstructing Gene Regulatory Networks (RRID:SCR_000220) Copy   


https://omictools.com/context-likelihood-of-relatedness-tool

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. A software that infers regulatory interactions between transcription factors and their targets using a compendium of gene expression profiles.

Proper citation: Context Likelihood of Relatedness (RRID:SCR_000216) Copy   


http://www.csir.co.za/

A leading scientific and technology research, development and implementation organization in Africa that undertakes directed research and development for socio-economic growth and improving the quality of life of South African citizens.

Proper citation: Council for Scientific and Industrial Research; Gauteng; South Africa (RRID:SCR_000214) Copy   


http://www.cdisc.org/

A global, open, multidisciplinary, non-profit organization that has established standards to support the acquisition, exchange, submission and archive of clinical research data and metadata. Its mission is to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of healthcare. CDISC standards are vendor-neutral, platform-independent and freely available via the CDISC website.

Proper citation: Clinical Data Interchange Standards Consortium (RRID:SCR_000219) Copy   


  • RRID:SCR_000217

    This resource has 10+ mentions.

https://github.com/vahuynh/dynGENIE3

An algorithm for the inference of gene regulatory networks from expression data.

Proper citation: GENIE3 (RRID:SCR_000217) Copy   


  • RRID:SCR_000218

    This resource has 1+ mentions.

http://bonneaulab.bio.nyu.edu/networks.html

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. Algorithm for learning parsimonious regulatory networks from systems biology data sets de novo. Software that utilizes inference algorithm to model genetic regulatory networks.Inferelator 2.0 is scalable framework for reconstruction of dynamic regulatory network models., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: Inferelator (RRID:SCR_000218) Copy   


  • RRID:SCR_000212

    This resource has 1+ mentions.

http://cran.r-project.org/web/packages/c3net/index.html

Software package that allows inferring gene regulatory networks with direct physical interactions from microarray expression data using C3NET.

Proper citation: c3net (RRID:SCR_000212) Copy   


http://knightadrc.wustl.edu/

The Charles F. and Joanne Knight Alzheimer Disease Research Center (Knight ADRC) supports researchers and our surrounding community in their pursuit of answers that will lead to improved diagnosis and care for persons with Alzheimer disease (AD). The Center is committed to the long-term goal of finding a way to effectively treat and prevent AD. The Knight ADRC facilitates advanced research on the clinical, genetic, neuropathological, neuroanatomical, biomedical, psychosocial, and neuropsychological aspects of Alzheimer disease, as well as other related brain disorders.

Proper citation: Washington University School of Medicine Knight Alzheimers Disease Research Center (RRID:SCR_000210) Copy   


  • RRID:SCR_000204

http://fiduswriter.org/

An online collaborative editor for academics that use citations and/or formulas. The editor focuses on the content rather than the layout, so that with the same text, it can be published in multiple ways: On a website, as a printed book, or as an ebook.

Proper citation: Fiduswriter (RRID:SCR_000204) Copy   


  • RRID:SCR_000205

http://www.uniklinikum-saarland.de/einrichtungen/fachrichtungen/humangenetik/software/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. A software tool for predicting granzyme B and caspase cleavage sites.

Proper citation: GraBCas (RRID:SCR_000205) Copy   


http://ccd.biocuckoo.org/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on July 31,2025. A software package for the prediction of calpain cleavage sites.

Proper citation: GPS-Calpain Cleavage Detector (RRID:SCR_000202) Copy   


https://www.qcif.edu.au/

Provides digital infrastructure capabilities for research and innovation across Queensland and Australia. Provides services, infrastructure and support for computation and data driven collaborative research and its application in industry. Members are six Queensland universities – The University of Queensland, Queensland University of Technology, Griffith University, James Cook University, CQUniversity, and the University of Southern Queensland. The University of the Sunshine Coast is an associate member. Member employees provide support and development services.

Proper citation: Queensland Cyber Infrastructure Foundation Ltd (RRID:SCR_000208) Copy   


http://www.themmrf.org/

Research foundation that funds research to develop new treatments for multiple myeloma, an incurable blood cancer.

Proper citation: Multiple Myeloma Research Foundation (RRID:SCR_000207) Copy   


http://www.nitrc.org/projects/ontologyviz/

Software that allows user to do faceted search on an ontology and enables visualization of the search results on the 3D digital atlas. Currently supports faceted search of functional neuroanatomy.

Proper citation: Faceted Search Based Ontology Visualizer (RRID:SCR_000124) Copy   



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