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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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  • RRID:SCR_012191

    This resource has 100+ mentions.

http://goldenhelix.com/

Specializes in sequence and array-based SNP and copy number analysis, genetic association software, and analytic services. Their technologies empower scientists to determine the genetic causes of disease, transform drug discovery, develop genetic diagnostics, and advance the quest for personalized medicine.

Proper citation: Golden Helix Incorporated (RRID:SCR_012191) Copy   


  • RRID:SCR_010620

    This resource has 50+ mentions.

http://scienceexchange.com/

Access service resource which connects labs needing and offering experimental services. Users can search for academic and government labs and experimental services, request and compare service quotes, and directly communicate with labs to arrange orders.

Proper citation: ScienceExchange (RRID:SCR_010620) Copy   


  • RRID:SCR_001213

    This resource has 1+ mentions.

http://www.goldenhelix.com/GenomeBrowse/index.html

Software tool that delivers visualizations of your genomic data that give you the power to see what is occurring at each base pair in your samples. A high performance backend is paired with an user interface to make sure that your discovery process is fluid and streamlined.

Proper citation: Golden Helix GenomeBrowse (RRID:SCR_001213) Copy   


http://www.goldenhelix.com/SNP_Variation/CNV_Analysis_Package/index.html

A set of software tools for processing raw intensity data, identifying regions of copy number variation (CNV), visualizing copy number data, and performing association analyses on a variety of copy number covariates.

Proper citation: SNP and Variation Suite CNV Analysis (RRID:SCR_001286) Copy   


http://www.goldenhelix.com/SNP_Variation/SNP_Analysis_Package/index.html

SNP Analysis software for basic to advanced analyses that incorporates a number of intuitive workflows to lead you beyond single marker associations. With support for case-control and quantitative traits, whole genome and candidate gene data, you can run a breadth of statistical tests under several genetic models. Advanced regression can further help elucidate even the most complex gene-gene and gene-environment interactions.

Proper citation: SNP and Variation Suite SNP Analysis (RRID:SCR_001285) Copy   


http://www.goldenhelix.com/products/index.html

An integrated collection of user-friendly, yet powerful analytic tools for managing, analyzing, and visualizing multifaceted genomic and phenotypic data.

Proper citation: SNP and Variation Suite (RRID:SCR_011856) Copy   



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