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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 69 showing 1361 ~ 1380 out of 2,818 results
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http://www.mitomap.org/

Database of polymorphisms and mutations of the human mitochondrial DNA. It reports published and unpublished data on human mitochondrial DNA variation. All data is curated by hand. If you would like to submit published articles to be included in mitomap, please send them the citation and a pdf.

Proper citation: MITOMAP - A human mitochondrial genome database (RRID:SCR_002996) Copy   


  • RRID:SCR_010960

    This resource has 1+ mentions.

http://www.premierbiosoft.com/dnamicroarray/index.html

Oligo and cDNA Microarray Design Software that designs thousands of primers and probes for oligo and cDNA microarrays in seconds.

Proper citation: Array Designer (RRID:SCR_010960) Copy   


  • RRID:SCR_010972

    This resource has 1000+ mentions.

http://www.genomics.agilent.com/en/Microarray-Data-Analysis-Software/GeneSpring-GX/?cid=AG-PT-130&tabId=AG-PR-1061

Powerful, accessible statistical tools for fast visualization and analysis of microarrays - expression arrays, miRNA, exon arrays and genomics copy number data.

Proper citation: GeneSpring GX (RRID:SCR_010972) Copy   


http://www.exiqon.com/mirna-array-software

Software for fast and accurate analysis of miRCURY LNA microRNA Array data.

Proper citation: miRCURY LNA microRNA Array Analysis Software (RRID:SCR_010952) Copy   


  • RRID:SCR_010805

http://realtimegenomics.com/products/variant-1.0

The product line encompasses distinct products for the specific needs of clinical research, saving time and money while allowing customers to focus on the answers they need most.

Proper citation: RTG Variant (RRID:SCR_010805) Copy   


  • RRID:SCR_011949

http://realtimegenomics.com/products/metagenomics-1.0

Delivers comprehensive shotgun metagenomics sequence analysis for accurate species frequency composition and protein searching.

Proper citation: RTG Metagenomics (RRID:SCR_011949) Copy   


  • RRID:SCR_011855

http://www.genomatix.de/solutions/index.html

With their unique combination of proprietary algorithms and comprehensive data background, all our solutions do more than enable you to efficiently and effectively analyze and interpret biological data., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: Genomatix Solutions (RRID:SCR_011855) Copy   


  • RRID:SCR_011960

    This resource has 1+ mentions.

http://sbcb.bioch.ox.ac.uk/kdb/

A Database of Potassium Ion Channel Homology Models & Molecular Dynamics Simulations.

Proper citation: Potassium Channel Database (RRID:SCR_011960) Copy   


  • RRID:SCR_010020

http://www.omixon.com/blog/

We share commentaries, news and announcement that advance our goal of helping clinical labs to adopt next generation sequencing for the analysis of diagnostic gene targets.

Proper citation: Omixon blog (RRID:SCR_010020) Copy   


  • RRID:SCR_009395

    This resource has 10+ mentions.

http://mcg.ustc.edu.cn/sdap1/cpss/index.html

Computational Platform for analysis of Small RNA deep Sequencing data BioStaCs group., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: CPSS (RRID:SCR_009395) Copy   


  • RRID:SCR_010841

    This resource has 500+ mentions.

http://diana.imis.athena-innovation.gr/DianaTools/index.php?r=tarbase/index

Manually curated database of experimentally supported animal microRNA targets. Collection of experimentally supported miRNA gene interactions.

Proper citation: TarBase (RRID:SCR_010841) Copy   


  • RRID:SCR_010787

    This resource has 100+ mentions.

http://www.snps3d.org/

A website which assigns molecular functional effects of non-synonymous SNPs based on structure and sequence analysis.

Proper citation: SNPs3D (RRID:SCR_010787) Copy   


  • RRID:SCR_010833

    This resource has 10+ mentions.

http://tools.genxpro.net/omiras/

A web server for the annotation, comparison and visualization of interaction networks of non-coding RNAs derived from small RNA-Sequencing experiments of two different conditions.

Proper citation: omiRas (RRID:SCR_010833) Copy   


  • RRID:SCR_010923

    This resource has 10+ mentions.

http://compbio.med.harvard.edu/CGHweb/

Data analysis service enabling users to analyse their array-CGH data with multiple algorithms simultaneously.

Proper citation: CGHweb (RRID:SCR_010923) Copy   


  • RRID:SCR_010772

    This resource has 50+ mentions.

http://agvgd.iarc.fr/index.php

A freely available, web-based program that combines the biophysical characteristics of amino acids and protein multiple sequence alignments to predict where missense substitutions in genes of interest fall in a spectrum from enriched delterious to enriched neutral.

Proper citation: Align-GVGD (RRID:SCR_010772) Copy   


  • RRID:SCR_010897

http://cosmoss.org/bm/plantapdb

A phylogeny-based comprehensive database of plant transcription associated proteins.

Proper citation: PlanTAPDB (RRID:SCR_010897) Copy   


  • RRID:SCR_010777

    This resource has 1000+ mentions.

http://www.mutationtaster.org/

Evaluates disease-causing potential of sequence alterations.

Proper citation: MutationTaster (RRID:SCR_010777) Copy   


  • RRID:SCR_010909

    This resource has 10+ mentions.

http://hyperbrowser.uio.no/hb/

A generic web-based system, providing statistical methodology and computing power to handle a variety of biological inquires on genomic datasets.

Proper citation: Genomic HyperBrowser (RRID:SCR_010909) Copy   


  • RRID:SCR_011796

    This resource has 500+ mentions.

https://genome-cancer.ucsc.edu/

A suite of web-based tools to visualize, integrate and analyze cancer genomics and its associated clinical data. It is possible to display your own clinical data within one of their datasets.

Proper citation: UCSC Cancer Genomics Browser (RRID:SCR_011796) Copy   


  • RRID:SCR_011824

    This resource has 100+ mentions.

http://www.ebi.ac.uk/Tools/sss/wublast/

Tool to find regions of sequence similarity within selected protein databases quickly, with minimum loss of sensitivity.

Proper citation: WU-BLAST (RRID:SCR_011824) Copy   



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