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START YOUR OWN ANALYSIS
 
 
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Challenges in BioInformatics 

The foundation of Genomic Analysis is BioInformatics - the intersection of Biology and Information Technology. Yet, BioInformatics is often cited as the major bottleneck for progress and growth in Precision Medicine, Drug Development and Agri-Business.
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Complexity
By removing the complexity of the BioInformatics, we empower the researcher to analyze their own data through our engaging, intuitive online interface.
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Bottleneck
With only 15,000 bioinformaticians globally, there isn't enough support to handle demands of 2,000,000+
Researchers.
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Storage Cost
Through affordable all-in-one per-sample pricing, including compute, storage and data management costs, this booming industry is free to scale.
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STEP 1: DEFINE YOUR EXPERIMENT DESIGN

Self-Guided Interface (no code required)

    • Designed for Biologists and Researchers
    • - No Coding. Simple drag and drop intuitive interface
      - Enter the minimum meaningful information
      - Use the BioSample or BioProject data model
      - Select the species
    • - Nothing more complex than the Genome Build
      - Select the method: RNA-seq, ChIP-seq, Exome-seq, etc.

 

STEP 2: SET UP YOUR EXPERIMENT

Select Kits and the Attributes for Comparison

    • - Identify the Kit for optimal data processing
    • - Set replicates and controls
    • - Identify the number of samples

    Select the minimum attributes from the BioSample data models that define the experiment: Cell Line, Cell Type, Genotype, Age, Disease, Treatment, etc.

 

 

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STEP 3: UPLOAD FILES & GO!

Simplified Data Transfer 

  • - Tired of FTP? Simply drag and drop your RAW FASTQ data files
  • - Never worry about command-line interfaces!
  • - Single and paired-end data files supported
  • - Leave all the QC to Rosalindâ„¢

 

STEP 4: INTERACT WITH YOUR DATA

Interactively Explore Your Data

    • - Trust consistent, reproducible results with automated analysis pipelines
    • - Bring your results to life with engaging, interactive analyses 
    • Select areas of interest and enjoy the thrill of exploring your data
      - Explore highlighted genes and peaks
      - See critical pathways, disease and functional information

      Through our partnership with Advaita Bioinformatics, researchers can seamlessly explore relevant Pathways, Gene Ontologies, Variants and Diseases associated with their experiment results.
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