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    Variants

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    Mutation Discovery Made Easy

    Overview

    In life sciences, discovering molecular variations (SNPs and Indels) among individual microbes, plants, animals, and humans is a critical component of scientific innovations. As a known example, scientists have been sequencing coronaviruses and discovered different variants such as alpha, delta, omicron and more. The faster the molecular variations are discovered; the faster the scientists will find solutions for global problems in plants, animals, microbes, humans and other organisms.

    Karyosoft's next generation Variants platform key benefits

    1. Faster (hours vs days) and can save up to 168 days for 96 samples (https://www.karyosoft.com/uc-davis-testimonial )
    2. Being web-based, the users can access Variants on any browser and any device.
    3. With a user-friendly interface, Variants can be operated by anyone with any level of computational skills with just 5 clicks.
    4. Flexibility to use single or multiple samples by uploading public or private data
    5. With an integrated queue manager, the users can run any number of jobs and learn the status of each job.
    6. Simple uploading of only reference genome in fasta, gff3 and paired end sequence data of your samples in fastq (any number).
    7. Flexibility to use single or multiple samples by uploading the public or private data directly from NCBI-SRA databases or through FTP link/AWS-S3 bucket.
    8. The users have options for changing the parameters; if not, the users can automate to run with default parameters.
    9. Integrated QC report for all your samples and will get 11 different quality parameters for your sample sequence data.
    10. Download all files such as indexed reference, samples, BAM files, VCF with annotations and more for other downstream applications.

    The discovered mutations can be used for designing custom chip with highly informative SNPs/Indels for population screening, primer designing around mutations for amplicon sequencing, direct genotyping of your core population to discover allelic status from a single genomic locus through whole genome wide.

    Highlights

    • Faster (hours vs days) and can save up to 168 days for 96 samples
    • With a user-friendly interface, Variants can be operated by anyone with any level of computational skills with 3 files and just 5 clicks.
    • Integrated QC report for all your samples and will get 11 different quality parameters for your sample sequence data.

    Details

    Delivery method

    Deployed on AWS

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    Features and programs

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    Pricing

    Pricing is based on actual usage, with charges varying according to how much you consume. Subscriptions have no end date and may be canceled any time.
    Additional AWS infrastructure costs may apply. Use the AWS Pricing Calculator  to estimate your infrastructure costs.

    Usage costs (6)

     Info
    Dimension
    Cost/unit
    Application Host: Per Instance with 4 GPU / hr
    $4.212
    Storage: Per Instance for OS and Swap Storage minimum of 200 GB / hr
    $0.035
    Storage: Per Instance for Processing data minimum of 1TB /hr
    $0.178
    Storage Operational Speed: Per Storage of 3000 IOPS / hr
    $0.271
    Storage: Per Bucket minimum of 1TB / hr
    $0.189
    Variant App with 4 parallel computing / hr
    $10.115

    Vendor refund policy

    We do not currently support refunds, but you can cancel at any time.

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    Usage information

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    Delivery details

    Software as a Service (SaaS)

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    AWS infrastructure support

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