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Tute Genomics

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Provo, Utah, US

About Tute Genomics

Founded: 2012 Type: Privately Held Size: 11-50 employees

Tute Genomics has developed an innovative cloud-based software solution to accelerate genetic discovery and enable precision medicine. Tute's clinical genome interpretation platform assists researchers in identifying disease genes and biomarkers, and assists clinicians/labs in performing genetic diagnosis.... Show more »

Tute Genomics has developed an innovative cloud-based software solution to accelerate genetic discovery and enable precision medicine. Tute's clinical genome interpretation platform assists researchers in identifying disease genes and biomarkers, and assists clinicians/labs in performing genetic diagnosis. Given sequencing data on a genome or a panel of genes, Tute can return over 125 annotations on variants and genes, perform family-based, case/control or tumor sample analyses to identify causal disease genes, and generates clinical reports for clinicians to focus on clinically relevant and actionable findings.

Tute is built on the expertise that developed ANNOVAR, the most widely used genome annotation & interpretation technology with over 800 scientific publications. The genome revolution is here, and Tute envisions a future where clinical reports on genomes are interactive and integrated into medical records.

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Our Services (12)


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DNA Sequencing Data Analysis

Price on request
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Biomarker Discovery

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Gene expression profiling

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NGS Data Analysis

Next generation sequencing data analysis
Starting at $25.00 per sample

NGS Panel Data Analysis - $25/sample

How it works:

  1. Researcher uploads genome variant file
    All major file formats supported, such as VCF, CG masterVar, and more.

  2. Tute annotates every genetic variant
    Tute pulls in more databases than anyone else, including Clinvar, GWAS Catalog, Sift, PolyPhen, Phylo P, GERP++,... Show more »

NGS Panel Data Analysis - $25/sample

How it works:

  1. Researcher uploads genome variant file
    All major file formats supported, such as VCF, CG masterVar, and more.

  2. Tute annotates every genetic variant
    Tute pulls in more databases than anyone else, including Clinvar, GWAS Catalog, Sift, PolyPhen, Phylo P, GERP++, Allele Frequency, etc.

3.Tute allows for robust, user-driven filtering
Users have the flexibility to specify either a set of default pipelines or a customized pipeline for variant filtering and stepwise reduction

4.Tute prioritizes & scores genetic variants
Using proprietary machine-learning algorithms & probablistic modeling, a ‘Tute Score’ is assigned to prioritize all genetic variants


NGS Exome Data Analysis - $50/sample

How it works:

  1. Researcher uploads genome variant file
    All major file formats supported, such as VCF, CG masterVar, and more.

  2. Tute annotates every genetic variant
    Tute pulls in more databases than anyone else, including Clinvar, GWAS Catalog, Sift, PolyPhen, Phylo P, GERP++, Allele Frequency, etc.

3.Tute allows for robust, user-driven filtering
Users have the flexibility to specify either a set of default pipelines or a customized pipeline for variant filtering and stepwise reduction

4.Tute prioritizes & scores genetic variants
Using proprietary machine-learning algorithms & probablistic modeling, a ‘Tute Score’ is assigned to prioritize all genetic variants


NGS Genome Data Analysis - $100/sample

How it works:

  1. Researcher uploads genome variant file
    All major file formats supported, such as VCF, CG masterVar, and more.

  2. Tute annotates every genetic variant
    Tute pulls in more databases than anyone else, including Clinvar, GWAS Catalog, Sift, PolyPhen, Phylo P, GERP++, Allele Frequency, etc.

3.Tute allows for robust, user-driven filtering
Users have the flexibility to specify either a set of default pipelines or a customized pipeline for variant filtering and stepwise reduction

4.Tute prioritizes & scores genetic variants
Using proprietary machine-learning algorithms & probablistic modeling, a ‘Tute Score’ is assigned to prioritize all genetic variants


NGS Data Analysis - Unlimited Use Enterprise Cloud Software - $18,000/year

How it works:

  1. Researcher uploads genome variant file
    All major file formats supported, such as VCF, CG masterVar, and more.

  2. Tute annotates every genetic variant
    Tute pulls in more databases than anyone else, including Clinvar, GWAS Catalog, Sift, PolyPhen, Phylo P, GERP++, Allele Frequency, etc.

3.Tute allows for robust, user-driven filtering
Users have the flexibility to specify either a set of default pipelines or a customized pipeline for variant filtering and stepwise reduction

4.Tute prioritizes & scores genetic variants
Using proprietary machine-learning algorithms & probablistic modeling, a ‘Tute Score’ is assigned to prioritize all genetic variants

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Bioanalysis

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Pharmacology & Toxicology

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Nucleic Acid Data Analysis

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Biomarkers

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Biology

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Nucleic Acid Analysis

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Biochemistry & Molecular Biology

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Sequencing Data Analysis and Management

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Nucleic Acid Services

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Mary Brown

Director of Operations
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Kai Wang

President
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Brady Wright

Director of Partnerships

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