Resources

Frequently Asked Questions

Explore the GenomeQuest solution further including details on the GQ platform and some frequently asked questions from next-generation customers.
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Case Study: Next-generation quality assurance for a next-generation sequence service facility

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Case study: GenomeQuest platform provides access to annotated next-generation sequence data for immediate analysis by researchers

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Making sense of the data.

The first steps in making sense of the data from high–speed sequencing machines are initial evaluation and annotation — this can take months or up to a year depending on bioinformatics resources. With GenomeQuest's
High-speed Sequence Search Suite (HS³) algorithm and high-throughput compute resources, researchers or next-generation service facilities can – in hours – perform in-silico QA/QC checks, identify, align and annotate large data sets, and more. Execute functions directly from your desktop without the database, administration or IT burden. The resulting scientifically–significant dataset is then ready for analysis.

Putting the data to work for you.

Using GenomeQuest's web–based platform, researchers can view databases and perform identity and similarity comparisons between the next–generation data and sequence databases found in GenomeQuest or other in–house databases. Genome visualization and simple search interfaces fore end users to browse, sort , select, search, and visualize sequence data and annotation. In addition, GenomeQuest enables users to filter results based on multiple parameters, generate reports and share workflows with colleagues, all from the command–line or the GenomeQuest web interface.