Foundry

FEATURES

Experiment Design

Simple, rapid integration of the data necessary to support your analytics

New data dimensions for modeling and analytics has never been easier.

Workflows & Pipelines

Customized bioinformatics workflows and pipelines with unmatched speed

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Ingest NGS data, published research data or your own private data.

Eliminate dev-Ops and operational complexities with ease.

Interrogate results with RStudio, Jupyter notebook and Shiny apps.

BENEFITS

There are many reasons to love Foundry. These are a good place to start.

Additional Products

Supercharge Foundry and operate seamlessly within your unique compute environment.

Foundry empowers Researchers, Scientists and Computational Biologists

LATEST ARTICLE

The Sixth Time: What Building the Same Pipeline Taught Me About Reusability in Bioinformatics

Industries

ACROSS INDUSTRIES

Biotech & Pharmaceuticals

Unleash the power multi-omics analysis, data interrogation, and discovery to support your core R&D and therapeutic development efforts.

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Unify your research and analytics to power the R&D lifecycle of your lab, lab system, and to share your results.

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Elevate research and innovation with a unified bioinformatics platform designed to drive breakthroughs that advance your global mission to heal.

Company

MISSION

Learn about our “Science-First” Approach and our commitment to democratizing science.

PEOPLE

World-renowned scientists, bioinformaticians, AI experts, and entrepreneurs.

CAREERS

Current Openings

Learn about our values and job openings with our world-class team.

Resources

Articles about bioinformatics, data analysis, and advanced research methodologies in areas such as metagenomics, RNA sequencing, spatial transcriptomics, AI in biological sciences, and more.

Platform overview with guides for developers and users. An in-depth peek into the power of Foundry.

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What is the Germline Variant Calling Pipeline?

What is the Germline Variant Calling Pipeline?

Updated:

This Gatk4 pipeline is intended for calling variants in samples that are clonal – i.e. a single individual.

Related Questions

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What is the Somatic Variant Calling Pipeline from BAM for RNA-seq?

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