Powering insights across the life sciences

If it involves biology and big data, Watershed is the solution. With 100+ unique data analysis templates, customizable workflows, and a dedicated team of bioinformaticians, no analysis is too complex.

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Explore Applications

Whole Genome Sequencing (WGS) & Whole Exome Sequencing (WES)

Variant Calling

Long-Read Sequencing

Gene Editing

Public Datasets

Genome-Wide Association Studies (GWAS)

Mendelian Randomization

ATAC-Seq

ChIP-Seq

RNA-Seq

Single Cell RNA-Seq

Public Datasets

Geneformer

Spatial Sequencing

Immune Repertoire Sequencing

Mass Spectrometry

Olink

AlphaFold2

Custom Integrations

Public Datasets

Cellranger

Cell Labeling

Cell Segmentation

Metagenomics

de novo Assembly

Metatranscriptomics

Read the latest insights

Learn about new research, best data practices, and more.

Webinar

Bugs and Junk: Transforming data from emerging -omics fields into novel therapeutics

Watch our webinar with computational biologist Dr. Liyang Diao to learn how novel bioinformatics approaches are unlocking the therapeutic potential of emerging research areas.
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Blog

Science Chat with Dr. Andrew Spencley

Dr. Andrew Spencley is a Genome Editing Scientist at Novo Nordisk. We spoke to Dr. Spencley about navigating the scientific process from bench to analysis, the importance of mentorship, and more.
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Webinar

The limits of dimensionality reduction tools for single-cell analysis

Learn how to visualize single-cell data and interrogate the outputs of dimensionality reduction tools like t-SNE and uMAP.
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Webinar

Cytometry in the -Omics Era for All

Learn how to overcome computational and technical barriers in flow cytometry data analysis and access cytomics insights with Dr. Andrew Wight.
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