Basepair Help Center

Demo workspace with Basepair genomics flows

Getting Started

Welcome to Basepair
Add your first sample

Configuration

Run a variant-calling pipeline
Quantify gene expression with RNA-seq
Set the reference genome
Turn on run notifications

Results

Review your results

Analysis

Filter down to the variants that matter

Sharing

Share a project
Update a collaborator's access

Datasets

Browse your reference datasets
Add a custom dataset