Need to analyze NGS data? Basepair is fast and easy to use.

Quickly analyze RNA-seq, DNA-seq, ChIP-seq and ATAC-seq data with Basepair’s automated pipelines, no coding needed. Our cloud platform instantly scales to analyze thousands of samples in parallel.

Some of our Customers

 

Free Bioinformatics advice! We love great science and want to help you make sense of your data regardless of whether you use Basepair or not. Click here to submit a question or to register your interest for an upcoming open office hours session with one of our resident Bioinformaticians.

How Basepair Works

Step 1, Ingest

Manually upload or automate the ingestion of your NGS data into BasePair or connect to the compute and storage resources in your own cloud account. If needed, directly import metadata from a LIMS system using our API.

Step 2, Analyze

Either select the analysis you want to run from a built-in library of industry standard tools and pipelines, or deploy and run your own in a docker container. Automate or manually launch analyses and if needed our cloud platform instantly scales to analyze thousands of samples in parallel. Thanks to our unique architecture, AI-powered algorithms and cloud optimizations, sample analysis is extremely fast and cost effective.

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Step 3, Deploy

Deliver workflows to your colleagues or customers as white labeled web portals that look like your own company branded application. If desired, use our back-end coupon technology to bundle the analysis with the sale of your own kit or assay. Results are then available online in customizable, interactive reports that you or your customers can collaborate on with colleagues anywhere in the world, using out of the box advanced visualizations and analytics to make sense of your data.

Features At A Glance

Custom Portals

Deploy workflows to end users via white labeled web portals that look and feel like your own company branded solution. Create unique coupon codes for your kits, assays or diagnostic tests to seamlessly bundle the right amount of analysis at their point of sale.

True Connected Cloud

BasePair is available in a multitude of cloud regions around the world to allow you to operate globally. Connect the platform to both your compute and storage resources in your own cloud account to achieve economies of scale with your cloud provider, or, for plug and play, use the multi-tenanted version which manages everything for you.

Cost Effective

Flexible pricing models that include both pay as you go per sample or annual licenses with a variety of usage bands. Connecting to the compute and storage resources in your own cloud allows you to take advantage of any discounts or credits you have negotiated with your cloud provider.

Built-In Visualizations

From heatmaps to volcano plots, interact with NGS data directly in the online report. Use filters and sliders to adjust your parameters, download your figures in high resolution, or export files for additional analysis

Support

Basepair’s scientists are available to help troubleshoot by phone, email or in person. Partner with our bioinformatics team to port, build or extend custom pipelines.

Application Diversity

Fully automated pipelines for most application areas including WGS/WES/Panel, RNA-Seq, Single Cell, ChIP-Seq, ATAC-Seq, CRISPR etc.

Automation

Use the CLI or REST and Python APIs to interact with and automate workflows, as well as integrate with upstream and downstream third party applications (eg instruments, LIMS, data lakes etc)

Security

BasePair has all the necessary certifications you would expect of a genomic analysis platform and all data is encrypted during rest and transfer. For added security, connecting it to your own cloud account means no data ever leaves your IT approved environment.

Trusted Automated Pipelines for Most NGS Data

DNA-Seq

QC

Alignment

Process reads

Variant calling

Annotation

RNA-Seq

QC

Alignment

Expression count

Differential expression

ChIP-Seq

QC

Alignment

Peak calling and annotation

Motifs

ATAC-Seq

QC

Alignment

Peak calling and annotation

Open chromatin regions

Learn how automated workflows simplify NGS analysis.

Basepair Work is in Dozens of Peer-Reviewed Journals

"Fast, excellent and reasonably priced...you CAN get all three!! Thank you to the folks at Basepair for helping us deal with some difficult RNA Seq data."

Sharen Mckay

Yale University

"I really like how easy the website is to use. And how quickly the results are generated, including figures. I would have never thought about doing a new analysis like I just did."

Emilie Montenont

NYU Langone Health

"Support answers come fast and are always precise!"

 

Maria Hollnagel

Ulm University

Analyze your NGS data today.

Get results in hours.

You really can do it yourself.

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