NGS Analysis for Researchers
We’ve been expecting you
All researchers run into the same fundamental problems. Waiting for weeks to analyze NGS data just to get the output in long bleary files. The good news? Basepair solves these. Try Basepair free for 14 days
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.
The problems researchers deal with mostly boil down to waiting – waiting for the analysis, waiting for the results, just waiting, instead of doing and publishing.
This makes being a researcher frustrating and even underwhelming at times. It leads to unnecessary delays, communication overhead creates human errors and busy work.
Serial processing analysis tools and open-source software can’t fix this problem. Basepair is different. It combines all the NGS analysis tools researchers need in a single, straightforward package that makes research feel, well, more like research.
Stop waiting. Start publishing.
1,000+ researchers rely on Basepair to analyze their NGS data. Why? It helps them get more done in less time without all the chaos and confusion.
✔ Results in about an hour
✔ 30+ ready to use pipelines
✔ Publication-ready results
Work by researchers using Basepair for their NGS analysis is in dozens of peer-reviewed journals. See the list of published works.
Types of Analysis
An overview of Basepair workflows for NGS applications.
See Basepair powered NGS research in peer-reviewed journals.
The bread and butter of our platform
Trusted by top research hospitals worldwide
Read the latest from our blog
Basepair Awarded $300,000 Grant for Development of Software Platform for Pre-Implantation Genetic Testing
The Eunice Kennedy Shriver National Institute of Child Health & Human Development recently awarded Basepair a $300,000 Small Business Innovation Research grant for the development of a software platform for pre-implantation genetic testing of aneuploidy (PGT-A). ...
We are pleased to announce the release of our new pipeline for investigating changes in alternative splicing (AS) in RNA-seq. As a quick reminder, a gene may have many forms (isoforms) depending on which exons and transcription...
Key features We are pleased to announce the release of Basepair's significantly updated single cell RNA-seq (scRNA-seq) pipeline. It brings many improvements in new features, efficiency, and user friendliness: 1. Seurat version 3 Version 3 of the scRNA-seq software we...