Basepair

CDFD-CGC has partnered with Basepair to bring integrated, easy-to-use data analysis directly into the sample ordering experience. Through this collaboration, researchers working with CGC can now seamlessly add on downstream bioinformatics analysis.

Basepair is a cloud-native bioinformatics platform built to make next-generation sequencing (NGS) data analysis effortless, no coding or command-line expertise required. Designed to bridge the gap between wet-lab scientists and bioinformatics, Basepair turns raw sequencing data into clear, interactive, publication-ready reports through an intuitive point-and-click interface. The platform supports a wide range of applications, including RNA-seq, whole genome and exome sequencing (WGS/WES), single-cell RNA-seq, metagenomics, ChIP-seq, ATAC-seq, and infectious disease profiling, and is trusted by academic, clinical, and commercial genomics teams around the world. By automating the heavy lifting of data analysis, Basepair frees up scientists to focus on discovery rather than getting stuck waiting on bioinformatics support.

This partnership between CDFD and Basepair provides researchers with a streamlined platform that enables a faster, simpler journey from raw sequencing data to meaningful biological insights. Routine pipeline analysis is available at a fixed cost per sample. Users may get custom analysis done on a case by case basis.