BaseSpace Apps enable researchers to perform complex sequencing data analyses. From RNA sequencing to exome/enrichment, amplicon, whole-genome sequencing (WGS), 16S metagenomics, and more, BaseSpace Apps meet the diverse needs of any researcher, regardless of bioinformatics experience.
This web-based tool enables users to design their own custom Illumina targeted sequencing panels.
This fully validated software can be used to analyze and interpret a wide range of forensic casework and database samples.
This web-based tool provides a simple and powerful method for evaluating loci and creating successful custom genotyping assays.
Visualize and analyze data generated on Illumina microarray platforms with this powerful solution.
This software offers a direct path to reduce experimental microarray data size and facilitate data analysis for large experiments.
BlueFuse software provides molecular cytogenetic and in vitro fertilization (IVF) data analysis in a single framework.
This software provides clinical labs in the EU with a CE-IVD marked sequencing data analysis solution for use in noninvasive prenatal testing (NIPT).
*For In Vitro Diagnostic Use. Not available in all countries or regions.