BaseSpace Cohort Analyzer enables you to aggregate and analyze subject and genomic data with access to over 100 bioinformatics workflows. Academic centers and research hospitals, pharmaceutical and biotech companies, and population sequencing centers can accelerate biomarker and drug discovery, track longitudinal and outcome data, and compare subjects and cohorts for clinical trials.1
Explore a large repository of highly curated public and controlled-access data sets across a broad range of disease indications with over 17,000 samples. (Source: 2/20/2017 Cohort Analyzer Release Version v1.0.0-eea18c3)
Discover and validate biomarkers across multiple types of molecular data, clinical trial information, and cell line models.
Integrate and analyze comprehensive clinical and genomic information associated with each individual human subject, including longitudinal data.
An award-winning interface empowers any user to easily access content and analytics, not just those with bioinformatics or programmatic expertise.
Successfully passed an independent third-party audit of security controls for HIPAA in 2013 & 2015.
Developed under an ISO 13485 certified quality system.
Supports regional data centers.
BaseSpace Cohort Analyzer was previously known as NextBio Clinical.
Clarity LIMS is a laboratory information management system designed for genomics labs to track samples and manage workflows for an optimized and efficient lab.
Data management and simplified bioinformatics for labs getting started and for rapidly scaling next-generation sequencing (NGS) operations.
BaseSpace Variant Interpreter allows scientists to rapidly identify biologically significant variants from human genomic data.