Microarray and sequencing technologies are proving useful to increasingly diverse industries, requiring specialized bioinformatics applications for data analysis and interpretation.
We provide dedicated bioinformatics applications as well as the BaseSpace platform on which partners can build and deploy industry-specific analysis and visualization tools. Through these practices, we support a broad and growing range of bioinformatics applications.
Drug discovery and development programs are enhanced with specialized bioinformatics analyses. BaseSpace Cohort Analyzer and BaseSpace Correlation Engine support translational research programs by providing access to curated genomic data, allowing correlation of private experimental results and testing of new hypotheses. BaseSpace Cohort Analyzer maximizes clinical trial value by enabling researchers to assess the impact of therapies or drug effects in large subject populations.
Cancer researchers need simple-to-use bioinformatics applications to gain insights from complex genomic data. BaseSpace Cohort Analyzer allows biologists and researchers to make important discoveries without specialized bioinformatics skills. The retrospective analysis of clinical trial data can help inform future cancer research and drug development programs. BaseSpace Correlation Engine can mine genomic studies to get data-driven answers about cancer-related genes, experiments, drugs, and phenotypes.
Single-cell sequencing applications offer key insights into the functioning of individual cells, allowing a new level of resolution for biological researchers. Single-cell methods examine the genomes or transcriptomes of individual cells, enabling researchers to determine cell-specific contributions within complex tissues.
We provide a comprehensive solution for single-cell whole transcriptome analysis, including both BaseSpace Sequence Hub and partner analysis apps. BaseSpace Sequence Hub is used upon completion of sequencing to demultiplex base call files (BCL) to per-sample FASTQ files and perform secondary analysis with the BaseSpace SureCell RNA Single-Cell App.View App
We offer tools for microarray experimental design, sample tracking, and analysis. These solutions reduce time to answer, so you can spend more time doing research.Learn More
HLA typing with Illumina NGS generates unambiguous, phase-resolved HLA typing results using a single assay, system, and analysis program.Learn More
Sequence an organism without a reference genome using de novo assembly, and use Velvet De Novo Assembly and Prokka Genome Annotation Apps for analysis.Learn More
Microbial sequencing offers critical genetic insights into bacteria and viruses, supported by a range of BaseSpace Sequence Hub apps.Learn More
Perform genotyping data analysis of polyploid organisms such as wheat and potato using the Polyploid Genotyping Module in GenomeStudio.Learn More