Bioinformatics
For analyzing, comparing and visualizing human hereditary and cancer NGS data for biomarker discovery
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BioInformatics
Leveraging state of the art NGS and OMIC data analysis in the cloud
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BioInformatics
State of the art bioinformatics: statistics, visualization and analysis
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BioInformatics
State of the art bioinformatics: statistics, visualization and analysis
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BioInformatics
Public and private genomic data for disease research
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Bioinformatics
The gold standard resource for comprehensive data on published human inherited disease mutations.
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BioInformatics
For enhancing functionalities of CLC Genomics Workbench, Biomedical Genomics Workbench, and CLC Server solutions
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BioInformatics
For analyzing and interpreting real-time PCR or NGS data
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BioInformatics
For research use, clinical reporting or clinical diagnostic purposes
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BioInformatics
A high-performance computing solution for mapping reads to a reference and de novo assembly of next-generation sequencing data.
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BioInformatics
For advanced DNA, RNA, and protein analyses
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BioInformatics
For analyzing, comparing, and visualizing next-generation sequencing data
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BioInformatics
For flexible next-generation sequencing data analysis
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BioInformatics
CLC Genomics Cloud Engine
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BioInformatics
ANNOVAR
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Variant Analysis product
For identifying disease-causing variants from human whole genome, exome and gene panel next-generation sequencing studies
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Ingenuity Pathway Analysis IPA Causal network diagram
For modeling, analyzing, and understanding complex 'omics data
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NGS QCI Analyze
The bioinformatic complement to the GeneReader NGS System
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NGS QCI Interpret
For NGS data interpretation and reporting
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BioInformatics
For microbial profiling, pathogen typing and outbreak analysis using state-of-the-art bioinformatics
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