Highly tunable data output to run virtually any genome, sequencing method, and scale of project
Easy adoption with superior support across the entire workflow. Fast, simple library prep and enrichment workflow from Illumina.
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A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
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Bringing efficiency and high confidence to case management, variant analysis, and interpretation in rare disease
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
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Enables and accelerates research leveraging BaseSpace Correlation Engine
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Environmentally friendly packaging reduces waste from landfills and carbon emissions
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Three approaches to help researchers with sequencing
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Expanded portfolio enables comprehensive genomic profiling from blood and tissue
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This high-throughput NGS test detects SARS-CoV-2 in nasopharyngeal, oropharyngeal, and mid-turbinate nasal swabs
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A transformational approach to biodiversity monitoring
New library prep kits enhance research in rare genetic diseases
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Why he believes CGP is poised to become a standard of care in oncology
Find out why laboratories In Europe have implemented VeriSeq NIPT
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Determine the best kit for your project type, starting material, and method or application.
Generate end-to-end documentation tailored to your experiment.
Install the software for downloading BeadChip decode map (DMAP) files.
Determine reagents and sequencing runs for your desired coverage.
Dilute pooled libraries to the appropriate concentration for sequencing.
Convert library concentrations from nanogram/microliter (ng/µl) to nanomolar (nM).
Design custom oligos for targeted sequencing applications.
Design a custom assay for select microarray products.
Find the analysis modules compatible with your instrument and Local Run Manager configuration.
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