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Nextera DNA kits provide a fast and easy library prep workflow, delivering whole-genome sequencing libraries in under 90 min.
Custom target enrichment kit to rapidly interrogate those portions of the human genome most important to your specific research.
Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in less than 90 minutes, with a low DNA input requirement.
This library prep kit delivers sensitive and specific amplicon sequencing results from both low-input and FFPE DNA samples.
Focus on key genomic regions of interest with this targeted resequencing solution, useful for very high plexity pools or longer amplicons.
Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.
Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA.
DNA library preparation for use with the NeoPrep System, providing comprehensive genomic coverage with low DNA input and minimal hands-on time.
These kits provide a simple, cost-effective solution for generating miRNA and small RNA sequencing libraries directly from total RNA, for any species.
Targeted RNA assays for gene expression studies: custom sequencing panels with a simple workflow and automated data analysis.
MiniSeq Reagent Kits bring the power of Illumina NGS to labs of all sizes. Access cost-efficient sequencing, even for low numbers of samples.
PhiX Control v3 is a ready-to-use control library for Illumina sequencing runs.
BaseSpace Clarity LIMS is a laboratory information management system that helps laboratories track samples and optimize procedures and workflows.
BaseSpace Cohort Analyzer allows you to integrate and analyze subject and genomic data together using innovative visualization and analysis tools.
BaseSpace Correlation Engine mines over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research.
Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data.
BaseSpace Variant Interpreter (Beta) enables genetic testing labs to rapidly annotate, filter, and interpret genomic data.
The TruSeq Amplicon - Cancer Panel is a highly multiplexed targeted resequencing assay for detecting somatic mutations.
This expert-defined sequencing panel targets 94 genes and 284 SNPs associated with a predisposition towards various cancers.
This kit provides researchers with a comprehensive, cost-effective solution for identifying causal variants implicated in inherited cardiac conditions (ICCs).
Unambiguous, phase-resolved HLA typing in a single assay using proven Illumina NGS technology and Assign analysis software.
TruSight Inherited Disease is a targeted sequencing panel that focuses on 552 genes associated with severe, recessive pediatric onset diseases.
The TruSight Myeloid Sequencing Panel targets variants associated with myeloid malignancies such as AML, MDS, MPN, CML, CMML, and JMML.
This panel focuses on exonic regions harboring disease-causing variants. Labs can perform commonly ordered molecular assays on-site with one assay.
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and FFPE.
TruSight Rapid Capture all-in-one kits enable targeted sequencing library preparation and enrichment for up to 96 samples in only 1.5 days.
Focused sequencing panel to assess 15 genes that are commonly mutated in solid tumors in a single assay, with a simple, rapid workflow.
This targeted sequencing panel enables clinical researchers to identify low-frequency variation in solid tumors across 26 genes.