Next-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.
Targeted amplicon library prep kit for contiguous coverage (overlapping amplicons), comprises multiplexed PCR, indexing PCR, and Normalase™ reagents (target-specific panel and indexing primers sold separately).
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Oncology and infectious disease panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Metagenomics panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
Metagenomics panels that utilize multiple overlapping amplicons in a single tube; comprises a premixed target-specific primer pool.
EGFR amplicon panel utilizing UMIs for identification of mutations occurring at 0.25% allele frequency. Custom panels available upon request.
Tailored to meet your research needs, custom amplicon panels offer a completely curated targeted sequencing workflow to interrogate genomic targets relevant to you.
Monkeypox Virus panel that utilizes multiple overlapping amplicons in a single tube, comprises a premixed target-specific primer pool.
Chromium Single Cell Gene Expression Flex empowers your research in remarkable new ways, enabling you to take scRNA-seq further than it’s ever gone before. This advanced chemistry provides 10x Genomics' most sensitive whole transcriptome profiling with the ultimate flexibility to meet your experimental needs every step of the way.
Digital DNA sequencing to confidently detect low-frequency variants
An expanding portfolio of NGS panels for research into haematological and solid tumour cancers, as well as library preparation kits for the accurate detection of a wide range of genetic aberrations
The SureSeq™ Myeloid Plus NGS Complete Workflow combines the rapid Universal NGS Workflow hybridisation-based target enrichment method together with OGT’s expert bait design to detect 49 key genes implicated in myeloid disorders.
The SureSeq™ CLL + CNV Panel has been designed in collaboration with recognised cancer experts to detect 13 key genes and 5 chromosomal regions implicated in CLL progression (Table 1). The SureSeq CLL + CNV Panel alleviates the burden of running multiple assays and streamlines your CLL research to deliver a comprehensive genomic profile for each CLL sample using a single workflow
Myeloproliferative neoplasms (MPNs) are a heterogeneous group of diseases characterised by the overproduction of one or more types of blood cells. The SureSeq™ Core MPN Panel has been designed in collaboration with recognised cancer experts to detect somatic variants in 3 clinically relevant MPN associated genes; JAK2, MPL and CALR.
The complete library preparation solution for unparalleled next generation sequencing (NGS) results. Based on scientists’ feedback, we have redesigned our workflow to ensure scientists achieve the most optimal NGS libraries, with one library preparation workflow across both our SureSeq™ and CytoSure® Constitutional NGS products.
Interpret is OGT’s powerful and easy-to-use next-generation sequencing analysis solution.
