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.
KAPA Stranded mRNA-Seq Kits includes all the enzymes and buffers required for cDNA library preparation for Illumina Next-Generation Sequencing, utilizing 100 ng – 4 µg of total RNA. KAPA mRNA Capture Beads are included for isolation of poly(A)-tailed RNA. Kits provides precise measurement of strand orientation (>99%), uniform coverage, and high-confidence mapping of alternate transcripts, and are optimized for the improved…
The gold standard for NGS library amplification.
KAPA Library Quantification Kits contain all the reagents needed for the accurate, reliable and reproducible qPCR-based quantification of NGS libraries prior to pooling for capture or flow cell amplification. Kits contain KAPA SYBR® FAST qPCR Master Mix, optimized for high-performance SYBR Green I-based qPCR. The engineered KAPA SYBR FAST DNA Polymerase contained in the Master Mix amplifies GC- and AT-rich DNA fragments of…
Multiplex amplicon panels for Illumina® platform.
Multiplex amplicons for Illumina® platform.
Multiplex amplicon panels for Illumina® platform.
Simply track and manage samples within and between studies.
For automated Pyrosequencing with integrated template preparation for advanced methylation, mutation and SNP quantification
DNA library preparation of difficult samples for NGS on Illumina® platforms.
Optimal sequencing of your cfDNA, FFPE and ChIP DNA
Optimal sequencing of your cfDNA, FFPE and ChIP DNA
PCR-free NGS prep with highest library diversity, lowest inputs
PCR-free NGS prep with highest library diversity, lowest inputs
NGS library prep for hybridization capture
NGS library prep for hybridization capture
DNA library preparation on Ion Torrent platforms
DNA library preparation on Ion Torrent platforms
Single base-pair, high-throughput solution for analysis of methylated DNA regions
Comprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants
Fastest, most efficient methylated DNA enrichment method on the market
Comprehensive services for DNA enrichment and profiling of genomic regions marked by DNA methylation or DNA methyl variants
The Accel-NGS 2S MID Indexing Kits have been designed, optimized, and validated for use withAccel-NGS 2S DNA Library Kits on Illumina platforms, and aid in low frequency variant detection, as well as accurate de-duplication of single read sequencing and sequencing from samples with non-random fragmentation. Get the most out of your NGS sequencing data with this powerful tool. Improve detection of low frequency alleles…
The DriverMap™ Human Genome-Wide Targeted Expression Profiling Assay enables researchers to simultaneously measure the expression level of almost 19,000 human protein-coding genes in a single assay. By combining highly multiplexed RT-PCR amplification with the depth and precision of next-generation sequencing (NGS) quantitation, the Driver-Map assay provides convenient, comprehensive, highly sensitive, and quantitative meas…
