The NextSeq Series Whole-Genome Sequencing (WGS) Solution enables researchers and clinicians to explore the entire genome of
any species cost-effectively for a deeper understanding of biology.
It leverages industry-standard Illumina next-generation sequencing (NGS) technology responsible for most global WGS, delivering the best data quality and highest coverage to identify variants in coding and noncoding regions of the genome. High-quality library preparation kits are optimized for low-input, unbiased coverage, and rapid workflow. With push-button sequencing, simple data analysis, and minimal hands-on time, the NextSeq Series WGS Solution enables researchers to interrogate simple prokaryotic and complex eukaryotic genomes quickly and efficiently.
A Fast, Efficient WGS Workflow :
The NextSeq Series WGS workflow offers a simple, fast, end-to-end solution for characterization of any genome. It begins with streamlined library preparation using high-quality TruSeq® library preparation kits. The NextSeq Series offers dual density flow cell configurations and accompanying reagent kits deliver 20–120 Gb, enabling researchers to match sequencer output with sequencing of prokaryotic and eukaryotic genomes. New NextSeq v2 reagent kits are optimized to improve base calling and data quality even further.
Data analysis, from alignment and variant calling to annotation and beyond, can be performed in BaseSpace, the Illumina genomics computing environment. Utilizing the Illumina industry-leading NGS workflow, the NextSeq Series provides access to the world’s largest collection of commercial and open-source data analysis software tools.
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