Sequencing Platforms | Illumina NGS platforms
View benchtop and production-scale sequencers, compare features, and learn how to choose the right next-generation sequencing (NGS) platform for your needs. Benchtop sequencers Looking for information to determine if these platforms are well-suited to your needs, and guidance selecting the right one?
Illumina | Sequencing and array solutions to fuel genomic …
2024年11月20日 · Next-generation sequencing for beginners. Curious about using NGS in your research? Learn the basics of next-generation sequencing and find tips for getting started. Learn about NGS
DNA Sequencing | Understanding the genetic code - Illumina
A highly scalable technology, DNA sequencing can be applied to small, targeted regions or the entire genome through a variety of methods, enabling researchers to investigate and better understand health and disease.
Whole-Genome Sequencing (WGS) - Illumina
Whole-genome sequencing can detect single nucleotide variants, insertions/deletions, copy number changes, and large structural variants. Due to recent technological innovations, the latest genome sequencers can perform whole-genome sequencing more efficiently than ever.
Next-Generation Sequencing (NGS) | Explore the technology
Next-generation sequencing (NGS) is a massively parallel sequencing technology that offers ultra-high throughput, scalability, and speed. The technology is used to determine the order of nucleotides in entire genomes or targeted regions of DNA or RNA.
Next-generation sequencing for beginners - Illumina
The basic next-generation sequencing process includes fragmenting DNA/RNA into multiple pieces, adding adapters, sequencing the libraries, and reassembling them to form a genomic sequence. In principle, the concept is similar to capillary electrophoresis.
iSeq 100 Sequencing System | Compact, affordable sequencing
With a maximum output of 1.2 Gb for longest supported read length, the iSeq 100 System offers rapid, multiplexed sequencing for a range of DNA and RNA sequencing applications, including small-genome sequencing, targeted gene sequencing, and gene expression profiling.
MiSeq System | Rapid and cost-effective sequencing - Illumina
With automated paired-end reads, an output range of up to 15 Gb per run, and optimized library prep kits, the MiSeq System can accommodate a variety of applications, including targeted gene sequencing, small genome sequencing, amplicon sequencing, 16S …
NovaSeq 6000 System | Powerful sequencing with scalable
Unlock a full spectrum of genetic variation and biological function with high-throughput sequencing. See all NovaSeq 6000 applications The Illumina Genomics Architecture workflow enables sequencing of 100,000 genomes in Singapore
Cost of NGS | Comparisons and budget guidance - Illumina
With the simplicity and cost efficiencies of benchtop sequencing systems, NGS equipment is now accessible to laboratories of all sizes. Many laboratories are choosing to bring NGS in-house to increase lab efficiency, save time, and tighten control over data privacy and NGS projects.