Illumina sequencing and array technologies drive advances in life science research, translational and consumer genomics, and molecular diagnostics.

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) 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.

Illumina next-generation sequencing (NGS) technology uses clonal amplification and sequencing by synthesis (SBS) chemistry to enable rapid, accurate sequencing. The process simultaneously identifies DNA bases while incorporating them into a nucleic acid chain.

DNA Sequencing. Analyze the entire genome, focus on regions of interest with whole-exome and targeted sequencing, or study DNA-protein interactions.

Specifications are based on Illumina PhiX control library, or a TruSeq DNA Library created with NA12878 at supported cluster densities. Performance may vary based on library type and quality, insert size, loading concentration, and other experimental factors.

The basic NGS 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.

We offer a wide range of comprehensive and seamless next-generation sequencing (NGS) data analysis solutions, including push-button tools for DNA sequence alignment, variant calling, and data visualization. Analyze DNA sequencing data from large or small whole genomes, whole exomes, targeted gene regions, and more with our user-friendly software.

Human whole-genome sequencing (WGS) offers the most detailed view into our genetic code. WGS has the ability to evaluate every base in the genome and navigate the complexity of genomic variants that make us unique. Previously a challenging application, human whole-genome sequencing is now one of the simplest.

Illumina sequencing technology, sequencing by synthesis (SBS), is a widely adopted next-generation sequencing (NGS) technology worldwide. Illumina instruments and reagents use a proprietary method that detects single bases as they are incorporated into growing DNA strands with massively parallel capabilities.