Illumina Sequencing Platforms
Illumina sequencing overview
The standard sequence of events for a run involves preparing a DNA library from sample input, attaching library DNA strands to a glass slide known as a flowcell, growing clusters from each DNA strand by bridge PCR and then performing the fluorescence-based sequencing on either, the Illumina NovaSeq X or Illumina NextSeq 1000. The data is analysed in the standard Illumina pipeline to produce sequenced 50-300 bp fragments which can then be assembled de-novo or re-mapped to a given sequence depending on the application.
In summary:
- During library preparation dsDNA is fragmented to 200-600 bp, alternatively cDNA is synthesized from fragmented mRNA (either polyA or rRNA depleted)
- Adaptors are ligated to the ends of the strands
- Strands are attached to a flowcell and each strand is amplified several thousand times to form a cluster of identical sequences
- A sequencing primer is annealed to the DNA strand
- Complementary DNA is synthesized to 50 or 300 bp using reversibly blocked fluorescently labelled nucleotides
- Nucleotide incorporation is imaged for each read and bases are called
- For paired-end sequencing, the clusters are re-generated after the first read and sequenced from the complementary strand (this gives additional information since the distance between each end of the DNA fragment is known)
Illumina NovaSeq X
We use the Illumina NovaSeq X to provide a versatile platform to support a wide variety of applications from bacterial and fungal pathogenomics to whole human genome sequencing.
The NovaSeq X system provides a more scalable, cost effective architecture for sequencing compared to previous generations of short read sequencers. This is achieved using multiple flow cell types and read length combinations. The NovaSeq X 1.5B, 10B and 25B flow cells provide quick and powerful sequencing for the majority of high-throughput applications. The NovaSeq X 25B flow cell, the largest scaling available, enables the highest throughput of sequencing at the most cost-effective price for a range of applications, making in-house whole genome sequencing (WGS) or whole exome sequencing (WES) studies an attractive and affordable option for more projects.
Key features of the Illumina NovaSeq X:
- Cheaper cost per base compared to other Illumina instruments
- Faster sequencing runs
- Multiple flow cell and read sizes for a more scalable approach
- Largest 25B flow cell can sequence
- ~ 64 whole human genomes at 30X coverage or
- ~ 750 exomes at 100X coverage or
- ~ 520 transcriptomes at 50M reads coverage
Flowcell output / scalability:
Number of reads per run on each flowcell:
Amount of data in Gigabases (Gb) per run on each flowcell:
Typical applications:
- De novo genome sequencing (small to large genomes)
- Genome re-sequencing
- Amplicon sequencing
- RNA-seq transcriptome sequencing
- Epigenetics such as ChIP-Seq, ATAC-Seq, Whole Genome Bisulphite Sequencing (WGBS)
- Metagenomics
- Single cell sequencing
Illumina NextSeq 1000
We utilize the Illumina NextSeq for smaller scale projects as well as testing pooled libraries prior to loading on the Illumina NovaSeq X. It is capable of automated paired-end reads and up to 240 Gb per run, delivering over 600 bases of sequence data per read. Specifications can be found here NextSeq 1000 & 2000 System Specifications | Output, run time, & more. (Please note only P1 and P2 flow cells are available for the NextSeq 1000).
Typical applications:
- Targeted gene sequencing
- Small genomes
- Amplicon sequencing
- 16S metagenomics
N.B. Low diversity samples such as amplicons, including 16S, 18S, ITS and CO1, require lower loading concentration so the output and number of reads would typically be reduced to approximately 50% of those quoted above.
