The “sequencing-by-synthesis” technology now used by Illumina was originally developed by Shankar Balasubramanian and David Klenerman at the University of Cambridge. They founded the company Solexa in 1998 to commercialize their sequencing method. Illumina went on to purchase Solexa in 2007 and has built upon, and rapidly improved the original technology.
Millions of reactions and the reversible terminators
The Solexa/Illumina sequencing method is similar to Sanger sequencing, but it uses modified dNTPs containing a terminator which blocks further polymerization- so only a single base can be added by a polymerase enzyme to each growing DNA copy strand. The sequencing reaction is conducted simultaneously on a very large number (many millions in fact) of different template molecules spread out on a solid surface. The terminator also contains a fluorescent label, which can be detected by a camera. Only a single fluorescent color is used, so each of the four bases must be added in a separate cycle of DNA synthesis and imaging. Following the addition of the four dNTPs to the templates, the images are recorded and the terminators are removed. This chemistry is called “reversible terminators”. Finally, another four cycles of dNTP additions are initiated. Since single bases are added to all templates in a uniform fashion, the sequencing process produces a set of DNA sequence reads of uniform length.
Although the fluorescent imaging system used in Illumina sequencers is not sensitive enough to detect the signal from a single template molecule, the major innovation of the Illumina method is the amplification of template molecules on a solid surface. The DNA sample is prepared into a “sequencing library” by the fragmentation into pieces each around 200 bases long. Custom adapters are added to each end and the library is flowed across a solid surface (the “flow cell”) and the template fragments bind to this surface. Following this, a solid phase “bridge amplification” PCR process (cluster generation) creates approximately one million copies of each template in tight physical clusters on the flowcell surface. Illumina has improved its image analysis technology dramatically which allows for higher cluster density on the surface of the flowcell.
Number 1 in the world
Illumina is now the dominant vendor of high-throughput DNA sequencing machines. According to the OmicsMaps website, Illumina has 1145 machines in place worldwide compare to 836 for all other vendors combined! Since Illumina machines generally produce the highest yields, they are responsible for an even larger fraction of the total bases of DNA sequence information assayed worldwide. Illumina currently sells several versions of its DNA sequencing machine, all of which use essentially the same sample prep kits and sequencing technology. The ‘HiSeq’ produces the highest yields (up to 75 billion bases, or Gb) per sample with maximum read length of 100 bases from both ends of each template. A typical ‘HiSeq’ run processes eight samples in 11 days. The ‘MiSeq’ is a less expensive machine that sequences a single sample per run. The ‘MiSeq’ runs more quickly (4-24 hours), but produces much less data per sample- from 200 Mb to 2 GB depending on the number of cycles. The ‘MiSeq’ is capable of reading 150 bp from each end of a template molecule, but 250 bp reads are currently in beta testing.
Genomic Science has come a long way since the early days of Sanger sequencing in the 1970’s. Today, there are jazzy new sequencing technologies that include fragment analysis, epigenetic sequencing, RNA/transcriptome sequencing and Next Generation Sequencing (NGS). Increasingly these technologies are becoming more accessible, but they still require highly specialized (read: expensive) equipment. Unless your…
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One of the most powerful methods of modern cellular biology is creating and analyzing RNA libraries via RNA-sequencing (RNA-seq). This technique, also called whole transcriptome shotgun sequencing, gives you a snapshot of the transcriptome in question, and can be used to examine alternatively spliced transcripts, post-transcriptional modifications, and changes in gene expression, amongst other applications….
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