Sequencing Technologies
Our sequencing center currently has two main genome sequencing platforms – the Illumina platform (137 Illumina HiSeq 2000) and the Applied Biosystems platform (27 SOLiD™ 4 Systems).
Vendor | Illumina | Applied Biosystems |
Technology | Hi-Seq 2000 | SOLiD™4 |
Platform Number | 137 | 27 |
Read length (bp) | 2 x 100 | 2 x 50 |
Run time (day) | 8 | 12 |
Throughput (Gb/day) | 25 | 8 |
Illumina HiSeq 2000
The Illumina HiSeq 2000 system is a very rapid, high-throughput, next-generation sequencing platform based on the formation of clonal molecule clusters and the principle of synthesis-based-sequencing. It supports the following applications de novo sequencing, whole genome resequencing, RNA sequencing, disease research, epigenomics, microbial sequencing, and others.
Highlights:
- Highest sequencing output
- Fastest data generation rate - up to 200 Gb per run, 2 x 100-bp read length, up to 25 Gb per day, two billion paired-end reads per run.
- Parallel sequencing of millions of fragments using proprietary chemistry
- First commercially available sequencer to obtain 30x coverage of two human genomes in a single run for less than $10,000 per sample
- Four-color DNA sequencing-by-synthesis technology
- High accuracy and true base-by-base sequencing
- Eliminates sequence-context specific errors
- Wide range of applications including gene expression, small RNA discovery, and protein-nucleic acid interactions
- Lower cost due to bypassing cloning, transformation, and plasmid preparation
For more information, please visit Illumina.
Applied Biosystems SOLiD™ 4 System
The SOLiD™ 4 System is a highly accurate, massively parallel next-generation sequencing platform using on clonal amplification of bead-linked DNA, based on sequential ligation of fluorescently labeled oligonucleotides. It supports a wide range of applications such as whole genome resequencing, small RNA analysis, whole transcriptome analysis, chromatin immunoprecipitation sequencing (ChiP-Seq), and methylation analysis.
Highlights:
- Unparalleled high throughput
- 99.4% base-calling accuracy
- Able to polymerize and amplify single copy DNA
- Able to sequence large DNA fragments
- 80–100 GB of mappable sequence per run
- Performs double reads of each nucleotide to ensure reliability
For more information, please visit Applied Biosystems.