SOLiD™ 4hq System
The SOLiD™ 4hq System—
Lowest cost per sample
Up to 300 Gb mappable sequence with read lengths of up to 75 bp
Benefits:
- Superior Accuracy
Error correction capabilities provide 99.99% system accuracy - Lowest cost per sample
Up to 300 Gb mappable sequence with read lengths of up to 75 bp - Increased productivity
System checks such as reagent tracking, real-time monitoring of reagent usage, and automatic notification of run status - Agile data integration and processing
Easy data flow and streamlined analysis pipelines for rapid results
* Cost per genome represents US list pricing at optimal running efficiencies with use of the SOLiD™ EZ Bead™ System.
** The Quality Genome is a combination of accuracy and throughput that enables research studies to be conducted more cost-effectively than ever before.
The SOLiD™ System enables researchers to obtain higher accuracy and sensitivity for variant discovery with less coverage. Read a selection of peer-reviewed publications that demonstrate how the SOLiD™ System allows you to see what has never been seen before.
Publications
- Whole-genome resequencing reveals loci under selection during chicken domestication. Publication: Nature (2010)
- Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. Publication: N Eng J Med (2010)
- Development of personalized tumor biomarkers using massively parallel sequencing. Publication: Science Translational Medicine (2010)
- Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of Trisomy 21 Publication: Clinical Chemistry (2009)
- Complete Khoisan and Bantu genomes from southern Africa. Publication: Nature Online (2010)
Training
Get hands-on lab experience with the SOLiD™ System
