SOLiD™ System Accuracy
The new 5500 Series SOLiD™ Sequencers enable unsurpassed accuracy and sensitivity to detect biological variation.
What Level of Accuracy Do You Demand?
- Do you need to detect somatic mutations present at 1% in your sample?
- Do you want to detect variants present in 5% of your sample with 1/3 the sequence coverage needed with other platforms
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Demand the Most!
See for Yourself! - Data and Publications
See SNP detection with less false
positives | Uniform sequence coverage | |
- White paper: Demonstration of increased accuracy with Exact Call Chemistry (ECC)
- Breaking the 1000-gene barrier for Mimivirus using ultra-deep genome and transcriptome sequencing. Publication: Virology Journal (2011) Authors: Legendre, et al.
- Large-scale detection and analysis of RNA editing in grape mtDNA by RNA deep-sequencing. Publication: Nucleic Acids Research, 1–13 (2010) Authors: Picardi, et al.
- U87MG Decoded: The genomic sequence of a cytogenetically aberrant human cancer cell line. Publication: PLoS Genetics, volume 6, issue 1 (January 2010) Authors: Smith, et al.
- Evaluation of next generation sequencing platforms for population targeted sequencing studies. Publication: Genome Biology 2009, 10:R32 Authors: Harismendy, et al.
- Modeling non-uniformity in short-read rates in RNA-Seq data. Publication: Genome Biology, 11:R50 (2010) Authors: Li, et al.
- Limitations and possibilities of small RNA digital gene expression profiling. Publication: Nature Methods 6, 474-476 (2009) Authors: Linsen, et al.
Browse the complete list of publications by application
For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use.
Try the SNP Calculator to see how much accuracy you need)
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