The SOLiD™ 3 Plus System enables unsurpassed accuracy and sensitivity to detect biological variation across multiple samples in a single run.
- Superior accuracy—high quality bases, resulting in lower false positives and subsequently less validation
- Scalable throughput—60+ GB of mappable sequence or greater than 1 billion reads per run for rare variant detection in cancer and human diseases
- Standard base data formats—SAM format, with base calls and associated quality values, for streamlined data analysis
- Maximum experimental flexibility—unmatched accuracy and increased throughput translates to lower running costs and time savings, helping
maximize cost-effectiveness for individual project needs
Distribution of quality values for SOLiD™ System Reads
The SOLiD™ 3 Plus System enables the superior accuracy and sensitivity to detect biological variation. Learn more about the innate error-checking capabilities within 2 base encoding that results in highly accurate base sequence.
For Research Use Only. Not for use in diagnostic procedures.
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