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Member since: 2011
Organization: University Camerino
"I found it hard to get this machine fully working. There were problems with the chemistry and problems with after sales assistance."
Member since: 2008
Organization: The Broad Institute of MIT & Harvard
"Fantastic support and trouble shooting."
• Obtain more comprehensive data.
Generate more than 1,000,000 individual reads with improved Q20 read length of 400 bases per 10-hour instrument run.
• Expand your project capabilities.
Harness the power of DNA sequencing for your complete genome project with one versatile system. Combine long single reads and Long-Tag Paired end reads to completely assemble genomes-often within a single run.
• Reduce your cost per result.
Ultra-high throughput delivers the data you need at an affordable price while longer reads reduce over-sampling requirements, keeping data requirements manageable. Benefit from flexible sample-loading options that support various throughput and experimental design needs, enabling efficient use of reagents and consumables.
• Increase your productivity.
Streamline library preparation of genomics samples and eliminate the laborious tasks of cloning and colony picking - genomic libraries are constructed in hours in a single tube.
• Drive results, not the accumulation of data files.
Perform data analysis without the need for enterprise scale IT solutions with the included easy-to-use software tools - GS De Novo Assembler, GS Reference Mapper, and GS Amplicon Variant Analyzer. Straightforward interpretation of data means faster discovery of biologically meaningful results.