Genome Analyzer definition

Genome Analyzer means Illumina’s sequencing instrument. “Hardware” means the hardware provided under this Agreement, or as upgrades or options under future agreements, as specified in the Specifications, including any Hardware that is a third-party Component. “Intellectual Property Rights” means all patent rights, copyrights, trade secrets, know-how, trademark, service ▇▇▇▇ and trade dress rights and other intellectual property rights, current or future, under the laws of any jurisdiction, together with all applications therefore and registrations thereto. “iScan” means Illumina’s high-resolution scanner that supports imaging of BeadArray-based genetic analysis products, including such accessories or peripherals as are described in the Specifications. “Oligo Pool” (or “OPA”) means a standard or custom collection of oligonucleotides required to practice an Assay. “Reagent Kit” means a kit containing the chemicals and enzymes supplied by Illumina to practice an Assay. “Sample Preparation Kit” means a kit supplied by Illumina containing the reagents required to prepare a nucleic acid template for amplification on an Illumina Cluster Station. “Sequencing Kit” means a kit supplied by Illumina containing the sequencing reagents for use on Illumina’s Genome Analyzer. “SNP” means single nucleotide polymorphism. “Software” means the Software provided under this Agreement, or as upgrades or options under future agreements, or as incorporated or embedded in other Components provided under this Agreement, in object code form, whether or not there is a separate charge thereof, including any Software that is provided from a third party. All references in this Agreement to the “purchase” or “sale” of Software shall mean the acquiring or granting, respectively, of a license to use such Software to exercise the rights pertaining to such Software that are expressly set forth herein. “Specifications” means the specifications for the System, Components or Consumables contained in the written quotation provided to Customer. “Standard Oligo Pool” (or “Standard OPA”) means an Oligo Pool offered for sale by Illumina as a regular catalog item. “System” means Illumina’s BeadArray System, BeadXpress system, Cluster Station, Genome Analyzer, or iScan, as applicable.
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Examples of Genome Analyzer in a sentence

  • From each processed amplicon pool, a total of 6 pmol of the library were added to one lane of the Genome Analyzer (GA) flowcell (Illumina, San Diego, CA).

  • While Sanger sequencing costs approximately $0.50 per kilobase, Illumina Genome Analyzer (IGA) sequencing costs a mere $0.002 per kilobase, making large-scale sequencing projects more efficient and affordable (Shendure and Ji 2008).

Related to Genome Analyzer

  • Bioassay means the determination of kinds, quantities or concentrations, and, in some cases, the locations of radioactive material in the human body, whether by direct measurement, in vivo counting, or by analysis and evaluation of materials excreted or removed from the human body. For purposes of these regulations, "radiobioassay" is an equivalent term.

  • in vitro diagnostic medical device means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information:

  • Research Analyst means any individual employed by Loomis Sayles who has been designated as a Research Analyst or Research Associate by Loomis Sayles. A person is considered a Research Analyst only as to those Covered Securities which he or she is assigned to cover and about which he or she issues research reports to other Investment Persons or otherwise makes recommendations to Investment Persons beyond publishing their research. As to other securities, he or she is simply an Access Person.

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Diagnostic source assembly means the tube housing assembly with a beam-limiting device attached.