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BioQule V1.0.0 Release Notes
BioQule Release Notes
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Elevating Genetic Testing Excellence: NSAI Certified Services
We pride ourselves on offering the highest level of Screening and Confirmatory Tests that Relate to Indicators for Human Genetic Diseases Focused on Fetal, Maternal and Newborn Domain support available in the industry. We are National Standards Authority of Ireland certified.
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Highly Sensitive Detection of the Interaction Occurring Between Phage Displayed Peptides and their Target using AlphaScreen™
The AlphaScreen Phage display assay involves the capture of phage particles by Acceptor beads conjugated with anti-M13 antibodies whereas a biotinylated-target is captured by Streptavidin-Donor beads.
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CLIA-certified lab ensuring accuracy and compliance.
At our state-of-the-art facility, we adhere to the rigorous standards set by CLIA, ensuring the highest quality and precision in all diagnostic procedures.
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National Accreditation Board for Testing and Calibration Laboratories
Revvity Omics meets Quality and compliance standards. We are National Accreditation Board for Testing and Calibration Laboratories
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Certificate SWEDAC (ISO15189)
Revvity is accredited by SWEDAC in recognition of meeting the international standard requirements for quality and competence that specifies the quality management system requirements particular to medical laboratories
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Accreditation of Clinical Gene Amplification Laboratory
A certificate for Gene amplification in a Clinical lab.
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Accreditation of Biosafety Laboratory Level II
A certificate for Laboratory Biosafety.
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Training Calendar-12.11.2023 rev3.1
Training Calendar-12.11.2023 rev3.1
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Training Calendar-11.21.2023-final rev.11.21.2023 dbc
training calendar
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Short tandem repeat analysis by Whole Genome Sequencing
Short tandem repeat analysis by Whole Genome Sequencing to detect repeat expansion disorders.
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Whole Genome Sequencing - Secondary Findings - Carrier Status
Flyer contains carrier status genes as secondary findings; Carrier status tests can detect genetic changes that can cause hereditary disorders in future generations.
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