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This means that laboratories can continue to use older instruments which have been obsoleted by other software systems.
#Perkins elmer serial#
#Perkins elmer driver#
The launch of a dedicated driver for the Clarus range continues the tradition and offers full instrument and autosampler control of Perkin Elmer’s flagship GC’s. PerkinElmer Genomics’ position as an industry leader in Next-Generation Sequencing (NGS) testing solutions allow us to introduce unmatched automation and efficiencies in our clinical laboratory, and we are happy to pass on those cost savings to our patients in the form of industry-leading pricing for WGS.Chromatography Software - Instrument control Perkin Elmer Clarus 480, 580 and 680 GC’s For over three decades the Chromperfect data system has offered unparalleled choice for customers who demand a “best of breed” solution, allowing the widest choice in Chromatography instrumentation. Adding enriched phenotypic data and the power of artificial intelligence to our process allows us to achieve more efficient and accurate diagnoses.Īcceptance of multiple sample types including Saliva Swabs, Dried Blood Spots, Whole Blood, and Genomic DNA. PerkinElmer Genomics is the first global laboratory to fully integrate FDNA’s Next-Generation Phenotyping technologies into our variant analysis and interpretation workflows. STAT testing is also available with a TAT of just 10-12 days.Ĭhoose the options that make sense for your patients, including the integration of biochemical results from PerkinElmer’s StepOne® comprehensive biochemical profile in WGS results to aid in clinical correlation.Įnhanced variant analysis and interpretation efficiencies
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Genome TATs that beat most competitors Exome TATs: Average TAT of 6-8 weeks for our standard WGS offering. Combining superior coverage of the exome (complete coverage of >99% of the exome) with an average six week turn-around time, our whole genome sequencing test is designed to maintain the same quality and TAT that clients deserve from an exome sequencing test, while providing access to additional valuable information throughout the genome. PerkinElmer Genomics is one of the first laboratories to offer Whole Genome Sequencing on a clinical basis in effort to maximize clinical diagnostic yield for our clients and patients. The more uniform coverage offered through WGS can in fact provide better coverage of some regions of the exome than traditional exome sequencing, increasing the possibility of finding a disease causing mutation. The PCR-free sequencing methods used in Whole Genome Sequencing (WGS) provide for more uniform coverage across both coding and non-coding regions of DNA. Studies have suggested that up to 15% of disease-causing variants may be found in the non-coding regions of the genome, which are not covered by exome sequencing tests.