Molecular Genetics eNews
October 2018 edition
We’re delighted to include a number of software support tools in this Fall edition of Molecular Genetics eNews. Our upgraded version of SureSeq™ Interpret Software strengthens our SureSeq product range – helping you to present meaningful results for confident annotation and reporting of low frequency variants.
We know that you also love our CytoSure™ Interpret software videos, Peter Gray, FAS (Field Application Scientist) has developed a new video where you can learn more about the options CytoSure Interpret provides for automating, uploading and processing sample ID information to the database.
We’re sure you’ll find it useful, but if you need any further support don’t forget our FAS’s are here to provide you with all the help you need in your lab. Just email firstname.lastname@example.org and we’ll put you in contact with an FAS in your area. All support is free of charge.
Aysel Heckel, VP Sales, North America
SureSeq Interpret Software – upgraded version now available
SureSeq Interpret is a powerful and easy-to-use next generation sequencing analysis solution.
Optimised for use with SureSeq NGS panels it offers confident annotation and reporting of low frequency single nucleotide variants (SNVs) and Indels as well as structural variants such as copy number variants (CNVs) and internal tandem duplications (ITDs).
"The software provided quick and reliable alignment and variant analysis to interpret results from our core MPN sequencing." Joshua Landreth, Molecular Laboratory Supervisor, Genetic Associates Inc.
CytoSure™ Interpret Software – new videos to help you in your analysis
Learn more about the options that CytoSure Interpret offers for automatic upload and processing of sample information to the CytoSure Interpret database by watching our new short video by our field application Specialist, Peter Gray:
Interested in receiving more support around any of OGT’s products? Don’t hesitate to contact us at email@example.com.
Custom NGS panels – new content now covers 120 fully optimised cancer related genes
See our latest press release on our SureSeq myPanel™ NGS Custom Cancer Panel content - now covering 120 fully optimised cancer related genes giving you even more freedom to customise your sequencing experiments.
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