Covering NGS, array and FISH probe technologies and cancer, constitutional and rare disease applications.
CytoSure™ Interpret Software – Automatic Classification of Aberrations
Learn about the automatic CNV classification feature in CytoSure Interpret. The video covers the set up and customisation of classifier sets, how they can aid the interpretation process and provide a faster, more standardised analytical workflow.
CytoSure™ Interpret Software - Automatic Sample ID Detection and Processing
Learn about the options CytoSure Interpret provides for automating, uploading and processing sample ID information to the database.
CytoSure™ Interpret Software - Target regions
A guide to the new target regions feature available in CytoSure Interpret Software version 4.10 onwards, allowing the user to focus their analysis on specific regions of interest in the data.
CytoSure™ Interpret Software Workflow Part Two - Loading, reviewing and reporting the analysis of aCGH data
Learn about the most popular features offered by CytoSure Interpret for the Import and Interpretation of your data.
CytoSure™ Interpret Software Workflow Part One - Data processing and analysis of aCGH data
Learn about the different options CytoSure Interpret offers for processing your aCGH data.
Introduction - CytoSure™ Interpret Software for aCGH analysis
Learn about the workflow and basic feature of our software with our quick overview video.
SureSeq myPanel™ NGS Custom Cancer Panels
Getting started with your SureSeq myPanel NGS Custom Panel could not be simpler, find out more in this video…
Make our expertise work for you
See how you can discover more when you take advantage of our aCGH design expertise.
CytoSure™ Interpret Software - Updates in Version 4.9
CytoSure Interpret continues to improve, with several new features added since the previous release. Peter Gray, Field Application Scientist, details the new features and changes.
Use of NGS panels and microarrays for CNV detection
Hear Douglas Hurd describe some of our recent advances in next generation sequencing (NGS) panel design to allow detection of both copy number variation (CNV) and single nucleotide variation (SNV) from a single assay.
Customisable, single exon resolution CNV analysis complements NGS for additional insights into genetic disorders
Hear Dr Tracey Lewis from the R&D Molecular Genomics Group, ARUP Laboratories Salt Lake City, USA discuss the importance of single exon CNV changes in a variety of genetic conditions.
Analysing OGT’s SureSeq Myeloid Panel Data
Watch this short demonstration video to discover how OGT's SureSeq Myeloid Panel and complimentary SureSeq Interpret Software can make the analysis of myeloid samples simple.
AMP Workshop 2015
Held at the Austin Convention Center in Austin, this workshop looks at how to implement an integrated approach to tumour profiling.
Identifying a broader range of genetic syndromes using exon-focussed array designs
This workshop outlines the development of the new CytoSure Constitutional v3 arrays and how Emory University School of Medicine complements its NGS workflows using the CytoSure™ Medical Research Exome array.
Enhanced bait design strategies that deliver more reliable NGS panel assays
Hear Chris Mattocks, Senior Clinical Research Scientist at the National Genetics Reference Laboratory (Wessex), Salisbury, UK, discuss the advantages of hybridisation enrichment and the importance of optimal bait design.