Resources Cytosure Hero

CytoSure Interpret Software for aCGH analysis tutorials

CytoSure Interpret aCGH software tutorial 1: Introduction

Learn about the workflow and basic feature of our software with our quick overview video.

CytoSure Interpret aCGH software tutorial 2: Data processing and analysis of aCGH Data

Learn about the different options CytoSure Interpret offers for processing your aCGH data.

CytoSure Interpret aCGH software tutorial 3: 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 aCGH software tutorial 4: 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 aCGH software tutorial 5: 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 aCGH software tutorial 6: 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 aCGH software tutorial 7: Probe filtering

Learn about the wide range of user-defined probe filtering options in CytoSure Interpret. The video explores the various probe filter parameters available, how to apply them and how they can be used to refine data analysis.

CytoSure Interpret aCGH software tutorial 8: Updating annotation tracks

Learn more about the new annotation track update feature in CytoSure Interpret version 4.11. The video details how to check for annotation track updates and access the very latest versions.

CytoSure Interpret aCGH software tutorial 9: Case status

Learn how to track the progress of a case in the Case Status field. The video details the various stages, transitioning between them and how the function can be used to search for samples in database management.

CytoSure Interpret aCGH software tutorial 10: Setting up analysis protocols

Learn how to customise CNV detection protocols. The video focuses on the setting up of mosaic CNV analysis protocols and the selection of appropriate threshold factors for the accurate detection of mosaic gains and losses.

Customer presentations

Beyond CNV: leveraging SNP microarrays in cancer

Dr. Stephen Moore will share his experience utilising OGT's CytoSure® chromosomal microarrays in various tumour types. Specifically, he will highlight the different applications of the single nucleotide polymorphism (SNP) track beyond oligonucleotides confirmation.

The whole exome: Completing the genomic picture using exon-targeted aCGH

Lora Bean provides valuable insights into the use of microarrays and NGS in parallel for CNV detection. While CNV calls from NGS data are becoming increasingly popular, they must be confirmed due to the significant false positive rate associated with them.

Implementation of the CytoSure Constitutional v3 microarray in the UK NHS

Dom McMullan discusses the implementation of the CytoSure® Constitutional v3 microarray in the NHS laboratory, and how it facilitated cost-effective, evidence-based analysis of large populations.

Validation of the CytoSure Constitutional v3 microarrays in prenatal and postnatal analysis

Kris Van Den Bogaert discusses the evaluation of the CytoSure® Constitutional v3 microarrays in prenatal and postnatal research.

Advancing genomic interpretation: combining NGS and microarrays

Madhuri Hegde expands on her work with OGT combining NGS, microarrays — including OGT’s CytoSure® Disease-Focused Research arrays — and an all-inclusive genomic data interpretation platform for comprehensive analysis of genetic disorders.

Customisable, exon-focused aCGH microarrays complement NGS for additional insights into genetic disorders

Dr Tracey Lewis delve into the benefits of combining the study of copy number variations (CNVs) and single nucleotide variations (SNVs) for enhanced mutation detection across a range of genetic conditions.

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