Agilent CytoGenomics Software User Guide

Agilent CytoGenomics software is a complete solution for cytogenetic research data analysis. It streamlines the cytogenetic research workflow for finding copy number changes, copy-neutral aberrations, and copy-neutral loss of heterozygosity (LOH) and uniparental disomy (UPD). It supports manual sample analysis with in-house and external databases, provides full automation of the analysis process, and enables easy generation of customizable analysis reports.


Agilent CytoGenomics Software User Guide - cover page
Brand
Agilent
Document type
User Manual
Language
English
Pages
8
File format
PDF
File size
977 KB
Published
05 July, 2012
Updated
29 September, 2023
MD5 checksum
6FD86EF049EB470D5D0E3AE7789AD881

About this manual

The Agilent CytoGenomics software is designed to streamline the cytogenetic research workflow by detecting copy number changes (CNCs), copy-neutral loss of heterozygosity (LOH), and uniparental disomy (UPD). It supports efficient analysis using SurePrint G3 CGH+SNP microarrays, offering a statistically and visually powerful tool for researchers. The software enables full automation of the analysis process from data upload to report generation.

What's inside

  • Technical Overview
  • Data Import and Analysis
  • Manual Sample Analysis in the Triage View
  • Cyto Report
  • Auto Processing of Data Upload, Feature Extraction, and Data Analysis
  • Customization of the Sample Analysis Workflow

Frequently asked questions

What is the analysis time for a normal constitutional sample?

The software allows researchers to analyze a normal, constitutional sample in less than five minutes.

Can the analysis workflow be customized?

Yes, users can pre-set parameters with their choice of analysis settings, report settings, aberration classifications, and customized tracks.

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