BlueFuse Multi combines facilities for managing all your arrayCGH information, fully automated data analysis and sophisticated DecisionTrack visualization in one easy to use software package. Unlimited licences for BlueFuse Multi are provided free-of-charge with all CytoChip microarrays in order to address the major challenges presented by routine arrayCGH, interpretation and management of results.
Choose a sample and experiment and visualize arrayCGH results
Manage samples. Store information on sample phenotype, quality and origin in one secure, centralized and scalable database. Link these to records of array investigations to provide trend analysis and comparisons of genotype. The database may be fully networked to deliver information to wherever it is needed.
Accelerate interpretation. Use advanced algorithms, developed specifically for interpreting constitutional copy number variation, to deliver detailed lists of imbalances which may be reviewed in detail for gene content and CNV frequency using BlueGnome's novel DecisionTrack technology.
View imbalances alongside gene content and CNV frequency
Automate reporting. Generate ISCN compliant reports from scanned microarray images in a single click. Increase operator productivity, remove error and experimental variation. Generate extended reports documenting break points and gene content of all imbalances marked for follow up.
Data mining. Mine your arrayCGH data using sophisticated queries. Check the history of clones in your database, or investigate correlation between phenotype and copy number. Exploit the full power of your data.
To evaluate or download the latest version of BlueFuse Multi, please contact BlueGnome.
