BlueFuse Multi
BlueFuse Multi is a comprehensive software solution for managing arrayCGH datasets.
BlueFuse Multi has been developed in collaboration with the cytogenetics community to
enable arrayCGH investigations to be reported rapidly and with confidence.
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| Choose a sample and experiment and visualize arrayCGH results |
Sample and experiment management.
Store sample and technical information associated with arrayCGH experiments.
Track consumables, experimental design, and operator to provide a complete audit trail.
Integration.
Seamlessly import sample information from other databases to minimize human error and
maximize efficiency.
Workflow.
Store all arrayCGH data on a centralized database. Allow different users to access / add
to the database from different locations, and at different times, increasing
workflow efficiency.
Data processing.
Use the same powerful statistical technology as BlueFuse for Microarrays
to identify regions of genomic copy number variation. Generate comprehensive
quality control metrics to confirm experiments have worked correctly.
Visualization.
Visualize copy number changes against chromosomal ideograms, identify results in regions
of disease, and exclude polymorphisms based on the latest research(1).
Visualize multiple arrayCGH profiles on the screen at one time, allowing easy comparison
of different results.
Automated reporting.
Generate ISCN compliant reports fully automatically from scanned microarray images in a single click.
Increase operator productivity, and reduce experimental variation.
Generate extended reports on failed clones and disease region investigations.
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.
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| Interrogate your database to visualize the history of a clone |
To evaluate or download the latest version of BlueFuse Multi, please contact BlueGnome.
