Clinician Access™
Customizable to your level of involvement.
Welcome to Clinician Access 2.0, now with enhanced features, allowing you to stay involved with every test you submit to Signature Genomics. Here you can monitor the status of submitted tests from receipt through completion.
This customizable system can generate notifications sent directly to your email anytime a process step of interest to you has been completed at our laboratory. When the entire testing process is finished the finalized report will be available instantly in your account. Your complete history of electronic reports will remain available in your account at all times. You can opt out of receiving faxed reports and utilize electronic reports alone, or you can still have both.
Need more information regarding an abnormal region found in your constitutional microarray results? Clinician Access provides a link to Signature Genomics’ Interactive Genome Browser covering a 5MB region surrounding each abnormal area. Investigate deeper and bring context to the results by utilizing a variety of resources that are collected into one central location – UCSC, OMIM, DGV and Signature Genomics extensive database of over 50,000 cases. Go above and beyond the level of information accessible through a standard report with Clinician Access.
Features:
- Real time order status tracking
- Electronic report delivery
- Interactive Genome Browser for abnormal regions
- Order dashboard
- Resources and information
- All available exclusively to Signature Genomics’ clients at no additional cost
Databases available to search include:
- OMIM
- PubMed
- UCSC Genome Browser
- Access to Signature Genomics’ private database of abnormal cases identified from over 50,000 samples.
Clinician Access is a time-saver for clinicians, allowing a view of patient results in relationship to a variety of online resources, thus providing a tool to:
- Assist with explaining results
- Educate patients of their microarray-based CGH results
- Counsel Patients
- Gather up-to-date genetic information
- Allow for genotype-phenotype comparisons of other cases with similar or overlapping abnormalities seen by Signature Genomics.
Get a sneak peek at the interactive browser by viewing
Signature Genomics’ Genome Browser:
Signature Genomics’ Genome Browser allows users the ability to populate gene content, CNV data, publication and sequence data for a region of interest with multiple search options.
- Search by Genomic Coordinates
- Select a chromosome and then enter the starting and ending base pair coordinates
- Search by Chromosome Band
- Simply enter a chromosome band or band prefix, for example 2p23.3 or 2p2 for all bands beginning with 2p2.
- Search by Gene
- Enter the full name of the gene or part of the name for a list of all genes available for viewing
- Search for BAC ID
- Enter the BAC ID, for example: RP11-316L10
Contact Us
For more information on how you can gain access to this powerful tool, contact us at casupport@signaturegenomics.com or call 1.877.SigChip.