Request for Assistance

Policies

• We are willing to help investigators who are Rogel Cancer Center members on their cancer related research.
• The investigator requesting assistance should explain the project using the form below. The CDS-SR leadership will then assign an appropriate member to work with them.
• For longer term assistance and collaboration the investigator is expected to write a statistician/analyst into their grant application or provide salary support through other means. CDS-SR personnel contributing to various projects are expected to be listed as co-authors on any publications resulting from their work
• The investigator requesting assistance should contact the CDS-SR well in advance of any deadline. Recommended timelines that would significantly facilitate our planning process are 
  • Advance notice of 1 month towards meeting abstracts
  • 2-3 months towards manuscripts (biostatistical/bioinformatics analysis, figure preparation etc.)
  • 3-6 months for R01 submissions
  • 6-9 months for program projects (eg SPOREs, P01s)

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Project Intake Form

If you see this don't fill out this input box.

Name*

Email Address*

Phone Number*

Requestor name

Principal Investigator*

Departmental Affiliation*

Cancer Research Program Affiliation

Cancer Control and Population Sciences

Translational & Clinical Research

Cancer Hematopoiesis & Immunology

Cancer Genetics Research

Signaling and Tumor Microenvironment

Developmental Therapeutics

Other

If "other" selected above, please list here

Details of project

Type of Project (Please select best fit from provided choices)

Biostatistical Analyses

Clinical Trial Design

Bioinformatics Analyses (sequencing/molecular data)Informatics

Analytics

other (e.g: mutation detection, CyTOF, microbiome, image analysis)

Additional information on selection above

Brief Description of Project (Aims and Scope)*

Is this for a Paper or a Grant?

Paper

Grant

If for a grant, when is the due date?

Expected time-line of the project

Funding source(s) (if available)

Additional Details

Please add additional details (e.g. goals, hypothesis, expected results etc.)

Key question to ask of the data

Are there any batch effects to be aware of?

Experimental Approach

Treatment Groups, if applicable

Number of samples

Sequencing Platform (if applicable)

Has statistician been consulted for project to evaluate experimental design?

Yes

No

Provide the statistical analysis plan, if available

Do you need us to perform statistical analysis?

Yes

No

I don't know

If so, please describe:

Data Specifics

Where is data being stored?

How will this data be provided to us?

Do we have your permission to access and move data for this analysis?

Was this data generated at the University of Michigan or an external institution?

Does any of this data need HIPAA-compliant storage?

Is there an IRB/MTA/DUA in place for this study? Please indicate study number

Submit   Clear

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Interested investigators who need assistance with cancer related research should contact: