Cores & Resources
Medical School Office of Research

We are committed to offering state-of-the-art technology and expertise through centralized cores and services that adapt to the ever-changing research landscape.

Research staff in a lab using a pipette
Biomedical Research Core Facilities
Michigan Research Cores
Data Office
Michigan Experts
Central Biorepository
Research Project Route Map
Research Cores

The Biomedical Research Core Facilities (BRCF) at the Medical School offer state-of-the-art instruments, resources, and expertise to investigators at the U-M and beyond. Many of our biomedical cores are recognized nationally and internationally for enabling new research and developing novel techniques for their respective scientific fields. The Biomedical Research Core Facilities include:

  • Advanced Genomics Core - the largest sequencing facility in the Midwest
  • Bioinformatics Core - offers custom support in computational methods and algorithm development
  • Biomedical Research Store - researchers can purchase thousands of products for their projects
  • Epigenomics Core - prepares samples for analysis in epigenetic regulation
  • Flow Cytometry Core - offers instrumentation, phenotypic analysis, cell sorting, and data analysis
  • Metabolomics Core - offers state-of-the-art in-house metabolomics analysis tools
  • Microscopy Core - offers high resolution microscopy, instruments, services, and data analysis
  • Proteomics & Peptide Synthesis Core - provides custom sample prep and data interpretation
  • Proteomics Resource Facility -  state of the art instruments, technical expertise, advanced informatics support
  • Transgenic Animal Model Core - internationally recognized expertise in rodent models
  • Vector Core - in-house viral and plasmid stocks are ready the next business day

For more information, visit the BRCF website.

Cores are centralized facilities or labs that offer shared services, shared equipment, resources and expertise to investigators and their teams on a fee-for-service basis. There are over 100 different cores supporting research across the University of Michigan. For more information, view the full list of Research Cores.

Clinical Research

Clinical Trials Support Units (CTSUs) are business units that partner with investigators and their teams to ensure the timely and efficient activation and execution of clinical trials at Michigan Medicine.

The CTSUs allow investigators to focus on their research and patients, instead of administrative tasks. CTSUs use a standard set of work guides to harmonize elements across the clinical research enterprise while allowing for local flexibility to reflect the uniqueness of various types of research. CTSUs provide mandatory pre-/post-award support and optional study coordinator support.

When working with the Support Units, the six non-oncology units are referred to as M-CTSU and oncology as O-CTSU. Learn more about each Clinical Trials Support Unit.

Principal Investigators can ultimately find a smoother process and save time by taking advantage of the Clinical Trials Support Office's study coordinator pool, which can provide investigators with team members who are already on staff and fully trained. All CTSU study coordinators are Good Clinical Practice (GCP) trained, and many coordinators have obtained or are working towards becoming either Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) certified. The study coordinator services span the entire scope of clinical trial study coordination. For more information, visit the Study Coordinator Support page.

The Science Coordinator is an evolving role with roots in the science liaison role from industry. This service offers a great resource to study teams in clinical research: adjunct study team member, Angie Lyden ([email protected]), who can help with infrastructure logistics, and serve as a mentor and guide for early-career investigators and staff. Angie will work with study teams as an invested partner to navigate the new era of clinical research here at Michigan Medicine. For more information, visit the Study Coordinator Support page.

The Michigan Clinical Research Unit (MCRU), part of the Clinical Trials Support Office, provides clinical staff, resources, and infrastructure that are necessary to conduct adult and pediatric human clinical research protocols at the University of Michigan. MCRU offers the following services:

  • RN Nursing
  • Clinical Support
  • Laboratory Processing and Shipping
  • MCRU Space
  • Mobile Clinical Research Team (MCRU2U)

 

The Medical School Office of Research has partnered with the School of Public Health to offer MM investigators statistical support for large-scale clinical trials, tapping into the expertise of the Statistical Analysis of Biomedical and Educational Research (SABER) Group, a unit of the Department of Biostatistics.

SABER offers a variety of support options for investigator-initiated multi-site trials, including study design, data and project management, clinical monitoring, and even development of customized apps for clincial studies.

MICHR, partnering with the Clinical Trials Support Office, offers a number of resources for clinical trialists, including:

  • Pilot awards
  • IND/IDE application preparation and submission
  • Database development
  • Participant recruitment and retention consultation

The Research Pharmacy is located in the central pharmacy area in University Hospital level B2 (room UHB2 D400). Pharmacists and technicians are dedicated to the coordination of drug studies and the dispensing of investigational drugs to inpatients and outpatients.

Patient Data & Biospecimens

The Michigan Institute for Clinical & Health Research (MICHR) offers many services related to participant recruitment. They can help you:

  • Determine whether their engaged participant registry, UMHealthResearch.org is an appropriate recruitment tool for your study and, if it is, teach you how to maximize the potential of UMHealthResearch.org for your study.
  • Develop and review recruitment materials, identifying obstacles that may affect participant recruitment for your study through a participant recruitment and retention consultation.

The Data Office for Clinical & Translational Research and the Central Biorepository partner to help researchers gain secure access to thousands of available biospecimens and 15 years of patient clinical data. The intersection of these two services can help accelerate more targeted research, increasing your opportunities for collaboration, funding, and publication.

Data access through the Data Office for Clinical & Translational Research:
The Data Offices offers multiple self-serve tools, or you can request a custom data extract from their experienced programmers.

Biospecimen access through the Central Biorepository:
The Central Biorepository can connect you with thousands of biosamples for your research. For more information, visit their Get Access page, or view a sampling of what is available visit their Inventory page.

Data Office for Clinical & Translational Research consultations provide information on available data tailored to your needs and a deep dive into all patient health data resources that are available. From support for your new funding proposal to informing your study design to crafting limited patient data searches, they offer consultations to help with all of your data requests.

Central Biorepository consultations connect you with experts who can help with guidance on consent, IRB applications, and distributions agreements, whether accessing or storing biosamples.

The MiChart Research Team assists with all aspects of the electronic medical record including recruitment, ordering, and tip sheets. The Team can help you with setting up recruitment alerts, order set development, study and reporting needs, and other ways to maximize patient records for research.

There are two main types of MiChart-Research access: View Only access (which allows users to view virtually everything in MiChart) and Study Coordinator access (which allows for users to write to patients’ charts in the form of a research note and to place orders). The easiest way to request any of the services provided is to submit a Service Request via ServiceNow or contact Health Information Technology & Services (HITS) at 734-936-8000.

The Central Biorepository serves as a central storage facility, point-of-research access, and administrative hub for research using biospecimens and data associated with or derived from them.

The repository is populated through partnerships with investigators, departments, centers, and institutes that are looking to create a resource for their own use, as well as sharing biomaterials and developing collaborative opportunities within the research enterprise at the University of Michigan and beyond.

Are you a clinician researcher considering options for storing your patient samples? Accredited by the College of American Pathologists, the Central Biorepository's expert staff can help you collect, manage, and protect your biospecimens using highly-automated processes and the highest-quality control. For more information, visit their Biobank page.

Research Technology

The Health Information & Technology Services (HITS) department supports the IT needs of our research enterprise. In addition to oversight of enterprise-wide services such as MiChart, the IT team provides lab support, informatics, and high-end computing and data storage to help investigators leverage technology and data in ways that make meaningful contributions to research.

The Research Computing Package (RCP) offers computing services and data storage at no cost to Michigan Medicine faculty. RCP encourages faculty researchers to maximize the impact of their scholarly work through centralized, worry-free computing services and data storage. These services are offered in partnership with Advanced Research Computing – Technology Services.

The HITS managed computing service offers options for your PC and Mac general computing devices that help ensure your computer has the most up to date security and software updates, and device management features.

The Electronic Research Notebook (ERN) is a Software as a Service tool that provides a secure and compliant replacement for traditional paper lab notebooks. As modern research and lab data is largely digital and not well managed by paper notebooks, a software tool is a much better suited solution to the problem of managing modern research and laboratories.

The SignNow service at U-M supports the automation of processes for requesting and capturing signatures and information on documents. This service is used to support a diverse set of document workflows, some system-supported (automated) and some that had been manual. In addition, the U-M ITS e-signature service provides enabling support that includes single sign-on (SSO) access, SignNow service administration, contract and vendor management, and support and training.

Questions?
Contact Us
Office of Research
University of Michigan Medical School
Phone: 734-763-4272
7313 Medical Science I Building
1301 Catherine Street
Ann Arbor, MI 48109-5624

North Campus Research Complex (NCRC)
Building 520, 3rd Floor
2800 Plymouth Road
Ann Arbor, MI 48109-2800
Upcoming Office of Research Events All Office of Research Events
Advancing Behavioral Science through AI and Digital Health (a joint event with MIDAS, e-HAIL, and MICHR's BRISP)
The conference is designed for Behavioral and Social Science Research (BSSR) scientists to learn about AI and applications to their research. It brings together several AI experts on campus and features Keynote Speaker Amy Bucher, PhD, Chief Behavioral Officer at Lirio.
A speaker and attendees at an event in Kahn Auditorium at BSRB
Introduction to sIRBs
This course will identify the Single IRB model for Multi-Site research, show the regulatory requirements of sIRB review and the exceptions to sIRB requirements, and explain sIRB requests of IRBMED as sIRB (accepting oversight), External IRB as sIRB (ceding oversight), and UofM as the Coordinating Center.
A computer screen showing multiple people participating in a zoom event
FDA Research Involving Drugs and Devices
This course will review what research is subject to FDA oversight, highlight the differences between OHRP and FDA regulations, learn the responsibilities of sponsors, investigators, and the IRB when conducting and reviewing research involving drugs and devices, and examine the requirements for conducting research with a drug or biologic/medical device.
A man participating in a zoom event
Subparts B, C, and D - Special Populations
This course will examine the additional regulatory requirements for conducting research involving pregnant women, fetuses, neonates, children, and prisoners, including the requirements for these populations in a research project and obtaining informed consent.
A zoom event on a laptop
Opportunities for AI in Mental Health: e-HAIL In-Person Roundtable Conversation
Join e-HAIL for a discussion on AI-powered approaches and tools to improve mental health for individuals and at scale. At this interactive session, U-M researchers will briefly present some current “mental health & AI” projects, focusing on new collaborations and ways to utilize additional data sources as they become available. This will be followed by table discussions focused on different topics, including topics from the showcase and other topics/problems/innovations that participants are interested in exploring.
e-HAIL discussion 23
Federal and Institutional Requirements for Human Subject Research
This course will introduce the basics of conducting human subject research in compliance with federal regulations and institutional practices.
A man participating in a zoom event
Event Rescheduled
BRCF Bioinformatics Workshop: Reproducible Computing at the University of Michigan
This multi-day, virtual workshop is for researchers who manage lots of data and/or execute compute-intensive analyses.
An illustration of a very large laptop and several figures sitting around the edges in a variety of poses.
Elements of Informed Consent
This course offers an overview of informed consent in human subject research. The course will examine IRBMED’s standard consent template and focus on how it reflects federal requirements.
A zoom event on a laptop
Advanced Genomics Core and Singular Genomics: G4 Sequencing Platform and G4XTM Spatial Sequencer
Learn about the G4, a bench-top sequencer with novel high-performance chemistry and advanced engineering, optimized to deliver unmatched power, speed, and flexibility, and the G4XTM Spatial Sequencer, a high-throughput in situ spatial sequencer for transcriptomic and proteomic analysis from FFPE samples at subcellular resolution.
A man listens to a lecture. Others are in the background, also listening to the lecture.
Featured Office of Research News All Research News FFMI fastPACE spring 2024
Office of Research
Register Today! FFMI fastPACE Spring Cohort Begins Friday, May 10
Don't miss your chance to participate in this project-based, experiential course designed to help academics launch new innovations, including medical devices/diagnostics, digital solutions, drugs, educational/training interventions, research tools, and many others.
Image of Mio Nakamura, MD, MS
Office of Research
Clinical Trials Support Office Announces New Associate Medical Director
The Clinical Trials Support Office (CTSO) is pleased to announce that Mio Nakamura, MD, MS, Clinical Assistant Professor, Dermatology, has been appointed as the new Associate Medical Director of the Michigan Clinical Trials Support Unit (M-CTSU) and Michigan Clinical Research Unit (MCRU). Dr. Nakamura’s appointment will begin July 1, 2024, and is a 2-year term.
a closeup image of a laptop
Office of Research
Information Assurance Guidelines for Using Applications and Technologies in Research
Before seeking approval for a research project, it is crucial to ensure that the work complies with Information Assurance guidelines.