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CCTSI > Informatics > Video Learning Resources
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See the videos below on common topics in translational informatics:
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Reading Less: How to Put Yourself on an Information Diet Author: Addie Fletcher, MLIS Date: July 5, 2012 Time: 6:58 |
Reading Less 5 x 5 Resources:
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Genome Browsers Author: Addie Fletcher, MLIS Date: April 27, 2012 Time: 6:27 |
Genome Browser 5 x 5 Resources:
General:
For comparative information:
NCBI:
Ensembl:
UCSC:
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Researcher Networking Author: Addie Fletcher, MLIS Date: December 21, 2011 Time: 5:40 |
Researcher Networking Resources:
CTSA Strategic Goal Committee 3
VIVO
Profiles
VIVO Ontology
RDF Triples
Linked Open Data
Applications
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How to Jump Start Your Career with Bioinformatics, Part 1
Author: David Kao Date: June 20, 2011 Time: 6:05 |
How to Jump Start Your Career with Bioinformatics, Part 1 |
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How to Jump Start Your Career with Bioinformatics, Part 2
Author: David Kao Date: June 20, 2011 Time: 8:05 |
How to Jump Start Your Career with Bioinformatics, Part 2 |
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How to Jump Start Your Career with Bioinformatics, Part 3
Author: David Kao Date: June 20, 2011 Time: 7:28 |
How to Jump Start Your Career with Bioinformatics, Part 3 |
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How to Jump Start Your Career with Bioinformatics, Part 4
Author: David Kao Date: June 20, 2011 Time: 7:33 |
How to Jump Start Your Career with Bioinformatics, Part 4 |
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Regulatory Compliance: What you need to know
Author: Tim McCain Date: November 1, 2011 Time: 6:23 |
This "5x5" will provide the researcher a high level overview of three of the most predominant regulations they may be held to in their research, including when they apply to them, sanctions for violation and identifying resources to assist in compliance. Regulations covered include HIPAA, FISMA and 21 CFR Part 11 (FDA Part 11).
Regulatory Compliance Resources:
University of Colorado Denver
HIPAA
FISMA
CFR 21 Part 11
- Food and Drug Administration (FDA)
- CFR 21 Part 11
- Glossary of Computerized System and Software Development Terminology (Division of Field Investigations, Office of Regional Operations, Office of Regulatory Affairs, FDA 1995)
- General Principles of Software Validation; Final Guidance for Industry and FDA Staff (FDA, Center for Devices and Radiological Health, Center for Biologics Evaluation and Research, 2002)
- Guidance for Industry, FDA Reviewers, and Compliance on Off-The-Shelf Software Use in Medical Devices (FDA, Center for Devices and Radiological Health, 1999)
- Pharmaceutical CGMPs for the 21st Century: A Risk-Based Approach; A Science and Risk-Based Approach to Product Quality Regulation Incorporating an Integrated Quality Systems Approach (FDA 2002)
- FDA Guidance Documents (Medical Devices and Radiation-Emitting Products)
- The Good Automated Manufacturing Practice (GAMP) Guide for Validation of Automated Systems, GAMP 4 (ISPE/GAMP Forum, 2001)
- ISO/IEC 17799:2000 (BS 7799:2000) Information technology - Code of practice for information security management (ISO/IEC, 2000)
- ISO 14971:2002 Medical Devices- Application of risk management to medical devices (ISO, 2001)
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Best Practices in Research Forms Design
Author: Swan Ellert, Linda Carlin, Umit Kaya, Jessica Bondy Date: September 2, 2011 Time: 9:37 |
This "5x5" presentation describes form design best practices and how to design your study forms to gather data that can be easily analyzed.
Best Practices in Research Forms Design Resources:
Clinical Data Acquisition Standards Harmonization (CDASH); October 2008. Chapter 3.0 Best Practice Recommendations
Note: Login for CDISC members. A link is provided for non-members. For non-members a valid company email address will be required and the document will be emailed.
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REDCap Using Social Networking Sites for Medical Research Recruitment
Author: Adelaide Fletcher Date: July 21, 2011 Time: 5:22 |
Five things to consider if you wonder whether you can use social networking sites for clinical and patient engagement.
Social Networking in Medical Research Resources:
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REDCap Author: Linda Carlin, PhD and Jessica Bondy, MHA Date: December 14, 2010 Time: 7:18 |
This "5x5" presentation describes REDCap, the best-practice data collection software at UC Denver, and how it fits into the clinical trials lifecycle
REDCap Resources:
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Merging Files Author: Pam Wolfe, Jessica Bondy, Linda Carlin. Narrated by Ben Shulman. Date: October 26, 2010 Time: 10:48 |
This "5x5" will explain how to ensure that you are able to produce an integrated data file for the analyses required for your study.
Merging Files Resources:
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Managing Your Research Data Author: Linda Carlin, PhD Date: September 23, 2010 Time: 8:04 |
This "5x5" presentation discusses the phases of data management and best practices for obtaining high quality data from your research.
Managing Your Research Data Resources:
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Why not use Excel for data management? Author: Linda Carlin, PhD Date: September 23, 2010 Time: 7:47 |
This "5x5" presentation discusses why you should not use Excel to collect and manage your research data. An overview of data management best practices is included, as well as suggestions for better alternatives for data collection software.
Why Not Use Excel Resources:
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Explaining Risk to Patients: numeracy made easy Author: Adelaide Fletcher, MLIS Date: September 8, 2010 Time: 5:15 |
This “5x5” presentation (5 concepts in 5 minutes) discusses the importance of giving patients factual data about treatment and associated risks so that they can make informed decisions about their care. Techniques for presenting risk clearly and completely are given, along with suggestions on where to find decision aids.
Explaining Risk Resources:
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mRNA Expression Technology Author: Tzu Phang PhD Date: April 4, 2010 Time: 4:16 |
This “5x5” presentation (5 concepts in 5 minutes) introduces mRNA expression technology: how microarrays are used to measure tens of thousands of gene expression signals simultaneously. It discusses the conceptual basis of the technology, how it is performed, and when it may be employed in research.
mRNA Expression Array Technology Resources:
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Array Comparative Genomics Hybridization (aCGH) Author: Tzu Phang PhD Date: April 4, 2010 Time: 3:58 |
This “5x5” presentation (5 concepts in 5 minutes) introduces aCGH: a method to detect variations in the number of gene copies. This technique can be used to identify gene deletions and amplifications that can modify gene expression in potentially biologically significant ways (for instance, in tumorigenesis). It discusses the conceptual basis of the technology, how it is performed, and when it may be employed in research.
Array CGH Resources:
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EpiGenomics Author: Tzu Phang PhD Date: April 4, 2010 Time: 4:20 |
This “5x5” presentation (5 concepts in 5 minutes) introduces Epigenomics, the study of how chemical compounds modify and mark the genome and affect the behavior of genes. Epigenomics is a normal part of cell development (making cell specialization possible), but it may also be altered by environmental agents. Diseases and cancers can be induced not only through changes to the genome, but also through changes to the epigenome. This lecture discusses the concept of the epigenome, microarray techniques to study it, and when those techniques may be employed in research.
Epigenomics Resources:
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Alternative Splicing Array Technology Author: Tzu Phang PhD Date: April 4, 2010 Time: 5:20 |
This “5x5” presentation (5 concepts in 5 minutes) introduces alternative splicing (exon) array technology. It introduces the biological concept of alternative splicing: how different splice forms of the same gene produce different gene products. It describes the use of exon microarrays to evaluate alternative splicing, and when these may be employed in research.
Alternative Splicing Array Technology Resources:
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ChIP: Chromatin Immunoprecipitation on a Chip Author: Tzu Phang PhD Date: April 4, 2010 Time: 3:55 |
This “5x5” presentation (5 concepts in 5 minutes) introduces techniques chromatin immunopreciptation microarray techniques. Proteins may bind to specific sites on DNA to regulate gene expression. ChIP is used to locate these protein binding sites. This presentation discusses “ChIP-chip” microarray methods, and when they may be employed in research.
ChIP Resources:
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Health Literacy Author: Adelaide Fletcher MLIS Date: September 8, 2010 Time: 5:15
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This “5x5” presentation (5 concepts in 5 minutes) defines health literacy and describes why it is such an important issue in clinical research. Problems with health literacy are common, affecting one third of adults in the United States. This presentation discusses methods to assess the health literacy of patients, and methods to assess and improve the readability of documents. This information will be valuable to researchers who develop materials for recruitment, surveys, and informed consent.
Health Literacy Resources:
Health Literacy in General:
Assessment Tools:
Methods to Address Low Literacy:
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Trustworthy Information Resources for Patients Author: Adelaide Fletcher MLIS Date: April 4, 2010 Time:
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This “5x5” presentation (5 concepts in 5 minutes) discusses the high quality, trustworthy, and literacy-appropriate health information available to patients through the National Institutes of Health and related institutions. It describes some health information resources translational researchers may provide to patients who are enrolled in clinical trials, and guides that are available to assess patient health information. It also provides methods for patients and researchers to get help from a medical librarian.
Health Information For Patients Resources:
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Bioinformatics: From Lab Bench Sciences to the Public Author: Tzu Phang, PhD Date: April 4, 2010 Time: 25:04 |
This lecture discusses common high-throughput methods used in bioinformatics research: evaluation of DNA (genomics), RNA (the transcriptome), proteins (proteomics), and metabolic pathways (metabolomics). It discusses the “promise and hype” of applying these tools to individual patients in the clinical setting. |
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 Care and Feeding of Your Grant Part 1 Author: Diane Fairclough, PhD Date: April 15, 2010 Time: 16:57
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Diane Fairclough DrPH provides a practical "hidden curriculum" for researchers, describing how to establish effective collaborations with statitcians/analysts, how to develop an effective data management plan, how to design data collection instruments to facilitate abstraction and analysis, and considerations in selecting software applications for data storage.
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 Care and Feeding of Your Grant Part 2 Author: Diane Fairclough, PhD Date: April 15, 2010 Time: 13:27
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Diane Fairclough DrPH continues her "hidden curriculum" for researchers, describing how to avoid pitfalls in designing, naming, and encoding response variables, how to prepare for publication even before data collection has started, how to refine the analytic plan, and how to plan for closing single-site and multi-site studies well before the end of the study. | |
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Miss an Informatics Seminar Series presentation? Click on the titles below to view archived videos of these events.
- Using Health Information Technology to Improve Clinical Care
March 18, 2010 Ted Palen, MD, PhD
- Clinical Informatics Year in Review
February 18, 2010 Michael Kahn, MD, PhD
- Development of an Open Source Application for Local Health Departments | Presentation Slides
January 21, 2010 Joe Schruers
- CIO Panel Discussion: The Challenge of Supporting Clinical Research Informatics Needs (no video available)
November 19, 2009 Steve Hess, Mary Anne Leach, and Gregg Veltri
- American Recovery and Reinvestment Act (ARRA) and the Colorado Regional Information Organization (CORHIO)
October 15, 2009 Carrie Book , BBA, PMP
- Trick or Treat? How Information Technologies Will Change the nature of Psychiatric Treatment (no video available)
September 17, 2009 Jay H. Shore, M.D., MPH
- REDCap: Collecting, Storing, and Accessing Data Online
June 18, 2009 Sean Banks, MS (ABD)
- Personal Health Records: Tethered and Interoperable (Google Health and Microsoft Health Vault)
May 21, 2009 Steve Ross, MD
- The Internet: Changing Biomedical Publication and Scientific Discourse
April 16, 2009 Robert Dellavalle, MD, PhD, MSPH
- DARTNet: A Distributed Network for Research and Quality Improvement
March 19, 2009 Wilson Pace, MD
- Informatics Year in Review| Presentation Slides
February 19, 2009 Michael Kahn, MD PhD
- Creation of a HIPAA-Compliant integrated network for collecting and using patient information for research: The University of Pittsburgh's Honest Broker System
October 16, 2008 Dana Marie Grzybicki, MD, PhD
- Study Design by Metadata (SDM): A system for collecting clinical research data
September 18th, 2008 Ted Wade PhD and Jeff Magouirk M.S
- Biomedical Discovery Acceleration
May 15, 2008 Lawerence Hunter, PhD
- RHIOS: CORHIO and Challenges in Implementing RHIOs
April 17, 2008 Arthur Davidson, MD, MSPH |
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