Bioinformatics Training & Education Program

This one-hour online training offers an overview of the NIH-sponsored Generalist Repository Ecosystem Initiative (GREI) (Dataverse, Dryad, Figshare, Mendeley Data, Open Science Framework, Vivli, and Zenodo), and the role of participating in these repositories in the NIH data repository landscape for intramural researchers. The session will highlight how these repositories support compliance with the NIH Data Management and Sharing Policy.

By the end of this training, attendees will be able to:  

• Describe how generalist repositories fit into the NIH data repository landscape for intramural researchers.
• Understand how these repositories support compliance with the NIH Data Management and Sharing Policy
• Learn about the resources developed by GREI repositories to support data sharing workflows, including a generalist repository comparison chart, a generalist repository selection flowchart, a data submission checklist, and a data management and sharing plan guide.
• Gain practical insights from real-world examples, demonstrating  how researchers use generalist repositories for data sharing and reuse, and how these efforts contribute to the broader NIH data sharing ecosystem.

Attendees are not expected to have any prior knowledge of the NIH Data Repository Landscape.    

The role of computational science in biomedical research has typically been downstream of experiments, where it plays important roles in signal processing, data integration, pattern detection, and hypothesis testing. But this is changing, and predictive models are now being used to generate and test hypotheses in silico. In this talk, Dr. Pollard will share examples from human genetics, where they have built deep learning models of 3D chromatin interactions that take only sequence as input and then used them to interpret disease variants. This strategy leads to causal hypotheses and enables them to prioritize variants with predicted functional effects. Experiments designed using model outputs are accelerating the rate of discoveries, shedding light on genetic mechanisms in cancer and developmental disorders. This prediction-first strategy exemplifies Dr. Pollard's vision for a more proactive, rather than reactive, role for computational science in biomedical research.

This one-hour online training will provide a high-level overview of Python coding concepts, as well as some of the integrative development environments (IDEs, such as Jupyter notebooks) used for Python coding. Python is a programming language used for data science, specifically: data analysis, statistical analysis, and visualization of results. The training will feature the following IDEs: Google Colaboratory: Jupyter Notebook; and Anaconda’s: Spyder, Jupyter Notebook, and JupyterLab. This overview training will demonstrate how these skills can boost productivity, rigor, and transparency in reporting research findings.  

By the end of the training, attendees will be able to: 

• Recognize four freely available IDEs for python coding
• Identify fundamental components of python code
• Understand how and why notebooks support rigor and transparency in analysis 

Attendees are not expected to have any prior knowledge of python coding or the IDEs to be successful in this training.  

If you choose to follow along with Google Colab or Jupyter Notebooks, these IDEs should be installed and ready to go. Code will be provided during the training for this option. 

This one-hour online training provides an introduction on how to sign up and access complimentary SAS training resources available to NIH and HHS employees. 

By the end of this training, attendees will be able to:  

• Enroll in recommended SAS 9.4 trainings and courses
• Navigate complimentary SAS tutorials, programming courses, and eLearning 

Attendees are not expected to have any prior knowledge of SAS to be successful in this training. 

Partek Flow enables scientists to construct analysis workflows for multi-omics sequencing data including DNA, bulk and single cell RNA, spatial transcriptomics, ATAC and ChIP. It is a point-and-click software suitable for those who wish to avoid the steep learning curve involved with analyzing sequencing data through coding. In this class, taught by Partek scientist, participants will learn about conducting QA/QC, performing cell type classification, obtaining differential analysis results, performing pathway analysis, and creating visualizations for single cell RNA sequencing data. This session is a demonstration and not hands-on. Experience using or access to Partek Flow is not needed for participation. Attendance is restricted to NIH staff.

This one and a half-hour online training covers the basic principles of FAIR (Findable, Accessible, Interoperable, Reusable) data and why it is important to make your data FAIR.  

 By the end of this training, attendees will be able to:  

• Define FAIR data   

• Explain what purpose FAIR data serves 

• Apply FAIR data principles to make data findable, accessible, interoperable, and reusable 

This is an introductory level training.