Training Guide Library

Identify and gather the data you need to address a problem.

• Beginner
  • [Article] Generating and Collecting Data: The Basics | Get the fundamentals on what it is, why it matters, and how you can do it effectively.
  • [Training Video Recording] Genomic Data Commons Data Portal | Watch a tutorial on how this web-based platform allows you to search, analyze, and download data from cancer genomics studies.
  • [Training Video Recording] GARDE: Open-Source Platform for Population-based Genetic Testing of Hereditary Cancer Syndromes | Learn how to facilitate population-based genetic testing with the GARDE software platform, which harnesses algorithms and chatbots to identify individuals eligible for genetic testing for hereditary cancer syndromes.
  • [Training Video Recording] The Cancer Proteome Atlas | Get an introduction to RPPA (a high-throughput, antibody-based technique for protein profiling); receive an overview of the bioinformatics resource, “The Cancer Proteome Atlas” (or TCPA); and learn more about TCPA’s chatbot, “TCPAplus.”
  • [Training Video Recording] Unlocking Insights from Clinical Notes with the EMERSE Text Processing Tool | Use this tool to identify key data within free-text clinical notes from electronic health records systems.
  • [Training Video Recording] Data Management and Planning: Getting Started | Learn the fundamentals of data management, including how to define key stakeholders and outline plans.
  • [Training Video Recording] Good Data Stewardship | Listen to an experienced and an early career investigator discuss how good stewardship means applying FAIR (Findable, Accessible, Interoperable, Reusable) best practices, providing long-term data management strategies, and talking to the right resources.
• Advanced
  • [Training Video Recording] WebMeV | Discover how to use this intuitive, web-based, bioinformatics analysis toolkit designed for non-bioinformaticians. This walkthrough includes steps on how to upload data files, run a single-cell analysis (using the tools available within the toolkit), and how to navigate/create public data sets available within WebMeV.

Fix discrepancies and handle missing values in your data.

• Beginner
  • [Article] Cleaning Data: The Basics | Get the fundamentals on what it is, why it matters, and how you can do it effectively.

Study your data, then form a hypothesis.

• Beginner
  • [Article] Exploring and Analyzing Data: The Basics | Get the fundamentals on what it is, why it matters, and how you can do it effectively.
  • [Article] How to Use the Cancer Data Aggregator | Read about this resource and how it can help you in your search for data across NCI's Cancer Research Data Commons.
  • [Article] Copy Number Variation (CNV) Calling: The Basics | Get tips on generating CNV data and how to choose the right tool.
  • [Article] Spatial Transcriptomics (ST): The Basics | Describes the basics of using ST for cancer research, including spotlighting an NCI-funded tool that doesn’t require specialized skills in bioinformatics.
  • [Training Video Recording] WebMeV | Receive a demonstration on how this web-based software for genomic data analysis can upload data and perform various analyses such as normalization, clustering, and principal component analysis.
  • [Training Video Recording] XNAT | Learn about this open source imaging informatics software platform that enables data ingestion, curation, annotation, quality control, and computational workflows using Docker containers.
  • [Training Video Recording] User-Friendly Analysis of Spatial Transcriptomics with spatialGE | Learn more about this user-friendly web application that integrates the spatial R package. This package, enhanced with additional ST analysis methods (such as SpaGCN, STdeconvolve, and InSituType), makes it more valuable for the cancer research community.
  • [Training Video Recording] RNAseq Data Analysis in Qlucore | Import and analyze RNA-sequencing data in Qlucore Omics Explorer—software that visualizes the data in 3D plots and can help you identify hidden structures and patterns.
  • [Training Video Recording] An Introduction to Bioconductor for Genomic Data Science | Learn the basics of integrative data containers for genome-scale experiments and components of analytic workflows for transcriptomics and epigenetics. You will also discover resources for annotation of genomic data.
  • [Training Video Recording] Introduction to FlowJo™ Software | Learn about FlowJo’s workspace—including how to load files, evaluate sample quality, draw gates, and generate tabular and graphical layouts to perform single-cell flow cytometry analysis.
  • [Training Video Recording] Unveiling FlowJo Version 11 | Discover FlowJo with a modern language code base. This version makes visual comparisons faster to access, it comes with more built-in automation tools, and it’s built on a foundation compatible with cloud computer.
• Advanced
  • [Training Video Recording] User-Friendly Analysis of ST with spatialGE | Get an overview of ST, discover how it’s advancing cancer research, and watch a demonstration of the spatialGE web application that can help you with your ST data analysis.
  • [Training Video Recording] An Introduction to Gene Set Enrichment Analysis (GSEA) and the Molecular Signatures Database (MSigDB) | Learn how the GSEA analysis tool operates, how to use MSigDB to compare your data against well annotated gene sets, and how to run GSEA with MSigDB.
  • [Training Video Recording] TCIA Jupyter Learning Lab | Explore a variety of use cases for identifying The Cancer Imaging Archive (TCIA) data sets, and learn how to download them using Jupyter Notebooks. You’ll also learn how to utilize TCIA for data exploration and downloading data.
  • [Training Video Recording] TumorDecon | Discover how digital cytometry methods and their applications assist in tumor research.
  • [Training Video Recording] Decoding Epigenetic Complexity: Modeling Gene Regulation with the Cistrome Data Browser | Discover methods for integrating Cistrome Data Browser data into single cell ATAC-sequencing and RNA-sequencing multimodal analysis.
  • [Training Video Recording] HLA-Arena: Enabling Structure-Guided Pipelines for Personalized Cancer Immunotherapy Design | Study Human Leukocyte Antigens (HLA) in cancer with this computational platform that incorporates neoantigen markers and other bioinformatics pipelines.
  • [Training Video Recordings] NCI’s Containers and Workflows Interest Group Webinar Series | Hear from presenters—across NCI CBIIT, NIH, industry, and academia—as they discuss how cloud computing and container technologies, workflows, and data pipelines could drive cancer data science.
  • [Training Video Recording] QIAGEN Ingenuity Pathway Analysis (IPA) Webinar | Learn how to analyze large data sets (including RNA-sequencing and proteomics) using QIAGEN IPA to perform interactive core and pathway analyses.
  • [Training Video Recording] Using the Network Zoo Tools to Explore Biological Complexity and Its Consequences | Find out how you can use the Network Zoo Tools, a repository of computational tools, to tackle complex biological questions about gene regulation and network inference.
    [Training Video Recording] AmpliconSuite: Enabling Analysis of Focal Amplifications in Cancer Genomics | Learn about the AmpliconSuite, an integrated toolkit for detecting and classifying extrachromosomal DNA, from a member of one of the 2022 NCI Grand Challenges teams.

Use computational tools like machine learning models to make predictions with your data.

• Beginner
  • [Article] Predictive Modeling: The Basics | Get the fundamentals on what it is, why it matters, and how you can do it effectively.
• Advanced
  • [Training Video Recording] Pixels to Predictions: Designing Computational Imaging AI to Enable Precision Medicine | Learn more about the use of AI in precision medicine, specifically focusing on the development of computational imaging tools for different patient pathways.

Communicate your data findings using interactive images, plots, and charts.

• Beginner
  • [Training Video Recording] Introduction to UCSC Xena: A Tool for Multi-omics Data & Associate Clinical and Phenotypic Annotations | Learn about the features and capabilities of the Xena platform for genomics visualization and analysis, including data loading, filtering, statistical analysis, single-cell analysis, and various visualization options.
  • [Article] Visualizing Data: The Basics | Get the fundamentals on what it is, why it matters, and how you can do it effectively.
  • [Article] How to Use Circle Plots for Visualizing Multi-Omics Data | Get tips on ‘OmicCircos,’ an R-based program that lets you manage, analyze, and visualize your omics data.
  • [Training Video Recording] MATLAB: Now What? Post-Processing AI Techniques for Enhanced Accuracy | Familiarize yourself with post-processing AI techniques.
  • [Training Video Recording] The GenePattern Ecosystem for Cancer Genomics and Reproducible Research | Discover an environment for accessible and reproducible research that hosts hundreds of genomics analysis and visualization tools. GenePattern exists in a web-based format that requires no programming, along with extensive features for reproducibility and accessibility.
  • [Training Video Recording] The Cancer Digital Slide Archive (CDSA) Webinar | Explore this open-source, web-based platform for storing, visualizing, and managing digitized whole slide images. The platform addresses the growing need for pathology data management within the biomedical research community, enabling you to explore large, histological data sets.
• Advanced
  • [Training Video Recording] Data Visualization with R | Learn how to use the ggplot2 package in the programming language R to graph plots that can form the basis of analysis. Note: This video is one of six videos that make up a course series exclusive to NCI staff and provided by the Bioinformatics Training and Education Program. In this recording, R Studio is accessed via DNAnexus.
  • [Training Video Recording] DNASTAR Lasergene Software | Learn about this software and its applications in molecular biology, including topics such as enzyme labels, primer design, cloning processes, construct analysis, and clone verification using Sanger sequencing.
  • [Training Video Recording] Next-Generation Clustered Heat Maps (NG-CHMs) | Learn how NG-CHMs can help you navigate large omic databases, zoom in on patterns, access external metadata resources, produce high-resolution graphics, and save metadata for later use. NG-CHMs play a valuable role in NIH projects, encompassing phenotypic and genotypic data at DNA, RNA, protein, and metabolite levels in bulk and single-cell studies.

Accelerate discovery by making your data available to others.

• Beginner
  • [Article] Sharing Data: The Basics | Get the fundamentals on what it is, why it matters, and how you can do it effectively.
  • [Training Video Recording] Data Management and Planning: Introduction to the NIH Policy for Data Management and Sharing | Receive an overview of this NIH policy and an introduction to both NIH resources and data management planning tools.
  • [Training Video Recording] Jointly Developing an Approach to FAIRness | Listen to an experienced and an early career investigator discuss how and why to adopt FAIR principles. They also meet with their peers to discuss data storage (i.e., repository) options based on specific scenarios.
  • [Training Video Recording] Leveraging Publicly Accessible Data | Learn about the importance of findable, accessible, interoperable, sharable, and reusable data.
• Advanced
  • [Resources] Metadata Services for Cancer Research | Discover how to approach the Cancer Standards Registry and Repository (caDSR II) infrastructure, which helps investigators create and use data standards for cancer research.
  • [Blog] Semantics Primer | Get a snapshot of how semantics help create shared and consistent meanings for data so they can be used/reused and shared with researchers.
  • [Blog] A Deep Dive into Common Data Elements (CDEs) | Discover how CDEs help researchers like you define, map, use, and share data more efficiently.

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