Supported by CCR Office of Science and Technology Resources (OSTR)
ncibtep@nih.gov

Bioinformatics Training and Education Program

Featured

Upcoming Classes & Events

April

Description

Looking for an introduction to artificial intelligence (AI) or an opportunity to expand on what you already know? Attend this workshop hosted by the NIH-funded Bridge2AI CHoRUS network and the University of Florida College of Medicine. Whether you register for the beginner or advanced track, you’ll be equipped with knowledge and skills that you could transfer to your own cancer research.

If you have little-to-no experience using AI, join Read More

Looking for an introduction to artificial intelligence (AI) or an opportunity to expand on what you already know? Attend this workshop hosted by the NIH-funded Bridge2AI CHoRUS network and the University of Florida College of Medicine. Whether you register for the beginner or advanced track, you’ll be equipped with knowledge and skills that you could transfer to your own cancer research.

If you have little-to-no experience using AI, join the “AI Boot Camp” (beginner track). If you have experience, the “Generative AI with Diffusion Models Workshop” (advanced track) might be better for you. Learn more about each track below!

AI Boot Camp

Register if you have no prior programming experience and/or are an AI and machine learning novice. You’ll learn about:

  • the Jupyter Lab environment and how to create Jupyter notebooks.
  • the rules of the programming language “Python” and how to develop and execute the code for manipulating biomedical data.
  • important Python libraries for biomedical data science.
  • additional topics related to large language models (LLMs), multidisciplinary collaboration, AI, and more.
Generative AI with Diffusion Models Workshop

Register if you understand PyTorch and deep learning. You’ll learn:

  • how to improve the quality of generated images through the process of gradually diffusing the noise.
  • how to control the image output with context embeddings.
  • how to generate images from English text-prompts.
  • additional topics related to denoising diffusion models.

Upon completing either track, you’ll receive a digital Credly credentials badge and certificate.

Details
Organizer
CBIIT
When
Sun, Apr 21, 2024 - 7:30 am - 5:30 pm
Where
Online
Description

Dear Colleagues,
  
In this webinar, you'll get an introduction to XNAT. XNAT is an open-source platform for managing, processing, and sharing medical imaging and related data in research settings.
 
You can use XNAT's flexible architecture and extensive customization options to streamline your workflows and collaborate effectively. It can also help to accelerate discoveries in neuroscience and medical imaging research.
 
You'll learn about key features Read More

Dear Colleagues,
  
In this webinar, you'll get an introduction to XNAT. XNAT is an open-source platform for managing, processing, and sharing medical imaging and related data in research settings.
 
You can use XNAT's flexible architecture and extensive customization options to streamline your workflows and collaborate effectively. It can also help to accelerate discoveries in neuroscience and medical imaging research.
 
You'll learn about key features and benefits of XNAT, including example use cases in oncology research. 

For questions contact Daoud Meerzaman or Kayla Strauss.

Details
Organizer
CBIIT
When
Mon, Apr 22, 2024 - 10:00 am - 11:00 am
Where
Online
Description
Intended Audience

This webinar targets researchers interested in exploring genomic mutation analysis capabilities within the recently introduced NCI Genomic Data Commons (GDC) 2.0 platform. It aims to accommodate individuals interested in analyzing genes and mutations within a cancer disease type, irrespective of their prior genomics experience.

Abstract

GDC 2.0 adopts a "cohort-centric" approach, allowing users to construct custom sets of cases and conduct gene- and variant-level data analysis directly within their web browser. This Read More

Intended Audience

This webinar targets researchers interested in exploring genomic mutation analysis capabilities within the recently introduced NCI Genomic Data Commons (GDC) 2.0 platform. It aims to accommodate individuals interested in analyzing genes and mutations within a cancer disease type, irrespective of their prior genomics experience.

Abstract

GDC 2.0 adopts a "cohort-centric" approach, allowing users to construct custom sets of cases and conduct gene- and variant-level data analysis directly within their web browser. This webinar will demonstrate the new cohort-centric workflow, from cohort building to analyzing genes and mutations associated with a cohort. Additionally, participants may ask GDC experts questions and provide feedback on GDC 2.0.

Included Topics
  • Utilizing the Cohort Builder to create custom cohorts for specific cancer disease types
  • Employing the Mutation Frequency Tool to visualize the most frequently mutated genes within a cohort
  • Using OncoMatrix to analyze the top mutated genes affected by high-impact mutations in a cohort
  • Using ProteinPaint to explore mutations and their potential impact within protein coding regions of genes
Webex Information
  • Meeting number (access code): 2306 971 7385
  • Meeting password: TGwpjPf@283 (84975731 from phones and video systems)
Details
Organizer
NCI Genomic Data Commons
When
Mon, Apr 22, 2024 - 2:00 pm - 3:00 pm
Where
Online
Description

Dr. Stephanie Harmon obtained her Ph.D. in medical physics at the University of Wisconsin–Madison and did her postgraduate training at Leidos Biomedical Research where she worked within the Molecular Imaging Branch and investigated computational biomarkers in various state-of-the-art prostate imaging modalities. In 2020, she became a staff scientist within the newly formed Artificial Intelligence Resource of the NCI.

Dr. Harmon’s research interests focus on computational approaches, including computer Read More

Dr. Stephanie Harmon obtained her Ph.D. in medical physics at the University of Wisconsin–Madison and did her postgraduate training at Leidos Biomedical Research where she worked within the Molecular Imaging Branch and investigated computational biomarkers in various state-of-the-art prostate imaging modalities. In 2020, she became a staff scientist within the newly formed Artificial Intelligence Resource of the NCI.

Dr. Harmon’s research interests focus on computational approaches, including computer vision and artificial intelligence, for combining multiscale biological and clinicopathological data to model cancer and cancer-related outcomes. She investigates the functional relationship of imaging characteristics across biological scales and their role in phenotypic heterogeneity in various cancer types. Her research centers around the idea that the use of integrative biomarkers from various imaging scales could enhance the understanding of disease and the role of imaging in cancer diagnosis and treatment. Her long-term goal is to identify interpretable imaging-based biomarkers on histopathological images that can predict underlying molecular phenotypes and translate these findings to improve diagnosis, treatment, and patient outcomes in various cancers.

Dr. Harmon received many awards during her training, including the Prostate Cancer Foundation Young Investigator Award and the NCI Director’s Intramural Innovation Award.

Dr. Harmon has published over 75 peer-reviewed articles, including publications in the Journal of Nuclear Medicine, PLOS One, JAMA Oncology, Cancer Imaging, Radiology, American Journal of Pathology, Journal of Medical Imaging, Nature Medicine, Journal of Clinical Oncology, Clinical Cancer Research, and Nature Communications.

For more information, please contact Aniruddha Ganguly, Ph.D.

Meeting number (access code): 2319 301 4914

Meeting password: KpxUgxg$372

Details
Organizer
NCI
When
Tue, Apr 23, 2024 - 9:30 am - 10:30 am
Where
Online
Description

What’s the difference between “regular” statistics (i.e., what you may have been using in the past several years) and the “new” Bayesian statistics? Which one should you use for your next study?

This is Part 1 of a two-part lecture series intended for non-statisticians interested in understanding the basic, intuitive thinking behind the two schools of statistical inference: frequentist (known as classical) and Bayesian. Part 1 will Read More

What’s the difference between “regular” statistics (i.e., what you may have been using in the past several years) and the “new” Bayesian statistics? Which one should you use for your next study?

This is Part 1 of a two-part lecture series intended for non-statisticians interested in understanding the basic, intuitive thinking behind the two schools of statistical inference: frequentist (known as classical) and Bayesian. Part 1 will address the frequentist approach and will cover the concepts of hypothesis testing, confidence intervals, Type I and Type II errors, statistical power, and p-values. Technical details will be kept to an absolute minimum. The class will be taught by the NIH Clinical Center's Biostatistics and Clinical Epidemiology Service (BCES).

Although you may attend only one part of this series, attending both parts will give you a better sense of the contrast between these two statistical approaches. During the class, time will be devoted to questions from attendees, and references will be provided for in-depth self-study.

You must register separately for Part 2 of this class series.

Individuals who need reasonable accommodations to participate should contact the NIH Interpreting Office directly at nih@ainterpreting.com, or the NIH Library Information Desk at 301-496-1080. Requests should be made at least five business days in advance in order to ensure availability.

Details
Organizer
ORF/NIH Library
When
Tue, Apr 23, 2024 - 11:00 am - 1:00 pm
Where
Online
Description

Crunching of large data requires large resources. Exploration of holobiont metagenomes is considered a “big data” project and here I’ll be describing how I used the FRCE cluster to explore 794 metagenomes simultaneously to assess the biosynthetic capacity associated with lichens. This presentation will focus more on computational tools and techniques used to solve metagenomic problems. This presentation is aimed at beginner to intermediate users. A basic understanding of Bash and Read More

Crunching of large data requires large resources. Exploration of holobiont metagenomes is considered a “big data” project and here I’ll be describing how I used the FRCE cluster to explore 794 metagenomes simultaneously to assess the biosynthetic capacity associated with lichens. This presentation will focus more on computational tools and techniques used to solve metagenomic problems. This presentation is aimed at beginner to intermediate users. A basic understanding of Bash and Slurm would be beneficial but not vital. This will be a hybrid event. This session will be recorded, and materials will be posted on the ABCS training site and also shared with attendees a few days after the event.

For additional details and questions, please contact Natasha Pacheco (natasha.pacheco@nih.gov), Advanced Biomedical Computational Science group, Frederick National Laboratory for Cancer Research.

Details
Organizer
BACS
When
Tue, Apr 23, 2024 - 12:00 pm - 1:00 pm
Where
Building 549 Conference Room B, Frederick
Description

Join Dr. Kai Tan of the Children’s Hospital of Philadelphia as he discusses his cutting-edge technology, CytoCommunity, for the supervised and unsupervised discovery of tissue cellular neighborhoods. CytoCommunity offers a powerful and scalable method for de novo interpretation of cellular function and cell-cell communications in tissue microenvironments.

This event is part of the NCI Emerging Read More

Details
Organizer
CBIIT
When
Tue, Apr 23, 2024 - 2:00 pm - 3:00 pm
Where
Online
Description

Please join us on Wednesday, April 24, 2024, when Dr. Abhishek Jha, co-founder and CEO of Elucidata, will present " Data Quality for LLMs: Building a Reliable Data Foundation." The presentation starts at 11:00 a.m. ET and ends at noon.
 
If you use large language models (LLMs) in your cancer research, register for this seminar to hear Elucidata’s Dr. Abhishek Jha discuss how data quality impacts LLM performance.
 
A Read More

Please join us on Wednesday, April 24, 2024, when Dr. Abhishek Jha, co-founder and CEO of Elucidata, will present " Data Quality for LLMs: Building a Reliable Data Foundation." The presentation starts at 11:00 a.m. ET and ends at noon.
 
If you use large language models (LLMs) in your cancer research, register for this seminar to hear Elucidata’s Dr. Abhishek Jha discuss how data quality impacts LLM performance.
 
A reliable foundation that is well annotated and accessible to an LLM plays a major role in the value of its results.
 
You’ll see examples of how LLM-powered artificial intelligence (AI) agents query across three versions of the same gene expression corpus with differing results, including:

•    unstructured data from the public repository Gene Expression Omnibus.
•    structured data from the Crowd Extracted Expression of Differential Signatures project.
•    clean, linked, and harmonized data.
 
Dr. Jha will use these examples to discuss how the different quality in these data sources impacts LLM performance.

Details
Organizer
CBIIT
When
Wed, Apr 24, 2024 - 11:00 am - 12:00 pm
Where
Online
Getting Started with scRNA-Seq Seminar Series

Description

This seminar provides an introduction to R in the context of single cell RNA-Seq analysis with Seurat.  In this seminar, attendees will learn about options for analyzing scRNA-Seq data, resources for learning R, how to import scRNA-Seq data, and how to create, examine, and access data stored in a Seurat object.  

This seminar provides an introduction to R in the context of single cell RNA-Seq analysis with Seurat.  In this seminar, attendees will learn about options for analyzing scRNA-Seq data, resources for learning R, how to import scRNA-Seq data, and how to create, examine, and access data stored in a Seurat object.  

Register
Organizer
BTEP
When
Wed, Apr 24, 2024 - 1:00 pm - 2:00 pm
Where
Online Webinar
Description

Dear Colleagues,
  
In this webinar, you'll get an introduction to WebMeV. WebMeV aims to democratize bioinformatics analysis for biological sciences researchers.
 
The maturation of many bioinformatics processes in sequencing has enabled the standardization of protocols. This allows simple programmatic encapsulation of the analysis. New technology has also allowed increased accessibility and replication of the software environment itself.
 
WebMeV provides both transparency and reproducibility of Read More

Dear Colleagues,
  
In this webinar, you'll get an introduction to WebMeV. WebMeV aims to democratize bioinformatics analysis for biological sciences researchers.
 
The maturation of many bioinformatics processes in sequencing has enabled the standardization of protocols. This allows simple programmatic encapsulation of the analysis. New technology has also allowed increased accessibility and replication of the software environment itself.
 
WebMeV provides both transparency and reproducibility of the analysis code and build environment. It also provides an easy to use web-based graphical interface to count-based bioinformatics analyses of RNASeq, scRNASeq, and more.

For questions contact Daoud Meerzaman or Kayla Strauss.

 

Details
Organizer
CBIIT
When
Fri, Apr 26, 2024 - 10:00 am - 11:00 am
Where
Online
Description

Webinar attendees will hear tips and tricks to code efficiently in the Researcher Workbench using R and RStudio. Although Python and SAS are alternative programming languages available on the Researcher Workbench, this session will only focus on using R and RStudio. Participants should already have a general understanding of how to code in R prior to attending the session. This session will not cover the basics of coding in R.

Presenter:Read More

Webinar attendees will hear tips and tricks to code efficiently in the Researcher Workbench using R and RStudio. Although Python and SAS are alternative programming languages available on the Researcher Workbench, this session will only focus on using R and RStudio. Participants should already have a general understanding of how to code in R prior to attending the session. This session will not cover the basics of coding in R.

Presenter: Aymone Kouame is a Data Scientist at Vanderbilt University Medical Center. She leads the Data Science & Engineering efforts for Digital Health Technologies (Fitbit). She is involved in the back-end and front-end processes of the All of Us Researcher Workbench curated data repository, working closely with the Curation and the Research Support Teams. Aymone discovered her passion for Data Science after a few years working/studying in Business and Accounting. She holds Master Degrees of Science in Data Analytics, Information Systems, and Accounting and Business Management. Before VUMC, she worked on the Data Science team of a cyber security company.

This is the fourth of five sessions about NIH’s All of Us Research Program and Researcher Workbench. Attendees are encouraged to attend all sessions. Register for additional session below: 

  • Session 5 - May 3: Resources to Support Researchers

For questions about this webinar series, contact Cindy Sheffield, cynthia.sheffield@nih.gov

 

 

 

Details
Organizer
NIH Library
When
Fri, Apr 26, 2024 - 11:00 am - 12:00 pm
Where
Online
Description

What’s the difference between “regular” statistics (i.e., what you may have been using in the past several years) and the “new” Bayesian statistics? Which one should you use for your next study? 

This is Part 2 of a two-part lecture series intended for non-statisticians interested in understanding the basic, intuitive thinking behind the two schools of statistical inference: frequentist (known as classical) and Bayesian. Part 2 Read More

What’s the difference between “regular” statistics (i.e., what you may have been using in the past several years) and the “new” Bayesian statistics? Which one should you use for your next study? 

This is Part 2 of a two-part lecture series intended for non-statisticians interested in understanding the basic, intuitive thinking behind the two schools of statistical inference: frequentist (known as classical) and Bayesian. Part 2 will address the Bayesian approach and will cover the concepts of Bayes’ Theorem, prior and posterior distributions, and Bayes factor. Technical details will be kept to an absolute minimum. This class will be taught by the Clinical Center's Biostatistics and Clinical Epidemiology Service (CC/BCES). 

Although you may attend only one part of this series, attending both parts will give you a better sense of the contrast between these two statistical approaches. During the class, time will be devoted to questions from attendees, and references will be provided for in-depth self-study. 

You must register separately for Part 1 of this class series.

Details
Organizer
NIH Library
When
Tue, Apr 30, 2024 - 11:00 am - 12:30 pm
Where
Online

May

Getting Started with scRNA-Seq Seminar Series

Description

This lesson reviews many of the standard steps in a scRNA-Seq workflow: QC filtering, normalization, scaling, and clustering. 

This lesson reviews many of the standard steps in a scRNA-Seq workflow: QC filtering, normalization, scaling, and clustering. 

Register
Organizer
BTEP
When
Wed, May 01, 2024 - 1:00 pm - 2:00 pm
Where
Online Webinar
Description
To register to attend, you must log in to your SITC Cancer Immunotherapy CONNECT account. Don’t have an account? Create a free one.

Join Dr. Mullin of the Roswell Park Comprehensive Cancer Center and Dr. Bao of the UPMC Hillman Cancer Center as they talk about artificial intelligence’s (AI’s) role in Read More

To register to attend, you must log in to your SITC Cancer Immunotherapy CONNECT account. Don’t have an account? Create a free one.

Join Dr. Mullin of the Roswell Park Comprehensive Cancer Center and Dr. Bao of the UPMC Hillman Cancer Center as they talk about artificial intelligence’s (AI’s) role in real-time monitoring of patients who are receiving immunotherapy for immune-related adverse events (irAE).

If you attend, you’ll learn about:

  • the current application of AI in irAE monitoring and detection.
  • future applications of these technologies across the field.

This webinar is the first of the 2024 SITC-NCI Computational Immuno-oncology Webinar Series, which focuses on the application of AI in immuno-oncology. It consists of nine free webinars to help individual research labs overcome computational challenges while analyzing and integrating different assay data throughout the immuno-oncology spectrum using AI. The annual series aims to educate early-career scientists, increase participants’ awareness of and engagement in NCI-supported Cancer Moonshot℠ Immunotherapy Networks, and fulfill the Blue Ribbon Panel’s goal of accelerating progress in cancer research.

Details
Organizer
CBIIT
When
Thu, May 02, 2024 - 12:00 pm - 1:00 pm
Where
Online
AI in Biomedical Research @ NIH Seminar Series

Description

The explosion of biomedical big data and information in the past decade or so has created new opportunities for discoveries to improve the treatment and prevention of human diseases. As such, the field of medicine is undergoing a paradigm shift driven by AI-powered analytical solutions. This talk explores the benefits (and risks) of AI and ChatGPT, highlighting their pivotal roles in revolutionizing biomedical discovery, patient care, diagnosis, treatment, and medical research. By Read More

The explosion of biomedical big data and information in the past decade or so has created new opportunities for discoveries to improve the treatment and prevention of human diseases. As such, the field of medicine is undergoing a paradigm shift driven by AI-powered analytical solutions. This talk explores the benefits (and risks) of AI and ChatGPT, highlighting their pivotal roles in revolutionizing biomedical discovery, patient care, diagnosis, treatment, and medical research. By demonstrating their uses in some real-world applications such as improving biomedical literature searches (Nature Biotechnology 2018; Nature 2020; Nature Genetics 2023), accelerating patient trial matching (TrialGPT, in collaboration with NCI clinicians), and assisting gene set analysis (GeneAgent, in collaboration with NCI researchers), we underscore the potential of AI and ChatGPT in enhancing clinical decision-making, personalizing patient experiences, and accelerating knowledge discovery.

Alternative Meeting Information: Meeting number: 2300 950 8025 Password: qiQsnDx?923 Join by video system Dial 23009508025@cbiit.webex.com You can also dial 173.243.2.68 and enter your meeting number. Join by phone 1-650-479-3207 Call-in number (US/Canada) Access code: 2300 950 8025  
Register
Organizer
BTEP
When
Thu, May 02, 2024 - 1:00 pm - 2:00 pm
Where
Online Webinar
Description

Webinar attendees will learn how to use and navigate the All of Us Researcher Workbench’s User Support Hub, which provides video tutorials, help articles, and more. Attendees will also learn about opportunities to get support from the Researcher Workbench help desk and how to stay involved with the All of Us Research Program through the program’s network of partners. 

Presenters:

Rubin Baskir, Read More

Webinar attendees will learn how to use and navigate the All of Us Researcher Workbench’s User Support Hub, which provides video tutorials, help articles, and more. Attendees will also learn about opportunities to get support from the Researcher Workbench help desk and how to stay involved with the All of Us Research Program through the program’s network of partners. 

Presenters:

Rubin Baskir, Ph.D., Researcher Engagement and Outreach Branch Chief, All of Us Research Program
Rubin Baskir, Ph.D., is a Program Officer and the Researcher Engagement and Outreach Branch Chief within the NIH All of Us Research Program engagement team. He is excited to be working with a team that helps maintain the essential relationship between the program, participants, and community partners.  Prior to his current position, Baskir began working in the All of Us Research Program as part of an American Association for the Advancement of Science (AAAS) science and technology policy fellowship. His interest in health policy began during his graduate work at Vanderbilt University, where, in addition to researching mechanisms of disease and signal transduction, he gained an appreciation for the effects of policy on human health. Baskir received his doctorate in clinical and cellular biology from Vanderbilt University and his Bachelor’s degree in biology from Washington University in St. Louis.

Sydney McMaster, CHES, Program Officer, All of Us Research Program
As a passionate health equity advocate, Sydney McMaster has served as a Program Officer and Researcher Engagement Specialist for the NIH All of Us Research Program for over two years. In this role, she functions as a liaison between the researcher community and the national program, offering support and technical assistance to researchers interested in studying the program’s dataset. Prior to this role, Sydney served as a Public Health Analyst with the Health Resources and Services Administration (HRSA) for three years. As a previous participant in a pathways internship program with HRSA, Sydney is passionate about supporting equitable pathways for diverse professionals interested in research and public health careers. 

This is the fifth of five sessions about NIH’s All of Us Research Program and Researcher Workbench. Attendees are encouraged, but not required, to attend all sessions. 

For questions about this webinar series, contact Cindy Sheffield, cynthia.sheffield@nih.gov

 

 

 

Details
Organizer
NIH Library
When
Fri, May 03, 2024 - 11:00 am - 12:00 pm
Where
Online
Description

Have you been looking for ways to use artificial intelligence (AI) in clinical practice but not sure where to start? Attend this webinar for tips from Dr. Anant Madabhushi on applying AI in precision oncology. He’ll describe how AI can be affordable, easy to interpret, and help ensure more equitable care for every patient. Specifically, Dr. Madabhushi will discuss efforts by his group to develop AI-based approaches for measuring:

  • Read More

Have you been looking for ways to use artificial intelligence (AI) in clinical practice but not sure where to start? Attend this webinar for tips from Dr. Anant Madabhushi on applying AI in precision oncology. He’ll describe how AI can be affordable, easy to interpret, and help ensure more equitable care for every patient. Specifically, Dr. Madabhushi will discuss efforts by his group to develop AI-based approaches for measuring:

  • alterations in the immune architecture underlying diseases (i.e., collagen disorder) using AI and pathology images, and
  • changes in tumor blood vessels (vessel tortuosity) using AI and radiologic scans.

He’ll describe how biomarkers like these can help you predict how well a patient will respond to treatment, as well as monitor their response.

Dr. Madabhushi has been on the forefront of translating lab-created technologies into clinical practice. He’s pioneered the use of AI in precision oncology, offering new solutions for diagnosing cancers (i.e., breast, prostate, lung) and predicting how patients will respond to cancer treatments, such as chemotherapy, immunotherapy, and protein inhibitors (i.e., cyclin-dependent kinase 4 and 6).

The Cancer Imaging Program is part of NCI’s Division of Cancer Treatment & Diagnosis. The program hosts this monthly NCI Imaging Community Webinar Series for scientists and clinicians interested in advancing cancer imaging. If you want to learn about upcoming opportunities for engagement, interdisciplinary collaboration, and current research showcases, you can explore upcoming events on the webinar series’ webpage.

Dr. Anant Madabhushi is the Robert W. Woodruff Professor of Biomedical Engineering and serves on the faculty of the departments of pathology, biomedical informatics, urology, radiation oncology, radiology and imaging sciences, global health and computer and information sciences, all at Emory University. He’s also a research career scientist at the Atlanta Veterans Administration Medical Center. And he’s director of the Emory Empathetic AI for Health Institute at Emory University. Dr. Madabhushi has authored more than 500 peer-reviewed scientific publications and holds (or has pending) over 200 patents in the areas of AI, radiomics, medical image analysis, computer-aided diagnosis, and computer vision.

Details
Organizer
CBIIT
When
Mon, May 06, 2024 - 1:00 pm - 2:00 pm
Where
Online
Description

Macros are ways to use code to substitute in a value, and using macros makes a code in SAS easier to read, easier to edit, less prone to errors,  and often allows it to run more efficiently. This intermediate class will provide an overview of what is a macro and how macros work in SAS, including the macro facility. Examples of macro code will be made available to class participants for modification and Read More

Macros are ways to use code to substitute in a value, and using macros makes a code in SAS easier to read, easier to edit, less prone to errors,  and often allows it to run more efficiently. This intermediate class will provide an overview of what is a macro and how macros work in SAS, including the macro facility. Examples of macro code will be made available to class participants for modification and later use.

Details
Organizer
NIH Library
When
Tue, May 07, 2024 - 10:00 am - 11:00 am
Where
Online
Description

Galaxy is a scientific workflow, data integration, data analysis, and publishing platform that makes computational biology accessible to research scientists that do not have computer programming experience. This workshop will introduce RNA-seq data analysis followed by tutorials showing the use of popular RNA-seq analysis packages and preparing participants to independently run basic RNA-Seq analysis for expression profiling. The hands-on exercises will run on the Galaxy platform using Illumina paired-end RNA-seq data. The workshop will Read More

Galaxy is a scientific workflow, data integration, data analysis, and publishing platform that makes computational biology accessible to research scientists that do not have computer programming experience. This workshop will introduce RNA-seq data analysis followed by tutorials showing the use of popular RNA-seq analysis packages and preparing participants to independently run basic RNA-Seq analysis for expression profiling. The hands-on exercises will run on the Galaxy platform using Illumina paired-end RNA-seq data. The workshop will be taught by NCI staff and is open to NIH and HHS staff.

Details
Organizer
NIH Library
When
Tue, May 07, 2024 - 1:00 pm - 4:00 pm
Where
Online
Description

If you’re a researcher, clinician, informaticist, commercial partner, or policy maker interested in cancer data science, register to attend this Cancer Data Exchange Summit.

You’ll have the opportunity to hear (and take part in) discussions around current opportunities and challenges with the following topics:

  • How to use a patient’s data to determine their eligibility for clinical trials
  • How to identify Read More

If you’re a researcher, clinician, informaticist, commercial partner, or policy maker interested in cancer data science, register to attend this Cancer Data Exchange Summit.

You’ll have the opportunity to hear (and take part in) discussions around current opportunities and challenges with the following topics:

  • How to use a patient’s data to determine their eligibility for clinical trials
  • How to identify and develop data standards to detect immune-related adverse events
  • Ways to enhance the efficiency and timeliness of the collection of cancer registry data
  • Ways to support patient access, interoperability, and data sharing

You can also help identify cancer-specific elements; develop implementation guides; and define requirements to build large language models for extracting data.

The participant group will comprise researchers, clinicians, informatics/data scientists, patient advocates, standard-setting organizations (such as HL7/FHIR), policymakers, EHR vendors, and industry partners. Their collaborative efforts will focus on identifying current opportunities, challenges, and essential oncology-specific data requirements for the USCDI+ Cancer use cases (1) using real-world data to determine patient eligibility for clinical trials; (2) identifying immune-related adverse events; (3) enhancing the efficiency and timeliness of cancer registry data.

Details
Organizer
NCI
When
Wed, May 08 - Thu, May 09, 2024 -10:00 am - 5:00 pm
Where
NCI Shady Grove at 9609 Medical Center Drive, Rockville, MD 20850
Getting Started with scRNA-Seq Seminar Series

Description

This seminar provides an overview of differential expression testing workflows with Seurat.

This seminar provides an overview of differential expression testing workflows with Seurat.

Register
Organizer
BTEP
When
Wed, May 08, 2024 - 1:00 pm - 2:00 pm
Where
Online Webinar
Description

This one-hour session will introduce attendees to the world of Artificial Intelligence (AI) as we explore the fundamentals, applications, and ethical considerations of this transformative technology. Key topics will include machine learning, deep learning, data handling, and real-world AI applications across various industries. We'll delve into the ethical implications of AI and offer insights on how to become AI literate. Whether you're a seasoned professional or just starting your AI journey, this session will Read More

This one-hour session will introduce attendees to the world of Artificial Intelligence (AI) as we explore the fundamentals, applications, and ethical considerations of this transformative technology. Key topics will include machine learning, deep learning, data handling, and real-world AI applications across various industries. We'll delve into the ethical implications of AI and offer insights on how to become AI literate. Whether you're a seasoned professional or just starting your AI journey, this session will equip you with essential knowledge to navigate the AI landscape effectively and make informed decisions in our data-driven world.

Details
Organizer
NIH Library
When
Wed, May 08, 2024 - 1:00 pm - 2:00 pm
Where
Online
Description

This is the first class in the NIH Library Introduction to R Series. This class provides a basic overview of the functionality of R programming language and RStudio. R is a programming language and open source environment for statistical computing and graphics. The R class series is a comprehensive collection of training sessions offered by the NIH Library Data Services Read More

This is the first class in the NIH Library Introduction to R Series. This class provides a basic overview of the functionality of R programming language and RStudio. R is a programming language and open source environment for statistical computing and graphics. The R class series is a comprehensive collection of training sessions offered by the NIH Library Data Services and Bioinformatics programs that is designed to teach non-programmers how to write modular code and to introduce best practices for using R for data analysis and data visualization. Each class uses both evidence-based best practices for programming and practical hands-on lessons.

By the end of this class, students should be able to: list reasons for using R; describe the purpose of the RStudio Script, Console, Environment, and Plots panes; describe the various methods for finding help on R and RStudio; organize files and directories for a set of analyses as an R Project; define the following terms as they relate to R: object, assign, comment, call, function, and arguments; and assign values to objects in R.

Students are encouraged to install R and RStudio before the class so that they can follow along with the instructor. Please bring your laptop with R and RStudio installed.

Details
Organizer
NIH Library
When
Thu, May 09, 2024 - 11:00 am - 12:00 pm
Where
Online
Description

This in-person workshop will focus on data wrangling using tidy data principles. Tidy data describes a standard way of storing data that facilitates analysis and visualization within the tidyverse ecosystem. There will be a discussion of what makes data "tidy," and methods for reshaping your data using 

This in-person workshop will focus on data wrangling using tidy data principles. Tidy data describes a standard way of storing data that facilitates analysis and visualization within the tidyverse ecosystem. There will be a discussion of what makes data "tidy," and methods for reshaping your data using dplyr and tidyr functions. Prior to attending this class, you will need to have:

  • Installed R and RStudio
  • Taken the Introduction to R and RStudio class. If not, here are some resources for getting started:
  • Introduction to R
  • Introduction to RStudio
  • Introduction to Scripts in RStudio
  • By the end of this class, attendees will be able to demonstrate how to describe the purpose of the dplyr and tidyr packages, select certain columns in a data frame, select certain rows in a data frame according to filtering conditions, and add new columns to a data frame that are functions of existing columns.

    Note on Technology

    The NIH Library has 24 pre-configured Windows laptops that you are welcome to use during this training on a first come, first served basis. You are also welcome to bring your own laptop (PC or Mac). NIH Staff bringing their own NIH-laptop can easily connect to the staff Wi-Fi. If participants are bringing a personal laptop, they are restricted to using the NIH-Guest-Network Wi-Fi.

    Registrants will receive an email with information and instructions to install and verify access to R and RStudio before the class.  If you register the day before the class, you may not have time to download and properly install the necessary software. If you do not have the software installed, this training will be demo only.

    Details
    Organizer
    NIH Library
    When
    Mon, May 13, 2024 - 10:00 am - 12:00 pm
    Where
    Online
    Description

    Participants will learn how to develop artificial intelligence (AI) applications using MATLAB, even if they do not have a formal background in machine and deep learning. The goal of this course is to introduce tools and fundamental approaches for developing predictive models on biomedical signals. The course will cover the entire AI pipeline, from signal exploration to deployment, including: annotating time series biomedical signals automatically, creating deep learning models using Convolutional Neural Networks (CNNs) Read More

    Participants will learn how to develop artificial intelligence (AI) applications using MATLAB, even if they do not have a formal background in machine and deep learning. The goal of this course is to introduce tools and fundamental approaches for developing predictive models on biomedical signals. The course will cover the entire AI pipeline, from signal exploration to deployment, including: annotating time series biomedical signals automatically, creating deep learning models using Convolutional Neural Networks (CNNs) and Long Short-Term Memories (LSTMs) for biomedical signal data, creating machine learning models for biomedical signal data, applying advanced signal pre-processing techniques for automated feature extraction, and automatically generating code for edge deployment of AI models.

    This is an introductory level class. No installation of MATLAB is necessary.

    Details
    Organizer
    NIH Library
    When
    Tue, May 14, 2024 - 1:00 pm - 2:30 pm
    Where
    Online
    Description
    To register to attend, you must log in to your SITC Cancer Immunotherapy CONNECT account. Don’t have an account? Create a free one.

    Join Dr. Karchin of the Johns Hopkins School of Medicine and Dr. Krieg of the Medical University of South Carolina as they discuss the novel use of artificial intelligence (AI) in immunotherapy Read More

    To register to attend, you must log in to your SITC Cancer Immunotherapy CONNECT account. Don’t have an account? Create a free one.

    Join Dr. Karchin of the Johns Hopkins School of Medicine and Dr. Krieg of the Medical University of South Carolina as they discuss the novel use of artificial intelligence (AI) in immunotherapy target discovery.

    Attend this webinar to learn how:

    • AI advances could quickly improve clinical care.
    • you can use AI to better analyze large-scale data sets for biomarkers that can enhance immunotherapy research.

    This webinar is part of the 2024 SITC-NCI Computational Immuno-oncology Webinar Series, which focuses on the application of AI in immuno-oncology. This is the second of nine free webinars to help individual research labs overcome computational challenges while analyzing and integrating different assay data throughout the immuno-oncology spectrum using AI. The annual series aims to educate early-career scientists, increase participants’ awareness of and engagement in NCI-supported Cancer Moonshot℠ Immunotherapy Networks, and fulfill the Blue Ribbon Panel’s goal of accelerating progress in cancer research.

    Details
    Organizer
    CBIIT
    When
    Wed, May 15, 2024 - 12:00 pm - 1:00 pm
    Where
    Online
    Description

    Generalist repositories offer NIH researchers a flexible, trusted resource to share data for which there is no appropriate discipline specific repository as well as to share many other research outputs valuable for reproducibility and open science. This webinar, presented by participants of the NIH Generalist Repository Ecosystem Initiative (GREI) (Dataverse, Dryad, Figshare, Mendeley Data, Open Science Framework, Vivli, and Zenodo) will share generalist repository use cases and best practices for sharing and finding data Read More

    Generalist repositories offer NIH researchers a flexible, trusted resource to share data for which there is no appropriate discipline specific repository as well as to share many other research outputs valuable for reproducibility and open science. This webinar, presented by participants of the NIH Generalist Repository Ecosystem Initiative (GREI) (Dataverse, Dryad, Figshare, Mendeley Data, Open Science Framework, Vivli, and Zenodo) will share generalist repository use cases and best practices for sharing and finding data in generalist repositories. It will describe how generalist repositories fit into the NIH data repository landscape for intramural researchers and can be part of meeting the new NIH Data Management and Sharing Policy requirements. It will present both the key common features of generalist repositories that meet the NIH desirable repository characteristics as well as the unique features of these repositories that make them suited to specific types of data. 

    Details
    Organizer
    NIH Library
    When
    Wed, May 15, 2024 - 1:00 pm - 2:00 pm
    Where
    Online
    Description

    This course provides detailed information on managing and sharing data from the first data planning stage, through the data life cycle, to data archiving, and finally to selecting an appropriate repository for data preservation. By the end of this course, participants will have an understanding of data management best practices, data management tools, and resources that enable data sharing.

    This is an introductory two-part course for those who want to learn about Read More

    This course provides detailed information on managing and sharing data from the first data planning stage, through the data life cycle, to data archiving, and finally to selecting an appropriate repository for data preservation. By the end of this course, participants will have an understanding of data management best practices, data management tools, and resources that enable data sharing.

    This is an introductory two-part course for those who want to learn about research data management and sharing, or for those who are interested in a refresher. Part 1 of this training will cover understanding research data, how to manage research data, and how to work with data. Audience: Researchers, fellows, post-docs, and trainees. You must register separately for Part 2 of this class.

    Details
    Organizer
    NIH Library
    When
    Thu, May 16, 2024 - 12:00 pm - 1:00 pm
    Where
    Online
    Description

    Qiagen CLC Genomics Workbench is a point-and-click bioinformatics software that runs on a personal computer and enables bulk RNA sequencing, ChIP sequencing, long reads, and variant analysis. This software is available to NCI scientists.

    This hands-on training will guide participants through bulk RNA sequencing analysis using CLC Genomics Workbench. After the class, participants will be able to

    • Import files and illumina reads
    • Import and associate metadata with Read More

    Qiagen CLC Genomics Workbench is a point-and-click bioinformatics software that runs on a personal computer and enables bulk RNA sequencing, ChIP sequencing, long reads, and variant analysis. This software is available to NCI scientists.

    This hands-on training will guide participants through bulk RNA sequencing analysis using CLC Genomics Workbench. After the class, participants will be able to

    • Import files and illumina reads
    • Import and associate metadata with samples
    • Download reference genome and annotation
    • Obtain RNA sequencing expression counts and perform differential expression analysis
    • Construct PCA and heatmap to visualize RNA sequencing data

     

    To get the most of this hands-on session, please reach out to the NCI service desk (https://service.cancer.gov/ncisp) to get this software installed, preview the tutorial (https://resources.qiagenbioinformatics.com/tutorials/RNASeq-droso.pdf), and download the example dataset (http://resources.qiagenbioinformatics.com/testdata/RNA_Seq_Droso2.zip) prior to attending.

    Meeting link:
    https://cbiit.webex.com/cbiit/j.php?MTID=m07f826d16b67d3c3b8a86e275ebac5a5
    Meeting number:
    2300 281 6121
    Password:
    e7aEqhpy@34

    Join by video system
    Dial 23002816121@cbiit.webex.com
    You can also dial 173.243.2.68 and enter your meeting number.

    Join by phone
    1-650-479-3207 Call-in number (US/Canada)
    Access code: 2300 281 6121

    Register
    When
    Thu, May 16, 2024 - 1:00 pm - 2:30 pm
    Where
    Online Webinar
    Description

    The NIH Artificial Intelligence (AI) Symposium will take place on Friday, May 17th, 2024, in Masur Auditorium in Building 10 on the Bethesda NIH campus. This event is open to all NIH members - registration and abstract submission are now open https://forms.microsoft.com/g/4WpdBXcEu6

    Biomedical science is in a technological revolution, driven by innovations in deep learning architecture and computational power. These Read More

    The NIH Artificial Intelligence (AI) Symposium will take place on Friday, May 17th, 2024, in Masur Auditorium in Building 10 on the Bethesda NIH campus. This event is open to all NIH members - registration and abstract submission are now open https://forms.microsoft.com/g/4WpdBXcEu6

    Biomedical science is in a technological revolution, driven by innovations in deep learning architecture and computational power. These cutting-edge techniques are being applied to every sub-field of the biological sciences, and with ground-breaking advancements arriving constantly it is challenging for researchers to stay up to speed on what is possible. This one-day NIH AI Symposium will bring together researchers from a broad range of disciplines to share their AI-related research, with the goal of disseminating the newest AI research, providing an opportunity to network, and to cross-pollinate ideas across disciplines in order to advance AI research in biomedicine.

    Keynote speakers James Zou, Ph.D. (Stanford University) and Hari Shroff, Ph.D. (Janelia Research Campus) will share their research, and also participate in a Panel Discussion on the current and future potential of AI in biomedical sciences. There will also be short talks and posters from researchers on campus who are developing or using AI approaches.

    The NIH AI Symposium is sponsored by NHLBI, in partnership with FAES. Registration and abstract submission are open to all NIH members, including experts in AI-related fields and novices interested in gaining more exposure.

    Important dates:

    March 15th - Abstract submission deadline

    April 5th - Abstract notifications

    May 3rd – Registration deadline

    Sign language interpreting and CART services are available upon request to participate in this event. Individuals needing either of these services and/or other reasonable accommodations should contact Ryan O’Neill (oneillrs@nih.gov).

    Questions can be directed to Lead Organizer Ryan O’Neill, Ph.D. (oneillrs@nih.gov).

    Details
    Organizer
    NHLBI
    When
    Fri, May 17, 2024 - 9:00 am - 5:30 pm
    Where
    Main NIH Campus, Building 10 (Clinical Center); Masur Auditorium
    Description

    This course provides detailed information on managing and sharing data from the first data planning stage, through the data life cycle, to data archiving, and finally to selecting an appropriate repository for data preservation. By the end of this course, participants will have an understanding of data management best practices, data management tools, and resources that enable data sharing.

    This is an introductory two-part course for those who want to learn about Read More

    This course provides detailed information on managing and sharing data from the first data planning stage, through the data life cycle, to data archiving, and finally to selecting an appropriate repository for data preservation. By the end of this course, participants will have an understanding of data management best practices, data management tools, and resources that enable data sharing.

    This is an introductory two-part course for those who want to learn about research data management and sharing, or for those who are interested in a refresher. During Part 2 of this training, participants will learn about sharing and archiving data. Audience: Researchers, fellows, post-docs, and trainees. You must register separately for Part 1 of this class.

    Details
    Organizer
    NIH Library
    When
    Fri, May 17, 2024 - 12:00 pm - 1:00 pm
    Where
    Online
    Description

    Hybrid (in-person location in Rockville, MD)

    Virtual attending via WebEx Meeting, link will be available two weeks prior to the meeting date.

    Attend the 2024 Co-Clinical Imaging Research Resource Program (CIRP) Annual Hybrid Meeting to learn about optimized quantitative imaging methods in cancer research and precision oncology. Register Read More

    Hybrid (in-person location in Rockville, MD)

    Virtual attending via WebEx Meeting, link will be available two weeks prior to the meeting date.

    Attend the 2024 Co-Clinical Imaging Research Resource Program (CIRP) Annual Hybrid Meeting to learn about optimized quantitative imaging methods in cancer research and precision oncology. Register by 11:00 p.m. ET, May 6.

    You’ll hear from presenters about optimizing quantitative imaging methods to improve the quality of imaging results for co-clinical cancer trials. You’ll also learn about applications of co-clinical imaging to precision oncology.

    There will be poster presentations, demonstrations, and discussions.

    The CIRP network is a joint effort of the Cancer Imaging Program at the Division of Cancer Treatment and Diagnosis, the Division of Cancer Biology, and the Division of Cancer Prevention. CIRP’s mission is to advance precision medicine by establishing best practices for co-clinical imaging. CIRP also seeks to develop optimized translational quantitative imaging methodologies to advance cancer research and treatment.

    Details
    Organizer
    CBIIT
    When
    Mon, May 20 - Tue, May 21, 2024 -9:00 am - 4:00 pm
    Where
    9609 Medical Center Drive, Rockville, MD, 20850
    Description

    Are you attending the 2024 AMIA Clinical Informatics Conference? Join NCI Fellow, Austin Fitts, as he presents on the National Childhood Cancer Registry (NCCR) during the May 22 afternoon sessions. The NCCR links cancer registry data with harmonized real-world Read More

    Are you attending the 2024 AMIA Clinical Informatics Conference? Join NCI Fellow, Austin Fitts, as he presents on the National Childhood Cancer Registry (NCCR) during the May 22 afternoon sessions. The NCCR links cancer registry data with harmonized real-world data for population-level research in childhood cancer. He will also share how NCCR’s harmonization process allows for more longitudinal studies and can serve as a model for similar data harmonization initiatives. There are future plans to publish the NCCR data model and make an initial harmonized data set available to the cancer research community through the upcoming NCCR Data Platform.

    Session Title: Advancing the Usability of Healthcare Data


    Austin Fitts, Pharm.D., is a post-doctoral fellow at NCI’s Surveillance Research Program. He completed his Doctor of Pharmacy degree from University of Mississippi School of Pharmacy in 2021. Dr. Fitts completed residencies in hospital pharmacy at North Mississippi Medical Center and pharmacy informatics at Vanderbilt University Medical Center. His current professional interests include pharmacy informatics, pediatric oncology, and pharmacoepidemiology.

    Details
    Organizer
    CBIIT
    When
    Wed, May 22, 2024 - 4:00 pm - 5:00 pm
    Where
    Online
    Distinguished Speakers Seminar Series

    Description

    An exciting opportunity at the intersection of the biomedical sciences and machine learning stems from the growing availability of large-scale multi-modal data (imaging-based and sequencing-based, observational and perturbational, at the single-cell level, tissue-level, and organism-level). Traditional representation learning methods, although often highly successful in predictive tasks, do not generally elucidate underlying causal mechanisms. Dr. Uhler will present initial ideas towards building a statistical and computational framework for causal representation learning and its applications towards Read More

    An exciting opportunity at the intersection of the biomedical sciences and machine learning stems from the growing availability of large-scale multi-modal data (imaging-based and sequencing-based, observational and perturbational, at the single-cell level, tissue-level, and organism-level). Traditional representation learning methods, although often highly successful in predictive tasks, do not generally elucidate underlying causal mechanisms. Dr. Uhler will present initial ideas towards building a statistical and computational framework for causal representation learning and its applications towards identifying novel disease biomarkers as well as inferring gene regulation in health and disease.

    Alternative Meeting Information: Meeting number: 2312 523 4308 Password: rgE4DbPX$65 Join by video system Dial 23125234308@cbiit.webex.com You can also dial 173.243.2.68 and enter your meeting number. Join by phone 1-650-479-3207 Call-in number (US/Canada) Access code: 2312 523 4308  
    Register
    Organizer
    BTEP
    When
    Thu, May 23, 2024 - 1:00 pm - 2:00 pm
    Where
    Online Webinar
    Description

    NCI is launching the virtual Cancer AI Conversations series featuring multiple perspectives on timely topics and themes in artificial intelligence for cancer research! 

    Each event features short talks from 2-4 subject matter experts offering diverse views on the session topic. These talks will be followed by a moderated panel discussion.

    “Cancer AI Conversations” are bimonthly, 1-hour virtual events featuring timely topics related to the application Read More

    NCI is launching the virtual Cancer AI Conversations series featuring multiple perspectives on timely topics and themes in artificial intelligence for cancer research! 

    Each event features short talks from 2-4 subject matter experts offering diverse views on the session topic. These talks will be followed by a moderated panel discussion.

    “Cancer AI Conversations” are bimonthly, 1-hour virtual events featuring timely topics related to the application of artificial intelligence in cancer research. Each event features short talks from 2-4 subject matter experts offering diverse perspectives on the session topic. 

    All of the Cancer AI Conversations will be recorded and posted for future viewing.

    Details
    Organizer
    NCI
    When
    Tue, May 28, 2024 - 11:00 am - 12:00 pm
    Where
    Online
    Description

    This 90-minute course equips participants with essential knowledge and skills for effective interactions with Large Language Models (LLMs), such as ChatGPT. Explore the intricacies of prompt engineering and its pivotal role in optimizing the conversational capabilities of LLMs. Emphasizing best practices and practical applications, this course features live demonstrations and group discussion, and provides valuable skills for the effective use of LLMs. Attendees are encouraged to 

    This 90-minute course equips participants with essential knowledge and skills for effective interactions with Large Language Models (LLMs), such as ChatGPT. Explore the intricacies of prompt engineering and its pivotal role in optimizing the conversational capabilities of LLMs. Emphasizing best practices and practical applications, this course features live demonstrations and group discussion, and provides valuable skills for the effective use of LLMs. Attendees are encouraged to register for a free ChatGPT account prior to taking this class. 

    Details
    Organizer
    NIH Library
    When
    Thu, May 30, 2024 - 12:00 pm - 1:30 pm
    Where
    Online

    June

    Distinguished Speakers Seminar Series

    Description

    The Brooks Lab developed a computational tool called FLAIR (Full-Length Alternative Isoform Analysis of RNA) to produce confident transcript isoforms from long-read RNA-seq data with the aim of alternative isoform detection and quantification. With an increase in the usage of long-read RNA-seq, there is a growing need for a systematic evaluation of this approach. We are part of an international community effort called the Long-read RNA-seq Genome Annotation Assessment Project (LRGASP) to perform such Read More

    The Brooks Lab developed a computational tool called FLAIR (Full-Length Alternative Isoform Analysis of RNA) to produce confident transcript isoforms from long-read RNA-seq data with the aim of alternative isoform detection and quantification. With an increase in the usage of long-read RNA-seq, there is a growing need for a systematic evaluation of this approach. We are part of an international community effort called the Long-read RNA-seq Genome Annotation Assessment Project (LRGASP) to perform such an evaluation. The Brooks Lab is extending FLAIR to incorporate sequence variation, RNA editing, and RNA modification in isoform detection as well as detection of complex gene fusions from long-read sequencing data.

      Meeting number: 2311 656 4503 Password: ySkM7uW6B$5 Join by video system Dial 23116564503@cbiit.webex.com You can also dial 173.243.2.68 and enter your meeting number. Join by phone 1-650-479-3207 Call-in number (US/Canada) Access code: 2311 656 4503  
    Register
    Organizer
    BTEP
    When
    Thu, Jun 06, 2024 - 1:00 pm - 2:00 pm
    Where
    Online Webinar
    Distinguished Speakers Seminar Series

    Description
    Dr. Irizarry will share findings demonstrating limitations of current
    workflows that are popular in single cell RNA-Seq data analysis.
    Specifically, he will describe challenges and solutions to dimension
    reduction, cell-type classification, and statistical significance
    analysis of clustering. Dr. Irizarry will end the talk describing some of his
    work related to spatial transcriptomics. Specifically, he will describe
    approaches to cell type annotation that account for presence of
    multiple cell-types Read More
    Dr. Irizarry will share findings demonstrating limitations of current
    workflows that are popular in single cell RNA-Seq data analysis.
    Specifically, he will describe challenges and solutions to dimension
    reduction, cell-type classification, and statistical significance
    analysis of clustering. Dr. Irizarry will end the talk describing some of his
    work related to spatial transcriptomics. Specifically, he will describe
    approaches to cell type annotation that account for presence of
    multiple cell-types represented in the measurements, a common
    occurrence with technologies such as Visium and SlideSeq. He will
    demonstrate how this approach facilitates the discovery of spatially
    varying genes. Meeting link: https://cbiit.webex.com/cbiit/j.php?MTID=m9dcd9ce21f4fa6b1a8e2d998a88c2c2b    Meeting number: 2317 712 9095 Password: gUKZzp3u76? Join by video system Dial 23177129095@cbiit.webex.com You can also dial 173.243.2.68 and enter your meeting number. Join by phone 1-650-479-3207 Call-in number (US/Canada) Access code: 2317 712 9095  
    Register
    Organizer
    BTEP
    When
    Thu, Jun 20, 2024 - 1:00 pm - 2:00 pm
    Where
    Online Webinar
    AI in Biomedical Research @ NIH Seminar Series

    Description

    CARD is a collaborative initiative of the National Institute on Aging and the National Institute of Neurological Disorders and Stroke that supports basic, translational, and clinical research on Alzheimer’s disease and related dementias. CARD’s central mission is to initiate, stimulate, accelerate, and support research that will lead to the development of improved treatments and preventions for these diseases.

    Alternative Meeting Information:  Meeting number: 2310 497 7985 Password: mjPjjmi$473 Join by video Read More

    CARD is a collaborative initiative of the National Institute on Aging and the National Institute of Neurological Disorders and Stroke that supports basic, translational, and clinical research on Alzheimer’s disease and related dementias. CARD’s central mission is to initiate, stimulate, accelerate, and support research that will lead to the development of improved treatments and preventions for these diseases.

    Alternative Meeting Information:  Meeting number: 2310 497 7985 Password: mjPjjmi$473 Join by video system Dial 23104977985@cbiit.webex.com You can also dial 173.243.2.68 and enter your meeting number. Join by phone 1-650-479-3207 Call-in number (US/Canada) Access code: 2310 497 7985  
    Register
    Organizer
    BTEP
    When
    Thu, Jun 27, 2024 - 1:00 pm - 2:00 pm
    Where
    Online Webinar