From 7e49c006af9c4f7453c3578a7d4f1fc4d7bdf3ed Mon Sep 17 00:00:00 2001 From: Arthur Centeno Date: Tue, 15 Jun 2021 15:27:18 +0000 Subject: Adding new content to tutorials.html --- wqflask/wqflask/templates/tutorials.html | 572 ++++++++++++++++++++++++++++++- 1 file changed, 560 insertions(+), 12 deletions(-) (limited to 'wqflask') diff --git a/wqflask/wqflask/templates/tutorials.html b/wqflask/wqflask/templates/tutorials.html index ce5d0e3d..04eddfa4 100644 --- a/wqflask/wqflask/templates/tutorials.html +++ b/wqflask/wqflask/templates/tutorials.html @@ -2,18 +2,566 @@ {% block title %}Tutorials/Primers{% endblock %} {% block content %} -
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The NIDA Center of Excellence in Omics, Systems Genetics, and the Addictome has put together a webinar series, Quantitative Genetics Tools for Mapping Trait Variation to Mechanisms, Therapeutics, and Interventions. The goal of this series is to transverse the path from trait variance to QTL to gene variant to molecular networks to mechanisms to therapeutic and interventions. The target audience for this series are those new to the field of quantitative genetics, so please pass this information on to your trainees or colleagues.
+ +Title/Description | +Presentation | +
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Webinar #01 - Introduction to Quantitative Trait Loci (QTL) Analysis+Friday, May 8th, 2020 Goals of this webinar (trait variance to QTL): +
Presented by: |
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Webinar #02 - Mapping Addiction and Behavioral Traits and Getting at Causal Gene Variants with GeneNetwork+Friday, May 22nd. 2020 + 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT + +Goals of this webinar (QTL to gene variant): +
Presented by: |
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Webinar #03 - Introduction to expression (e)QTL and their role in connecting QTL to genes and molecular networks+Friday, June 12, 2020 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT + + Goals of this webinar (QTL to gene/molecular networks): +
Presented by: |
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Webinar #04 - From Candidate Genes to Causal Variants—Strategies for and Examples of Identifying Genes and Sequence Variants in Rodent Populations+Friday, June 26, 2020 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT + + Goals of this webinar (candidate genes to causal variants): +
Presented by:
+Link to course material |
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Webinar #05 - Identifying genes from QTL using RNA expression and the PhenoGen website (http://phenogen.org)+Friday, August 28, 2020 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar (candidate genes to causal variants): + Demonstrate how to use the PhenoGen website to identify transcripts: +
Presented by: |
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Webinar #06 - Sex as a Biological Covariate in QTL Studies+Friday, September 11th, 2020 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar (trait variance to QTL): + +
Presented by: |
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Webinar #07 - Introduction to Weighted Gene Co-expression Network Analysis+Friday, September 25th at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar (molecular networks): +
Background reading available at: http://bit.ly/osga_wgcna +Presented by: |
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Webinar #08 - Using genetic and non-genetic covariates in QTL studies+Friday, October 9th at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar (quantitative trait to genetic loci): +
Presented by: |
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Webinar #09 - Introduction to GeneWeaver: Integrating and analyzing heterogeneous functional genomics data+Friday, October 23th at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar: +
Presented by:
+Dr. Erich Baker |
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Webinar #10 - Sketching alternate realities: An introduction to causal inference in genetic studies+Friday, November 20th at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar: + Determination of cause is an important goal of biological studies, and genetic studies provide unique opportunities. In this introductory lecture we will frame causal inference as a missing data problem to clarify challenges, assumptions, and strategies necessary for assigning cause. We will survey the use of directed acyclic graphs (DAGs) to express causal information and to guide analytic strategies. +
Presented by: |
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Webinar #11 - Beginner's guide to bulk RNA-Seq analysis+Friday, February 12th, 2021 at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar: + The use of high throughput short read RNA sequencing has become common place in many scientific laboratories. The analysis tools for quantitating a transcriptome have matured becoming relatively simple to use. The goals of this webinar are: +
Presented by: This webinar series is sponsored by the NIDA Center of Excellence in Omics, Systems Genetics, and the Addictome (P30 DA044223) and the NIAAA-funded PhenoGen Website (R24 AA013162). + |
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Webinar #12 - From GWAS to gene: What are the essential analyses and how do we bring them together using heterogeneous stock rats?+Friday, February 26th at 10am PST/ 11am MST/ 12pm CST/ 1pm EST Goals of this webinar: + Heterogeneous stock (HS) rats are an outbred population that was created in 1984 by intercrossing 8 inbred strains. The Center for GWAS in Outbred Rats (www.ratgenes.org) has developed a suite of analysis tools for analyzing genome wide association studies (GWAS) in HS rats +
Presented by: Link to course material in pptx: Palmer_talk_2-26-21.pptx + +This webinar series is sponsored by the NIDA Center of Excellence in Omics, Systems Genetics, and the Addictome (P30 DA044223) and the NIDA-funded Center for GWAS in Outbred Rats (P50 DA037844). + |
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Webinar #13 - Become a UseR: A brief tour of R+Friday, March 12th at 10am PST/ 11am MST/ 12pm CST/ 1pm EST We will introduce R programming language and outline the benefits of learning R. We will give a brief tour of basic concepts and tasks: variables, objects, functions, basic statistics, visualization, and data import/export. We will showcase a practical example demonstrating statistical analysis. + + Goals of this webinar: +
Presented by: |
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Webinar #14 - Landing on Jupyter: A guided tour of interactive notebooks+Friday, March 26th at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Jupyter is an interactive interface to data science and scientific computing across a variety of programming languages. We will present the Jupyter notebook, and explain some key concepts (e.g., kernel, cells). We will show how to create a new notebook; modify an existing notebook; save, export, and publish a notebook. We will discuss several possible use cases: developing code, writing reports, taking notes, and teaching/presenting. + + Goals of this webinar: +
Presented by: |
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Webinar #15 – Introduction to Metabolomics Platforms and Data Analysis+Friday, April 9th at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar: + The use of metabolomics to profile small molecules is now widespread in biomedical research. The goals of this webinar are: +
Presented by: |
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Webinar #16 – Introduction to the Hybrid Rat Diversity Panel: A renewable rat panel for genetic studies of addiction-related traits+Friday, April 23rd at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar: + The Hybrid Rat Diversity Panel (HRDP) is an inbred panel of rats that included two recombinant inbred panels and a panel of classic inbred strains. +
Presented by:
+Dr. Laura Saba | + |
Webinar #17 – Identifying sample mix-ups in eQTL data+Friday, June 11th at 10am PDT/ 11am MDT/ 12pm CDT/ 1pm EDT Goals of this webinar: + Sample mix-ups interfere with our ability to detect genotype-phenotype associations. However, the presence of numerous eQTL with strong effects provides the opportunity to not just identify sample mix-ups, but also to correct them. +
Presented by: + + +Link to course material:kbroman.org/Talk_OSGA2021 + + + |
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Bonus 1 - Data structure, disease risk, GXE, and causal modeling+Friday, November 20th at 9am PDT/ 11pm CDT/ 12pm EDT Human disease is mainly due to complex interactions between genetic and environmental factors (GXE). We need to acquire the right "smart" data types—coherent and multiplicative data—required to make accurate predictions about risk and outcome for n = 1 individuals—a daunting task. We have developed large families of fully sequenced mice that mirror the genetic complexity of humans. We are using these Reference Populations to generate multiplicatively useful data and to build and test causal quantitative models of disease mechanisms with a special focus on diseases of aging, addiction, and neurological and psychiatric disease. + + Speaker Bio: Robert (Rob) W. Williams received a BA in neuroscience from UC Santa Cruz (1975) and a Ph.D. in system physiology at UC Davis with Leo M. Chalupa (1983). He did postdoctoral work in developmental neurobiology at Yale School of Medicine with Pasko Rakic where he developed novel stereological methods to estimate cell populations in brain. In 2013 Williams established the Department of Genetics, Genomics and Informatics at UTHSC. He holds the UT Oak Ridge National Laboratory Governor’s Chair in Computational Genomics. Williams is director of the Complex Trait Community (www.complextrait.org) and editor-in-chief of Frontiers in Neurogenomics. One of Williams’ more notable contributions is in the field of systems neurogenetics and experimental precision medicine. He and his research collaborators have built GeneNetwork (www.genenetwork.org), an online resource of data and analysis code that is used as a platform for experimental precision medicine. + +Presented by: |
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