Population genomics in practice
Date: 16 September 2024
Timezone: Stockholm
Course content
The aim of this workshop is to provide an introduction to commonly used methods in population genomics. As the focus of the course is on hands-on work, the topics have been designed to cover the fundamental analyses that are common in many population genomics studies. The course consists of lectures and exercises, with a focus on the practical aspects of analyses. Whereas lectures introduce some background theory, their primary aim is to set the stage for accompanying exercises.
Important dates and information
Application opens: 2024-09-09
Application closes: 2024-10-15
Confirmation to accepted students: 2024-10-30
Course fee
A course fee* of 3000 SEK for academic participants and 15000 SEK for non-academic participants will be invoiced to accepted participants. The fee includes lunches, coffee and snacks.
*Please note that NBIS cannot invoice individuals
Topics covered will include:
- Foundations of population genetics
- Introduction to simulation and the coalescent
- Basics of variant calling
- Variant filtering and sequence masks
- Characterization and interpretation of DNA sequence variation
- Calculation and interpretation of summary statistics from variation data
- Investigating population structure with admixture modelling and principal component analyses
- Demographic modelling using sequentially Markovian coalescent models and linkage disequilibrium
- Selection scans
Due to limited space the course can accommodate a maximum of 25 participants. If we receive more applications, participants will be selected based on selection criteria, including (but not limited to) correct entry requirements, motivation to attend the course, as well as gender and geographical balance.
Contact: The course is instructed by: Per Unneberg (CL), André Soares (CL), Nikolay Oskolkov, Jason Hill In case you miss information on any of the above dates, please contact: edu.population-genomics-in-practice@nbis.se
Keywords: genomics, bioinformatics
Venue: SciLifeLab Uppsala, Navet BMC, Husaregatan 3
City: Uppsala
Country: Sweden
Prerequisites:
The following is a list of skills required for being able to follow the course and complete the exercises:
- Basic knowledge in R or Python
- Basic knowledge of variant calling, or the equivalent of NBIS course “Introduction to Bioinformatics using NGS data”
- Basic knowledge of population genetics
- Basic understanding of frequentist statistics
- A computer
Desirable, but not essential, skills increasing the output of the course, include:
- Experience with analysis of NGS and other omic data
Learning objectives:
Upon completion of this course, you will be able to:
- describe the different forces of evolution and how they influence genetic variation
- understand and interpret genealogical trees and how they relate to genetic variation data
- describe the basics of the coalescent
- perform simple coalescent simulations with msprime
- run simple SLiM forward simulation models
- describe and run the steps of a variant calling pipeline, including quality control of raw reads, read mapping, and - variant calling
- know how and when to filter raw variant calls using manual coverage filters
- describe and calculate nucleotide diversity from variation data
- analyse population structure with admixture modelling and dimensionality reduction methods
- perform demographic modelling with sequential Markovian coalescent models
- describe methods that identify regions undergoing adaptation and selection
- run selection scans, score identified regions and interpret findings in the context of genome annotations
Target audience: postdocs, PhD Students, group leaders, industry professionals, healthcare professionals, everyone
Event types:
- Workshops and courses
Activity log
