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Dear all,
we have the last places available for our course on "Comparative Genomics" (1-5 October 2018) at the Freie Universität Berlin, Königin-Luise-Straße 6-8, Berlin (Germany).
Application deadline is September 5th, 2018. Attendees are seated on a first-come, first-served basis.
Our instructors are :
Dr Fritz J. Sedlazeck (https://fritzsedlazeck.github.io/)
Prof. Dr. Ingo Ebersberger (https://scholar.google.com/citations...3kYAAAAJ&hl=en)
Course overview
This course will introduce biologists and bioinformaticians into the field of comparative genomics. Different techniques will be introduced to identify single nucleotide polymorphism (SNP) and structural variations (SVs) as well as the annotation of these variations and the assessment for their functional impact.
TARGETED AUDIENCE & ASSUMED BACKGROUND
The course is aimed at researchers interested in learning how to compare genomes and what can be learned from genomic similarities as well as variations. It will include information useful for both beginners and more advanced users. We will start by introducing general concepts of comparative genomics. On this basis, we will then continue to describe all major analysis steps from the raw sequencing data via the identification of variations to an assessment of their impact on the phenotype.
Attendees should have a background in biology. There will be a mix of lectures and hands-on practical exercises using command line Linux. We will therefore dedicate one session to introduce basic and advanced Linux concepts for processing data on Amazon cloud (AWS). Attendees should have also some familiarity with genomic data such as that arising from NGS sequencing experiments.
LEARNING OUTCOMES
Identification of SNPs and SVs using de novo genome assembly and read mapping strategies
Assessment of strengths and weaknesses of the different DNA sequencing technologies, Illumina, Pacific Bioscience, Oxford Nanopore, for the detection of variations
Strengths and pitfalls of de novo assembly and mapping approaches for comparative genomics
Hands on experience of state of the art methods to compare multiple genomes
Annotation of variations and comparative genomics analysis
For more information about the course, please visit our website: https://www.physalia-courses.org/cou...hops/course34/
Here is the full list of our courses and Workshops: https://www.physalia-courses.org/courses-workshops/
Best regards,
Carlo
--------------------
Carlo Pecoraro, Ph.D
Physalia-courses DIRECTOR
[email protected]
Twitter: @physacourses
mobile: +49 15771084054
we have the last places available for our course on "Comparative Genomics" (1-5 October 2018) at the Freie Universität Berlin, Königin-Luise-Straße 6-8, Berlin (Germany).
Application deadline is September 5th, 2018. Attendees are seated on a first-come, first-served basis.
Our instructors are :
Dr Fritz J. Sedlazeck (https://fritzsedlazeck.github.io/)
Prof. Dr. Ingo Ebersberger (https://scholar.google.com/citations...3kYAAAAJ&hl=en)
Course overview
This course will introduce biologists and bioinformaticians into the field of comparative genomics. Different techniques will be introduced to identify single nucleotide polymorphism (SNP) and structural variations (SVs) as well as the annotation of these variations and the assessment for their functional impact.
TARGETED AUDIENCE & ASSUMED BACKGROUND
The course is aimed at researchers interested in learning how to compare genomes and what can be learned from genomic similarities as well as variations. It will include information useful for both beginners and more advanced users. We will start by introducing general concepts of comparative genomics. On this basis, we will then continue to describe all major analysis steps from the raw sequencing data via the identification of variations to an assessment of their impact on the phenotype.
Attendees should have a background in biology. There will be a mix of lectures and hands-on practical exercises using command line Linux. We will therefore dedicate one session to introduce basic and advanced Linux concepts for processing data on Amazon cloud (AWS). Attendees should have also some familiarity with genomic data such as that arising from NGS sequencing experiments.
LEARNING OUTCOMES
Identification of SNPs and SVs using de novo genome assembly and read mapping strategies
Assessment of strengths and weaknesses of the different DNA sequencing technologies, Illumina, Pacific Bioscience, Oxford Nanopore, for the detection of variations
Strengths and pitfalls of de novo assembly and mapping approaches for comparative genomics
Hands on experience of state of the art methods to compare multiple genomes
Annotation of variations and comparative genomics analysis
For more information about the course, please visit our website: https://www.physalia-courses.org/cou...hops/course34/
Here is the full list of our courses and Workshops: https://www.physalia-courses.org/courses-workshops/
Best regards,
Carlo
--------------------
Carlo Pecoraro, Ph.D
Physalia-courses DIRECTOR
[email protected]
Twitter: @physacourses
mobile: +49 15771084054
