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2019 Edition

JUNE 24-28, 2019, Château’form Seine-Port (77)

The programme will cover statistical methodologies and bioinformatics tools used in genomics and metagenomics in the context of a comprehensive approach to pathological mechanisms.
The course will include lectures by guest speakers as well as hands-on computer sessions* with experts in the field.

Program - Summer School 2019

Conferences

Mihai POP, Professor, Department of Computer Science
Director, Institute for Advanced Computer Studies (UMIACS)
Title To Be confirmed (topic on metagenomics in human health and disease)

Marco Antonio MENDOZA-PARA, team leader, Genoscope - Centre National de Séquençage · Laboratory of Synthetic and Systems Biology LISSB
Title : Quality Control Assessment of ChIP-Seq and Related Deep Sequencing-Generated Datasets

Practical sessions

Generation and analysis of data

Nicolas WIART CNRGH, CEA
→ "Workflow optimisation and data analysis on HPC facilities"

Valentin LOUX, INRA,
→ “Quality control, alignment and variant calling”

Variation in the human genome (SNPs, CNV...)
Vincent MEYER, Lilia MESROB and Florian SANDRON, CNRGH, CEA
→ Content on Whole Exome/Genome Sequencing as a strategy to identify the genetic bases of common Mendelian disorders and rare diseases.

Statistical methods (1)
Christophe AMBROISE, Université d’Evry-Val d’Essonne
Guillem RIGAILL, Inra Université d’Evry Val d’Essonne
→ Transcriptome / RNA-Seq analysis (Whole Transcriptome Sequencing) : quantification and differential expression
→ How to choose the appropriate statistical methodologies : detecting bias and troubleshoots and interpreting statistical results
→ Statistical inference /hypothesis testing
→ Quantitative genetics

Strategies for metagenomics

Katarzyna HOOKS, Université de Bordeaux , CNRS UMR 5800,
→ bioinformatic tools for the study of microbial communities in the scope of human health
Outcome of this session : After this workshop you will be able to : find a suitable tool to analyse the metagenomic sequencing, extract publicly available data from repositories (e.g. EBI Metagenomic), analyse and visualise it using web-based resources.

Visualization of genomics data
Andrei ZINOVYEV, Inserm U900-Institut Curie
→ Network-based visualization of genomics data
After this session, students will master using several popular platforms for network-based visualization of genomics data : Cytoscape, NaviCell, MINERVA. The students will be able to visualize a transcriptomic, proteomic, mutational, copy-number profile on an existing biological network (for example, from Atlas of Cancer Signaling Network), or to construct an ad hoc biological network from a pathway database, and use it for data visualization.

Transcriptomics
Fariza TAHI, Université d’Evry-Val d’Essonne
→ RNA secondary structure prediction and identification and prediction of ncRNAs in large-scale genomic sequences

Sponsors & Partners

GenMEd UPS - investissement Avenir France Genomique    
 
 
Ile de France IFB INRA CNRS Institut Curie