20 June 2012
New York, United States of AmericaTranslational Control http://meetings.cshl.edu/meetings/transc12.shtml https://tess.elixir-europe.org/events/translational-control 2012-06-20 16:32:54 UTC 2012-06-20 16:32:54 UTC Cold Spring Harbor Laboratory Cold Spring Harbor Laboratory, New York, United States of America Cold Spring Harbor Laboratory New York United States of America    meetings_and_conferences  Viruses&CellSignalingCancer&DiseasesmiRNAs
RNA-Seq Data Analysis Using Galaxy
26 May 2016
Sydney, AustraliaRNA-Seq Data Analysis Using Galaxy http://www.bioplatforms.com/rna-seq-using-galaxy-may-2016/ https://tess.elixir-europe.org/events/rna-seq-data-analysis-using-galaxy RNA-Seq Analysis Using Galaxy is a one-day, workshop that introduces the concepts of RNA-Seq analysis. This workshop provides hands-on experience with RNA-Seq data preparation, statistical testing for differential gene expression, identifying novel transcription features and generating graphical summaries of RNA-Seq data. The workshop will focus on the use of Galaxy, a platform that provides a simple and user-friendly interface to bioinformatics tools, and will also feature an introduction to the R environment used widely by bioinformaticians. 2016-05-26 09:00:00 UTC 2016-05-26 00:00:00 UTC Children’s Medical Research Institute Children’s Medical Research Institute, Westmead, Sydney, Australia Children’s Medical Research Institute, Westmead Sydney Australia Data architecture, analysis and design RNA-Seq    workshops_and_courses  BPAABRGalaxy
Variant Detection Using Galaxy
27 May 2016
Sydney, AustraliaVariant Detection Using Galaxy http://www.bioplatforms.com/variant-detection-using-galaxy-may-2016/ https://tess.elixir-europe.org/events/variant-detection-using-galaxy Variant Detection using Galaxy is a one-day, hands-on workshop that will cover the concepts of detecting small variants, including SNPs and small indels, from next-generation sequencing data. You will use and compare a number of popular detection tools, visualise variants using a genome browser, and annotate SNPs for predicting biological effects. Course Outline -During this course you will learn about; -The tool and workflows of SNP and indel detection -Quality filtering and other techniques for improving SNP prediction accuracy -Comparison of variant detection software -the use of the Galaxy platform for variant detection analysis 2016-05-27 09:00:00 UTC 2016-05-27 00:00:00 UTC Children’s Medical Research Institute Children’s Medical Research Institute, Sydney, Australia Children’s Medical Research Institute Sydney Australia Data architecture, analysis and design    workshops_and_courses  ABRBPAGalaxyvariantcalling
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