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  • High-thoughput Omics & Data Integration Workshop

    14 - 16 February 2013

    Barcelona, Spain

    High-thoughput Omics & Data Integration Workshop https://tess.elixir-europe.org/events/high-thoughput-omics-data-integration-workshop 2013-02-14 00:00:00 UTC 2013-02-16 00:00:00 UTC SeqAhead Hospital Duran i Reynals, Barcelona, Spain Hospital Duran i Reynals Barcelona Spain Bioinformatics [] [] [] workshops_and_courses [] NGSdataintegrationmethodologystatisticsEMBnet
  • 3-day Fundamentals in NGS Data Analysis

    12 - 14 July 2016

    Perth, Australia

    3-day Fundamentals in NGS Data Analysis https://tess.elixir-europe.org/events/3-day-fundamentals-in-ngs-data-analysis Fundamentals in NGS Data Analysis is a three-day, hands-on workshop that offers attendees a basic understanding of NGS data analysis workflows. The workshop provides hands-on computational experience in analysis of NGS data using common analytical approaches for ChIP-Seq, RNA-Seq data and de novo genome assembly. Workshop Outline Topics covered by this workshop include: -An introduction to the command line interface and NGS file formats -Assessment of the quality of NGS sequence reads -Sequence alignment algorithms -Basic ChIP-Seq analysis -Basic RNA-Seq analysis -de novo genome assembly 2016-07-12 09:00:00 UTC 2016-07-14 00:00:00 UTC Curtin University, Perth, Australia Curtin University Perth Australia Data architecture, analysis and design [] [] [] workshops_and_courses [] ABRBPANGSIntroduction
  • RNA-Seq Next Generation Sequencing Analysis Workshop

    26 - 28 October 2016

    Leicester, United Kingdom

    RNA-Seq Next Generation Sequencing Analysis Workshop https://tess.elixir-europe.org/events/rna-seq-next-generation-sequencing-analysis-workshop This course will provide an introduction to next generation sequencing (NGS) platforms, data analysis and tools for data quality control, read alignment (mapping), differential expression, de novo and referenced based transcriptome assembly, annotation and gene discovery of RNA sequencing (RNA-Seq) data. The course will be delivered using a mixture of lectures and computer based hands on practical sessions using real data. This course is aimed at wet-lab biologists who are involved in research projects that will require the handling and analysis of NGS data. A significant proportion of the course will be computer-based using command line tools in the Unix environment, therefore, in order to gain maximum benefit from the course all attendees will be required to have basic Unix skills. This means applicants must at a minimum be able to move easily around the file system and make directories (e.g. pwd, cd, ls, mkdir), manage files (e.g. cp, mv, ln, rm, less, head, tail, wc) and search with grep. 2016-10-26 00:00:00 UTC 2016-10-28 00:00:00 UTC University of Leicester University of Leicester - College Court Conference Centre, Leicester, United Kingdom University of Leicester - College Court Conference Centre Leicester United Kingdom LE2 3UF Bioinformatics Sequencing RNA-Seq [] [] [] workshops_and_courses [] NGSRNA-SeqBioinformatics
  • ELIXIR Workshop Genomics

    7 - 8 November 2016

    Bruxelles, Belgium

    Elixir node event
    ELIXIR Workshop Genomics https://tess.elixir-europe.org/events/elixir-workshop-genomics Goal The fast generation of large amounts of data is fundamentally changing the way how research is done today. Many domains of research are challenged with managing, analyzing and sharing genomics data. This is not just a challenge, it is an oppurtunity to implement this workshop for researchers to learn basic handling of genomics concepts, skills and tools. This workshop is aimed at researchers in the life sciences at all career stage and is designed for learners with little to no prior knowledge of Linux and command line tools or biological networks in Cytoscape. A basic knowledge of programming in R is recommended. ​ Workshop Topics The main ambition or this workshop is that researchers get more familiar with genomics data and handle it in a more efficient way. The following topics will be covered during the workshop.   DAY 1 Introduction to Linux and the command line The first session will introduce you to the use of Linux and the command line for managing and analyzing genomics data.   DAY 2​ Data manipulation in R This session gives an introduction to the use of the R packages plyr and ggplot2 for data manipulation and subsequent graphing. Initiation Cytoscape In this tutorial, you will be introduced to the basics of Cytoscape (how to make a network, change the visualisation parameters such as the layout, ...), and to more advanced functionalities such as data integration and data analysis using Cytoscape plugins. 2016-11-07 09:00:00 UTC 2016-11-08 17:00:00 UTC ELIXIR Belgium Belgian Science Policy (BELSPO), 231, Avenue Louise, Bruxelles, Belgium Belgian Science Policy (BELSPO), 231, Avenue Louise Bruxelles Belgium Data visualisation Molecular interactions, pathways and networks Bioinformatics VIB christof.debo@vib.be ELIXIR-BE PhD studentsPost Docs [] [] Cytoscape R-programming Linux
  • Large-scale analytical workflows on the cloud using Galaxy and Globus

    16 November 2016

    Large-scale analytical workflows on the cloud using Galaxy and Globus https://tess.elixir-europe.org/events/large-scale-analytical-workflows-on-the-cloud-using-galaxy-and-globus We would like to invite you to attend the 8th webinar in BioExcel’s webinar series on computational methods and applications for biomolecular research, which will take place on 16th November 2016: Presenter: Ravi Madduri (introduction by Stian Soiland-Reyes) When: Wed 16th November 2016 16:00 CET (2016-11-16 15:00 UTC) Registration: Free In this BioExcel webinar we are delighted to have Ravi Madduri from Argonne National Laboratory and University of Chicago present Globus Genomics, a system developed for rapid analysis of large quantities of next-generation sequencing (NGS) genomic data, combining Galaxy workflows with cloud technologies like Amazon EC2 and Globus File Transfer. This system achieves a high degree of end-to-end automation that encompasses every stage of data analysis including initial data retrieval from remote sequencing centers or storage (via the Globus file transfer system); specification, configuration, and reuse of multi-step processing pipelines (via the Galaxy workflow system); creation of custom Amazon Machine Images and on-demand resource acquisition via a specialized elastic provisioner (on Amazon EC2); and efficient scheduling of these pipelines over many processors (via the HTCondor scheduler). The system allows biomedical researchers to perform rapid analysis of large NGS datasets in a fully automated manner, without software installation or a need for any local computing infrastructure. Ravi’s work is part of the BD2K center Big Data for Discovery Science, building infrastructure for reproducible workflows using minids (minimal viable identifiers), analyzing data at scale using identified Docker containers, publish results in to Globus Publication services thus providing an end-to-end framework for reproducible research. In this BioExcel webinar, Ravi will present Globus Genomics and the technologies used to achieve large-scale analytical Galaxy workflows on the cloud. We think this will be of interest not just for the genomics community, but for any scientific workflow users who need to consider distributed deployments, data management and scalability. 2016-11-16 15:00:00 UTC 2016-11-16 16:00:00 UTC BioExcel Whole genome sequencing High-throughput sequencing Genomics Workflows University of ManchesterUniversity of ChicagoArgonne National Laboratory Please register at https://attendee.gotowebinar.com/register/5808939110698431491. You will then receive an email with details of how you can connect to the webinar. [] bioinformaticianssoftware engineersGalaxy usersCloud users workshops_and_courses first_come_first_served CloudGalaxyGlobusNGSNext generation sequencing data analysis
  • COMBINE R for Bioinformatics workshop

    18 - 19 May 2017

    Carlton, Australia

    COMBINE R for Bioinformatics workshop https://tess.elixir-europe.org/events/combine-r-for-bioinformatics-workshop Bioconductor is an Open-Source repository for bioinformatics software in R Statistical Programming Language. Bioconductor provides core technologies and infrastructures that facilitates day-to-day bioinformatics data analysis, including data retrieval, data processing and data analysis. This is a one-day intensive workshop on Bioconductor core packages such as GenomicFeatures, GenomicRanges, GenomicAlignments, Biostrings, Rsamtools, GEOquery, AnnotationHub and other annotation packages. An intermediate knowledge of R is required. Instructors: Anna Quaglieri, Paul Harrison, Maria Doyle, Agnieszka Aleksandra Golicz and Soroor Hediyeh-Zadeh Details: What: COMBINE R for Bioinformatics workshop Date: 19th May 2017 Time: 9am – 5pm Location: Lab14, 700 Swanston St, Carlton VIC 3053 Registration: http://www.abacbs.org/combineworkshops/bioconductor-melb-may-2017 Price: Student $15, Non-student $30 This event is sponsored by Melbourne Bioinformatics. 2017-05-18 23:00:00 UTC 2017-05-19 07:00:00 UTC Soroor Hediyeh-Zadeh combine@combine.org.au LAB-14, 700, Swanston Street, Carlton, Australia LAB-14, 700, Swanston Street Carlton Melbourne City Australia Genomics Bioinformatics [] Melbourne Bioinformatics [] workshops_and_courses first_come_first_served R-programming
  • Genome Annotation with Monica Munoz-Torres

    27 June 2017

    University of Melbourne, Australia

    Genome Annotation with Monica Munoz-Torres https://tess.elixir-europe.org/events/genome-annotation-with-monica-munoz-torres 2017-06-27 09:00:00 UTC 2017-06-27 17:00:00 UTC Melbourne Bioinformatics 161 Barry St, Carlton, University of Melbourne, Australia 161 Barry St, Carlton University of Melbourne Australia Bioinformatics Genomics Data submission, annotation and curation Melbourne Bioinformatics [] [] [] [] BioinformaticsGenomics
  • Introduction to NGS Data Analysis

    27 - 29 June 2017

    Camperdown, Australia

    Introduction to NGS Data Analysis https://tess.elixir-europe.org/events/introduction-to-ngs-data-analysis-8290433d-ac97-4f5c-99ed-8a9bec24a058 Introduction to NGS Data Analysis is a three-day, hands-on workshop that offers attendees a basic understanding of NGS data analysis workflows. The workshop provides hands-on computational experience in analysis of NGS data using common analytical approaches for ChIP-Seq, RNA-Seq data and de novo genome assembly. 2017-06-27 09:00:00 UTC 2017-06-29 17:00:00 UTC Bioplatforms Australia Johns Hopkins Centre, Camperdown, Australia Johns Hopkins Centre Camperdown Australia 2006 Bioinformatics University of Sydney kchamp@bioplatforms.com [] [] workshops_and_courses [] Genomics
  • Genopole Summer School

    4 - 7 July 2017

    Seine-Port, France

    Elixir node event
    Genopole Summer School https://tess.elixir-europe.org/events/bioinformatic-and-biostatistic-tools-in-medical-genomics Bioinformatic and Biostatistic tools in medical genomics 2017-07-04 09:00:00 UTC 2017-07-07 00:00:00 UTC Genopole, IFB and France Genomique Châteauform' Seine Port (77), Seine-Port, France Châteauform' Seine Port (77) Seine-Port Seine-et-Marne France 77240 Medicines research and development Metagenomics Functional genomics [] goo.gl/bzEdQ2 [] BioinformaticiansResearcher in life sciences workshops_and_courses first_come_first_served Statistical-model Variant-callingSNPbioinformaticsBiomarker discoverymetagenomicsNext generation sequencing data analysisWorkflowscomputer-science
  • Introduction to R

    12 - 13 July 2017

    Clayton, Australia

    Introduction to R https://tess.elixir-europe.org/events/introduction-to-r-ab6dceb1-f7e0-4583-9b7e-4344a50535f3 This workshop will teach the fundamentals of R. You will learn to quickly visualize and summarize data from experiments involving multiple experimental factors and measurements. Register here: https://www.eventbrite.com/e/introduction-to-r-tickets-34994825465 2017-07-12 23:00:00 UTC 2017-07-13 06:00:00 UTC Monash Bioinformatics Platform Room E365 (Level 3, East wing, 20 Chancellors Walk- Menzies Building), Monash University Clayton Campus, Wellington Road, Clayton, Australia Room E365 (Level 3, East wing, 20 Chancellors Walk- Menzies Building), Monash University Clayton Campus, Wellington Road Clayton Australia Bioinformatics Monash University [] [] workshops_and_courses [] bioinformatics R-programming
  • GATK Best Practices for Variant Discovery

    17 - 19 July 2017

    Edinburgh, United Kingdom

    Elixir node event
    GATK Best Practices for Variant Discovery https://tess.elixir-europe.org/events/gatk-best-practices-for-variant-discovery This workshop will focus on the core steps involved in calling variants with the Broad’s Genome Analysis Toolkit, using the Best Practices developed by the GATK team. You will learn why each step is essential to the variant discovery process, what are the operations performed on the data at each step, and how to use the GATK tools to get the most accurate and reliable results out of your dataset. In the course of this workshop, we highlight key functionalities such as the GVCF workflow for joint variant discovery in cohorts, RNAseq-specific processing, and somatic variant discovery using MuTect2. We also preview capabilities of the upcoming GATK version 4, including a new workflow for CNV discovery, and we demonstrate the use of pipelining tools to assemble and execute GATK workflows. 2017-07-17 09:00:00 UTC 2017-07-19 17:00:00 UTC The King's Buildings, The University of Edinburgh, Edinburgh, United Kingdom The King's Buildings, The University of Edinburgh Edinburgh United Kingdom Bioinformatics Genomics Edinburgh Genomics Bert Overduin - bert.overduin@ed.ac.uk [] [] workshops_and_courses [] Variant discoveryGenomicsBioinformatics
  • Long-read Data Analysis workshop

    18 - 19 July 2017

    Kensington, Australia

    Long-read Data Analysis workshop https://tess.elixir-europe.org/events/long-read-data-analysis-workshop Workshop Content: Introduction to long-read sequencing Practical considerations when performing long-read sequencing and analysis Introduction to the command line interface and NGS file formats Short and long-read de novo genome assembly (microbial) Comparison between short and long-read assemblies This workshop will be delivered using a mixture of lectures, hands-on practical sessions, and open discussions. 2017-07-18 09:00:00 UTC 2017-07-19 17:00:00 UTC Bioplatforms Australia Red Centre Building, Kensington, Australia Red Centre Building Kensington Australia 2033 Bioinformatics University of New South Wales [] [] workshops_and_courses [] Genomics
  • An Introduction to Genomics with R

    18 July 2017

    Adelaide, Australia

    An Introduction to Genomics with R https://tess.elixir-europe.org/events/an-introduction-to-genomics-with-r 2017-07-18 09:00:00 UTC 2017-07-18 17:00:00 UTC University of Adelaide Room 422, Horace Lamb Building, The University of Adelaide, Adelaide, Australia Room 422, Horace Lamb Building, The University of Adelaide Adelaide SA Australia Bioinformatics University of Adelaide [] [] workshops_and_courses [] R-programminggenomics
  • Introduction to R

    24 July 2017

    Clayton, Australia

    Introduction to R https://tess.elixir-europe.org/events/introduction-to-r-fa4063f1-c129-4635-8b07-6e906e39750c 2017-07-24 10:00:00 UTC 2017-07-24 17:00:00 UTC Monash Bioinformatics Training Room 2 (T2), Matheson Library, Monash University, Clayton, Australia Training Room 2 (T2), Matheson Library, Monash University Clayton Australia Bioinformatics Monash University [] [] workshops_and_courses [] R-programming
  • Cancer Genomics workshop

    25 - 27 July 2017

    University of Sydney, Australia

    Cancer Genomics workshop https://tess.elixir-europe.org/events/cancer-genomics-workshop-4a98d5cd-8e5d-42d0-9845-3a52e9fee96d The Cancer Genomics workshop aims to provide an introduction to cancer genomics analytical pipelines for single nucleotide variations (SNV), copy number variations (CNV) and structural variations (SV). 2017-07-25 09:00:00 UTC 2017-07-27 17:00:00 UTC Bioplatforms Australia Charles Perkins Centre, University of Sydney, Australia Charles Perkins Centre University of Sydney Australia Bioinformatics University of Sydney kchamp@bioplatforms.com [] [] workshops_and_courses [] BioinformaticsCancerGenomics
  • Introduction to Programming with R

    27 July 2017

    Sydney, Australia

    Introduction to Programming with R https://tess.elixir-europe.org/events/introduction-to-programming-with-r-607032a5-9a9f-443a-b6a8-fe4358cdeb19 2017-07-27 09:30:00 UTC 2017-07-27 16:30:00 UTC Intersect Australia UNSW Kensington, Computer Lab G16-G17, ground floor, Wallace Wurth Building , Sydney, Australia UNSW Kensington, Computer Lab G16-G17, ground floor, Wallace Wurth Building Sydney Australia Bioinformatics University of New South Wales [] [] workshops_and_courses [] R-programming
  • Software Carpentry - Introduction to Programming in R

    8 August 2017

    Melbourne, Australia

    Software Carpentry - Introduction to Programming in R https://tess.elixir-europe.org/events/software-carpentry-introduction-to-programming-in-r 2017-08-08 09:30:00 UTC 2017-08-08 16:30:00 UTC Intersect Australia HS3 401, La Trobe University - Bundoora , Melbourne, Australia HS3 401, La Trobe University - Bundoora Melbourne Australia Bioinformatics La Trobe University [] [] workshops_and_courses [] R-programming
  • Data preparation, processing and reporting using R

    9 August 2017

    Saint Lucia, Australia

    Data preparation, processing and reporting using R https://tess.elixir-europe.org/events/data-preparation-processing-and-reporting-using-r 2017-08-09 09:00:00 UTC 2017-08-09 17:00:00 UTC QFAB Bioinformatics Multimedia room 3.141, Queensland Bioscience Precinct, The University of Queensland, Saint Lucia, Australia Multimedia room 3.141, Queensland Bioscience Precinct, The University of Queensland Saint Lucia Brisbane Australia Data management University of Queensland [] [] workshops_and_courses [] R-programmingBioinformatics
  • Sequences and genomic features in R

    4 September 2017

    Melbourne, Australia

    Sequences and genomic features in R https://tess.elixir-europe.org/events/sequences-and-genomic-features-in-r This course introduces Bioconductor, a comprehensive collection of R packages related to bioinformatics. We will demonstrate the Bioconductor way of doing things and how to work with biological data types, and equip you to confidently approach whichever specific Bioconductor packages you need. Pre-requisite To attend this class, you must have attended our introductory R course or be reasonably familiar with the R language. 2017-09-04 14:00:00 UTC 2017-09-04 16:00:00 UTC Monash Bioinformatics Platform Melbourne, Melbourne, Australia Melbourne Melbourne Australia Bioinformatics Monash University Dr Sonika Tyagi, bioinformatics.platform@monash.edu [] PhD studentsPost-docsBioinformaticiansResearchers workshops_and_courses registration_of_interest R-programmingbioinformaticsBioconductor
  • Introduction to R

    6 September 2017

    Australia

    Introduction to R https://tess.elixir-europe.org/events/introduction-to-r-94807d72-1f91-4c1b-8376-52ca3947b838 2017-09-06 09:00:00 UTC 2017-09-06 17:00:00 UTC QFAB Bioinformatics Room 3.141, Queensland Bioscience Precinct, The University of Queensland, Australia Room 3.141, Queensland Bioscience Precinct, The University of Queensland Brisbane Australia Bioinformatics University of Queensland [] [] workshops_and_courses [] Bioinformatics R-programming
  • 3Gb-TEST NGS Course Ljubljana 2017

    25 - 27 September 2017

    Ljubljana, Slovenia

    3Gb-TEST NGS Course Ljubljana 2017 https://tess.elixir-europe.org/events/3gb-test-ngs-in-a-diagnostic-setting A 3-day course on NGS Ljubljana, Slovenia in the period of 25-27 September 2017. The focus of the course is on clinical diagnostics using exome/genome sequences, variant identification and analysis including afternoon practical sessions. 2017-09-25 08:00:00 UTC 2017-09-27 18:00:00 UTC 3Gb-TEST Best Western Premier Hotel Slon, Ljubljana, Slovenia Best Western Premier Hotel Slon Ljubljana Slovenia Sequencing Exome sequencing Sequence analysis [] J.A.Lopez_Hernandez@lumc.nl In collaboration with RD-Connect [] 100 workshops_and_courses registration_of_interest NGSDiagnosisWESWGSELSI
  • Training Course on Best practices for RNA-Seq data analysis

    27 - 29 September 2017

    Fisciano, Italy

    Training Course on Best practices for RNA-Seq data analysis https://tess.elixir-europe.org/events/training-course-on-best-practices-for-rna-seq-data-analysis Next-generation sequencing (NGS) of RNA libraries (RNA-Seq) has become increasingly common and it largely replaced microarray technology for gene expression profiling. The aim of this course is to get a deeper understanding of RNA-Seq experiments, providing a theoretical introduction to the data processing steps, together with practical sessions illustrating the use of the most popular data analysis tools. The classroom size is limited to 25 participants to optimize the learning and the interaction with the instructors. Starting from the raw sequenced data coming from different phenotypical samples (e.g disease vs healthy control samples), genes which are differentially expressed between the two conditions are determine. Some strategies are illustrated for detecting alternative splicing products, predicting novel isoforms and gene fusion events. Some methods for downstream analysis are described to give insight into how biological knowledge can be generated from RNA-Seq experiments. A lecture on single-cell RNA-Seq will provide an idea of how transcriptome data from individual cells is now emerging as a powerful tool, allowing the study of cell-to-cell gene expression heterogeneity in the same tissue. 2017-09-27 09:15:00 UTC 2017-09-29 16:30:00 UTC Anna Marabotti (University of Salerno and ELIXIR-IIB Training Team, Italy), Roberto Tagliaferri (University of Salerno, Italy), Alessandro Weisz (University of Salerno, Italy), Loredana Le Pera (ELIXIR-IIB Training Team and IIT, Italy), Allegra Via (ELIXIR-IIB Training Coordinator, CNR-IBPM, Italy) Campus di Fisciano, Università degli Studi di Salerno, Via Giovanni Paolo II, n. 132, Fisciano, Italy Campus di Fisciano, Università degli Studi di Salerno, Via Giovanni Paolo II, n. 132 Fisciano Provincia di Salerno Italy 84084 Transcriptomics RNA splicing Sequencing Bioinformatics RNA-Seq Gene expression Campus di Fisciano, University of Salerno, Italy elixir.ita.training@gmail.com, amarabotti@unisa.it ELIXIR Italy PhD students and young researchers in the life science and computational biology field who are planning to use RNA-seq data and are looking for the best practices to analyze these types of data 25 workshops_and_courses first_come_first_servedregistration_of_interest NGSRNA-SeqBioinformaticsData analysisHigh Throughput Sequencing AnalysisGene Expression
  • 3Gb-TEST NGS Course Mexico 2017

    10 - 13 October 2017

    México City, Mexico

    3Gb-TEST NGS Course Mexico 2017 https://tess.elixir-europe.org/events/3gb-test-ngs-course-mexico-2017 The focus of the course is on clinical diagnostics using exome/genome sequences, variant identification and analysis including afternoon practical sessions in dry lab as well as in wetlab. *Event mostly in Spanish 2017-10-10 08:00:00 UTC 2017-10-13 14:30:00 UTC 3Gb-TEST Centro Médico Nacional 20 de Noviembre, México City, Mexico Centro Médico Nacional 20 de Noviembre México City DF Mexico Data quality management Whole genome sequencing Exome sequencing Bioinformatics ISSSTE genomicatraslacional@gmail.com [] [] 200 workshops_and_courses [] NGS bioinformaticsNGSDiagnosisDatabases
  • Introduction to ChIP-seq Data Analysis and Visualisation using Ensembl

    23 - 24 November 2017

    Edinburgh, United Kingdom

    Elixir node event
    Introduction to ChIP-seq Data Analysis and Visualisation using Ensembl https://tess.elixir-europe.org/events/introduction-to-chip-seq-data-analysis-and-visualisation-using-ensembl-d125d464-c708-4919-8322-19d50246c22d ChIP-seq (Chromatin ImmunoPrecipitation followed by Sequencing) is a popular high-throughput sequencing assay to identify binding sites of DNA-associated proteins and histone modifications. Determining how proteins interact with DNA and the epigenetic landscape is essential for elucidating the regulation of gene expression. The aim of this workshop is to familiarise the participants with the primary analysis of ChIP-seq data sets by providing a balanced set of lectures and practicals on analysis methodologies. Practicals include publicly available ChIP-seq datasets, processed using widely used and open-source software programs (e.g. FASTQC, BWA, samtools, bedtools, wiggletools, MACS2, MEME, TOMTOM, ngsplot) and visualised on the Ensembl genome browser. 2017-11-23 09:00:00 UTC 2017-11-24 17:00:00 UTC The King's Buildings, The University of Edinburgh, Edinburgh, United Kingdom The King's Buildings, The University of Edinburgh Edinburgh United Kingdom EH9 3JN Genomics ChIP-seq Bioinformatics Edinburgh Genomics Bert Overduin - bert.overduin@ed.ac.uk [] [] workshops_and_courses [] BioinformaticsChIP-seqGenomics
  • Introduction to Programming with R

    29 November 2017

    Armidale, Australia

    Introduction to Programming with R https://tess.elixir-europe.org/events/introduction-to-programming-with-r-30c9bb71-d64d-40fe-9de6-d1af1649c943 2017-11-29 09:30:00 UTC 2017-11-29 16:30:00 UTC Intersect Australia University of New England, Armidale, Australia University of New England Armidale Australia 2350 Bioinformatics Computer science University of New England [] [] workshops_and_courses [] R-programming
  • CESNET e-infrastructure workshop

    11 December 2017

    Prague, Czechia

    Elixir node event
    CESNET e-infrastructure workshop https://tess.elixir-europe.org/events/cesnet-e-infrastructure-workshop In Czech, CESNET, GEANT, DataCare, Metacentrum, HPC, ELIXIR, EDGAIN, SAGElab, Cloud computing 2017-12-11 08:30:00 UTC 2017-12-11 16:45:00 UTC CESNET Thákurova 550/1, 1, Thákurova, Prague, Czechia Thákurova 550/1, 1, Thákurova Prague Hlavní město Praha Czechia Data security Database management Data management Computer science [] [] PhD studentspostdocLife Science Researchers 200 meetings_and_conferences registration_of_interest Cloud computingcomputer-scienceDatabases
  • Handle your data the tidy way: Data science using R and the tidyverse

    13 December 2017

    Leuven, Belgium

    Handle your data the tidy way: Data science using R and the tidyverse https://tess.elixir-europe.org/events/handle-your-data-the-tidy-way-data-science-using-r-and-the-tidyverse The use of R in the data science field has increased enormously the last few years. One very useful toolkit for a wide variety of analyses is the ‘tidyverse’: a collection of R-packages used for data manipulation, exploration and visualization that share a common design philosophy. Tidyverse packages are intended to make statisticians and data scientists more productive by guiding them through workflows that facilitate communication, and result in reproducible work products. In this workshop you will learn: The difference between tidy and untidy data How to create tidy datasets and manipulate them using the main tidyr and dplyr verbs Make your results reproducible by using Rmarkdown and Rstudio Integrate data visualisation into your workflow using ggplot2 Apply the tidyverse to biological problems LEVEL: A very basic knowledge of the R programming language (or any other programming language) is expected. We expect a little bit of R-experience for this workshop. If you’re already an R-wizard but never did anything using Tidyverse, then this workshop is a great introduction to it! If you’re not an R-wizard but now a little bit of R, then this course is a great way to improve your R-skills fast. If you’re already pretty good with Tidyverse, I guess we can not help you as this is an introduction Please remember to bring your own laptop with the last version of R installed. Location: Campus Gusthuisberg O&N2 HP5 (05.204) and HP7 (05.208) classrooms 2017-12-13 14:00:00 UTC 2017-12-13 18:00:00 UTC Stijn Wittouck and Sander Wuyts UCLL Campus Gasthuisberg, 49, Herestraat, Leuven, Belgium UCLL Campus Gasthuisberg, 49, Herestraat Leuven Vlaams-Brabant Belgium KU Leuven Daniele Parisi dparisi@esat.kuleuven.be Elixir Belgium bioinformaticians [] [] R-programmingtidyverse
  • RNA-Seq analysis in R

    22 - 23 February 2018

    Perth, Australia

    RNA-Seq analysis in R https://tess.elixir-europe.org/events/rna-seq-analysis-in-r 2018-02-22 09:00:00 UTC 2018-02-23 15:00:00 UTC COMBINE Australia Pawsey Supercomputing Centre, 26 Dick Perry Ave, Perth, Australia Pawsey Supercomputing Centre, 26 Dick Perry Ave Perth Australia Pawsey Supercomputing Centre [] [] [] [] bioinformatics RNA-Seq R-programming
  • CWLEXEC: Run Common Workflow Language on HPC with IBM Spectrum LSF

    28 February 2018

    CWLEXEC: Run Common Workflow Language on HPC with IBM Spectrum LSF https://tess.elixir-europe.org/events/cwlexec-a-new-open-source-tool-to-run-cwl-workflows-on-lsf The [Common Workflow Language (CWL)](http://www.commonwl.org/) is a community-led specification for describing analysis _workflows_ and tools in a way that makes them portable and scalable across a variety of software and hardware environments, from workstations to cluster, cloud, and _high performance computing_ (HPC) environments. [IBM Spectrum LSF](https://www.ibm.com/us-en/marketplace/hpc-workload-management) (formerly IBM Platform LSF) is a complete workload management solution for demanding HPC environments. Featuring intelligent, policy-driven scheduling, it helps organizations accelerate research and design while controlling costs through superior resource utilization. Recognizing the popularity of CWL among LSF users, we introduce a new open source project **CWLEXEC** to support running CWL workflows on LSF. The project will feature smooth integration with LSF with high efficiency and scalability, self-healing of workflows, support user-specified submission options while keeping CWL definitions portable, and other benefits. * **Title**: CWLEXEC: A new open source tool to run CWL workflows on LSF * **Presenter:** Qingda Wang, Principal Architect, IBM Spectrum LSF Family Products and OEM * **Time**: 2018-02-28 14:00 GMT / 15:00 CET 2018-02-28 14:00:00 UTC 2018-02-28 15:00:00 UTC BioExcel Bioinformatics Genomics Workflows University of ManchesterBioExcel CoE Stian Soiland-Reyes http://ask.bioexcel.eu/ [] bioinformaticiansHPC users workshops_and_courses registration_of_interest WorkflowsCWLHPCLSF
  • Introduction to Galaxy and the GVL

    20 March 2018

    Carlton, Australia

    Introduction to Galaxy and the GVL https://tess.elixir-europe.org/events/introduction-to-galaxy-and-the-gvl 2018-03-20 09:30:00 UTC 2018-03-20 12:30:00 UTC Melbourne Bioinformatics Melbourne Bioinformatics, 187 Grattan St, Carlton, Australia Melbourne Bioinformatics, 187 Grattan St Carlton Australia 3053 Bioinformatics University of Melbourne [] [] workshops_and_courses [] GalaxyGenomics
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