Training eSupport System
  • Log In
    • Log in with LS Login
    • Login
    • Register
  • About
  • Events
  • Materials
  • e-Learning
  • Workflows
  • Collections
  • Learning paths
  • Directory
    • Providers
    • Nodes
    • Spaces

TeSS makes use of some necessary cookies to provide its core functionality. Additionally, we make use of Google Analytics to discover how people are using TeSS in order to help us improve the service. To opt out of this, choose the "Allow necessary cookies" option.

See our Privacy Policy for more information.

You can modify your cookie preferences at any time here, or from the link in the footer.

Allow necessary cookies Allow all cookies
  1. Home
  2. Materials

Filter

  • Sort

  • Filter Clear filters

    • Date added
    • In the last 24 hours
    • In the last 1 week
    • In the last 1 month
    • Scientific topic
    • Genomics
    • MicroRNA sequencing125
    • RNA sequencing125
    • RNA-Seq125
    • RNA-Seq analysis125
    • Small RNA sequencing125
    • Small RNA-Seq125
    • Small-Seq125
    • Transcriptome profiling125
    • WTSS125
    • Whole transcriptome shotgun sequencing125
    • miRNA-seq125
    • Genome annotation111
    • Exomes103
    • Genomes103
    • Personal genomics103
    • Synthetic genomics103
    • Viral genomics103
    • Whole genomes103
    • R92
    • R program92
    • R script92
    • Comparative transcriptomics89
    • Transcriptome89
    • Transcriptomics89
    • Data management74
    • Metadata management74
    • Research data management (RDM)74
    • Chromosome walking70
    • Clone verification70
    • DNA-Seq70
    • DNase-Seq70
    • High throughput sequencing70
    • High-throughput sequencing70
    • NGS70
    • NGS data analysis70
    • Next gen sequencing70
    • Next generation sequencing70
    • Panels70
    • Primer walking70
    • Sanger sequencing70
    • Sequencing70
    • Targeted next-generation sequencing panels70
    • Bayesian methods66
    • Biostatistics66
    • Descriptive statistics66
    • Gaussian processes66
    • Inferential statistics66
    • Markov processes66
    • Multivariate statistics66
    • Probabilistic graphical model66
    • Probability66
    • Statistics66
    • Statistics and probability66
    • Active learning50
    • Ensembl learning50
    • Kernel methods50
    • Knowledge representation50
    • Machine learning50
    • Neural networks50
    • Recommender system50
    • Reinforcement learning50
    • Supervised learning50
    • Unsupervised learning50
    • Python41
    • Python program41
    • Python script41
    • py41
    • FAIR data38
    • Findable, accessible, interoperable, reusable data38
    • Rare diseases36
    • Bioinformatics34
    • Single-cell genomics34
    • Single-cell sequencing34
    • Antimicrobial stewardship32
    • Medical microbiology32
    • Microbial genetics32
    • Microbial physiology32
    • Microbial surveillance32
    • Microbiological surveillance32
    • Microbiology32
    • Molecular infection biology32
    • Molecular microbiology32
    • Data rendering31
    • Data visualisation31
    • Metagenomics31
    • Shotgun metagenomics31
    • Pipelines30
    • Software integration30
    • Tool integration30
    • Tool interoperability30
    • Workflows30
    • Bottom-up proteomics28
    • Discovery proteomics28
    • MS-based targeted proteomics28
    • MS-based untargeted proteomics28
    • Metaproteomics28
    • Peptide identification28
    • Protein and peptide identification28
    • Proteomics28
    • Show N_FILTERS more
    • Tool
    • Bioconductor8
    • BridgeDb1
    • Data Stewardship Wizard1
    • RDMkit1
    • UCSC Genome Browser1
    • Show N_FILTERS more
    • Standard database or policy
    • European Nucleotide Archive1
    • FAIRsharing1
    • Genomics England | PanelApp1
    • RDA DMP Common Standard for Machine-Actionable Data Management Plans1
    • Show N_FILTERS more
    • Content provider
    • Glittr.org52
    • ERGA Knowledge Hub20
    • European Bioinformatics Institute (EBI)12
    • Bioconductor8
    • Centre for Genomic Regulation (CRG)3
    • Bioinformatics and Biomathematics Training Hub1
    • CNAG-CRG1
    • Department of Bioinformatics - BiGCaT, Maastricht University1
    • ELIXIR Norway1
    • VHP4Safety1
    • Show N_FILTERS more
    • Keyword
    • Genomics76
    • Next generation sequencing26
    • R13
    • RNA-seq13
    • Genome assembly11
    • Variant analysis11
    • Long read sequencing8
    • Transcriptomics8
    • Unix/Linux8
    • Comparative genomics6
    • Data visualization6
    • General6
    • Metagenomics5
    • Population genetics5
    • Genome annotation4
    • Single-cell sequencing4
    • ATAC-seq3
    • Data management3
    • Epidemiology3
    • Epigenetics3
    • Machine learning3
    • Multiomics3
    • Statistics3
    • Version control3
    • Artificial intelligence2
    • ChIP-seq2
    • Cloud computing2
    • FAIR data2
    • FEGA2
    • Federated EGA2
    • Galaxy2
    • Phylogenetics / Phylogenomics2
    • Python2
    • Reproducibility2
    • bioinformatics2
    • API1
    • Assembly Curation1
    • Assembly Evaluation1
    • Biocuration1
    • BridgeDb1
    • ChIP-Seq1
    • Conservation genomics1
    • Containerization1
    • Data Life Cycle1
    • Data Management Plan1
    • Data Steward1
    • Data Stewardship Wizard1
    • Data management planning1
    • Data science1
    • Database Management1
    • Designing functional genomics experiments1
    • ELIXIR Converge1
    • ELIXIR RIR, BridgeDb1
    • ELIXIR-CONVERGE1
    • Enrichment analysis1
    • FASTA1
    • FASTQC1
    • GTF1
    • Gene lists1
    • Genome browser1
    • Genome sequencing1
    • Gramene database1
    • High performance computing1
    • IBERS1
    • Identifiers1
    • Institute of Biological, Environmental and Rural Sciences1
    • Introduction1
    • Julia1
    • Large language models1
    • Microbiology1
    • Nextflow1
    • Ontology1
    • Pathways and Networks1
    • Perl1
    • Programmatic access1
    • Quality Control1
    • Research Data Management1
    • Research Infrastructure1
    • Rmarkdown1
    • Sequence alignments1
    • Singularity1
    • Snakemake1
    • Spatial omics1
    • Workflows1
    • covid191
    • e-learning1
    • evolution1
    • human disease1
    • multi-omics data integration1
    • transcriptomics1
    • Show N_FILTERS more
    • Competency level
    • Not specified100
    • Beginner3
    • Show N_FILTERS more
    • Licence
    • License Not Specified
    • Creative Commons Attribution 4.0 International73
    • GNU General Public License v3.0 only11
    • MIT License11
    • Creative Commons Attribution Non Commercial No Derivatives 4.0 International5
    • Creative Commons Zero v1.0 Universal4
    • Creative Commons Attribution Non Commercial 4.0 International1
    • Creative Commons Attribution Share Alike 4.0 International1
    • Show N_FILTERS more
    • Target audience
    • Clinicians4
    • PhD students4
    • Bioinformaticians2
    • Biologists2
    • Clinical Scientists2
    • Life Science Researchers2
    • Researchers2
    • Bioinformatician, Bioanalysts1
    • Biologists with little or no prior computational experience1
    • Data Access Committeses from the EGA1
    • Data Managers1
    • Data Scientists1
    • Data stewards1
    • Life Scientists1
    • Microbiologists1
    • PhD Scholars, Graduates and Post Graduates, Professors, Associate Professors, Assistant Professors, Bio instruments Professionals, Bio-informatics Professionals, Directors, CEO’s of Organizations, Supply Chain companies, Manufacturing Companies, Software development companies, Research Institutes and members1
    • PhD candidates1
    • PhD students in Genomics datascience1
    • Principal Investigators1
    • Principal Investigators (PIs)1
    • Professors1
    • Public Health Professionals1
    • Researchers and bioinformaticians in other projects interested in depositiong data at the EGA1
    • Researchers and bioinformaticians involved in the VEIS project1
    • clinicians and informaticians interested in cancer genetics1
    • Show N_FILTERS more
    • Author
    • Data Carpentry6
    • bioinformatics.ca6
    • Martin Morgan4
    • The Gulbenkian Training Programme in Bioinformatics4
    • Canadian Bioinformatics Workshops3
    • Hervé Pagès2
    • Michael Lawrence2
    • The Carpentries Lab2
    • Andries Marees1
    • Applied Genomics1
    • Biocore@CRG1
    • Bioinformatics, Rockefeller University1
    • BiotrAIn1
    • Computational Genomics with R1
    • Computational Metagenomics1
    • Egon Willighagen1
    • Ellen McDonagh1
    • Espen Åberg1
    • Federico Bianchini1
    • Friederike Ehrhart1
    • Functional Genomics Laboratory1
    • Global Biodiversity Information Facility1
    • IB-ULFRI1
    • Illimar Rekand1
    • Jan Paces1
    • Jonathan Mélius1
    • Korbinian Bösl1
    • Kristyna Kupkova1
    • Leonardo Collado-Torres1
    • Luca Cozzuto1
    • Melbourne Bioinformatics1
    • Michael Squance1
    • Mike Lee1
    • NBIS - National Bioinformatics Infrastructure Sweden1
    • Nanopore for Educators1
    • Nazeefa Fatima1
    • Pachter Lab1
    • Papenfuss Lab1
    • Raf Winand1
    • Raphael Mourad1
    • Rebecca Foulger1
    • SciLifeLab-Training1
    • St. Jude Children's Research Hospital1
    • Stephen Turner1
    • Steven M. Van Belleghem1
    • Teaching materials at the Harvard Chan Bioinformatics Core1
    • The McDonnell Genome Institute1
    • Toni Hermoso Pulido1
    • Vasilis Lenis1
    • Wellcome Connecting Science1
    • cambiotraining1
    • genomicsclass1
    • gladstone-institutes1
    • nullranges1
    • rapidspeciation1
    • Show N_FILTERS more
    • Contributor
    • Canadian Bioinformatics Workshops8
    • Erin Becker8
    • François Michonneau8
    • Toby Hodges8
    • maneesha8
    • Jason Williams7
    • Tracy Teal7
    • Zhian N. Kamvar7
    • Bianca Peterson6
    • C. Titus Brown6
    • Taylor Reiter6
    • Amanda Charbonneau5
    • Dan Kerchner5
    • Rayna M Harris5
    • Robert Davey5
    • Anita Schürch4
    • Mark Fernandes4
    • Nelly Sélem4
    • Pete4
    • Sarah Stevens4
    • The Gulbenkian Training Programme in Bioinformatics4
    • Annajiat Alim Rasel3
    • Bob Freeman3
    • Brittany N. Lasseigne, PhD3
    • Bérénice Batut3
    • David Pérez-Suárez3
    • Fotis E. Psomopoulos3
    • Hilmar Lapp3
    • JCSzamosi3
    • Jemma Stachelek3
    • Kari L. Jordan, PhD3
    • Katrin Leinweber3
    • Michael R. Crusoe3
    • Naupaka Zimmerman3
    • Paula Andrea Martinez3
    • Sam Nooij3
    • Sarah Brown3
    • murraycadzow3
    • zhibinlu3
    • Aaron E. Jaime2
    • Abby Cabunoc Mayes2
    • AbrahamAvelar2
    • Ahmed Moustafa2
    • Alana Alexander2
    • Allen Lee2
    • Andrew Sanchez2
    • Andy Boughton2
    • Aziz Khan2
    • Brandon Curtis2
    • Charlie Barclay2
    • Christina K.2
    • CladoniaRang2
    • Clara2
    • Claudia Zirión Martínez2
    • Darian2
    • David Mawdsley2
    • Dinindu Senanayake2
    • EWheeler1232
    • Edmund Miller2
    • Erik Garrison2
    • EvanWill2
    • Finlay Maguire2
    • Gabriel A. Devenyi2
    • Graeme Grimes2
    • Ian Lee2
    • Idowu Olawoye2
    • J. Abel Lovaco2
    • Jared Simpson2
    • Jeff Oliver2
    • JesseKerkvliet2
    • Joel Nothman2
    • Jon Pipitone2
    • Jonah Duckles2
    • Karen Cranston2
    • Karen Word2
    • Katie Anne Mills2
    • Kevin Weitemier2
    • Lex Nederbragt2
    • M. Foos2
    • Mateusz Kuzak2
    • Matthew Kweskin2
    • Maxim Belkin2
    • Michael Hansen2
    • Michael Love2
    • Miguel Cardoso2
    • Nick Young2
    • Niclas Jareborg2
    • Piotr Banaszkiewicz2
    • Raniere Silva2
    • Remi Rampin2
    • Salehkarim212
    • Sangram K Sahu2
    • Sheldon McKay2
    • Stephen Turner2
    • Sue McClatchy2
    • Val Gartner2
    • W. Trevor King2
    • William L. Close2
    • alanaschick2
    • annmeyer2
    • Show N_FILTERS more
    • Resource type
    • Recorded webinar8
    • Video4
    • e-learning4
    • Tutorial3
    • Presentation2
    • Course materials1
    • Slides1
    • Training materials1
    • knowledgebase1
    • Show N_FILTERS more
    • Related resource
    • Beacon v2: a discovery tool for genomic and pheno-clinical data1
    • DisGeNET: a discovery platform designed to address a variety of questions concerning the genetic underpinning of human diseases1
    • GPAP: the RD-Connect Genome-Phenome Analysis Platform for diagnosis and gene discovery in rare disease research1
    • Genomics England PanelApp1
    • Introduction to the EGA and sharing sensitive data1
    • Slides | Beacon v2: a discovery tool for genomic and pheno-clinical data1
    • Slides | DisGeNET: a discovery platform designed to address a variety of questions concerning the genetic underpinning of human diseases1
    • Slides | GPAP: the RD-Connect Genome-Phenome Analysis Platform for diagnosis and gene discovery in rare disease research1
    • Slides | Introduction to the EGA and sharing sensitive data1
    • VEIS webinar: The essentials of DUO codes | Presentation1
    • VEIS webinar: The essentials of DUO codes | Video1
    • Video of the course1
    • Show N_FILTERS more
    • Node
    • Switzerland72
    • EMBL-EBI12
    • Spain4
    • Netherlands2
    • Belgium1
    • Czech Republic1
    • Norway1
    • United Kingdom1
    • Show N_FILTERS more
    • Collection
    • VEIS - Value of the EGA for Industry and Society3
    • ELIXIR Federated Human Data Community2
    • ELIXIR Biodiversity Community1
    • Show N_FILTERS more
    • Status
    • Active3
    • Show N_FILTERS more
  • Show materials from all spaces
  • Show disabled materials
  • Hide materials with broken links
  • Show archived materials

Training materials

  • Subscribe via email

Email Subscription

Register training material

Scientific topics: Genomics

and Licence: License Not Specified

and Include broken links: true

103 materials found
  • gbif/training

    ELIXIR node event
    Genomics FAIR data Metagenomics Genomics Population genetics FAIR data Metagenomics
  • bioinformaticsdotca/Genomic_Med_2017

    ELIXIR node event
    Epigenetics Genomics Sequencing Variant pattern analysis Genomics Next generation sequencing Epigenetics Variant analysis
  • IB-ULFRI/instructor-notes

    ELIXIR node event
    Genomics Genomics
  • SciLifeLab-Training/BGE-HiC-course

    ELIXIR node event
    Genomics Genome assembly Genome assembly Genomics
  • GTPB/AM22

    ELIXIR node event
    Genomics Metagenomics Sequencing Metagenomics Next generation sequencing Genomics
  • GTPB/CPANG22

    ELIXIR node event
    Comparative genomics Genomics Genome assembly Genomics Comparative genomics Genome assembly
  • bioinformaticsdotca/PGE_2025

    ELIXIR node event
    Public health and epidemiology Genomics Sequencing Epidemiology Genomics Next generation sequencing
  • bioinformaticsdotca/GPO_Hal-2511

    ELIXIR node event
    Genomics Variant pattern analysis Genomics Variant analysis
  • bioinformaticsdotca/HTG_2021

    ELIXIR node event
    Genomics Sequencing Genomics Next generation sequencing
  • bioinformaticsdotca/PGX_2024

    ELIXIR node event
    Genomics Multiomics RNA-Seq Multiomics RNA-seq R Genomics
  • 1
  • 2
  • 3
  • 4
  • 5
  • 6
  • 7
  • 8
  • 9
  • 10
  • 11
Training eSupport System
[email protected]
Contribute
About TeSS
Browse Spaces
Funding & acknowledgements
Privacy
Cookie preferences
Version: 1.5.1
Source code
API documentation
Bioschemas testing tool

TeSS has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 676559.