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
    • Comparative genomics16
    • Genome annotation13
    • Exomes9
    • Genomes9
    • Genomics9
    • Personal genomics9
    • Synthetic genomics9
    • Viral genomics9
    • Whole genomes9
    • Functional genome annotation7
    • Metagenome annotation7
    • Structural genome annotation7
    • Breakend assembly6
    • Genome assembly6
    • Genomic assembly6
    • Sequence assembly (genome assembly)6
    • Comparative transcriptomics2
    • Metagenomics2
    • Shotgun metagenomics2
    • Transcriptome2
    • Transcriptomics2
    • DNA methylation1
    • Data management1
    • Data rendering1
    • Data visualisation1
    • Enrichment1
    • Enrichment analysis1
    • Epigenetics1
    • Functional enrichment1
    • Genetic variation analysis1
    • Genetic variation annotation1
    • Histone modification1
    • Metadata management1
    • Methylation profiles1
    • MicroRNA sequencing1
    • Over-representation analysis1
    • Phylogenetics1
    • Pipelines1
    • Population genetics1
    • RNA sequencing1
    • RNA-Seq1
    • RNA-Seq analysis1
    • Research data management (RDM)1
    • Sequence read processing1
    • Sequence variation analysis1
    • Small RNA sequencing1
    • Small RNA-Seq1
    • Small-Seq1
    • Software integration1
    • Tool integration1
    • Tool interoperability1
    • Transcript variant analysis1
    • Transcriptome profiling1
    • Variant analysis1
    • Variant pattern analysis1
    • WTSS1
    • Whole transcriptome shotgun sequencing1
    • Workflows1
    • miRNA-seq1
    • Show N_FILTERS more
    • Content provider
    • Glittr.org9
    • ERGA Knowledge Hub8
    • Show N_FILTERS more
    • Keyword
    • Comparative genomics
    • R297
    • Python121
    • Genomics119
    • Transcriptomics115
    • Next generation sequencing113
    • RNA-seq110
    • Data management74
    • Statistics74
    • Data science64
    • Machine learning61
    • Unix/Linux60
    • Single-cell sequencing59
    • FAIR data57
    • Reproducibility56
    • Variant analysis48
    • Data visualization47
    • Version control47
    • Genome assembly39
    • General36
    • Genome annotation34
    • training30
    • Long read sequencing26
    • Metagenomics26
    • Workflows26
    • Containerization22
    • High performance computing21
    • Shiny21
    • Spatial transcriptomics21
    • FAIR20
    • Docker18
    • Microbiology18
    • Nextflow18
    • ChIP-seq16
    • Artificial intelligence15
    • Image analysis14
    • Quarto14
    • Epigenetics13
    • Galaxy13
    • Pathways and Networks13
    • ATAC-seq12
    • Clinical data11
    • Enrichment analysis11
    • Rmarkdown11
    • Cloud computing10
    • Julia10
    • Proteomics10
    • Singularity10
    • Snakemake10
    • genes and genomes10
    • Epidemiology9
    • FAIRsharing9
    • Knowledge graph9
    • Multiomics9
    • Population genetics9
    • SPARQL9
    • databases9
    • policies9
    • reproducibility9
    • standards9
    • Database Management8
    • Ontology8
    • RDF8
    • Science Communication8
    • medicine and health8
    • data management7
    • next generation sequencing7
    • programming7
    • ABS6
    • Data submission6
    • Interoperability6
    • Quality Control6
    • biostatistics6
    • data visualisation6
    • services and resources6
    • Assembly Evaluation5
    • CWL5
    • Citizen Science5
    • Educational resources5
    • Large language models5
    • Metabolomics5
    • Nagoya5
    • Phylogenetics / Phylogenomics5
    • Query data5
    • SARS-CoV-25
    • alan bridge group5
    • torsten schwede & thierry sengstag group5
    • Open Science4
    • SQL4
    • Standards4
    • basic research4
    • environmental science4
    • infectious disease4
    • mark ibberson group4
    • Data mining3
    • GNU Make3
    • GraphDB3
    • Java3
    • SNOMED CT3
    • Semantic Framework3
    • Show N_FILTERS more
    • Competency level
    • Not specified17
    • Show N_FILTERS more
    • Licence
    • License Not Specified9
    • Creative Commons Attribution 4.0 International5
    • MIT License2
    • Creative Commons Zero v1.0 Universal1
    • Show N_FILTERS more
    • Author
    • The Gulbenkian Training Programme in Bioinformatics3
    • Galaxy Project1
    • Genome Informatics Facility1
    • SIB Swiss Institute of Bioinformatics1
    • SLU Global Bioinformatics Centre1
    • Steven M. Van Belleghem1
    • ebp-nor1
    • Show N_FILTERS more
    • Contributor
    • The Gulbenkian Training Programme in Bioinformatics3
    • Erik Garrison2
    • Miguel Cardoso2
    • Aleksandra E. Badaczewska-Dawid1
    • Andrea Guarracino1
    • Andrew Severin1
    • Antonin Thiébaut1
    • Arun Seetharam1
    • Benedicte Garmann-Aarhus1
    • Bram Danneels1
    • Christopher Bottoms1
    • Ephantus Wambui1
    • Galaxy Project1
    • GitBook Bot1
    • Hadrien Gourlé1
    • Helle Tessand Baalsrud1
    • Jacques Dainat1
    • Jennifer Chang1
    • Lars Grønvold1
    • Maryam1
    • Mikko Rautiainen1
    • Natasha Glover1
    • Ole Kristian Tørresen1
    • Rick Masonbrink1
    • Sharu Paul Sharma1
    • Siva Chudalayandi1
    • Steven M. Van Belleghem1
    • Tayab Soomro1
    • Thu-Hien To1
    • VSatheesh1
    • dependabot-support1
    • hsiao yi1
    • jhayer1
    • margaretwoodhouse1
    • sm301
    • usha-m1
    • Show N_FILTERS more
    • Node
    • Switzerland
    • Norway1
    • Show N_FILTERS more
  • Show materials from all spaces
  • Show disabled materials
  • Show materials with broken links
  • Show archived materials

Training materials

  • Subscribe via email

Email Subscription

Register training material

Keywords: Comparative genomics

and Node: Switzerland

17 materials found
  • Tutorials for analysis of low-coverage whole genome sequencing data

    ELIXIR node event
    Genomics Comparative genomics Genetic variation analysis Genomics Variant analysis Comparative genomics
  • Biodiversity Genomics course

    ELIXIR node event
    Genomics Comparative genomics Population genetics Phylogenetics Genomics Next generation sequencing Comparative genomics Population genetics Phylogenetics / Phylogenomics
  • sib-swiss/biodiversity-bioinformatics

    ELIXIR node event
    Comparative genomics Transcriptomics Enrichment analysis Genome annotation Comparative genomics Transcriptomics Enrichment analysis Genome annotation Ontology
  • StevenVB12/stevenvb12.github.io

    ELIXIR node event
    Comparative genomics Genomics Comparative genomics Genomics
  • GTPB/CPANG19

    ELIXIR node event
    Comparative genomics Genomics Comparative genomics Genomics
  • ISUgenomics/bioinformatics-workbook

    ELIXIR node event
    Workflows Data management Comparative genomics Epigenetics Metagenomics Transcriptomics Data visualisation Genome annotation Genome assembly RNA-Seq …
  • galaxyproject/training-material

    ELIXIR node event
    Data management FAIR data ChIP-seq Comparative genomics Epigenetics Genomics Metagenomics Microbiology Sequencing Transcriptomics …
  • 1
  • 2
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.