Please note: This instance is for testing/development, and any content submitted may be changed or deleted without warning.
Training eSupport System
  • Log In
    • Login
    • Register
  • About
  • Events
  • Materials
  • e-Learning
  • Workflows
  • Collections
  • Learning paths
  • Directory
    • Trainers
    • Providers
    • Nodes

TeSS makes use of some necessary cookies to provide its core functionality.

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
  1. Home
  2. Materials

Filter

  • Sort

  • Filter Clear filters

    • Scientific topic
    • Polymorphism
    • DNA variation6
    • Genetic variation6
    • Genomic variation6
    • Mutation6
    • Somatic mutations6
    • Biological sequences2
    • Sequence analysis2
    • Sequence databases2
    • Assembly1
    • Sequence assembly1
    • Show N_FILTERS more
    • Tool
    • Galaxy6
    • BWA4
    • SAMtools4
    • FreeBayes3
    • GEMINI3
    • Trimmomatic3
    • BCFtools2
    • Falco2
    • FastQC2
    • MultiQC2
    • EGA1
    • FREEC1
    • Galactic Circos1
    • MAFFT1
    • QualiMap1
    • UCSC Genome Browser Utilities1
    • VarScan1
    • compute_sequence_length1
    • fastp1
    • iVar1
    • Show N_FILTERS more
    • Content provider
    • Galaxy Training6
    • Show N_FILTERS more
    • Keyword
    • Variant Analysis6
    • cyoa1
    • one-health1
    • virology1
    • Show N_FILTERS more
    • Difficulty level
    • Beginner4
    • Advanced2
    • Show N_FILTERS more
    • Licence
    • Creative Commons Attribution 4.0 International6
    • Show N_FILTERS more
    • Target audience
    • Students6
    • Show N_FILTERS more
    • Author
    • Wolfgang Maier
    • Anton Nekrutenko4
    • Khaled Jum'ah2
    • Simon Gladman2
    • Alex Ostrovsky1
    • Anika Erxleben1
    • Anna Syme1
    • Björn Grüning1
    • Bérénice Batut1
    • Daniel Blankenberg1
    • Dave Clements1
    • David Salgado1
    • Helena Rasche1
    • Jasper Ouwerkerk1
    • Jörg Wennmann1
    • Katarzyna Kamieniecka1
    • Krzysztof Poterlowicz1
    • Marius van den Beek1
    • Nick Stoler1
    • Nicola Soranzo1
    • Peter van Heusden1
    • Saskia Hiltemann1
    • Thoba Lose1
    • Tomas Klingström1
    • Torsten Houwaart1
    • Torsten Seemann1
    • Show N_FILTERS more
    • Contributor
    • Helena Rasche6
    • Saskia Hiltemann6
    • Wolfgang Maier6
    • Björn Grüning5
    • Bérénice Batut3
    • Niall Beard2
    • Nicola Soranzo2
    • Simon Gladman2
    • Verena Moosmann2
    • Anton Nekrutenko1
    • Armin Dadras1
    • Ekaterina Polkh1
    • Gildas Le Corguillé1
    • Jasper Ouwerkerk1
    • Katarzyna Kamieniecka1
    • Khaled Jum'ah1
    • Lucille Delisle1
    • Martin Čech1
    • Teresa Müller1
    • Show N_FILTERS more
    • Resource type
    • e-learning6
    • Show N_FILTERS more
    • Related resource
    • Associated Workflows
    • Associated Training Datasets5
    • Show N_FILTERS more
  • Show disabled materials
  • Show archived materials
    • Date added
    • In the last 24 hours
    • In the last 1 week
    • In the last 1 month

Training materials

  • Subscribe via email

Email Subscription

Register training material

Authors: Wolfgang Maier

and Scientific topics: Polymorphism

and Related resources: Associated Workflows

6 materials found
  • e-learning

    Trio Analysis using Synthetic Datasets from RD-Connect GPAP

    ••• advanced
    Genetic variation Variant Analysis cyoa
  • e-learning

    Pox virus genome analysis from tiled-amplicon sequencing data

    ••• advanced
    Genetic variation Variant Analysis one-health virology
  • e-learning

    Somatic Variant Discovery from WES Data Using Control-FREEC

    • beginner
    Genetic variation Variant Analysis
  • e-learning

    Exome sequencing data analysis for diagnosing a genetic disease

    • beginner
    Genetic variation Variant Analysis
  • e-learning

    Mapping and molecular identification of phenotype-causing mutations

    • beginner
    Genetic variation Variant Analysis
  • e-learning

    Identification of somatic and germline variants from tumor and normal sample pairs

    • beginner
    Genetic variation Variant Analysis
Training eSupport System
contact@example.com
Contribute
About TeSS
Funding & acknowledgements
Privacy
Cookie preferences
Version: 1.5.0
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.