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
    • Somatic mutations
    • DNA variation3
    • Genetic variation3
    • Genomic variation3
    • Mutation3
    • Polymorphism3
    • Comparative transcriptomics2
    • Transcriptome2
    • Transcriptomics2
    • Antimicrobial stewardship1
    • Biological sequences1
    • ChIP-exo1
    • ChIP-seq1
    • ChIP-sequencing1
    • Chip Seq1
    • Chip sequencing1
    • Chip-sequencing1
    • Communicable disease1
    • DNA polymorphism1
    • Epigenomics1
    • Evolution1
    • Evolutionary biology1
    • Exomes1
    • Genome annotation1
    • Genomes1
    • Genomics1
    • Infectious disease1
    • Medical microbiology1
    • Microbial genetics1
    • Microbial physiology1
    • Microbial surveillance1
    • Microbiological surveillance1
    • Microbiology1
    • Microsatellites1
    • Molecular infection biology1
    • Molecular microbiology1
    • Personal genomics1
    • RFLP1
    • SNP1
    • Sequence analysis1
    • Sequence databases1
    • Single nucleotide polymorphism1
    • Synthetic genomics1
    • Transmissible disease1
    • VNTR1
    • Variable number of tandem repeat polymorphism1
    • Viral genomics1
    • Whole genomes1
    • snps1
    • Show N_FILTERS more
    • Tool
    • Trimmomatic
    • Galaxy16
    • BWA9
    • SAMtools7
    • FreeBayes6
    • FastQC5
    • BCFtools4
    • GEMINI4
    • fastp4
    • MultiQC3
    • QualiMap3
    • Vcflib3
    • BamTools2
    • Falco2
    • MAFFT2
    • SRA Software Toolkit2
    • iVar2
    • snippy2
    • COMBAT-TB Workbench1
    • EGA1
    • FREEC1
    • Galactic Circos1
    • JBrowse1
    • Jvarkit1
    • NCBI Resources1
    • Nextclade1
    • Trim Galore1
    • UCSC Genome Browser Utilities1
    • VAPOR1
    • VarScan1
    • compute_sequence_length1
    • ggplot21
    • iqtree1
    • kraken21
    • lofreq1
    • pangolin1
    • seqtk1
    • snpEff1
    • tb-profiler1
    • Show N_FILTERS more
    • Content provider
    • Galaxy Training3
    • Show N_FILTERS more
    • Keyword
    • Variant Analysis3
    • Show N_FILTERS more
    • Difficulty level
    • Beginner3
    • Show N_FILTERS more
    • Licence
    • Creative Commons Attribution 4.0 International3
    • Show N_FILTERS more
    • Target audience
    • Students3
    • Show N_FILTERS more
    • Author
    • Wolfgang Maier3
    • Anika Erxleben1
    • Björn Grüning1
    • Bérénice Batut1
    • David Salgado1
    • Katarzyna Kamieniecka1
    • Khaled Jum'ah1
    • Krzysztof Poterlowicz1
    • Torsten Houwaart1
    • Show N_FILTERS more
    • Contributor
    • Björn Grüning3
    • Helena Rasche3
    • Saskia Hiltemann3
    • Wolfgang Maier3
    • Bérénice Batut2
    • Simon Gladman2
    • Verena Moosmann2
    • Armin Dadras1
    • Ekaterina Polkh1
    • Gildas Le Corguillé1
    • Katarzyna Kamieniecka1
    • Khaled Jum'ah1
    • Martin Čech1
    • Niall Beard1
    • Nicola Soranzo1
    • Teresa Müller1
    • Show N_FILTERS more
    • Resource type
    • e-learning
    • Show N_FILTERS more
    • Related resource
    • Associated Training Datasets3
    • Associated Workflows3
    • 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

e-Learning

  • Subscribe via email

Email Subscription

Register training material

Scientific topics: Somatic mutations

and Tools: Trimmomatic

and Resource type: e-learning

3 e-learning materials found
  • 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

    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.