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
    • Assembly3
    • DNA variation3
    • Genetic variation3
    • Genomic variation3
    • Mutation3
    • Polymorphism3
    • Sequence assembly3
    • Somatic mutations3
    • Biological sequences2
    • Sequence analysis2
    • Sequence databases2
    • Antimicrobial stewardship1
    • Comparative transcriptomics1
    • DNA polymorphism1
    • Exomes1
    • Genome annotation1
    • Genomes1
    • Genomics1
    • Medical microbiology1
    • Microbial genetics1
    • Microbial physiology1
    • Microbial surveillance1
    • Microbiological surveillance1
    • Microbiology1
    • Microsatellites1
    • Molecular infection biology1
    • Molecular microbiology1
    • Personal genomics1
    • RFLP1
    • SNP1
    • Single nucleotide polymorphism1
    • Synthetic genomics1
    • Transcriptome1
    • Transcriptomics1
    • VNTR1
    • Variable number of tandem repeat polymorphism1
    • Viral genomics1
    • Whole genomes1
    • snps1
    • Show N_FILTERS more
    • Tool
    • FastQC
    • Galaxy46
    • BWA7
    • SAMtools7
    • BEDTools6
    • DeepTools5
    • FreeBayes4
    • JBrowse4
    • MultiQC4
    • BamTools3
    • Falco3
    • Stacks3
    • Trimmomatic3
    • Bandage2
    • Cutadapt2
    • GEMINI2
    • HISAT22
    • QUAST2
    • SPAdes2
    • Unicycler2
    • Vcflib2
    • VelvetOptimiser2
    • bx-python2
    • lofreq2
    • mothur2
    • taxonomy_krona_chart2
    • BCFtools1
    • Bowtie 21
    • Bwa-mem21
    • Circos1
    • DESeq21
    • FASTQE1
    • FeatureCounts1
    • GOseq1
    • Galactic Circos1
    • HUMAnN21
    • HiCExplorer1
    • IWTomics1
    • Krona1
    • MEME1
    • MetaPhlAn1
    • MethylDackel1
    • NanoPlot1
    • Newick Utilities1
    • Peakachu1
    • R1
    • RCAS1
    • RSeQC1
    • SRA Software Toolkit1
    • STAR1
    • Salmon1
    • UMI-tools1
    • UniProt1
    • WoLF PSORT1
    • compute_sequence_length1
    • fastp1
    • ggplot21
    • msConvert1
    • pathview1
    • pyGenomeTracks1
    • pycoQC1
    • seqtk1
    • snippy1
    • snpEff1
    • Show N_FILTERS more
    • Content provider
    • GTN7
    • Show N_FILTERS more
    • Keyword
    • Variant Analysis3
    • Assembly2
    • Sequence analysis1
    • Transcriptomics1
    • microgalaxy1
    • prokaryote1
    • Show N_FILTERS more
    • Competency level
    • Beginner7
    • Show N_FILTERS more
    • Licence
    • Creative Commons Attribution 4.0 International7
    • Show N_FILTERS more
    • Target audience
    • Students7
    • Show N_FILTERS more
    • Author
    • Bérénice Batut3
    • Anton Nekrutenko2
    • Simon Gladman2
    • Alex Ostrovsky1
    • Alexandre Cormier1
    • Anika Erxleben1
    • Anthony Bretaudeau1
    • Björn Grüning1
    • Daniel Maticzka1
    • Erwan Corre1
    • Florian Heyl1
    • Laura Leroi1
    • Nick Stoler1
    • Stéphanie Robin1
    • Torsten Houwaart1
    • Wolfgang Maier1
    • Show N_FILTERS more
    • Contributor
    • Niall Beard
    • Helena Rasche34
    • Saskia Hiltemann31
    • Björn Grüning27
    • Bérénice Batut23
    • Cristóbal Gallardo19
    • Nicola Soranzo13
    • Anthony Bretaudeau7
    • Wolfgang Maier7
    • Gildas Le Corguillé6
    • William Durand6
    • Lucille Delisle5
    • Maria Doyle5
    • Mehmet Tekman5
    • Paul Zierep5
    • Teresa Müller4
    • Tristan Reynolds4
    • Wendi Bacon4
    • Alexandre Cormier3
    • Florian Heyl3
    • Martin Čech3
    • Mateo Boudet3
    • Pavankumar Videm3
    • Anna Syme2
    • Anne Fouilloux2
    • Anup Kumar2
    • Armin Dadras2
    • Beatriz Serrano-Solano2
    • Christine Oger2
    • David López2
    • Deepti Varshney2
    • Engy Nasr2
    • Hans-Rudolf Hotz2
    • Joachim Wolff2
    • Leily Rabbani2
    • Linelle Abueg2
    • Morgan Howells2
    • Mélanie Petera2
    • Natalie Kucher2
    • Simon Gladman2
    • Swathi Nataraj2
    • Yvan Le Bras2
    • Ahmed Hamid Awan1
    • Alex Ostrovsky1
    • Anika Erxleben1
    • Anton Nekrutenko1
    • Antonia Taiani1
    • Ava Hoffman1
    • Bazante Sanders1
    • Bert Droesbeke1
    • Candace Savonen1
    • Ekaterina Polkh1
    • Elizabeth Humphries1
    • Frederick Tan1
    • José Manuel Domínguez1
    • Katarzyna Kamieniecka1
    • Katherine Cox1
    • Khaled Jum'ah1
    • Marie Josse1
    • Marisa Loach1
    • Marius van den Beek1
    • Matthias Bernt1
    • Matti Hoch1
    • Matúš Kalaš1
    • Miaomiao Zhou1
    • Mira Kuntz1
    • Mohua Das1
    • Natalie Whitaker-Allen1
    • Nate Coraor1
    • Nuwan Goonasekera1
    • Peter van Heusden1
    • Phil Reed1
    • Polina Polunina1
    • Sanjay Kumar Srikakulam1
    • Simon Bray1
    • Siyu Chen1
    • Subina Mehta1
    • Timon Schlegel1
    • Verena Moosmann1
    • Vijay1
    • Show N_FILTERS more
    • Resource type
    • e-learning5
    • slides2
    • Show N_FILTERS more
    • Related resource
    • Associated Training Datasets7
    • Associated Workflows7
    • 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

Tools: FastQC

and Contributors: Niall Beard

7 materials found
  • e-learning

    Exome sequencing data analysis for diagnosing a genetic disease

    • Beginner
    Genetic variation Variant Analysis
  • e-learning

    Calling variants in non-diploid systems

    • Beginner
    Genetic variation Genomics Sequence assembly DNA polymorphism Microbiology Sequence analysis Variant Analysis microgalaxy prokaryote
  • e-learning

    Calling very rare variants

    • Beginner
    Genetic variation Variant Analysis
  • e-learning

    An Introduction to Genome Assembly

    • Beginner
    Sequence assembly Assembly
  • e-learning

    CLIP-Seq data analysis from pre-processing to motif detection

    • Beginner
    Transcriptomics Transcriptomics
  • slides

    An Introduction to Genome Assembly

    • Beginner
    Sequence assembly Assembly
  • slides

    Quality Control

    • Beginner
    Sequence analysis Sequence analysis
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.