Materials - TeSS (Training eSupport System)

Filter Clear filters
- Date added
- In the last 24 hours
- In the last 1 week
- In the last 1 month
- Scientific topic
- Exomes75
- Genome annotation75
- Genomes75
- Genomics75
- Personal genomics75
- Synthetic genomics75
- Viral genomics75
- Whole genomes75
- Chromosome walking20
- Clone verification20
- DNA-Seq20
- DNase-Seq20
- High throughput sequencing20
- High-throughput sequencing20
- NGS20
- NGS data analysis20
- Next gen sequencing20
- Next generation sequencing20
- Panels20
- Primer walking20
- Sanger sequencing20
- Sequencing20
- Targeted next-generation sequencing panels20
- MicroRNA sequencing13
- RNA sequencing13
- RNA-Seq13
- RNA-Seq analysis13
- Small RNA sequencing13
- Small RNA-Seq13
- Small-Seq13
- Transcriptome profiling13
- WTSS13
- Whole transcriptome shotgun sequencing13
- miRNA-seq13
- Breakend assembly11
- Genome assembly11
- Genomic assembly11
- Sequence assembly (genome assembly)11
- Variant pattern analysis11
- Comparative transcriptomics8
- Transcriptome8
- Transcriptomics8
- Comparative genomics6
- Data rendering6
- Data visualisation6
- Sequence read processing5
- Functional genome annotation4
- Metagenome annotation4
- Metagenomics4
- Population genetics4
- Shotgun metagenomics4
- Single-cell genomics4
- Single-cell sequencing4
- Structural genome annotation4
- Active learning3
- Bayesian methods3
- Biostatistics3
- DNA methylation3
- Descriptive statistics3
- Ensembl learning3
- Epidemiology3
- Epigenetics3
- Gaussian processes3
- Histone modification3
- Inferential statistics3
- Integrative omics3
- Kernel methods3
- Knowledge representation3
- Machine learning3
- Markov processes3
- Methylation profiles3
- Multi-omics3
- Multiomics3
- Multivariate statistics3
- Neural networks3
- Pan-omics3
- Panomics3
- Probabilistic graphical model3
- Probability3
- Public health3
- Public health and epidemiology3
- Recommender system3
- Reinforcement learning3
- Statistics3
- Statistics and probability3
- Supervised learning3
- Unsupervised learning3
- Bioinformatics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Data management2
- Metadata management2
- Phylogenetics2
- Research data management (RDM)2
- Antimicrobial stewardship1
- Content management1
- Show N_FILTERS more
- Standard database or policy
- Genomics England | PanelApp1
- Show N_FILTERS more
- Content provider
- Glittr.org51
- ERGA Knowledge Hub20
- Centre for Genomic Regulation (CRG)3
- GOBLET2
- Show N_FILTERS more
- Keyword
- Genomics
- R191
- Python69
- Next generation sequencing67
- Transcriptomics67
- RNA-seq66
- Data management46
- Statistics45
- Data science42
- Reproducibility36
- Machine learning32
- Single-cell sequencing32
- Unix/Linux32
- FAIR data30
- Data visualization29
- Genome28
- Molecular28
- Version control26
- Variant analysis22
- Metagenomics21
- Bioinformatics20
- Workflows20
- General18
- FAIR17
- Genome assembly17
- life-sciences17
- Containerization16
- Phylogenetics16
- Microbiology15
- Anatomy Physiology and Atlases14
- Shell13
- Spatial transcriptomics13
- Docker12
- Introduction12
- health-informatics12
- Cells and Organisms11
- Cloud computing11
- Genome annotation11
- Introduction bioinformatics11
- Long read sequencing11
- Nextflow11
- Pathway11
- plant phenotyping11
- Europe PMC10
- Extras10
- Programming10
- databases10
- Comparative genomics9
- FAIRsharing9
- High performance computing9
- Python biologists9
- computer-science9
- policies9
- standards9
- Artificial intelligence8
- Epidemiology8
- Galaxy8
- Git8
- Inferential statistics8
- Literature search8
- PDBe8
- Pathways and Networks8
- Populations8
- Quarto8
- Regex8
- Rmarkdown8
- algorithms8
- Biomedical Literature7
- ChIP-seq7
- Image analysis7
- Information visualisation7
- Intro7
- Make7
- NGS7
- Protein families7
- Proteomics7
- Ref7
- Snakemake7
- Systems biology7
- Communication6
- Enrichment analysis6
- Epigenetics6
- Genome sequencing6
- Julia6
- Multiomics6
- Network analysis6
- Protein sequence analysis6
- Sequence alignments6
- Variants6
- biotic interactions6
- insects6
- intercropping6
- plant disease6
- AI based tools5
- ATAC-seq5
- Biocuration5
- Hg5
- Independent and dependent events5
- Matlab5
- Multiple sequence alignment5
- Show N_FILTERS more
- Competency level
- Not specified
- Show N_FILTERS more
- Licence
- License Not Specified
- Creative Commons Attribution 4.0 International33
- MIT License12
- GNU General Public License v3.0 only11
- Creative Commons Zero v1.0 Universal4
- Creative Commons Attribution Non Commercial 4.0 International1
- Show N_FILTERS more
- Target audience
- Life Science Researchers2
- Researchers2
- Clinical Scientists1
- Data Access Committeses from the EGA1
- Master students1
- Professors1
- 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
- healthcare professionals1
- postgrad1
- Show N_FILTERS more
- Author
- Data Carpentry6
- bioinformatics.ca6
- The Gulbenkian Training Programme in Bioinformatics4
- Canadian Bioinformatics Workshops3
- The Carpentries Lab2
- Andries Marees1
- Applied Genomics1
- Biocore@CRG1
- Bioinformatics, Rockefeller University1
- BiotrAIn1
- Celia van Gelder1
- Computational Genomics with R1
- Computational Metagenomics1
- Ellen McDonagh1
- Functional Genomics Laboratory1
- IB-ULFRI1
- Jan Paces1
- Jan Taylor1
- Kristyna Kupkova1
- Leonardo Collado-Torres1
- Melbourne Bioinformatics1
- Mike Lee1
- NBIS - National Bioinformatics Infrastructure Sweden1
- Nanopore for Educators1
- Pachter Lab1
- Papenfuss Lab1
- 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
- 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
- Video3
- Presentation2
- 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
- EGA Submitter Portal Tutorial1
- 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
- Show N_FILTERS more
- Node
- Switzerland71
- Spain3
- Czech Republic1
- Show N_FILTERS more
- Collection
- ELIXIR Federated Human Data Community3
- VEIS - Value of the EGA for Industry and Society3
- ELIXIR Biodiversity Community1
- Show N_FILTERS more
- Status
- Active1
- Show N_FILTERS more
Show materials from all spaces
Show disabled materials
Show materials with broken links
Show archived materials

Training materials

Register training material

Keywords: Genomics

and Competency level: Not specified

and Licence: License Not Specified

78 materials found

Results per page:

1
2
3
4
5
6
7
8