- Home
- Materials
Filter
Sort
-
-
Filter Clear filters
-
-
Scientific topic
- Genomics
- Pipelines22
- Software integration22
- Tool integration22
- Tool interoperability22
- Workflows22
- Variant pattern analysis4
- CWL3
- Common Workflow Language3
- CommonWL3
- Data rendering3
- Data visualisation3
- DNA methylation2
- Epigenetics2
- Genome annotation2
- Histone modification2
- Metagenomics2
- Methylation profiles2
- MicroRNA sequencing2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Shotgun metagenomics2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Transcriptome profiling2
- WTSS2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Active learning1
- Applied ontology1
- Breakend assembly1
- ChIP-exo1
- ChIP-seq1
- ChIP-sequencing1
- Chip Seq1
- Chip sequencing1
- Chip-sequencing1
- Chromosome walking1
- Clone verification1
- Comparative genomics1
- Comparative transcriptomics1
- DNA-Seq1
- DNase-Seq1
- Data management1
- Ensembl learning1
- Exomes1
- Functional genome annotation1
- Genome assembly1
- Genomes1
- Genomic assembly1
- High throughput sequencing1
- High-throughput sequencing1
- Kernel methods1
- Knowledge representation1
- Machine learning1
- Metadata management1
- Metagenome annotation1
- NGS1
- NGS data analysis1
- Neural networks1
- Next gen sequencing1
- Next generation sequencing1
- Ontologies1
- Ontology1
- Ontology and terminology1
- Ontology relations1
- Panels1
- Personal genomics1
- Primer walking1
- Recommender system1
- Reinforcement learning1
- Research data management (RDM)1
- Sanger sequencing1
- Sequence assembly (genome assembly)1
- Sequencing1
- Single-cell genomics1
- Single-cell sequencing1
- Structural genome annotation1
- Supervised learning1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Terminology1
- Transcriptome1
- Transcriptomics1
- Unsupervised learning1
- Upper ontology1
- Viral genomics1
- Whole genomes1
- Show N_FILTERS more
-
-
-
Content provider
- Glittr.org1
- Show N_FILTERS more
-
-
-
Keyword
- Workflows
- Genomics52
- Next generation sequencing23
- microgalaxy17
- Variant analysis16
- R14
- RNA-seq10
- Unix/Linux10
- prokaryote10
- Transcriptomics9
- General8
- ATAC-seq6
- ChIP-seq6
- Data visualization6
- Epigenetics6
- Genome Annotation6
- Single-cell sequencing6
- gmod6
- jbrowse16
- Metagenomics5
- Statistics5
- illumina5
- Assembly4
- Genome assembly4
- Version control4
- bacteria4
- one-health4
- Comparative genomics3
- Data management3
- Epidemiology3
- Genome annotation3
- Long read sequencing3
- Reproducibility3
- Variant Analysis3
- Cloud computing2
- Data science2
- Evolution2
- FAIR data2
- Galaxy2
- Multiomics2
- Python2
- Snakemake2
- amr2
- assembly2
- API1
- CWL1
- Containerization1
- Designing functional genomics experiments1
- Docker1
- Ecology1
- Enrichment analysis1
- Genome sequencing1
- Gramene database1
- High performance computing1
- Introduction1
- Julia1
- Machine learning1
- Metabolomics1
- Microbiology1
- Nextflow1
- Perl1
- Programmatic access1
- Proteomics1
- Rmarkdown1
- Sequence alignments1
- Sequence analysis1
- Singularity1
- Spatial omics1
- Spatial transcriptomics1
- annotation1
- apollo21
- cookbook1
- essential genes1
- eukaryote1
- evolution1
- multi-omics data integration1
- nanopore1
- phylogenetics1
- tnseq1
- tuberculosis1
- vgp1
- Show N_FILTERS more
-
-
-
Difficulty level
- Not specified1
- Show N_FILTERS more
-
-
-
Contributor
- The McDonnell Genome Institute1
- Show N_FILTERS more
-
- Show disabled materials
- Show archived materials