- Home
- Materials
Filters
Sort
-
-
Filter Clear filters
-
-
Scientific topic
- Variant pattern analysis29
- Chromosome walking18
- Clone verification18
- DNA-Seq18
- DNase-Seq18
- High throughput sequencing18
- High-throughput sequencing18
- NGS18
- NGS data analysis18
- Next gen sequencing18
- Next generation sequencing18
- Panels18
- Primer walking18
- Sanger sequencing18
- Sequencing18
- Targeted next-generation sequencing panels18
- Genome annotation17
- Exomes16
- Genomes16
- Genomics16
- Personal genomics16
- Synthetic genomics16
- Viral genomics16
- Whole genomes16
- MicroRNA sequencing8
- RNA sequencing8
- RNA-Seq8
- RNA-Seq analysis8
- Small RNA sequencing8
- Small RNA-Seq8
- Small-Seq8
- Transcriptome profiling8
- WTSS8
- Whole transcriptome shotgun sequencing8
- miRNA-seq8
- Comparative transcriptomics7
- Transcriptome7
- Transcriptomics7
- ChIP-exo6
- ChIP-seq6
- ChIP-sequencing6
- Chip Seq6
- Chip sequencing6
- Chip-sequencing6
- DNA methylation6
- Epigenetics6
- Histone modification6
- Methylation profiles6
- Pipelines4
- Single-cell genomics4
- Single-cell sequencing4
- Software integration4
- Tool integration4
- Tool interoperability4
- Workflows4
- Bayesian methods3
- Biostatistics3
- Breakend assembly3
- Data rendering3
- Data visualisation3
- Descriptive statistics3
- Functional genome annotation3
- Gaussian processes3
- Genome assembly3
- Genomic assembly3
- Inferential statistics3
- Markov processes3
- Metagenome annotation3
- Metagenomics3
- Multivariate statistics3
- Probabilistic graphical model3
- Probability3
- Sequence assembly (genome assembly)3
- Shotgun metagenomics3
- Statistics3
- Statistics and probability3
- Structural genome annotation3
- CWL2
- Common Workflow Language2
- CommonWL2
- Comparative genomics2
- Data management2
- FAIR data2
- Findable, accessible, interoperable, reusable data2
- Metadata management2
- Research data management (RDM)2
- Active learning1
- Antimicrobial stewardship1
- Bottom-up proteomics1
- Discovery proteomics1
- Enrichment1
- Enrichment analysis1
- Ensembl learning1
- Exometabolomics1
- Functional enrichment1
- Kernel methods1
- Knowledge representation1
- LC-MS-based metabolomics1
- MS-based metabolomics1
- MS-based targeted metabolomics1
- Show N_FILTERS more
-
-
-
Content provider
- Glittr.org1
- Show N_FILTERS more
-
-
-
Keyword
- Variant analysis
- Metabolomics14
- Galaxy2
- Metabolites2
- Metabolome2
- ATAC-seq1
- ChIP-seq1
- Comparative genomics1
- Data management1
- Data science1
- ELIXIR RIR, BridgeDb1
- Epigenetics1
- FAIR data1
- General1
- Genome annotation1
- Genome assembly1
- Genomics1
- Identifiers1
- Long read sequencing1
- MGnify1
- Machine learning1
- Mass spectrometry1
- Metagenomics1
- Microbiology1
- NMR spectroscopy1
- Next generation sequencing1
- Proteomics1
- Python1
- R1
- RDM1
- RNA-seq1
- Reproducibility1
- Single-cell sequencing1
- Small molecules1
- Snakemake1
- Spatial omics1
- Statistics1
- Transcriptomics1
- Unix/Linux1
- Version control1
- Workshop1
- hologenomics1
- metagenomics1
- multi-omics data integration1
- networks and pathways1
- single-cell transcriptomics1
- Show N_FILTERS more
-
-
-
Difficulty level
- Not specified1
- Show N_FILTERS more
-
-
-
Licence
- MIT License1
- Show N_FILTERS more
-
-
-
Contributor
- Galaxy Project1
- Show N_FILTERS more
-
- Show archived materials