- Home
- Materials
Filter
Sort
-
-
Filter Clear filters
-
-
Scientific topic
- Panels
- MicroRNA sequencing2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Transcriptome profiling2
- WTSS2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- ChIP-exo1
- ChIP-seq1
- ChIP-sequencing1
- Chip Seq1
- Chip sequencing1
- Chip-sequencing1
- Chromosome walking1
- Clone verification1
- Comparative transcriptomics1
- DNA methylation1
- DNA-Seq1
- DNase-Seq1
- Epigenetics1
- Exomes1
- Genome annotation1
- Genomes1
- Genomics1
- High throughput sequencing1
- High-throughput sequencing1
- Histone modification1
- Methylation profiles1
- NGS1
- NGS data analysis1
- Next gen sequencing1
- Next generation sequencing1
- Personal genomics1
- Pipelines1
- Primer walking1
- Sanger sequencing1
- Sequencing1
- Software integration1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Tool integration1
- Tool interoperability1
- Transcriptome1
- Transcriptomics1
- Variant pattern analysis1
- Viral genomics1
- Whole genomes1
- Workflows1
- Show N_FILTERS more
-
-
-
Content provider
- Glittr.org1
- Show N_FILTERS more
-
-
-
Keyword
- Galaxy
- Next generation sequencing38
- Transcriptomics17
- RNA-seq16
- Genomics14
- R9
- Variant analysis7
- Metagenomics5
- Single-cell sequencing5
- General4
- ATAC-seq3
- ChIP-seq3
- Epigenetics3
- Unix/Linux3
- Cloud computing2
- Data management2
- FAIR data2
- Microbiology2
- Spatial transcriptomics2
- Statistics2
- Containerization1
- Data visualization1
- Docker1
- Environmental DNA1
- Genome assembly1
- Long read sequencing1
- Multiomics1
- Proteomics1
- Python1
- Reproducibility1
- Snakemake1
- Workflows1
- eDNA1
- Show N_FILTERS more
-
-
-
Difficulty level
- Not specified1
- Show N_FILTERS more
-
-
-
Contributor
- Erasmus Medical Center1
- Show N_FILTERS more
-
- Show disabled materials
- Show archived materials
