- Home
- Materials
Filters
Sort
-
-
Filter Clear filters
-
-
Scientific topic
- Software integration
- R141
- R program141
- R script141
- Comparative transcriptomics88
- Transcriptome88
- Transcriptomics88
- MicroRNA sequencing82
- RNA sequencing82
- RNA-Seq82
- RNA-Seq analysis82
- Small RNA sequencing82
- Small RNA-Seq82
- Small-Seq82
- Transcriptome profiling82
- WTSS82
- Whole transcriptome shotgun sequencing82
- miRNA-seq82
- Chromosome walking65
- Clone verification65
- DNA-Seq65
- DNase-Seq65
- High throughput sequencing65
- High-throughput sequencing65
- NGS65
- NGS data analysis65
- Next gen sequencing65
- Next generation sequencing65
- Panels65
- Primer walking65
- Python65
- Python program65
- Python script65
- Sanger sequencing65
- Sequencing65
- Targeted next-generation sequencing panels65
- py65
- Bayesian methods61
- Biostatistics61
- Descriptive statistics61
- Gaussian processes61
- Inferential statistics61
- Markov processes61
- Multivariate statistics61
- Probabilistic graphical model61
- Probability61
- Statistics61
- Statistics and probability61
- Genome annotation55
- Exomes52
- Genomes52
- Genomics52
- Personal genomics52
- Synthetic genomics52
- Viral genomics52
- Whole genomes52
- Active learning51
- Ensembl learning51
- Kernel methods51
- Knowledge representation51
- Machine learning51
- Neural networks51
- Recommender system51
- Reinforcement learning51
- Supervised learning51
- Unsupervised learning51
- Single-cell genomics49
- Single-cell sequencing49
- Data management41
- Metadata management41
- Research data management (RDM)40
- Data rendering35
- Data visualisation35
- FAIR data34
- Findable, accessible, interoperable, reusable data34
- Variant pattern analysis29
- Pipelines21
- Tool integration21
- Tool interoperability21
- Workflows21
- Metagenomics18
- Shotgun metagenomics18
- ChIP-exo15
- ChIP-seq15
- ChIP-sequencing15
- Chip Seq15
- Chip sequencing15
- Chip-sequencing15
- DNA methylation11
- Epigenetics11
- Histone modification11
- Image analysis11
- Methylation profiles11
- R markdown10
- Bottom-up proteomics8
- Breakend assembly8
- Discovery proteomics8
- Genome assembly8
- Genomic assembly8
- MS-based targeted proteomics8
- Show N_FILTERS more
-
-
-
Keyword
- Workflows21
- Nextflow10
- Snakemake5
- Containerization4
- Variant analysis4
- CWL3
- Data visualization3
- Docker3
- Reproducibility3
- ATAC-seq2
- Epigenetics2
- Metagenomics2
- Python2
- R2
- RNA-seq2
- Unix/Linux2
- ChIP-seq1
- Comparative genomics1
- Data management1
- General1
- Genome annotation1
- Genome assembly1
- Genomics1
- Long read sequencing1
- Machine learning1
- Next generation sequencing1
- Single-cell sequencing1
- Singularity1
- Transcriptomics1
- Version control1
- Show N_FILTERS more
-
-
-
Difficulty level
- Not specified21
- Show N_FILTERS more
-
-
-
Author
- carpentries-incubator4
- Biocore@CRG3
- Biodata Analysis Group1
- BovReg1
- CRUK CI Bioinformatics Core1
- Dockstore1
- Fred Hutch Data Science Lab1
- Genome Informatics Facility1
- NIAID BCBB1
- PeriMatrix IT Consultancy1
- R. Burke Squires1
- Romain Feron1
- SIB Swiss Institute of Bioinformatics1
- Sateesh_Peri1
- Seqera1
- The McDonnell Genome Institute1
- VIB Technologies: Training material and software projects1
- Workflow Languages in R1
- Show N_FILTERS more
-
-
-
Contributor
- carpentries-incubator4
- Biocore@CRG3
- Biodata Analysis Group1
- BovReg1
- CRUK CI Bioinformatics Core1
- Dockstore1
- Fred Hutch Data Science Lab1
- Genome Informatics Facility1
- NIAID BCBB1
- PeriMatrix IT Consultancy1
- R. Burke Squires1
- Romain Feron1
- SIB Swiss Institute of Bioinformatics1
- Sateesh_Peri1
- Seqera1
- The McDonnell Genome Institute1
- VIB Technologies: Training material and software projects1
- Workflow Languages in R1
- Show N_FILTERS more
-
- Show archived materials
