Training materials
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fhdsl/Choosing_Genomics_Tools
ChIP-seq Epigenetics Genome annotation Genomics Sequencing RNA-Seq Single-cell sequencing Transcriptomics Variant pattern analysis ATAC-seq Next generation sequencing RNA-seq Spatial transcriptomics Variant analysis
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ErasmusMC-Bioinformatics/galaxy-courses
Sequencing RNA-Seq Transcriptomics Variant pattern analysis Galaxy Next generation sequencing RNA-seq Variant analysis
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griffithlab/pmbio.org
CWL Genomics Sequencing Transcriptomics Variant pattern analysis Next generation sequencing Variant analysis
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liulab-dfci/bioinfo-combio
ChIP-seq Epigenetics Genomics Sequencing Single-cell sequencing Transcriptomics Variant pattern analysis General ATAC-seq Next generation sequencing Variant analysis
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ISUgenomics/bioinformatics-workbook
Workflows Data management Data visualisation Comparative genomics Epigenetics Genome annotation Genome assembly Metagenomics RNA-Seq Transcriptomics Variant pattern analysis Nextflow General Data visualization Unix/Linux ATAC-seq RNA-seq Variant analysis
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hbctraining/Training-modules
FAIR data Data visualisation R markdown Enrichment analysis RNA-Seq Transcriptomics Variant pattern analysis General Data visualization Python R Rmarkdown Unix/Linux Version control RNA-seq Variant analysis
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galaxyproject/training-material
Data management FAIR data ChIP-seq Comparative genomics Epigenetics Genome annotation Genome assembly Genomics Metagenomics Microbiology Sequencing RNA-Seq Single-cell sequencing Transcriptomics Variant pattern analysis Machine learning Statistics and probability Metabolomics Proteomics Galaxy Snakemake General Reproducibility Python R Unix/Linux Version control ATAC-seq Next generation sequencing RNA-seq Variant analysis Data science Statistics Long read sequencing