Training materials
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genome/bfx-workshop
Workflows Data visualisation ChIP-seq Epigenetics Genomics Metagenomics Sequencing RNA-Seq Single-cell sequencing Variant pattern analysis Docker Data visualization Python R Unix/Linux ATAC-seq Next generation sequencing RNA-seq Variant analysis Long read sequencing
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Functional-Genomics-Lab/Applied-Genomics
ChIP-seq Epigenetics Genomics RNA-Seq Variant pattern analysis Containerization High performance computing Nextflow Singularity Reproducibility Unix/Linux Version control RNA-seq Variant analysis Julia
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IFB-ElixirFr/EBAII
ChIP-seq Sequencing RNA-Seq Variant pattern analysis R Unix/Linux Next generation sequencing RNA-seq Variant analysis
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WCSCourses/SARS-COV-2_B4B
Genomics Variant pattern analysis Unix/Linux Variant analysis
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eriqande/eca-bioinf-handbook
Genome assembly Genomics Variant pattern analysis General R Unix/Linux Version control 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