Training materials
-
stjude/learngenomics.dev
Genomics Sequencing Variant pattern analysis General Next generation sequencing Variant analysis
-
eriqande/eca-bioinf-handbook
Genome assembly Genomics Variant pattern analysis General R Unix/Linux Version control Variant analysis
-
liulab-dfci/bioinfo-combio
ChIP-seq Epigenetics Genomics Sequencing Single-cell sequencing Transcriptomics Variant pattern analysis General ATAC-seq Next generation sequencing Variant analysis
-
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
-
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
-
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