Training materials
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Introduction to Bayesian Inference using Stan with Applications to Cancer Genomics
Statistics and probability
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Analyzing splice events from RNA-seq data with SGSeq
RNA-Seq
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Hello Ranges: An Introduction to Analyzing Genomic Ranges in R
Genomics
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Low-level exploratory data analysis and methods development for RNA-seq
RNA-Seq
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Annotating high throughput data using Bioconductor resources
Annotation
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Managing big biological sequence data with Biostrings and DECIPHER
Sequence Analysis
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Building and running automated NGS analysis workflows
workflows
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R Graphics
Graphics
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Independent Hypothesis Weighting
Statistics and probability
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Reproducible research and R authoring with markdown and knitr
Git