A practical guide to setting up the Integrative Genomics Viewer for personal whole-genome, RNA-seq, and copy-number data, including file indexing, pileup interpretation, batch scripting, and the failure modes that produce false confidence.
A working guide to loading your own BAM/CRAM, VCF, and RNA-seq files into IGV and igv.js: reference builds, indexing, annotation tracks, batch screenshots, and the visual checks that catch bad variant calls.
A working guide to building the handful of plots that matter for a personal molecular dataset: coverage tracks, variant pileups, copy-number profiles, expression MA and volcano plots, and a genome-wide circular summary. With real commands, file formats, and the failure modes that produce misleading pictures.
A step-by-step guide to turning transcript quantifications into plots that tell you something: sample-level QC, longitudinal gene trajectories, differential expression views, and pathway summaries, with the R and command-line code to produce them.
A step-by-step guide to producing a volcano plot from a count matrix with DESeq2 and ggplot2, choosing thresholds that mean something, and reading the resulting shape correctly, including the single-cell and mass-spectrometry variants.
A working guide to turning RNA-seq FASTQs into the handful of plots that matter: sample PCA, distance heatmaps, MA and volcano plots, and longitudinal gene trajectories, with the commands, parameters, and failure modes.
A practical guide to building violin plots from bulk and single-cell RNA-seq counts: which normalization to plot, how to set kernel bandwidth and trimming, and how to read the shapes without fooling yourself.