User guide
How to drive JBrowse once it is running. New here? Start with the JBrowse Web or JBrowse Desktop quickstart.
General usage
Track types
Views
Sequence tools
Analysis
JBrowse 2Clustering rowsReorder a multi-row track's rows by similarity, read the dendrogram, and filter to a subtree
SV visualizationReading structural variant evidence off the reads
Tutorials
Getting started
genomes.jbrowse.org
- Basic usage of genomes.jbrowse.org
- Synteny on genomes.jbrowse.org
- Proteins on genomes.jbrowse.org
- RepeatMasker as one row per class
Synteny & comparative genomics
Whole-genome alignments
- Synteny visualization (pairwise minimap2)
- Comparing one genome's two haplotypes (T2T-HG002)
- Synteny from liftOver chains (hg38 and eight vertebrates)
- Synteny from a Cactus alignment (T2T apes)
- Synteny visualization (all-vs-all minimap2)
- Rearrangements between genomes by type (SyRI)
- Synteny on a circle (human and mouse)
Ortholog tables
- Synteny from MCScan anchors (grape, peach)
- Synteny from an ortholog table (grape, peach, cacao)
- Synteny visualization (OrthoFinder orthogroups)
- Synteny from gene symbols (eight primates)
- Synteny from gene symbols (E. coli genomes)
- Synteny by ancestral linkage group (sponge, comb jelly, jellyfish)
- Selection pressure between two genomes (dN/dS)
- Synteny visualization (a polyploid against itself)
Pangenomes
Building a graph
HPRC release 2
- Pangenome (HPRC) part 1: the graph's alleles and the haplotypes that have them
- Pangenome (HPRC) part 2: haplotypes against each other
- Pangenome (HPRC) part 3: repeat lengths across haplotypes
Mouse and cattle
Structural variation
- CNV across a population (1000 Genomes)
- Structural variants (1000 Genomes)
- Structural variants from Hi-C
- Low-mappability regions (SMN)
Cancer genomics
- Complex rearrangements and derivative alleles
- Gene fusion calls and the DNA behind them
- Reviewing a whole SV callset
- Structural variants (Cancer GIAB) part 1: breakpoints
- Structural variants (Cancer GIAB) part 2: copy number
- Mutation cohort (TCGA)
- CNV cohort (TCGA)
Population genomics
- Selection scans (Drosophila DGRP)
- Phased trio analysis (1000 Genomes)
- LD at a selective sweep (human)
- LD across an inversion (mosquitoes)
- QTL mapping (BXD mice)
Dog10K
- A selected haplotype (Dog10K)
- A loss-of-function allele across breeds (Dog10K)
- Structural variants (Dog10K)
- Local ancestry (Dog10K)
Epigenomics & single cell
- Methylation (long-read)
- Methylation (bisulfite)
- ChromHMM chromatin states
- Single-cell ATAC pseudobulk
- Single-cell RNA pseudobulk
- AlphaGenome predictions
Transcriptomics & proteins
Variants on protein structures
- Variants on protein structures part 1: sickle cell from GWAS hit to haemoglobin S
- Variants on protein structures part 2: degenerative myelopathy in dogs
- Variants on protein structures part 3: seedless grapes on an AlphaFold model
- Variants on protein structures part 4: KRAS G12 in the GTP pocket
- Variants on protein structures part 5: TP53 R248 and R273 on DNA
- Variants on protein structures part 6: BRAF V600 in the activation loop
Genes & annotation
- Reviewing a gene prediction (Tiberius)
- Protein domains on gene models
- Gene density and transposon density along a chromosome
- A map of the human mitochondrial genome
Grammar of graphics
- A grammar of graphics over a BED (RepeatMasker Alu age)
- A grammar of graphics over a BAM (NA12878 insert size)