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We created a new website at https://genomes.jbrowse.org that features new JBrowse 2 instances for over 50,000 species. This massive effort is primarily driven by bulk loading data from UCSC, both their main browsers and GenArk hubs, which have data for thousands of NCBI RefSeq (curated) and GenBank genomes
All of these JBrowse 2 instances are available on both the web and on the desktop app
Users can even browse "synteny views" between the different hubs by opening a liftOver track, see https://genomes.jbrowse.org/demos/ for example
Screenshot of hg38 vs hs1, as seen in the demos page
Synteny and dotplot viewer improvements
We added some new features to the dotplot and synteny view, including:
Opacity/transparency slider
Min length slider
Easy picker for new color schemes
Auto-diagonalization to reorder chromosomes
"Location markers" for helping see where you are in large alignments
A screenshot of the grape vs peach with "Color by Query" enabled in the dotplot and synteny view
Screenshot of the location markers, which help orient where you are in large alignments
Draw amino acids on Gene glyphs
The setting "Color by CDS" added the ability to draw amino acid letters (and was thus renamed "Color by CDS and draw amino acids").
This can help with detailed investigations of protein structures, which is an area we are actively developing (see https://github.com/GMOD/proteinbrowser for more information)
Create 'Linked read display' for Alignments tracks
Users can now see paired-end reads and supplementary alignments as linked entities using the "Linked reads display". This can be particularly useful for structural variant inspection.
We included a variety of specialized options to help users dig into their data, including:
Show/hide proper pairs
Show/hide 'singletons' (reads without pairs or supplementary alignments)
Coloring schemes that highlight misoriented pairs and abnormally large insert sizes
And more
Screenshot showing the "Linked reads display" with PacBio, Nanopore, and Illumina paired-end reads. The long reads with split alignments are colored salmon and light blue so that you can see the flip in orientation from positive to negative, and back to positive again. The short paired-end reads are colored navy and green to show the misoriented pairs
Screenshot showing a variety of SV types with our mock test data
Improved modified reads plotting
Some of the code for handling modifications was given a fresh refactor, which fixed bugs with 'duplex' data where modifications are stored on both a positive and negative pass on the same read
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Hi everyone,
This is a big release on many fronts! Here are some highlights
JBrowse 2 genome hubs https://genomes.jbrowse.org
We created a new website at https://genomes.jbrowse.org that features new JBrowse 2 instances for over 50,000 species. This massive effort is primarily driven by bulk loading data from UCSC, both their main browsers and GenArk hubs, which have data for thousands of NCBI RefSeq (curated) and GenBank genomes
All of these JBrowse 2 instances are available on both the web and on the desktop app
Users can even browse "synteny views" between the different hubs by opening a liftOver track, see https://genomes.jbrowse.org/demos/ for example
Screenshot of hg38 vs hs1, as seen in the demos page
Synteny and dotplot viewer improvements
We added some new features to the dotplot and synteny view, including:
A screenshot of the grape vs peach with "Color by Query" enabled in the dotplot and synteny view
Screenshot of the location markers, which help orient where you are in large alignments
Draw amino acids on Gene glyphs
The setting "Color by CDS" added the ability to draw amino acid letters (and was thus renamed "Color by CDS and draw amino acids").
This can help with detailed investigations of protein structures, which is an area we are actively developing (see https://github.com/GMOD/proteinbrowser for more information)
Create 'Linked read display' for Alignments tracks
Users can now see paired-end reads and supplementary alignments as linked entities using the "Linked reads display". This can be particularly useful for structural variant inspection.
We included a variety of specialized options to help users dig into their data, including:
Screenshot showing the "Linked reads display" with PacBio, Nanopore, and Illumina paired-end reads. The long reads with split alignments are colored salmon and light blue so that you can see the flip in orientation from positive to negative, and back to positive again. The short paired-end reads are colored navy and green to show the misoriented pairs
Screenshot showing a variety of SV types with our mock test data
Improved modified reads plotting
Some of the code for handling modifications was given a fresh refactor, which fixed bugs with 'duplex' data where modifications are stored on both a positive and negative pass on the same read
Here is an example of a screenshot showing chromatin accessibility via introduced 6mA methylation from a Nanopore dataset (source: https://epi2me.nanoporetech.com/chromatin-acc-hg002/)
Conclusion
Let us know if you have any feedback on these new features! Enjoy
3.7.0 (2025-11-07)
🚀 Enhancement
core🐛 Bug Fix
core@jbrowse/clipackage.json (@garrettjstevens)🏠 Internal
coreCommitters: 2
Done in 0.96s.
This discussion was created from the release Release v3.7.0.
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