@jbrowse/cli 5.0.0-beta.1 → 5.0.0-beta.2

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package/README.md CHANGED
@@ -59,6 +59,7 @@ COMMANDS
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  admin-server Start up a small admin server for JBrowse configuration
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  upgrade Upgrades JBrowse 2 to latest version
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  make-pif Creates pairwise indexed PAF (PIF), with bgzip and tabix
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+ make-density Counts feature starts per bin into a bigWig density sidecar, with bedGraphToBigWig
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  sort-gff Sort a GFF/GTF for tabix: sort -k1,1 -k4,4n, header kept on top
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  sort-bed Sort a BED for tabix: sort -k1,1 -k2,2n, header kept on top
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  add-connection Add a connection to a JBrowse 2 configuration
@@ -310,6 +311,11 @@ Options:
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  --bed2 Used only for mcscan anchors/simpleAnchors types
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+ --density Path or URL of a features-per-bin bigWig (jbrowse
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+ make-density) to attach as the adapter's
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+ densityAdapter. A local <file>.density.bw beside
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+ the track file is attached without this flag
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+
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  Notes:
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  --load controls how the data file is placed relative to config.json: copy, move,
@@ -337,6 +343,14 @@ or a .json file with an array of BigWig locations or subadapter objects (each
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  carrying its own name/color/group). With --load, local list entries are copied
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  like any other track file.
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+ --density attaches a features-per-bin bigWig (jbrowse make-density) as the
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+ adapter's densityAdapter, the band a display draws where the region is too large
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+ to fetch features. A local <file>.density.bw beside the track file is attached
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+ without the flag; a URL cannot be probed, so a remote sidecar needs it. The
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+ adapters carrying the slot are BamAdapter, CramAdapter, HtsgetBamAdapter,
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+ Gff3TabixAdapter, GtfTabixAdapter, BedTabixAdapter, BigBedAdapter,
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+ VcfTabixAdapter and SplitVcfTabixAdapter.
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+
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  For pairwise synteny adapters (PAF/Delta/Chain) --assemblyNames is query,target
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  — the reverse of the minimap2/nucmer input order. For the all-vs-all adapters
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  (AllVsAllPAFAdapter, AllVsAllIndexedPAFAdapter) it is instead the full list of
@@ -371,6 +385,9 @@ $ jbrowse add-track --multiwig a.bw,b.bw,c.bw --load copy --name "Coverage"
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  # ...or from a sources.json carrying per-row name/color for each BigWig
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  $ jbrowse add-track --multiwig sources.json --name "CATlas ATAC"
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+
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+ # attach a remote density sidecar (a local genes.gff3.density.bw needs no flag)
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+ $ jbrowse add-track https://mywebsite.com/genes.gff3.gz --density https://mywebsite.com/genes.gff3.density.bw
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  ```
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@@ -398,14 +415,14 @@ nothing. That is what this command is mainly for.
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  Two levels are reported:
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  error JBrowse accepts it and silently does the wrong thing — an unknown
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- slot, a track naming an assembly the config never defines, a
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- defaultSession naming a trackId that does not exist, a duplicate
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- trackId. Exits 1.
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+ slot, a key a defaultSession view or display does not declare, a
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+ track naming an assembly the config never defines, a defaultSession
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+ naming a trackId that does not exist, a duplicate trackId. Exits 1.
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  warning JBrowse will complain by itself on load, or handles it — a type name
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  the core plugins do not register (expected if one of your plugins
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- registers it), or a legacy key a migration rewrites. Never fails
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- the run.
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+ registers it), or a legacy key a migration rewrites, such as a view
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+ nesting its settings under "init". Never fails the run.
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  Types registered by plugins are not known to this command, so they come through
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  as warnings rather than errors.
@@ -637,16 +654,22 @@ Options:
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  --csi Create a CSI index for the PIF file instead of TBI
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- --coarse Minimum insertion/deletion length (bp) at which a
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- coarse-tier row is split into multiple pieces so
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- each row stays tight — 0 emits an unsplit coarse
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- tier. Defaults to 10000. The no-CIGAR coarse tier
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- (prefix T/Q) is emitted alongside the per-row CIGAR
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- fine tier by default so whole-genome synteny views
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- can auto-switch to it; pass --no-coarse to omit it.
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+ --coarse Accuracy bound (bp) of the coarse tier. A coarse
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+ row replaces its CIGAR with a coarse CIGAR (cr:Z:)
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+ that keeps every indel longer than half this length
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+ and folds the rest into runs, each run staying
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+ within this many bp of the real alignment. Defaults
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+ to 10000. The coarse tier (prefix T/Q) is emitted
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+ alongside the per-row CIGAR fine tier by default so
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+ whole-genome synteny views can auto-switch to it;
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+ pass --no-coarse to omit it.
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+
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+ --no-coarse Do not emit the coarse tier; write only the per-row
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+ CIGAR fine tier.
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- --no-coarse Do not emit the coarse no-CIGAR tier; write only
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- the per-row CIGAR fine tier.
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+ --threads Compression threads for bgzip. Defaults to 4. Raise
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+ it on a machine with cores to spare, or set 1 to
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+ leave the rest of the machine alone.
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  Notes:
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@@ -666,11 +689,70 @@ $ jbrowse make-pif input.paf --out output.pif.gz
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  # use a CSI index for assemblies with chromosomes longer than ~512 Mb
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  $ jbrowse make-pif input.paf --csi
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- # emit an unsplit coarse tier (alongside the fine tier)
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- $ jbrowse make-pif input.paf --coarse 0
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+ # a looser coarse tier: runs within 50kb of the alignment, indels over 25kb kept
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+ $ jbrowse make-pif input.paf --coarse 50000
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  # emit only the per-row CIGAR fine tier, skipping the coarse tier
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  $ jbrowse make-pif input.paf --no-coarse
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+
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+ # give bgzip more (or fewer) compression threads than the default 4
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+ $ jbrowse make-pif input.paf --threads 8
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+ ```
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+
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+ ## jbrowse make-density
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+ ```
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+ Counts feature starts per bin into a bigWig, the density sidecar a track draws
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+ where the region is too large to fetch its features
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+ Usage: jbrowse make-density <file> [options]
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+ Options:
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+ -h, --help Show help
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+ --bin Width of each bin, in bp [default: 1000]
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+ --chrom-sizes Two-column reference name and length table for the
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+ assembly the file is on
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+ --assembly FASTA of the assembly the file is on; its .fai
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+ supplies the reference lengths, in place of
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+ --chrom-sizes
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+ --out Where to write the bigWig. Defaults to
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+ <file>.density.bw beside the input, which is where
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+ add-track looks for it
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+ Notes:
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+ The sidecar is attached to a track through its adapter's densityAdapter slot,
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+ which BamAdapter, CramAdapter, HtsgetBamAdapter, Gff3TabixAdapter,
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+ GtfTabixAdapter, BedTabixAdapter, BigBedAdapter, VcfTabixAdapter and
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+ SplitVcfTabixAdapter declare. add-track attaches it on its own when the default
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+ <file>.density.bw sits beside the track file, so building it before adding the
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+ track is all it takes; --density attaches one by path or URL.
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+
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+ GFF3 counts only top-level features — a line whose attributes carry no Parent= —
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+ so a gene is one count rather than one per exon. GTF, BED and VCF have no parent
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+ link to follow, so every record counts.
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+ BAM and CRAM are out of scope: read depth is not feature density, and the tools
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+ that compute it already write bigWig. Point add-track --density at what they
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+ produce.
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+ Requires bedGraphToBigWig (UCSC) on the PATH.
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+ Examples:
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+ # writes genes.gff3.density.bw beside the input, in 1kb bins
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+ $ jbrowse make-density genes.gff3.gz --chrom-sizes hg38.chrom.sizes
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+ # take the reference lengths from the assembly FASTA index instead
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+ $ jbrowse make-density variants.vcf.gz --assembly hg38.fa
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+ # coarser bins, and a name of your own
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+ $ jbrowse make-density genes.gff3.gz --assembly hg38.fa --bin 10000 --out genes.10kb.bw
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  ```
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