Releases
v4.12
Alignment path in config files and new features
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[4.12]
Added
Accepts alignment_path in load config to pass bam/cram files
Display all phenotypes on variant page
Display hgvs coordinates on pinned and causatives
Clear panel pending changes
Adds option to setup the database with static files
Adds cli command to download the resources from CLI that scout needs
Adds dummy files for merged somatic SV and CNV; as well as merged SNV, and INDEL part of #1279
Allows for upload of OMIM-AUTO gene panel from static files without api-key
Fixed
Cancer case HPO panel variants link
Fix so that some drop downs have correct size
First IGV button in str variants page
Cancer case activates on SNV variants
Cases activate when STR variants are viewed
Always calculate code coverage
Pinned/Classification/comments in all types of variants pages
Null values for panel's custom_inheritance_models
Discrepancy between the manual disease transcripts and those in database in gene-edit page
ACMG classification not showing for some causatives
Fix bug which caused IGV.js to use hg19 reference files for hg38 data
Bug when multiple bam files sources with non-null values are available
Changed
Renamed requests file to scout_requests
Cancer variant view shows two, instead of four, decimals for allele and normal
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