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GUDMAP_RBK
RNA-seq
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60d3fa8b9177613db3986cff2476f7761f97e9b2
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2
develop
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master
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v2.0.1
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v2.0.0rc02
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v1.0.1
v1.0.0
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Merge branch 'develop' into 'master'
Update errors in readme
Merge branch '108-samtools.mem' into 'develop'
Update DAG
Use 1 less process for samtools threading and limit memto 75% of available
Make sampled align use > 32GB nodes on BioHPC
Catch error if fastq file error grep
Fix fastqc error detection
Add back ends manual to parse ci unit
Add back ends manual to ci unit for parse, but manual
Add unexpected meta and fastq structure error ci integration tests
Add excape to bracket in echo
Remove ends manual from parse metadata unit ci
Add premature fail execution run upload with fastq file error
Fix no fastq error detail
Fix no fastq's present in inputBag
Upgrade version to v1.0.3
Fix file structure error detection
Fix if then
Fix endsManual assignment
Fix fastq file error detection
Make dummy fastqc output if fail
Detect malformed fastqs
Fix spike/species asignment for unexpected
Fix python else syntac
Further remove parsing restrictions from stranded/spike/species
Remove ability to count fastqs manually from file.csv
Don't parse manual ends from file.csv anymore
Fix elif
Handle blank endness better
Remove redundant check for multiple fastqs in parse metadata
Allow .R[1,2] and _R[1,2] fastqs
Filter input bag export config to only get fastq's matching convention
Only used fastq's named correctly
Physically move fastqc process up
Fix fastq run before trim
Move fastqc before trim
Update changelog
Allow unexpected values for stranded/spike/species
Update changelog