tag v1.7.1
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@ -4,23 +4,22 @@ All notable changes to this project will be documented in this file.
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The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.1.0/),
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and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0.html).
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## [Unreleased]
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## [v1.7.1]
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### Changed
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- Updated to wf-template v5.6.2, changing:
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- Reduce verbosity of debug logging from fastcat which can occasionally occlude errors found in FASTQ files during ingress.
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- Log banner art to say "EPI2ME" instead of "EPI2ME Labs" to match current branding. This has no effect on the workflow outputs.
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- pre-commit configuration to resolve an internal dependency problem with flake8. This has no effect on the workflow.
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- Stringtie updated to v2.2.3, which fixes stalling at transcriptome assembly step.
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- Gffcompare updated to v0.12.6, which fixes issue where ref_gene_id was assigned an nan value.
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- Stringtie updated to v2.2.3, which fixes stalling at transcriptome assembly step.
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- Gffcompare updated to v0.12.6, which fixes issue where ref_gene_id was assigned an nan value.
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### Fixed
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- Updated to wf-template v5.6.2, fixing:
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- dacite.exceptions.WrongTypeError during report generation when barcode is null.
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- Sequence summary read length N50 incorrectly displayed minimum read length, it now correctly shows the N50.
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- Sequence summary component alignment and coverage plots failed to plot under some conditions.
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- Error in `deAnalysis` process - `mode(counts) %in% "numeric" is not TRUE` - caused by hyphens in sample sheet aliases.
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- Error in `deAnalysis` process - `values in 'transcripts$tx_strand' must be "+" or "-"`.
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- The workflow will now filter out any unstranded annotations from downstream analysis and log a warning.
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- Output the `results_dexseq.tsv` file when `--de_analysis` enabled.
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- Missing `results_dexseq.tsv` file when `--de_analysis` enabled.
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## [v1.7.0]
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### Changed
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@ -107,7 +107,7 @@ manifest {
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description = 'Transcriptome analysis including differential expression as well as assembly and annotation of cDNA and direct RNA sequencing data.'
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mainScript = 'main.nf'
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nextflowVersion = '>=23.04.2'
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version = 'v1.7.0'
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version = 'v1.7.1'
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}
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epi2melabs {
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