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Releases: epi2me-labs/wf-transcriptomes

v1.6.1

03 Jan 14:52
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Fixed

  • merge_gff_compare failing with empty GFF files.

v1.6.0

13 Dec 15:31
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Fixed

  • v1.5.0 bug; access to undefined channel output bug when using precomputed transcriptome.
  • Bug where incorrect gene_id assigned in the DE tables.

v1.5.0

11 Nov 15:08
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Updated

  • Workflow report updated to use ezcharts.

Fixed

  • Exons per isoforms histogram reporting incorrect numbers.
  • Output the results_dexseq.tsv file when --de_analysis enabled.

Removed

  • per-class gffcompare tracking files as there exists a combine tracking file.

v1.4.0

16 Sep 13:02
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Added

  • --igv parameter (default: false) for outputting IGV config allowing visualisation of read alignments in the EPI2ME App.
  • If required for IGV, reference indexes are output in to a igv_reference directory

Changed

  • BAMS are output in to a BAMS directory.
  • Reconcile with template 5.2.6.

v1.3.0

08 Aug 14:42
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Removed

  • Fusion detection subworkflow, as the functionality is not robust enough for general use at this time.

Changed

  • Updated pychopper to 2.7.10

Added

  • new cdna_kit options: PCS114 and PCB111/114

v1.2.1

05 Jul 14:06
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Changed

  • Increase some memory and CPU allocations.

v1.2.0

05 Jun 06:19
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Added

  • Workflow now accepts BAM or FASTQ files as input (using the --bam or --fastq parameters, respectively).

Changed

  • MA plot in the results_dge.pdf has been updated to match the MA plot in the report.

v1.1.1

05 Mar 16:27
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Changed

  • Improved handling of different annotation file types (eg. .gtf/.gff/.gff3) in de_analysis mode.
  • Improved handling of annotation files that do not contain version numbers in transcript_id (such as gtf's from Ensembl).

Fixed

  • Differential expression failing with 10 or more samples.
  • Regression causing the DE analysis numeric parameters to not be evaluated correctly.

v1.1.0

13 Feb 14:20
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Changed

  • Improve documentation around filtering of transcripts done before DTU analysis.
  • Renamed files:
    • de_analysis/all_counts_filtered.tsv to de_analysis/filtered_transcript_counts_with_genes.tsv
    • de_analysis/de_tpm_transcript_counts.tsv to de_analysis/unfiltered_tpm_transcript_counts.tsv
  • Minimum memory requirements to 32 GB.

Added

  • Published isoforms table to output directory.
  • Output additional de_analysis/cpm_gene_counts.tsv with counts per million gene counts.
  • Output additional de_analysis/unfiltered_transcript_counts_with_genes.tsv with unfiltered transcript counts with associated gene IDs.
  • Add gene name column to the de_analysis counts TSV files.

Fixed

  • Mapping stage using a single thread only.

Changed

  • More memory assigned to the fusion detection process.
  • When no --ref_annotation is provided the workflow will still run but the output transcripts will not be annotated. However --de_analysis mode still requires a --ref_annotation.

v1.0.0

12 Dec 09:59
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Added

  • Published minimap2 and pychopper results to output directory.
  • Two extra pychopper parameters --cdna_kit and --pychopper_backend. --pychopper_options is still available to define any other options.
  • Memory requirements for each process.

Changed

  • Documentation.

Fixed

  • When Jaffa is run only output one report.