Releases: epi2me-labs/wf-basecalling
Releases · epi2me-labs/wf-basecalling
v1.4.5
v1.4.4
v1.4.3
Changed
- Reconciled workflow with wf-template v5.3.3.
v1.4.2
v1.4.1
v1.4.0
Added
- IGV configuration file with
--ref --igv
options and either--output_fmt bam
or--output_fmt cram
. - Support for gzipped reference genomes.
output_fmt
selects the output format for basecalled and aligned files.
Changed
- Updated Dorado to v0.8.0
- Reconciled workflow with wf-template v5.2.6.
- Do not emit the reference FASTA file.
- Collapse redundant RG and PG header lines when emitting BAM or CRAM.
Fixed
- Workflow starting with
--duplex --barcode_kit
, despite duplex not supporting barcoding. - Workflow crashing with
--ref {{ reference }} --barcode_kit
. - Aligned reads will no longer be trimmed when demuxing to preserve mapping information.
- Workflow emits confusing warning about Bonito filtering when using Dorado.
Removed
fastq_only
andoutput_bam
options replaced byoutput_fmt
.--output_fmt fastq
can be used to output unaligned FASTQ instead of unaligned CRAM.--output_fmt bam
can be used to output unaligned or aligned BAM instead of CRAM.
v1.3.0
Added
- Modified base calling with
--duplex
. - APK 5.0.0 model.
Changed
- Updated Dorado to v0.7.2 (see https://github.com/nanoporetech/dorado/releases/tag/v0.7.2)
v1.2.2
Changes
- Bug fix for downstream workflows and
--poly_a_config
which does not affect normal workflow use.
v1.2.1
Added
- Output channel for demuxed BAM files for downstream use.
v1.2.0
### Added
- Support for
dorado demux
to demultiplex barcoded runs. Specify your--barcode_kit
to activate demultiplexing. - Support for poly(a) tail length estimation with
--poly_a_config
. You can configure by providng a TOML file to--poly_a_config
which is described in detail here
Changed
- Updated Dorado to v0.7.1 (see https://github.com/nanoporetech/dorado/releases/tag/v0.7.1)