The format is based on Keep a Changelog and this project adheres to Semantic Versioning.
- Add DNA variant calling functionality
- Add RNA modification and fusion detection functionalities
- Add
demux_fast5
module to output demultiplexed fast5 files when--output_demultiplex_fast5
is set - Add
--trim_barcodes
in Guppy basecaller to trim the barcodes from output fastq - Port pipeline to the updated Nextflow DSL2 syntax adopted on nf-core/modules
- Removed
--publish_dir_mode
as it is no longer required for the new syntax - Bump minimum Nextflow version from 21.04.0 -> 21.10.3
- Update pipeline template to nf-core/tools
2.2
- Update
bambu
version from1.0.2
to2.0.0
- Update
multiqc
version from1.10.1
to1.11
- Added
--output_demultiplex_fast5
to output demultiplexed fast5 - Added
--trim_barcodes
in Guppy basecaller to trim the barcodes from output fastq - Added
--call_variants
to detect DNA variants - Added
--split_mnps
to split multi-nucleotide polymorphisms into single nucleotide polymorphisms when using medaka - Added
--phase_vcf
to output a phased vcf when using medaka - Added
--deepvariant_gpu
to use gpu with docker pepper_margin_deepvariant - Added
--skip_vc
to skipvariant_calling
- Added
--skip_sv
to skipstructural_variant_calling
- Added
--variant_caller
to specify variant caller. - Added
--structural_variant_caller
to specify structural variant caller - Added
--skip_modification_analysis
to skip RNA modification detection - Added
--skip_xpore
to skipxpore
- Added
--skip_m6anet
to skipm6anet
- Added
--skip_fusion_analysis
to skip RNA fusion detection - Added
--jaffal_ref_dir
to indicate the reference directory path required byJAFFAL
Dependency | Old version | New version |
---|---|---|
bioconductor-bambu |
1.0.2 | 2.0.0 |
bioconductor-bsgenome |
1.58.0 | 1.62.0 |
cutesv |
1.0.12 | |
deepvariant |
1.0.3 | |
jaffa |
2.0 | |
m6anet |
1.0 | |
medaka |
1.4.4 | |
multiqc |
1.10.1 | 1.11 |
ont_fast5_api |
4.0.0 | |
pepper_margin_deepvariant |
0.8 | |
pepper_margin_deepvariant_gpu |
0.8 | |
samtools |
1.14 | 1.15 |
sniffles |
1.0.12 | |
xpore |
2.1 |
- The
GET_TEST_DATA
process now uses checks for any file in the path.
NB: Dependency has been updated if both old and new version information is present. NB: Dependency has been added if just the new version information is present. NB: Dependency has been removed if version information isn't present.
- The
UCSC_BEDGRAPHTOBIGWIG
process now uses theucsc-bedgraphtobigwig
container - The full-size and minimal AWS tests have successfully finished after changing to the
ucsc-bedgraphtobigwig
container
- Pipeline has been re-implemented in Nextflow DSL2
- Software containers are now obtained from Biocontainers
- Update pipeline template to nf-core/tools
2.1
- #77 - Skipped alignment steps
- #97 - Add optional DNA cleaning option
- Added
--run_nanolyse
to run NanoLyse for DNA cleaning of FastQ files - Added
--nanolyse_fasta
to provide a fasta file for nanolyse to filter against
Dependency | Old version | New version |
---|---|---|
bioconductor-bambu |
1.0.0 | 1.0.2 |
nanolyse |
1.2.0 | |
r-base |
4.0.3 | 4.0.2 |
NB: Dependency has been updated if both old and new version information is present. NB: Dependency has been added if just the new version information is present. NB: Dependency has been removed if version information isn't present.
- Transcript reconstruction and quantification (
bambu
orStringTie2
andfeatureCounts
) - Differential expression analysis at the gene-level (
DESeq2
) and transcript-level (DEXSeq
) - Ability to provide BAM input to the pipeline
- Change samplesheet format to be more flexible to BAM input files
- Add pycoQC and featureCounts output to MultiQC report
- Add AWS full-sized test data
- Add parameter JSON schema for pipeline
- Add citations file
- Update pipeline template to nf-core/tools
1.11
- Collapsible sections for output files in
docs/output.md
- Replace
set
withtuple
andfile
withpath
ininput
section of all processes - Capitalise process names
- Added
--gpus all
to DockerrunOptions
when using GPU as mentioned here - Cannot invoke method
containsKey()
on null object when--igenomes_ignore
is set #76
- Added
--barcode_both_ends
requires barcode on both ends for Guppy basecaller - Added
--quantification_method
to specify the transcript quantification method to use - Added
--skip_quantification
to skip transcript quantification and differential analysis - Added
--skip_differential_analysis
to skip differential analysis with DESeq2 and DEXSeq - Added
--publish_dir_mode
to customise method of publishing results to output directory nf-core/tools#585
Dependency | Old version | New version |
---|---|---|
Guppy |
3.4.4 | 4.0.14 |
markdown |
3.1.1 | 3.3.3 |
multiqc |
1.8 | 1.9 |
nanoplot |
1.28.4 | 1.32.1 |
pygments |
2.5.2 | 2.7.2 |
pymdown-extensions |
6.0 | 8.0.1 |
python |
3.7.3 | 3.8.6 |
samtools |
1.9 | 1.11 |
ucsc-bedgraphtobigwig |
357 | 377 |
ucsc-bedtobigbed |
357 | 377 |
bioconductor-bambu |
- | 1.0.0 |
bioconductor-bsgenome |
- | 1.58.0 |
bioconductor-deseq2 |
- | 1.30.0 |
bioconductor-dexseq |
- | 1.36.0 |
bioconductor-drimseq |
- | 1.18.0 |
bioconductor-stager |
- | 1.12.0 |
r-base |
- | 4.0.3 |
seaborn |
- | 0.10.1 |
stringtie |
- | 2.1.4 |
subread |
- | 2.0.1 |
psutil |
- | - |
NB: Dependency has been updated if both old and new version information is present. NB: Dependency has been added if just the new version information is present. NB: Dependency has been removed if version information isn't present.
Initial release of nf-core/nanoseq, created with the nf-core template.