The format is based on Keep a Changelog and this project adheres to Semantic Versioning.
v2.2.2 - 2023-09-04
- [#253] - Remove globs from process alias when using ECR containers
- [#237] - Fix illumina protocol clip parameters to default
- Remove public_aws_ecr profile
- [#269] - Updated miRBase URLs with new location (old ones were broken)
Dependency | Old version | New version |
---|---|---|
multiqc |
1.13 | 1.15 |
fastp |
0.23.2 | 0.23.4 |
v2.2.1 - 2023-05-12
- [#238] - Restored the missing mirtop outputs
- [#242] - Fixed mirtrace using wrong input fastq files (untrimmed)
v2.2.0 - 2023-04-26
- [#220] - Fixed an issue where miRTrace reports fastq basename instead of sample ID
- [#208] - Fixed usability of
--skip_qc
parameter - Updated FASTP module to allow direct addition of adapter_fasta file to it
- [#205] - Fix mirTrace Report to be a single report again instead of per sample reports
- [#206] - Use % as separator in sed commands to enable conda working properly on OSX and Linux
- [#207] - Fix Samplesheet print error
- Group samples by adapter sequence before running mirtrace
- Remove
--skip_qc
parameter
v2.1.0 - 2022-10-20 Maroon Tin Dalmatian
- [#12] - Enabled the use of
MirGeneDB
as an alternative database insted ofmiRBase
- [#113] - Added a optional contamination filtering step, including MultiQC plot
- [#137] - Fixed issue with mirTop and MultiQC by upgrading to MultiQC V1.13dev
- [#159] - Index files were not collected when
bowtie_index
was used and thus mapping was failing - [#161] - Trimmed output was not as documented and not correctly published
- [#168] - Removed
mirtrace_protocol
as the parameter was redundant andparams.protocol
is entirely sufficient - Updated pipeline template to nf-core/tools 2.6.0
- [#188] - Dropped TrimGalore in favor of fastp QC and adapter trimming, improved handling of adapters and trimming parameters
- [#194] - Added default adapters file for FastP improved miRNA adapter trimming
Old parameter | New parameter |
---|---|
--mirgenedb |
|
--mirgenedb_species |
|
--mirgenedb_gff |
|
--mirgenedb_mature |
|
--mirgenedb_hairpin |
|
--contamination_filter |
|
--rrna |
|
--trna |
|
--cdna |
|
--ncrna |
|
--pirna |
|
--other_contamination |
v2.0.0 - 2022-05-31 Aqua Zinc Chihuahua
- Updated pipeline template to nf-core/tools 2.4.1
- [#137] - Update mirtop container to version
0.4.25
to fix multiqc error - Port pipeline to the updated Nextflow DSL2 syntax adopted on nf-core/modules
- Bump minimum Nextflow version from
20.04.0
->21.10.3
- Point to the proper test data branch
- Software version(s) will now be reported for every module imported during a given pipeline execution
- Updated
nextflow_schema.json
should now display correctly on Nextflow Tower - Added mirtop logs to multiqc
- Allow a gene to be associated to a non null number of reads in all samples (in
edgeR_miRBase.r
script)
- #134 - Fixed colSum of zero issues for edgeR_miRBase.R script
- #55 - update seqcluster to fix UMI-detecting bug
Old parameter | New parameter |
---|---|
--conda |
--enable_conda |
--clusterOptions |
|
--publish_dir_mode |
NB: Parameter has been updated if both old and new parameter information is present. NB: Parameter has been added if just the new parameter information is present. NB: Parameter has been removed if parameter information isn't present.
Note, since the pipeline is now using Nextflow DSL2, each process will be run with its own Biocontainer. This means that on occasion it is entirely possible for the pipeline to be using different versions of the same tool. However, the overall software dependency changes compared to the last release have been listed below for reference.
Dependency | Old version | New version |
---|---|---|
bioconductor-edger |
3.26.5 | 3.36.0 |
bioconductor-limma |
3.40.2 | 3.50.0 |
mirdeep2 |
2.0.1.2 | 2.0.1.3 |
mirtop |
0.4.23 | 0.4.25 |
multiqc |
1.10.1 | 1.12.0 |
python |
3.7.3 | 3.8.3 |
r-base |
3.6.3 | 4.0.3 |
r-data.table |
1.12.4 | 1.14.2 |
r-gplots |
3.0.1.1 | 3.1.1 |
r-statmod |
1.4.32 | 1.4.36 |
samtools |
1.12 | 1.13 |
seqcluster |
1.2.7 | 1.2.9 |
seqkit |
0.16.0 | 2.0.0 |
trim-galore |
0.6.6 | 0.6.7 |
bioconvert |
- | 0.4.3 |
htseq |
- | - |
markdown |
- | - |
pymdown-extensions |
- | - |
pygments |
- | - |
r-r.methodss3 |
- | - |
bowtie2 |
- | 2.4.5 |
blat |
- | 36 |
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.
v1.1.0 - 2021-06-15
This release contains several major (potentially breaking) changes:
- The main input parameter has been changed from
--reads
to--input
to standardize the pipeline with other nf-core pipelines - All parameter documentation has moved into a new
nextflow_schema.json
file - A
lib
folder with groovy helper classes has been added to the pipeline. This includes validation of input parameters using the schema defined in thenextflow_schema.json
file
- remove spaces in genome headers and replace special nt by N in hairpin file for mirdeep2 to work. [#69]
- Accept custom genome and remove non-canonical letters in the genome. Thanks to @sdjebali. Follow up from [#63]
- Fix error when only one sample is in the input [#31]
- Made
CamelCase
pipeline parameterssnake_case
and lower caseclip_R1
->clip_r1
three_prime_clip_R1
->three_prime_clip_r1
saveReference
->save_reference
skipQC
->skip_qc
skipFastqc
->skip_fastqc
skipMultiqc
->skip_multiqc
- Update with the latest
TEMPLATE
version for nf-core1.12.1
- Update conda environment with new packages and updates
- Added
--protocol custom
to allow custom adapter trimming modes [#41]] - Fix error when UMI is on the reads header: [#35]
- Updated
params.mirtrace_species
to be properly initialised when using--genome
, for all iGenomes species - Made
params.mature
andparams.hairpin
default to miRBase FTP URL so that the file is automatically downloaded if not provided - Allow
.fa
or.fa.gz
files for mature and hairpin FASTA files. - Add full-size benchmark / test dataset to run on AWS for each release (see
test_full.config
) - Add
-f
flag togunzip
commands to deal with soft-links - Add
--mirtrace_protocol
parameter to allow for more flexible selection of this parameter - Added
--trim_galore_max_length
option [#77] - Solved memory usage issue for mirtrace in the main process and in the
get_software_versions
process [#68] - Removed logging of
single_end
parameter and added missing parameters to schema and config files - Added "custom" as option for
--protocol
in thenextflow_schema.json
fastqc=0.11.8
->0.11.9
trim-galore=0.6.3
->0.6.5
bowtie=1.2.2
->1.2.3
multiqc=1.7
->1.9
mirtop=0.4.22
->0.4.23
seqcluster=1.2.5
->1.2.7
htseq=0.11.2
->0.11.3
fastx_toolkit=0.0.14
->0.0.14
seqkit=0.10.1
->0.12.0
mirtrace=1.0.0
->1.0.1
- Added
conda-forge::python=3.7.3
- Added
conda-forge::markdown=3.1.1
- Added
conda-forge::pymdown-extensions=6.0
- Added
conda-forge::pygments=2.5.2
- Removed
conda-forge::r-markdown=1.0
v1.0.0 - 2019-09-19
- Figures to output documentation
- Samtools stats for genome alignments
- Seqkit and remove razers
- Mirtop and razers tools
- Adapt code and docs to nf-core template
- Update tools and Dockerfile/Singularity to match current template
- openjdk 8.0.144 -> 11.0.1
- fastqc 0.11.7 -> 0.11.8
- trim-galore 0.5.0 -> 0.6.2
- bioconductor-edger 3.20.7 -> 3.26.0
- bioconductor-limma 3.34.9 -> 3.40.0
- conda-forge::r-data.table 1.11.4 -> 1.12.2
- conda-forge::r-gplots 3.0.1 -> 3.0.1.1
- conda-forge::r-r.methodss3 1.7.1 -> 1.7.1
- htseq 0.9.1 -> 0.11.2
- r-markdown 0.9
- Added mirtop 0.4.18a
- Removed razers3 3.5.3
- Added seqkit 0.10.1-1
- Added seqcluster 1.2.5
- conda-forge::r-base=3.5.1 -> 3.6.1
- conda-forge::r-statmod=1.4.30 -> 1.4.32
- conda-forge::r-markdown=0.9 -> 1.0
- trim-galore=0.6.2 -> 0.6.3
- mirtop=0.4.18a -> 0.4.22
- bioconductor-edger=3.26.0 -> 3.26.5
- bioconductor-limma=3.40.0 -> 3.40.2
- "protocol" with pre-defined settings
- miRTrace in the pipeline.
- multiqc 1.6 -> 1.7.
- Port original pipeline SciLifeLab/NGI-smRNAseq to nf-core/smrnaseq.
- Use Bowtie 1 instead of Bowtie 2 for the alignment to host reference genome.
- Option for sequencing centre in BAM file.
- trim-galore 0.4.5 -> 0.5.0
- samtools 1.8 -> 1.9
- multiqc 1.5 -> 1.6