155 lines
6.0 KiB
Markdown
155 lines
6.0 KiB
Markdown
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# biobox x.x.x
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## BREAKING CHANGES
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* `star/star_align_reads`: Change all arguments from `--camelCase` to `--snake_case` (PR #62).
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* `star/star_genome_generate`: Change all arguments from `--camelCase` to `--snake_case` (PR #62).
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## NEW FUNCTIONALITY
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* `star/star_align_reads`: Add star solo related arguments (PR #62).
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* `bd_rhapsody/bd_rhapsody_make_reference`: Create a reference for the BD Rhapsody pipeline (PR #75).
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* `umitools/umitools_dedup`: Deduplicate reads based on the mapping co-ordinate and the UMI attached to the read (PR #54).
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* `seqtk`:
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- `seqtk/seqtk_sample`: Subsamples sequences from FASTA/Q files (PR #68).
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- `seqtk/seqtk_subseq`: Extract the sequences (complete or subsequence) from the FASTA/FASTQ files
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based on a provided sequence IDs or region coordinates file (PR #85).
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* `agat`:
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- `agat/agat_convert_sp_gff2gtf`: convert any GTF/GFF file into a proper GTF file (PR #76).
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- `agat/agat_convert_bed2gff`: convert bed file to gff format (PR #97).
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- `agat/agat_convert_embl2gff`: convert an EMBL file into GFF format (PR #99).
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- `agat/agat_convert_sp_gff2tsv`: convert gtf/gff file into tabulated file (PR #102).
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- `agat/agat_convert_sp_gxf2gxf`: fixes and/or standardizes any GTF/GFF file into full sorted GTF/GFF file (PR #103).
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* `bedtools`:
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- `bedtools/bedtools_intersect`: Allows one to screen for overlaps between two sets of genomic features (PR #94).
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- `bedtools/bedtools_sort`: Sorts a feature file (bed/gff/vcf) by chromosome and other criteria (PR #98).
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- `bedtools/bedtools_bamtofastq`: Convert BAM alignments to FASTQ files (PR #101).
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- `bedtools/bedtools_bedtobam`: Converts genomic feature records (bed/gff/vcf) to BAM format (PR #111).
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* `qualimap/qualimap_rnaseq`: RNA-seq QC analysis using qualimap (PR #74).
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* `rsem/rsem_prepare_reference`: Prepare transcript references for RSEM (PR #89).
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## MINOR CHANGES
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* `busco` components: update BUSCO to `5.7.1` (PR #72).
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* Update CI to reusable workflow in `viash-io/viash-actions` (PR #86).
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* Update several components in order to avoid duplicate code when using `unset` on boolean arguments (PR #133).
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* Bump viash to `0.9.0-RC7` (PR #134)
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## DOCUMENTATION
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* Extend the contributing guidelines (PR #82):
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- Update format to Viash 0.9.
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- Descriptions should be formatted in markdown.
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- Add defaults to descriptions, not as a default of the argument.
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- Explain parameter expansion.
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- Mention that the contents of the output of components in tests should be checked.
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* Add authorship to existing components (PR #88).
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## BUG FIXES
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* `pear`: fix component not exiting with the correct exitcode when PEAR fails (PR #70).
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* `cutadapt`: fix `--par_quality_cutoff_r2` argument (PR #69).
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* `cutadapt`: demultiplexing is now disabled by default. It can be re-enabled by using `demultiplex_mode` (PR #69).
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* `multiqc`: update multiple separator to `;` (PR #81).
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# biobox 0.1.0
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## NEW FEATURES
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* `arriba`: Detect gene fusions from RNA-seq data (PR #1).
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* `fastp`: An ultra-fast all-in-one FASTQ preprocessor (PR #3).
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* `busco`:
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- `busco/busco_run`: Assess genome assembly and annotation completeness with single copy orthologs (PR #6).
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- `busco/busco_list_datasets`: Lists available busco datasets (PR #18).
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- `busco/busco_download_datasets`: Download busco datasets (PR #19).
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* `cutadapt`: Remove adapter sequences from high-throughput sequencing reads (PR #7).
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* `featurecounts`: Assign sequence reads to genomic features (PR #11).
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* `bgzip`: Add bgzip functionality to compress and decompress files (PR #13).
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* `pear`: Paired-end read merger (PR #10).
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* `lofreq/call`: Call variants from a BAM file (PR #17).
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* `lofreq/indelqual`: Insert indel qualities into BAM file (PR #17).
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* `multiqc`: Aggregate results from bioinformatics analyses across many samples into a single report (PR #42).
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* `star`:
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- `star/star_align_reads`: Align reads to a reference genome (PR #22).
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- `star/star_genome_generate`: Generate a genome index for STAR alignment (PR #58).
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* `gffread`: Validate, filter, convert and perform other operations on GFF files (PR #29).
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* `salmon`:
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- `salmon/salmon_index`: Create a salmon index for the transcriptome to use Salmon in the mapping-based mode (PR #24).
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- `salmon/salmon_quant`: Transcript quantification from RNA-seq data (PR #24).
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* `samtools`:
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- `samtools/samtools_flagstat`: Counts the number of alignments in SAM/BAM/CRAM files for each FLAG type (PR #31).
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- `samtools/samtools_idxstats`: Reports alignment summary statistics for a SAM/BAM/CRAM file (PR #32).
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- `samtools/samtools_index`: Index SAM/BAM/CRAM files (PR #35).
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- `samtools/samtools_sort`: Sort SAM/BAM/CRAM files (PR #36).
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- `samtools/samtools_stats`: Reports alignment summary statistics for a BAM file (PR #39).
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- `samtools/samtools_faidx`: Indexes FASTA files to enable random access to fasta and fastq files (PR #41).
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- `samtools/samtools_collate`: Shuffles and groups reads in SAM/BAM/CRAM files together by their names (PR #42).
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- `samtools/samtools_view`: Views and converts SAM/BAM/CRAM files (PR #48).
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- `samtools/samtools_fastq`: Converts a SAM/BAM/CRAM file to FASTQ (PR #52).
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- `samtools/samtools_fastq`: Converts a SAM/BAM/CRAM file to FASTA (PR #53).
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* `umi_tools`:
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-`umi_tools/umi_tools_extract`: Flexible removal of UMI sequences from fastq reads (PR #71).
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* `falco`: A C++ drop-in replacement of FastQC to assess the quality of sequence read data (PR #43).
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* `bedtools`:
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- `bedtools_getfasta`: extract sequences from a FASTA file for each of the
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intervals defined in a BED/GFF/VCF file (PR #59).
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## MINOR CHANGES
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* Uniformize component metadata (PR #23).
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* Update to Viash 0.8.5 (PR #25).
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* Update to Viash 0.9.0-RC3 (PR #51).
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* Update to Viash 0.9.0-RC6 (PR #63).
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* Switch to viash-hub/toolbox actions (PR #64).
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## DOCUMENTATION
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* Update README (PR #64).
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## BUG FIXES
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* Add escaping character before leading hashtag in the description field of the config file (PR #50).
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* Format URL in biobase/bcl_convert description (PR #55).
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