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## CHANGELOG
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#### 0.9.2 - June 30th 2021
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* Data updates: ClinVar, GWAS catalog, CIViC, CancerMine, dbNSFP, KEGG, ChEMBL, Disease Ontology/EFO, Open Targets Platform, UniProt KB, GENCODE
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* Software upgrades: R v4.1, Bioconductor v3.13, VEP (104) ++
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##### Changed
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* TOML-based configuration for PCGR is abandoned, all options to PCGR are now configured through command-line parameters
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* __NOTE__: We recommend to turn on `--show_noncoding` and `--vcf2maf` (prevously turned on by default in TOML). For tumor-only runs, we recommend to include `--exclude_dbsnp_nonsomatic` and `exclude_nonexonic`
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##### Added
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* Command-line options
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* Previously set in TOML file)
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* Allelic support
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* `--tumor_dp_tag`
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* `--tumor_af_tag`
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* `--control_dp_tag`
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* `--control_af_tag`
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* `--call_conf_tag`
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* Tumor-only options
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* `--maf_onekg_eur`
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* `--maf_onekg_amr`
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* `--maf_onekg_afr`
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* `--maf_onekg_eas`
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* `--maf_onekg_sas`
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* `--maf_onekg_global`
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* `--maf_gnomad_nfe`
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* `--maf_gnomad_asj`
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* `--maf_gnomad_fin`
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* `--maf_gnomad_oth`
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* `--maf_gnomad_amr`
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* `--maf_gnomad_afr`
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* `--maf_gnomad_eas`
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* `--maf_gnomad_sas`
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* `--maf_gnomad_global`
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* `--exclude_pon`
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* `--exclude_likely_het_germline`
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* `--exclude_likely_hom_germline`
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* `--exclude_dbsnp_nonsomatic`
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* `--exclude_nonexonic`
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* `--report_theme`
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* `--preserved_info_tags` (previously `custom_tags (TOML)`)
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* `--show_noncoding` (previously `list_noncoding (TOML)`)
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* `--vcfanno_n_proc` (previously `n_vcfanno_proc (TOML)`)
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* `--vep_n_forks` (previously `n_vep_forks (TOML)`)
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* `--vep_pick_order`
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* `--vep_no_intergenic` (previously `vep_skip_intergenic (TOML)`)
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* `--vcf2maf`
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* New options
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* `--report_nonfloating_toc` (**NEW**) - add the TOC at the top of the HTML report, not floating at the left of the document
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* `--cpsr_report` (**NEW**) - add a dedicated section in PCGR with main germline findings from CPSR analysis - (use the gzipped JSON output from CPSR as input)
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* `--vep_regulatory` (**NEW**) - append regulatory annotations to variants (TF binding sites etc.)
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* `--include_artefact_signatures` (**NEW**) - include sequencing artefacts in the reference collection of mutational signatures (COSMIC v3.2)
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##### Fixed
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* Bug in writing (large) report contents to JSON (issue [#118](https://github.com/sigven/pcgr/issues/118))
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* Bug (typo) in merge of clinical evidence items from different sources (CIVIC + CGI) (issue [#126](https://github.com/sigven/pcgr/issues/126))
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* Bug in value box for number of (high-confident) kataegis events - rmarkdown (issue [#122](https://github.com/sigven/pcgr/issues/122))
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* Bug in value box for tumor purity/ploidy -rmarkdown (issue [#129](https://github.com/sigven/pcgr/issues/129))
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##### Removed
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* Command-line options
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* `--conf` - TOML-based configuration file
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#### 0.9.1 - November 30th 2020
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* Data updates: ClinVar, GWAS catalog, CIViC, CancerMine, dbNSFP, KEGG, ChEMBL/DGIdb, Disease Ontology, Experimental Factor Ontology
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