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4ccd547
Merge changes from main into develop (#703)
github-actions[bot] Jun 22, 2026
b15805e
Enabled explicit local access for wkhtmltopdf
ESapenaVentura Jun 23, 2026
abf31f1
Updated CHANGELOG
ESapenaVentura Jun 23, 2026
8a82362
Updated wkhtmltopdf required version
victor5lm Jul 1, 2026
a2d7a4b
Fixed linting for github actions
victor5lm Jul 1, 2026
fd1d76e
Updated assembly config for multiqc
victor5lm Jul 1, 2026
142ad81
Updated assembly results lablog
victor5lm Jul 1, 2026
969e2e8
Updated CHANGELOG.md
victor5lm Jul 1, 2026
1656275
Updated exomeeb template
victor5lm Jul 2, 2026
3085402
Updated DROP template
victor5lm Jul 2, 2026
68647dd
Updated exometrio template
victor5lm Jul 2, 2026
863e25c
Updated wgstrio template
victor5lm Jul 2, 2026
676f7d0
Updated missing paths
victor5lm Jul 2, 2026
8831064
Updated CHANGELOG.md
victor5lm Jul 2, 2026
91dcf0c
Updated assembly template
victor5lm Jul 2, 2026
84e6c68
Updated characterization template
victor5lm Jul 2, 2026
a695555
Updated pikavirus template
victor5lm Jul 2, 2026
46c717e
Updated viralrecon template
victor5lm Jul 2, 2026
9e5ba0c
Update CHANGELOG.md
victor5lm Jul 2, 2026
a746a3d
Updated CHANGELOG.md
victor5lm Jul 2, 2026
2d7074c
Updated pyproject.toml
victor5lm Jul 2, 2026
9c6bcac
Updated __main__.py
victor5lm Jul 2, 2026
72774ba
updated bacass to version 2.6.1, no need to skip busco
saramonzon Jul 9, 2026
0559972
updated changelog
saramonzon Jul 9, 2026
462b626
include R1 and R2 in assembly sample names for cleaning
saramonzon Jul 15, 2026
fd3ebd8
fix assembly Bacass output handling
saramonzon Jul 15, 2026
de91d01
support Bacass numeric sample IDs downstream
saramonzon Jul 15, 2026
7e65929
fix Snippy IQ-TREE model reuse workflow
saramonzon Jul 15, 2026
02ab651
enhance outbreak summary workbook reporting
saramonzon Jul 15, 2026
ddc5eb7
document template improvements for PR 718
saramonzon Jul 15, 2026
acfa2b0
linting
saramonzon Jul 15, 2026
f8d7470
add Snippy SNP distance and close-pair QC tools
saramonzon Jul 15, 2026
e7673d6
document Snippy SNP QC tools for PR 718
saramonzon Jul 15, 2026
b648f53
linting
saramonzon Jul 15, 2026
6eb9bd6
Fix IRMA stats for flu and rsv when having missing readcounts
PauPascualMas Jul 10, 2026
0e67670
Updated CHANGELOG.md
PauPascualMas Jul 10, 2026
fba4f72
Updated CHANGELOG.md
PauPascualMas Jul 20, 2026
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2 changes: 1 addition & 1 deletion .github/workflows/python_lint.yml
Original file line number Diff line number Diff line change
Expand Up @@ -4,7 +4,7 @@ on:
push:
branches: "**"
pull_request:
types: [opened, reopened, synchronize, closed]
types: [opened, reopened, synchronize]
branches: "**"

jobs:
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31 changes: 31 additions & 0 deletions CHANGELOG.md
Original file line number Diff line number Diff line change
Expand Up @@ -4,6 +4,37 @@ All notable changes to this project will be documented in this file.

The format is based on [Keep a Changelog](https://keepachangelog.com/en/1.0.0/), and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0.html).

## [2.3.4] - 2026-07-02 : https://github.com/BU-ISCIII/buisciii-tools/releases/tag/2.3.4

### Credits

- [Enrique Sapena](https://github.com/ESapenaVentura)
- [Victor Lopez](https://github.com/victor5lm)

### Template fixes and updates

- Updated assembly config for MultiQC and RESULTS lablog [#708](https://github.com/BU-ISCIII/buisciii-tools/pull/708)
- Updated iGenomes paths [#710](https://github.com/BU-ISCIII/buisciii-tools/pull/710)
- Updated the assembly template to skip busco and some paths in correspondence to refgenie system [#711](https://github.com/BU-ISCIII/buisciii-tools/pull/711)

### Modules

#### Implementation

#### Added enhancements

#### Fixes

- Fixed local file access for PDF generation via wkhtmltopdf [#705](https://github.com/BU-ISCIII/buisciii-tools/pull/705)

#### Changed

#### Removed

### Requirements

- Updated wkhtmltopdf version requirement from 0.12.4 to 0.12.6.1 [#708](https://github.com/BU-ISCIII/buisciii-tools/pull/708)

## [2.3.3] - 2026-06-22 : https://github.com/BU-ISCIII/buisciii-tools/releases/tag/2.3.3

### Credits
Expand Down
2 changes: 1 addition & 1 deletion buisciii/__main__.py
Original file line number Diff line number Diff line change
Expand Up @@ -66,7 +66,7 @@ def run_buisciii():
highlight=False,
)

__version__ = "2.3.3"
__version__ = "2.3.4"
stderr.print(
"[grey39] BUISCIII-tools version {}".format(__version__), highlight=False
)
Expand Down
5 changes: 4 additions & 1 deletion buisciii/bioinfo_doc.py
Original file line number Diff line number Diff line change
Expand Up @@ -552,7 +552,10 @@ def convert_to_pdf(self, html_file):
pdf_file = html_file.replace(".html", ".pdf")
try:
pdfkit.from_file(
html_file, output_path=pdf_file, configuration=self.config_pdfkit
html_file,
output_path=pdf_file,
configuration=self.config_pdfkit,
options={"enable-local-file-access": ""},
)
log.info(f"PDF file created successfully: {pdf_file}")
except OSError as e:
Expand Down
Original file line number Diff line number Diff line change
Expand Up @@ -9,7 +9,7 @@ sampleAnnotation: sample_annotation_AE.tsv
geneAnnotation:
gencode29: /data/ucct/bi/references/refgenie/alias/hg19/gtf/gencode29/gencode.v29lift37.annotation.gtf
genomeAssembly: hg19
genome: /data/ucct/bi/references/igenomes/Homo_sapiens/Ensembl/GRCh37/Sequence/WholeGenomeFasta/genome.fa
genome: /data/ucct/bi/references/refgenie/alias/Homo_sapiens_Ensembl_GRCh37/fasta/v20230419/genome.fa
# You can define multiple reference genomes in yaml format, ncbi: path/to/ncbi, ucsc: path/to/ucsc
# the keywords that define the path should be in the GENOME column of the sample annotation table

Expand Down
Original file line number Diff line number Diff line change
Expand Up @@ -9,7 +9,7 @@ sampleAnnotation: sample_annotation_AS.tsv
geneAnnotation:
gencode29: /data/ucct/bi/references/refgenie/alias/hg19/gtf/gencode29/gencode.v29lift37.annotation.gtf
genomeAssembly: hg19
genome: /data/ucct/bi/references/igenomes/Homo_sapiens/Ensembl/GRCh37/Sequence/WholeGenomeFasta/genome.fa
genome: /data/ucct/bi/references/refgenie/alias/Homo_sapiens_Ensembl_GRCh37/fasta/v20230419/genome.fa
# You can define multiple reference genomes in yaml format, ncbi: path/to/ncbi, ucsc: path/to/ucsc
# the keywords that define the path should be in the GENOME column of the sample annotation table

Expand Down
Original file line number Diff line number Diff line change
Expand Up @@ -9,7 +9,7 @@ sampleAnnotation: sample_annotation_MAE.tsv
geneAnnotation:
gencode29: /data/ucct/bi/references/refgenie/alias/hg19/gtf/gencode29/gencode.v29lift37.annotation.gtf
genomeAssembly: hg19
genome: /data/ucct/bi/references/igenomes/Homo_sapiens/Ensembl/GRCh37/Sequence/WholeGenomeFasta/genome.fa
genome: /data/ucct/bi/references/refgenie/alias/Homo_sapiens_Ensembl_GRCh37/fasta/v20230419/genome.fa
# You can define multiple reference genomes in yaml format, ncbi: path/to/ncbi, ucsc: path/to/ucsc
# the keywords that define the path should be in the GENOME column of the sample annotation table

Expand Down
Original file line number Diff line number Diff line change
Expand Up @@ -123,6 +123,7 @@ nextflow run /data/ucct/bi/pipelines/nf-core-bacass/nf-core-bacass-2.5.0/main.nf
--save_trimmed ${SAVETRIMMED} \\
--skip_kraken2 true \\
--skip_kmerfinder false \\
--skip_busco true \\
--kmerfinderdb /data/ucct/bi/references/kmerfinder/latest/bacteria \\
--ncbi_assembly_metadata /data/ucct/bi/references/bacteria/20240626/assembly_summary_refseq.txt \\
${PROKKA_ARGS} \\
Expand Down
3 changes: 2 additions & 1 deletion buisciii/templates/assembly/DOC/hpc_slurm_assembly.config
Original file line number Diff line number Diff line change
Expand Up @@ -221,7 +221,8 @@ process {
saveAs: { filename -> filename.equals('versions.yml') ? null : filename }
]
}
withName: 'MULTIQC_CUSTOM' {
withName: 'CUSTOM_MULTIQC' {
ext.args = '--interactive'
publishDir = [
[
path: { "${params.outdir}/99-stats/multiqc" },
Expand Down
4 changes: 2 additions & 2 deletions buisciii/templates/assembly/RESULTS/lablog_assembly_results
Original file line number Diff line number Diff line change
Expand Up @@ -6,8 +6,8 @@ mkdir -p $DELIVERY_FOLDER/assembly
cd $DELIVERY_FOLDER/assembly

# Links to reports
ln -s ../../../ANALYSIS/*ASSEMBLY/multiqc/multiqc_report.html .
ln -s ../../../ANALYSIS/*ASSEMBLY/multiqc/summary_assembly_metrics_mqc.csv .
ln -s ../../../ANALYSIS/*ASSEMBLY/99-stats/multiqc/multiqc_report.html .
ln -s ../../../ANALYSIS/*ASSEMBLY/99-stats/summary_assembly_metrics_mqc.csv .
ln -s ../../../ANALYSIS/*ASSEMBLY/Kmerfinder/kmerfinder_summary.csv .
ln -s ../../../ANALYSIS/*ASSEMBLY/03-assembly/quast/global_report/report.html quast_global_report.html

Expand Down
Original file line number Diff line number Diff line change
@@ -1,3 +1,3 @@
# module load singularity

cp /data/ucct/bi/references/ariba/databases.txt .
cp /data/ucct/bi/references/refgenie/alias/ariba/databases.txt .
Original file line number Diff line number Diff line change
Expand Up @@ -6,7 +6,7 @@ mkdir MLVA_output
scratch_dir=$(pwd | sed 's|/data/ucct/bi/scratch_tmp|/scratch|g')
cp ../../*_ASSEMBLY/03-assembly/unicycler/*.fasta* assemblies/
gzip -d assemblies/*.fasta.gz
available_primers=$(ls /data/ucct/bi/references/MLVA/*primer* | rev | cut -d "/" -f1 | rev | cut -d "_" -f1)
available_primers=$(ls /data/ucct/bi/references/refgenie/alias/MLVA/primers/v20231004/*primer* | rev | cut -d "/" -f1 | rev | cut -d "_" -f1)

echo "Available primers:"
select primer in $available_primers; do
Expand All @@ -18,6 +18,6 @@ select primer in $available_primers; do
fi
done

primer_file=$(ls /data/ucct/bi/references/MLVA/${primer}*)
primer_file=$(ls /data/ucct/bi/references/refgenie/alias/MLVA/primers/v20231004/${primer}*)

echo "srun --partition short_idx --chdir ${scratch_dir} --output logs/MLVA.log --job-name MLVA python /data/ucct/bi/pipelines/mlva/MLVA_finder.py -c -i assemblies -o MLVA_output -p ${primer_file} --full-locus-name --predicted-PCR-size-table --flanking-seq 20 &" > _01_mlva.sh
Original file line number Diff line number Diff line change
Expand Up @@ -38,7 +38,7 @@ nextflow run /data/ucct/bi/pipelines/nf-core-sarek/nf-core-sarek_3.4.4/3_4_4/mai
--dbsnp '/data/ucct/bi/references/eukaria/homo_sapiens/hg19/1000genomes_b37/variants/20131208/dbsnp_138_mod.b37.vcf.gz' \\
--dbsnp_tbi '/data/ucct/bi/references/eukaria/homo_sapiens/hg19/1000genomes_b37/variants/20131208/dbsnp_138_mod.b37.vcf.gz.tbi' \\
--igenomes_ignore \\
--igenomes_base '/data/ucct/bi/references/igenomes/' \\
--igenomes_base '/data/ucct/bi/references/refgenie/alias/' \\
--tools 'haplotypecaller' \\
--joint_germline \\
-resume
Expand Down
32 changes: 16 additions & 16 deletions buisciii/templates/exomeeb/DOC/hpc_slurm_sarek.config
Original file line number Diff line number Diff line change
Expand Up @@ -26,23 +26,23 @@ params {
max_time = '48.h'
genomes {
'GATK.GRCh37' {
ascat_alleles = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/ASCAT/G1000_alleles_hg19.zip"
ascat_alleles = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-ASCAT/v20230419/G1000_alleles_hg19.zip"
ascat_genome = 'hg19'
ascat_loci = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/ASCAT/G1000_loci_hg19.zip"
ascat_loci_gc = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/ASCAT/GC_G1000_hg19.zip"
ascat_loci_rt = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/ASCAT/RT_G1000_hg19.zip"
bwa = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/BWAIndex/"
chr_dir = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/Chromosomes"
dict = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/WholeGenomeFasta/human_g1k_v37_decoy.dict"
fasta = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/WholeGenomeFasta/human_g1k_v37_decoy.fasta"
fasta_fai = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/WholeGenomeFasta/human_g1k_v37_decoy.fasta.fai"
germline_resource = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/af-only-gnomad.raw.sites.vcf.gz"
germline_resource_tbi = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/af-only-gnomad.raw.sites.vcf.gz.tbi"
intervals = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/intervals/wgs_calling_regions_Sarek.list"
known_snps = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/1000G_phase1.snps.high_confidence.b37.vcf.gz"
known_snps_tbi = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/1000G_phase1.snps.high_confidence.b37.vcf.gz.tbi"
known_indels = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/{1000G_phase1,Mills_and_1000G_gold_standard}.indels.b37.vcf.gz"
known_indels_tbi = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/{1000G_phase1,Mills_and_1000G_gold_standard}.indels.b37.vcf.gz.tbi"
ascat_loci = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-ASCAT/v20230419/G1000_loci_hg19.zip"
ascat_loci_gc = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-ASCAT/v20230419/GC_G1000_hg19.zip"
ascat_loci_rt = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-ASCAT/v20230419/RT_G1000_hg19.zip"
bwa = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/bwa_index/v20230419/"
chr_dir = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/chromosomes/v20230419/"
dict = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/fasta/v20230419/human_g1k_v37_decoy.dict"
fasta = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/fasta/v20230419/human_g1k_v37_decoy.fasta"
fasta_fai = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/fasta/v20230419/human_g1k_v37_decoy.fasta.fai"
germline_resource = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/af-only-gnomad.raw.sites.vcf.gz"
germline_resource_tbi = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/af-only-gnomad.raw.sites.vcf.gz.tbi"
intervals = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-intervals/v20230419/wgs_calling_regions_Sarek.list"
known_snps = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/1000G_phase1.snps.high_confidence.b37.vcf.gz"
known_snps_tbi = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/1000G_phase1.snps.high_confidence.b37.vcf.gz.tbi"
known_indels = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/{1000G_phase1,Mills_and_1000G_gold_standard}.indels.b37.vcf.gz"
known_indels_tbi = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/{1000G_phase1,Mills_and_1000G_gold_standard}.indels.b37.vcf.gz.tbi"
snpeff_db = 'GRCh37.87'
snpeff_genome = 'GRCh37'
snpeff_version = '5.1'
Expand Down
Original file line number Diff line number Diff line change
Expand Up @@ -58,7 +58,7 @@ nextflow run /data/ucct/bi/pipelines/nf-core-sarek/nf-core-sarek_3.4.4/3_4_4/mai
--save_reference \\
--joint_germline \\
--igenomes_ignore \\
--igenomes_base '/data/ucct/bi/references/igenomes/' \\
--igenomes_base '/data/ucct/bi/references/refgenie/alias/' \\
-resume
EOF

Expand Down
32 changes: 16 additions & 16 deletions buisciii/templates/exometrio/DOC/hpc_slurm_sarek.config
Original file line number Diff line number Diff line change
Expand Up @@ -26,23 +26,23 @@ params {
max_time = '48.h'
genomes {
'GATK.GRCh37' {
ascat_alleles = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/ASCAT/G1000_alleles_hg19.zip"
ascat_alleles = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-ASCAT/v20230419/G1000_alleles_hg19.zip"
ascat_genome = 'hg19'
ascat_loci = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/ASCAT/G1000_loci_hg19.zip"
ascat_loci_gc = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/ASCAT/GC_G1000_hg19.zip"
ascat_loci_rt = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/ASCAT/RT_G1000_hg19.zip"
bwa = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/BWAIndex/"
chr_dir = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/Chromosomes"
dict = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/WholeGenomeFasta/human_g1k_v37_decoy.dict"
fasta = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/WholeGenomeFasta/human_g1k_v37_decoy.fasta"
fasta_fai = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Sequence/WholeGenomeFasta/human_g1k_v37_decoy.fasta.fai"
germline_resource = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/af-only-gnomad.raw.sites.vcf.gz"
germline_resource_tbi = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/af-only-gnomad.raw.sites.vcf.gz.tbi"
intervals = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/intervals/wgs_calling_regions_Sarek.list"
known_snps = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/1000G_phase1.snps.high_confidence.b37.vcf.gz"
known_snps_tbi = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/1000G_phase1.snps.high_confidence.b37.vcf.gz.tbi"
known_indels = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/{1000G_phase1,Mills_and_1000G_gold_standard}.indels.b37.vcf.gz"
known_indels_tbi = "${params.igenomes_base}/Homo_sapiens/GATK/GRCh37/Annotation/GATKBundle/{1000G_phase1,Mills_and_1000G_gold_standard}.indels.b37.vcf.gz.tbi"
ascat_loci = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-ASCAT/v20230419/G1000_loci_hg19.zip"
ascat_loci_gc = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-ASCAT/v20230419/GC_G1000_hg19.zip"
ascat_loci_rt = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-ASCAT/v20230419/RT_G1000_hg19.zip"
bwa = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/bwa_index/v20230419/"
chr_dir = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/chromosomes/v20230419/"
dict = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/fasta/v20230419/human_g1k_v37_decoy.dict"
fasta = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/fasta/v20230419/human_g1k_v37_decoy.fasta"
fasta_fai = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/fasta/v20230419/human_g1k_v37_decoy.fasta.fai"
germline_resource = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/af-only-gnomad.raw.sites.vcf.gz"
germline_resource_tbi = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/af-only-gnomad.raw.sites.vcf.gz.tbi"
intervals = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-intervals/v20230419/wgs_calling_regions_Sarek.list"
known_snps = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/1000G_phase1.snps.high_confidence.b37.vcf.gz"
known_snps_tbi = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/1000G_phase1.snps.high_confidence.b37.vcf.gz.tbi"
known_indels = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/{1000G_phase1,Mills_and_1000G_gold_standard}.indels.b37.vcf.gz"
known_indels_tbi = "${params.igenomes_base}/Homo_sapiens_GATK_GRCh37/annotation-GATKBundle/v20230419/{1000G_phase1,Mills_and_1000G_gold_standard}.indels.b37.vcf.gz.tbi"
snpeff_db = 'GRCh37.87'
snpeff_genome = 'GRCh37'
snpeff_version = '5.1'
Expand Down
Original file line number Diff line number Diff line change
Expand Up @@ -10,7 +10,7 @@ process {
params {
config_profile_name = 'ISCIII HPC profile'
config_profile_description = 'Profile designed for the High Performance Computer in the ISCIII'
kraken2_db = "/data/ucct/bi/references/kraken/minikraken_8GB_20200312"
kraken2_db = "/data/ucct/bi/references/refgenie/alias/kraken/minikraken_8GB/v20200312"
vir_ref_dir = "/data/ucct/bi/references/PikaVirus/viral_assemblies_for_pikavirus"
vir_dir_repo = "/data/ucct/bi/references/PikaVirus/viral_assemblies.tsv"
bact_ref_dir = "/data/ucct/bi/references/PikaVirus/bacteria_assemblies_for_pikavirus"
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Expand Up @@ -10,7 +10,7 @@ process {
withName: 'ARTIC_MINION' {
ext.args = [
'--normalise 500',
'--scheme-directory /data/ucct/bi/references/virus/2019-nCoV/primer_schemes/',
'--scheme-directory /data/ucct/bi/references/refgenie/alias/coronaviridae/primer_schemes/',
'--medaka'
].join(' ').trim()
}
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Expand Up @@ -52,7 +52,7 @@ nextflow run /data/ucct/bi/pipelines/nf-core-sarek/nf-core-sarek_3.4.4/3_4_4/mai
--dbsnp '/data/ucct/bi/references/eukaria/homo_sapiens/hg19/1000genomes_b37/variants/20131208/dbsnp_138_mod.b37.vcf.gz' \\
--dbsnp_tbi '/data/ucct/bi/references/eukaria/homo_sapiens/hg19/1000genomes_b37/variants/20131208/dbsnp_138_mod.b37.vcf.gz.tbi' \\
--igenomes_ignore \\
--igenomes_base '/data/ucct/bi/references/igenomes/' \\
--igenomes_base '/data/ucct/bi/references/refgenie/alias/' \\
--tools 'haplotypecaller' \\
--joint_germline \\
-resume
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