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bump viral docker images to ones based on viral-core 2.1.12 (#180)
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tomkinsc authored Dec 14, 2020
1 parent 7b6dd91 commit 87066a4
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Showing 13 changed files with 57 additions and 54 deletions.
14 changes: 7 additions & 7 deletions pipes/WDL/tasks/tasks_assembly.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -15,7 +15,7 @@ task assemble {
String sample_name = basename(basename(reads_unmapped_bam, ".bam"), ".taxfilt")

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-assemble:2.1.10.0"
String docker="quay.io/broadinstitute/viral-assemble:2.1.12.0"
}

command {
Expand Down Expand Up @@ -80,7 +80,7 @@ task scaffold {
Float? scaffold_min_pct_contig_aligned

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-assemble:2.1.10.0"
String docker="quay.io/broadinstitute/viral-assemble:2.1.12.0"

# do this in multiple steps in case the input doesn't actually have "assembly1-x" in the name
String sample_name = basename(basename(contigs_fasta, ".fasta"), ".assembly1-spades")
Expand Down Expand Up @@ -226,7 +226,7 @@ task align_reads {
Boolean? skip_mark_dupes=false

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"

String sample_name = basename(basename(basename(reads_unmapped_bam, ".bam"), ".taxfilt"), ".clean")
}
Expand Down Expand Up @@ -342,7 +342,7 @@ task refine_assembly_with_aligned_reads {
Int? min_coverage=3

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-assemble:2.1.10.0"
String docker="quay.io/broadinstitute/viral-assemble:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -434,7 +434,7 @@ task refine {
Int? min_coverage=1

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-assemble:2.1.10.0"
String docker="quay.io/broadinstitute/viral-assemble:2.1.12.0"

String assembly_basename=basename(basename(assembly_fasta, ".fasta"), ".scaffold")
}
Expand Down Expand Up @@ -504,7 +504,7 @@ task refine_2x_and_plot {
String? plot_coverage_novoalign_options="-r Random -l 40 -g 40 -x 20 -t 100 -k"

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-assemble:2.1.10.0"
String docker="quay.io/broadinstitute/viral-assemble:2.1.12.0"

# do this in two steps in case the input doesn't actually have "cleaned" in the name
String sample_name = basename(basename(reads_unmapped_bam, ".bam"), ".cleaned")
Expand Down Expand Up @@ -636,7 +636,7 @@ task run_discordance {
String out_basename = "run"
Int min_coverage=4

String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down
4 changes: 2 additions & 2 deletions pipes/WDL/tasks/tasks_demux.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -6,7 +6,7 @@ task merge_tarballs {
String out_filename

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -60,7 +60,7 @@ task illumina_demux {
Boolean? forceGC=true

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down
8 changes: 4 additions & 4 deletions pipes/WDL/tasks/tasks_interhost.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -9,7 +9,7 @@ task multi_align_mafft_ref {
Float? mafft_gapOpeningPenalty

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}

String fasta_basename = basename(reference_fasta, '.fasta')
Expand Down Expand Up @@ -53,7 +53,7 @@ task multi_align_mafft {
Float? mafft_gapOpeningPenalty

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}

command {
Expand Down Expand Up @@ -142,7 +142,7 @@ task index_ref {
File? novocraft_license

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -252,7 +252,7 @@ task merge_vcfs_gatk {
File ref_fasta

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"

String output_prefix = "merged"
}
Expand Down
6 changes: 3 additions & 3 deletions pipes/WDL/tasks/tasks_intrahost.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -11,7 +11,7 @@ task isnvs_per_sample {
Boolean removeDoublyMappedReads=true

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"

String sample_name = basename(basename(basename(mapped_bam, ".bam"), ".all"), ".mapped")
}
Expand Down Expand Up @@ -52,7 +52,7 @@ task isnvs_vcf {
Boolean naiveFilter=false

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -125,7 +125,7 @@ task annotate_vcf_snpeff {
String? emailAddress

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"

String output_basename = basename(basename(in_vcf, ".gz"), ".vcf")
}
Expand Down
16 changes: 8 additions & 8 deletions pipes/WDL/tasks/tasks_metagenomics.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -11,7 +11,7 @@ task krakenuniq {
File krona_taxonomy_db_tgz # taxonomy.tab
Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -136,7 +136,7 @@ task build_krakenuniq_db {
Int? zstd_compression_level

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

command {
Expand Down Expand Up @@ -202,7 +202,7 @@ task kraken2 {
Int? min_base_qual

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -334,7 +334,7 @@ task build_kraken2_db {
Int? zstd_compression_level

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -472,7 +472,7 @@ task blastx {
File krona_taxonomy_db_tgz

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -559,7 +559,7 @@ task krona {
Int? magnitude_column

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

command {
Expand Down Expand Up @@ -658,7 +658,7 @@ task filter_bam_to_taxa {
String out_filename_suffix = "filtered"

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

String out_basename = basename(classified_bam, ".bam") + "." + out_filename_suffix
Expand Down Expand Up @@ -743,7 +743,7 @@ task kaiju {
File krona_taxonomy_db_tgz # taxonomy/taxonomy.tab
Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

String input_basename = basename(reads_unmapped_bam, ".bam")
Expand Down
12 changes: 6 additions & 6 deletions pipes/WDL/tasks/tasks_ncbi.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -25,7 +25,7 @@ task download_fasta {
Array[String]+ accessions
String emailAddress

String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}

command {
Expand Down Expand Up @@ -56,7 +56,7 @@ task download_annotations {
String emailAddress
String combined_out_prefix

String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}

command {
Expand Down Expand Up @@ -100,7 +100,7 @@ task annot_transfer {
File reference_fasta
Array[File]+ reference_feature_table

String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -153,7 +153,7 @@ task align_and_annot_transfer_single {
Array[File]+ reference_fastas
Array[File]+ reference_feature_tables

String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -208,7 +208,7 @@ task biosample_to_genbank {
Int num_segments=1
Int taxid

String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}
String base = basename(biosample_attributes, ".txt")
command {
Expand Down Expand Up @@ -254,7 +254,7 @@ task prepare_genbank {
String? assembly_method_version

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker="quay.io/broadinstitute/viral-phylo:2.1.12.0"
}

parameter_meta {
Expand Down
2 changes: 1 addition & 1 deletion pipes/WDL/tasks/tasks_nextstrain.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -263,7 +263,7 @@ task mafft_one_chr {
Boolean large = false
Boolean memsavetree = false
String docker = "quay.io/broadinstitute/viral-phylo:2.1.10.0"
String docker = "quay.io/broadinstitute/viral-phylo:2.1.12.0"
Int mem_size = 60
Int cpus = 32
}
Expand Down
8 changes: 4 additions & 4 deletions pipes/WDL/tasks/tasks_read_utils.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -11,7 +11,7 @@ task merge_and_reheader_bams {
File? reheader_table
String out_basename

String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -71,7 +71,7 @@ task rmdup_ubam {
String method="mvicuna"

Int? machine_mem_gb
String? docker="quay.io/broadinstitute/viral-core:2.1.10"
String? docker="quay.io/broadinstitute/viral-core:2.1.12"
}

parameter_meta {
Expand Down Expand Up @@ -125,7 +125,7 @@ task downsample_bams {
Boolean? deduplicateAfter=false

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -184,7 +184,7 @@ task FastqToUBAM {
String? platform_name
String? sequencing_center

String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}
parameter_meta {
fastq_1: { description: "Unaligned read1 file in fastq format", patterns: ["*.fastq", "*.fastq.gz", "*.fq", "*.fq.gz"] }
Expand Down
18 changes: 9 additions & 9 deletions pipes/WDL/tasks/tasks_reports.wdl
Original file line number Diff line number Diff line change
Expand Up @@ -10,7 +10,7 @@ task plot_coverage {
Boolean bin_large_plots=false
String? binning_summary_statistic="max" # max or min
String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -85,7 +85,7 @@ task coverage_report {
Array[File] mapped_bam_idx # optional.. speeds it up if you provide it, otherwise we auto-index
String out_report_name="coverage_report.txt"

String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -115,7 +115,7 @@ task fastqc {
input {
File reads_bam

String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

String reads_basename=basename(reads_bam, ".bam")
Expand Down Expand Up @@ -148,7 +148,7 @@ task align_and_count {
Int topNHits = 3

Int? machine_mem_gb
String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

String reads_basename=basename(reads_bam, ".bam")
Expand Down Expand Up @@ -191,7 +191,7 @@ task align_and_count_summary {

String output_prefix="count_summary"

String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -222,7 +222,7 @@ task aggregate_metagenomics_reports {
String aggregate_taxlevel_focus = "species"
Int aggregate_top_N_hits = 5

String docker="quay.io/broadinstitute/viral-classify:2.1.10.0"
String docker="quay.io/broadinstitute/viral-classify:2.1.12.0"
}

parameter_meta {
Expand Down Expand Up @@ -365,7 +365,7 @@ task tsv_join {
String join_type="inner"
String out_basename

String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -406,7 +406,7 @@ task tsv_stack {
input {
Array[File]+ input_tsvs
String out_basename
String docker="quay.io/broadinstitute/viral-core:2.1.10"
String docker="quay.io/broadinstitute/viral-core:2.1.12"
}

command {
Expand Down Expand Up @@ -436,7 +436,7 @@ task compare_two_genomes {
File genome_two
String out_basename

String docker="quay.io/broadinstitute/viral-assemble:2.1.10.0"
String docker="quay.io/broadinstitute/viral-assemble:2.1.12.0"
}

command {
Expand Down
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