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Merge pull request #566 from nf-core/multiqc-tweak
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Tweak order of MultiQC sections to better match workflow
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CarsonJM authored Feb 1, 2024
2 parents 601114d + 2a3eb28 commit 61376a8
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1 change: 1 addition & 0 deletions CHANGELOG.md
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Expand Up @@ -20,6 +20,7 @@ and this project adheres to [Semantic Versioning](https://semver.org/spec/v2.0.0
### `Fixed`

- [#558](https://github.com/nf-core/mag/pull/558) - Fix bug in run merging when dealing with single end data (reported by @roberta-davidson, fix by @jfy133)
- [#566](https://github.com/nf-core/mag/pull/566) - More logical ordering of MultiQC sections (assembly and bin sections go together respectively) (fix by @jfy133)

### `Dependencies`

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28 changes: 14 additions & 14 deletions assets/multiqc_config.yml
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Expand Up @@ -33,6 +33,7 @@ top_modules:
- "*trimmed*"
- "fastp"
- "adapterRemoval"
- "porechop"
- "fastqc":
name: "FastQC: after preprocessing"
info: "After trimming and, if requested, contamination removal."
Expand All @@ -48,12 +49,6 @@ top_modules:
info: "Mapping statistics of reads mapped against host genome and subsequently removed."
path_filters:
- "*_host_removed.bowtie2.log"
- "bowtie2":
name: "Bowtie2: assembly"
info: "Mapping statistics of reads mapped against assemblies."
path_filters_exclude:
- "*_host_removed.bowtie2.log"
- "*_phix_removed.bowtie2.log"
- "kraken":
name: "Kraken2"
anchor: "Kraken2"
Expand All @@ -70,21 +65,26 @@ top_modules:
extra: "ℹ️: plot title will say Kraken2 due to Centrifuge producing the same output format as Kraken. If activated, see the actual Kraken2 results in the section above."
path_filters:
- "*.centrifuge_kreport.txt"
- "porechop"
- "bcftools"
- custom_content
- "busco":
info: "assesses genome assembly and annotation completeness with Benchmarking Universal Single-Copy Orthologs. In case BUSCO's automated lineage selection was used, only generic results for the selected domain are shown and only for genome bins and kept, unbinned contigs for which the BUSCO analysis was successfull, i.e. not for contigs for which no BUSCO genes could be found. Bins for which a specific virus lineage was selected are also not shown."
- "quast":
name: "QUAST: assembly"
info: "Assembly statistics of raw assemblies."
path_filters:
- "*rawassemblies.tsv"
- "bowtie2":
name: "Bowtie2: assembly"
info: "Mapping statistics of reads mapped against assemblies."
path_filters_exclude:
- "*_host_removed.bowtie2.log"
- "*_phix_removed.bowtie2.log"
- "bcftools"
- custom_content
- "quast":
name: "QUAST: bins"
info: "Assembly statistics of binned assemblies."
path_filters_exclude:
- "*rawassemblies.tsv"
- "busco":
info: "assesses genome assembly and annotation completeness with Benchmarking Universal Single-Copy Orthologs. In case BUSCO's automated lineage selection was used, only generic results for the selected domain are shown and only for genome bins and kept, unbinned contigs for which the BUSCO analysis was successfull, i.e. not for contigs for which no BUSCO genes could be found. Bins for which a specific virus lineage was selected are also not shown."
- "prokka"

custom_data:
Expand Down Expand Up @@ -140,7 +140,6 @@ table_columns_visible:
after_filtering_gc_content: False
pct_surviving: True
pct_adapter: True
"Bowtie2: assembly": False
"Kraken2": False
"Centrifuge": False
"QUAST: assembly":
Expand All @@ -150,6 +149,7 @@ table_columns_visible:
"Largest contig": True
"Total length": True
N50: True
"Bowtie2: assembly": False
"QUAST: bins":
N75: True
L50: True
Expand Down Expand Up @@ -190,8 +190,6 @@ table_columns_placement:
overall_alignment_rate: 5000
"Bowtie2: host removal":
overall_alignment_rate: 6000
"Bowtie2: assembly":
overall_alignment_rate: 7000
"Kraken2":
"% root": 8000
"% Top 5": 8100
Expand All @@ -203,6 +201,8 @@ table_columns_placement:
"QUAST: assembly":
"N50": 10000
"Total length": 11000
"Bowtie2: assembly":
overall_alignment_rate: 7000
"QUAST: bins":
"N50": 10000
"Total length": 11000
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