Benchmarking Universal Single Copy Orthologs
meta
:map
Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]
fasta
:file
Nucleic or amino acid sequence file in FASTA format.
*.{fasta,fna,fa,fasta.gz,fna.gz,fa.gz}
mode
:string
The mode to run Busco in. One of genome, proteins, or transcriptome
{genome,proteins,transcriptome}
lineage
The BUSCO lineage to use, or “auto”, “auto_prok” or “auto_euk” to automatically select lineage
busco_lineages_path
:directory
Path to local BUSCO lineages directory.
config_file
Path to BUSCO config file.
clean_intermediates
:boolean
Flag to remove intermediate files.
batch_summary
Groovy Map containing sample information e.g. [ id:‘test’ ]
*-busco.batch_summary.txt
Summary of all sequence files analyzed
short_summaries_txt
short_summary.*.txt
Short Busco summary in plain text format
short_summaries_json
short_summary.*.json
Short Busco summary in JSON format
log
*-busco.log
BUSCO main log
full_table
*-busco/*/run_*/full_table.tsv
Full BUSCO results table
full_table.tsv
missing_busco_list
*-busco/*/run_*/missing_busco_list.tsv
List of missing BUSCOs
missing_busco_list.tsv
single_copy_proteins
*-busco/*/run_*/single_copy_proteins.faa
Fasta file of single copy proteins (transcriptome mode)
single_copy_proteins.faa
seq_dir
*-busco/*/run_*/busco_sequences
BUSCO sequence directory
busco_sequences
translated_dir
*-busco/*/translated_proteins
Six frame translations of each transcript made by the transcriptome mode
busco_dir
*-busco
BUSCO lineage specific output
downloaded_lineages
busco_downloads/lineages/*
Lineages downloaded by BUSCO when running the analysis, for example bacteria_odb12
single_copy_faa
*-busco/*/run_*/busco_sequences/single_copy_busco_sequences/*.faa
Single copy .faa sequence files
single_copy_fna
*-busco/*/run_*/busco_sequences/single_copy_busco_sequences/*.fna
Single copy .fna sequence files
versions
versions.yml
File containing software versions
BUSCO provides measures for quantitative assessment of genome assembly, gene set, and transcriptome completeness based on evolutionarily informed expectations of gene content from near-universal single-copy orthologs selected from OrthoDB.