Bio Binning QC
Bin metagenomic contigs, route bins by domain, run domain-specific quality checks, and join the results into normalized tables.
Instructions
Tool guides and versions: docs/README.md.
- Map each sample's reads back to the assembly (BBMap or
bwa-mem2for short reads, minimap2 for long reads; see/bio-reads-qc-mapping), then compute per-sample contig depth from the sorted BAMs with CoverM v0.7.0+. - Bin contigs with QuickBin from Bryce Foster's BBTools container (
bryce911/bbtools:39.85; record the digest when pulled). QuickBin is the default for short-read and long-read assemblies (docs/quickbin.md). On a CUDA GPU node, SemiBin2 v2.3.0+ is the alternative. Use MetaBAT2 v2.18+ only to reproduce a prior pipeline. - Run
/tracking-taxonomy-updatesfor BBTools-container QuickClade domain triage on the bin directory and the source assembly withpercontig. Persist the per-contig screen so mixed bins are visible. - Route bins by the QuickClade domain screen:
- Bacteria or Archaea -> run GTDB-Tk taxonomy assignment. If the GTDB-Tk reference package is missing, set it up under
$BIO_DB_ROOT, exportGTDBTK_DATA_PATH, rungtdbtk check_install, and record the release before classification. - Eukaryota -> run EukCC v2.1.3+ for eukaryotic bins.
- Viral or virus-like -> remove from MAG QC and route candidate contigs/genomes to
/bio-viromics; use vConTACT3 for phage/prokaryotic-virus evidence and GVClass for giant-virus/Nucleocytoviricota candidates. - Mixed or low-confidence -> flag as potential chimeras and inspect per-contig assignments before QC scoring.
- Bacteria or Archaea -> run GTDB-Tk taxonomy assignment. If the GTDB-Tk reference package is missing, set it up under
- Run domain-specific QC:
- CheckM2 v1.1.0+ for bacterial and archaeal bins (v1.1.0 is a breaking upgrade: update the pinned Pixi environment and refresh the DIAMOND v3 database from Zenodo DOI 10.5281/zenodo.14897628).
- EukCC v2.1.3+ for eukaryotic bins.
- GUNC v1.1.0+ (needed for the
progenomes_3andgtdb_214databases) for bacterial and archaeal bins only, as a chimerism check next to CheckM2. Do not apply GUNC to eukaryotic bins.gunc runreads.fafiles from--input_dirby default; set--file_suffixto match other bin suffixes.
- Normalize routed outputs with
scripts/build_bin_qc_tables.py. The join rejects GUNC rows for non-prokaryotic routes, refuses prokaryotic or eukaryotic bins that lack their domain-specific QC or taxonomy outputs, and refuses to overwrite existing outputs. Accepted routes areprokaryote,eukaryote,prokaryotic_virus,giant_virus, andmanual_review.
Quick Reference
| Task | Action |
|------|--------|
| Build normalized tables | uv run --script skills/bio-binning-qc/scripts/build_bin_qc_tables.py --routing domain_routing.tsv --checkm2 quality_report.tsv --gunc GUNC.progenomes_3.maxCSS_level.tsv --eukcc eukcc.csv --gtdbtk gtdbtk.bac120.summary.tsv --out-dir results/bio-binning-qc |
| Input tables | Native tool outputs, tab-separated: CheckM2 (Name, Completeness, Contamination), GUNC (genome, clade_separation_score, pass.GUNC), EukCC folder mode (bin, completeness, contamination, ncbi_lng), GTDB-Tk (user_genome, classification). FASTA suffixes on bin names are stripped before joining. When GTDB-Tk writes both bac120 and ar53 summaries, concatenate them with a single header line. |
Input Requirements
Prerequisites:
- Tools declared in the project's pinned Pixi environment. See
docs/README.mdfor expected tools. - Reference DB root: set
BIO_DB_ROOTto the project or site-local database directory. - Coverage/depth tables or reads available to compute coverage.
- Docker or Apptainer/Singularity available for
bryce911/bbtoolsQuickBin runs, or a documented local BBTools install. Inputs: - contigs.fasta
- coverage.tsv (per-sample depth table)
Output
- results/bio-binning-qc/bins/ (QuickBin or SemiBin2 output)
- results/bio-binning-qc/quickclade_percontig.tsv and domain_routing.tsv (from
/tracking-taxonomy-updates) - results/bio-binning-qc/bin_metrics.tsv (one row per routed bin; written by
build_bin_qc_tables.py) - results/bio-binning-qc/gtdbtk_taxonomy.tsv (one row per prokaryotic bin; written by
build_bin_qc_tables.py) - results/bio-binning-qc/bin_qc_report.json (routed-bin counts by domain; written by
build_bin_qc_tables.py) - results/bio-binning-qc/logs/
Quality Gates
- [ ] Completeness, contamination, and GUNC chimerism results are reported against project thresholds (for example MIMAG, see docs/README.md).
- [ ] On execution failure, preserve logs and report the failed command; retry only after diagnosing the cause and recording the changed parameters. Report unmet biological thresholds as results; never tune parameters solely to pass a gate.
- [ ] Verify contigs.fasta and coverage.tsv are non-empty.
- [ ] Verify reference DBs for QC tools exist under the reference root.
- [ ] QuickClade
percontigscreen exists for the source assembly and bin set before CheckM2/EukCC/GTDB-Tk decisions. - [ ] Bacterial and archaeal bins have GTDB-Tk taxonomy with the database release recorded.
- [ ] Viral/virus-like bins are routed to
/bio-viromicsinstead of reported as MAGs. - [ ] Mixed-domain bins are flagged as possible contamination/chimeras with per-contig evidence.
- [ ]
bin_metrics.tsvcovers every routed bin, including viral and manual-review rows, andgtdbtk_taxonomy.tsvcovers every prokaryotic bin.
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