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implementing-new-modules

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Create a new MultiQC module from scratch. Parse a bioinformatics tool's output, register search patterns and entry points, add general stats columns, build plots and sections, write tests, open a PR. Use when implementing a `module: new` GitHub issue, when the user asks to add support for a new tool, or when adding a parser for a new tool output format.

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How to use this skill

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  3. Review the proposed files and risks before you approve installation.
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Source SKILL.md: https://github.com/MultiQC/MultiQC/blob/HEAD/.claude/skills/implementing-new-modules/SKILL.md

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Implement New MultiQC Module

Workflow

  1. Research the tool: read its docs, get example output files (check MultiQC/test-data/data/modules/ first), find similar existing modules for reference. Note version- and flag-dependent output variations.
  2. Pick architecture: single-tool or multi-subtool (see below).
  3. Build the module: parser, general stats, sections, plots. Full step-by-step in implementation-checklist.md.
  4. Register: add to search_patterns.yaml and pyproject.toml entry points.
  5. Test: unit tests for parsers, integration test via pytest tests/test_modules_run.py -k "toolname" -v, and multiqc … --strict on test data.
  6. Quality gate: prek run, ruff check, python .github/workflows/code_checks.py, mypy.
  7. PR: brief summary, <details> for the full write-up, Closes #XXXX.

Architecture decision

Single-tool (FastQC, Qualimap): one output format, one parser.

multiqc/modules/toolname/
├── __init__.py
└── toolname.py

Multi-subtool (samtools, seqkit, picard): distinct subcommands with different output formats, or more subcommands likely to be added.

multiqc/modules/toolname/
├── __init__.py
├── toolname.py        # Orchestrator
├── subtool1.py        # parse_toolname_subtool1() function
├── subtool2.py        # parse_toolname_subtool2() function
└── tests/

Class skeletons and full file templates: module-structure.md. Patterns for code inside a module (parsing, plots, alerts, etc.): code-patterns.md.

Common Pitfalls

  1. Forgetting add_software_version() — required by linting, even if version is None.
  2. Calling write_data_file() too early — must be at end, after all sections.
  3. Raising UserWarning instead of ModuleNoSamplesFound.
  4. Not handling both tab- and space-separated output when both are valid.
  5. Hardcoding values instead of using f["s_name"] and other dynamic variables.
  6. Manually cleaning sample names instead of self.clean_s_name().
  7. Inappropriate colour scales — e.g. RdYlGn for GC% (which is not "higher is better").
  8. Silently defaulting on known fields — parsed.get(key, 0) for fields the tool always emits (or try/except: return {} over the whole parse) hides real format breakage behind a fake-looking report. Access documented keys directly; reserve .get(default) for genuinely optional fields. Catching a parse error to raise a friendlier message is fine; silently producing zeros is not.
  9. Trivial single-statement helpers — a helper that wraps one or two lines, or just renames a one-liner, adds indirection without aiding readability. Per-section / per-parser helpers (_add_adapter_section, _parse_log) are fine and often clearer; one-liner wrappers (_add_filtered_section calling add_section with no real logic) are not.
  10. Using raw parsed dict keys in user-facing text — total_counts and pct_dup belong in code, never in plot/column titles, axis labels, or section names. Convert to "Total Counts", "% Duplicates".
  11. Dropping the whole section when all samples are zero — keep the section, pass plot=None, and add a SectionAlert via the alerts= parameter on add_section() listing affected samples. Don't append raw <div class="alert ..."> HTML to description — use the alerts API.
  12. Pre-filtering samples at parse time — keep every sample in the main data dict so write_data_file is complete; filter at plot-render time.
  13. Em-dashes (—) in any user-facing text — descriptions, docstrings, alerts, PR text. AI tell. Use commas or split sentences.