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vdjdb-format

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Standardise a raw or partially-formatted VDJdb TSV chunk — normalising species names, IMGT V/D/J gene IDs, IMGT-HLA MHC alleles, and method vocabulary — and produce a properly-named chunk file ready for proofreading.

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/format — VDJdb Chunk Formatting Skill

Purpose

Take the output of /extract (or any TSV resembling a chunk file) and standardise all controlled-vocabulary fields to the VDJdb / IMGT specification. Cross-check naming conventions against existing chunks/ files to ensure internal consistency. This is the second stage: extract → format → proofread.

Invocation

/format [path-to-tsv]

The TSV must have a VDJdb-compatible header (see canonical column order in /extract). If the file has structural problems (missing columns, wrong separator), halt and report — this is a job for /proofread Step 1, not format.


Standardisation Rules

1. Species Names

Normalise to the exact VDJdb-accepted values (case-sensitive):

Normalise FROMNormalise TO
Homo sapiens, human, H. sapiens, hs, HumanHomoSapiens
Mus musculus, mouse, M. musculus, mm, MouseMusMusculus
Rattus norvegicus, rat, RattusRattusNorvegicus
Macaca mulatta, rhesus, macaque, NHPMacacaMulatta

If a species is not in the above list:

  1. Log it as a candidate for extending speciesList in py_src/ChunkQC.py
  2. Ask the user whether to include or exclude those rows

2. IMGT V/D/J Gene IDs

Primary authority: proofreading/imgt_alleles.tsv.gz (column imgt_gene_id) Conversion table: patches/nomenclature.conversions Secondary fallback: patches/IGM_nomenclature_table.tsv

Rules (apply in order):

  1. Strip whitespace: remove all spaces within the gene name (TRBV 7 → TRBV7, TRAV 12-2 → TRAV12-2)

  2. Detect and convert Adaptive Biotech ImmunoSEQ names (see proofreading/imgt.md §9.2 for full details):

    • Full Adaptive prefix (TCRB, TCRA, TCRG, TCRD): replace with TRB, TRA, TRG, TRD
      • TCRBV06-05*01 → strip TCR prefix → TRBV06-05*01
    • Zero-padded subgroup: strip leading zeros from subgroup number
      • TRBV06-5 → TRBV6-5
    • Zero-padded cluster: strip leading zeros from cluster number
      • TRBV7-06 → TRBV7-6, TRBV4-01 → TRBV4-1
    • Verify result in imgt_alleles.tsv.gz: if gene-cluster is not found, try the bare gene name (Adaptive always appends -01 to single-cluster genes that IMGT names without a cluster)
      • TRBV19-01 → TRBV19-1 not found → TRBV19 found ✓
      • TRBV11-02 → TRBV11-2 found ✓
    • When source is Adaptive, note in format log: ADAPTIVE_NAME → IMGT_NAME (Adaptive ImmunoSEQ normalisation)
  3. Look up in imgt_alleles.tsv.gz (strip allele suffix *NN before lookup):

    • If found → keep (or correct capitalisation to match)
    • If not found → check patches/nomenclature.conversions for a mapping
    • If found in conversions → apply the conversion and log old_name → new_name
    • If not found in either → flag as unresolvable; ask user
  4. Validate allele (if present, e.g., TRBV12-3*02):

    • Look up the full allele name in imgt_allele_id column: gzip -dc proofreading/imgt_alleles.tsv.gz | awk -F'\t' '$3=="TRBV12-3*02"'
    • If not found as a complete allele: flag as invalid; check whether the gene itself exists (gene-level lookup)
  5. Check functionality: if functionality is P (pseudogene) in imgt_alleles.tsv.gz: flag as biologically suspicious

  6. Consistency check against existing chunks:

    grep -h "" chunks/*.txt | cut -f3 | sort -u | grep "^TRAV"  # check v.alpha values
    

    If the same gene appears with different notation in existing chunks (e.g., TRAV13-1 vs TRAV13), standardise to the IMGT-canonical form.

  7. Multiple gene possibilities (comma-separated ambiguous assignments): check each against imgt_alleles.tsv.gz, keep all valid candidates comma-separated without spaces (e.g., TRBV7-2,TRBV7-3)


3. MHC Alleles

Primary authority: proofreading/mhc_alleles.tsv.gz (column allele_name) Reference: proofreading/mhc.md

Human MHC (HLA)

Target format: HLA-<GENE>*<FIELD1>:<FIELD2> (e.g., HLA-A*02:01)

ProblemFix
A02, A0201 (old serological)→ HLA-A*02:01 if unambiguous; flag if ambiguous
A*0201 (old format, no colon)→ HLA-A*02:01 (add prefix + insert colon)
HLA-A*02 (low resolution, 1-field)Keep as-is; note in log that higher resolution preferred
HLA-A*02:01:01 or *02:01:01:01 (high-res)Keep full string as-is
HLA-A 02:01 (space)→ HLA-A*02:01
HLA-A*02:01N, *02:01L (expression suffix)Keep suffix; note in log
Confirmed status from mhc_alleles.tsv.gzgzip -dc proofreading/mhc_alleles.tsv.gz | awk -F'\t' '$2=="HLA-A*02:01"{print $3}'

MHC-I second chain: always normalise to literal B2M — never beta-2-microglobulin, β2m, b2m, B2M*01, etc.

mhc.class cross-check:

If mhc.a starts with...mhc.class must bemhc.b must be
HLA-A, HLA-B, HLA-C, HLA-E, HLA-F, HLA-GMHCIB2M
HLA-DR, HLA-DQ, HLA-DP, HLA-DOMHCIIHLA β-chain allele

Mouse MHC (H-2)

Normalise FROMNormalise TO
H2-Db, H2DbH-2Db
IAb, I-Ab, IA-bI-Ab
H-2D^bH-2Db

For mouse class I: mhc.b = B2M For mouse class II: mhc.b = the β-chain name (e.g., I-Ab)


4. Method Vocabulary

Normalise method.identification and method.verification to VDJdb-recognised terms.

The governing rule: use what the source says. Do not upgrade or downgrade based on prevalence in VDJdb.

Author writesNormalise toReasoning
tetramer, pMHC tetramer, tetramer sorttetramer-sortSource specifies tetramers
dextramer, dextramer sortdextramer-sortSource specifies dextramers
pentamer, pentamer sortpentamer-sortSource specifies pentamers
multimer, pMHC multimer, multimer sortmultimer-sortSource gives no more specific reagent type
Reagent type not stated (only "sort" or "FACS")multimer-sortCannot assume tetramer; use generic
ELISpotDo NOT map automaticallyLog and ask user
51Cr release assayDo NOT map automaticallyLog and ask user

Example: A readme that says only "tetramer-sort" → tetramer-sort. A readme that says only "multimer-sort" with no other information → multimer-sort, even if tetramers are the most common reagent in VDJdb. Never infer the reagent type from context or database prevalence.

Rule: If an identification or verification method has no close equivalent in the current VDJdb vocabulary, do NOT force it. Instead:

  1. Leave a descriptive string in the field (for reference)
  2. Document it under "Vocabulary gaps" in the format log
  3. Suggest adding it as a new term via a note to the database maintainers

5. Reference IDs

Enforce correct format:

ProblemFix
https://doi.org/10.1016/...→ doi:10.1016/... (remove URL prefix)
http://dx.doi.org/10.1016/...→ doi:10.1016/...
doi: 10.1016/... (space after colon)→ doi:10.1016/...
pubmed:12345678 or PubMed:12345678→ PMID:12345678
Bare number 12345678Ask if it is a PMID; if confirmed → PMID:12345678

6. Antigen Fields

Cross-reference patches/antigen_epitope_species_gene.dict:

  • If antigen.epitope exists in the dict → use the dict's antigen.gene and antigen.species (this ensures consistency with the full database)
  • If the epitope is new → keep author-provided gene/species values, note in log

7. Chunk ID

After all formatting changes, renumber chunk.id sequentially from 1 (integer, no leading zeros).


Output Filename

Prefer PMID_<pubmed_id>.txt (e.g., PMID_28975614.txt).

If no PMID is available:

  1. Ask the user for the preferred name
  2. Alternatives: doi_<mangled_doi>.txt, submitter-date format
  3. Check that the chosen name does not duplicate an existing file in chunks/

Suggested placement: chunks_unformatted/ if uncertain about QC status; chunks/ only after /proofread passes.


Format Log

Write <output_basename>_format_log.txt containing:

  1. Changes made: for each change — field name, old value, new value, source of normalisation (imgt_alleles.tsv.gz / mhc_alleles.tsv.gz / nomenclature.conversions / manual)
  2. Unresolvable fields: fields that could not be normalised and why
  3. Vocabulary gaps: novel method/verification terms encountered
  4. Allele resolution notes: alleles that exist in mhc_alleles.tsv.gz at low resolution only
  5. Consistency discrepancies: naming differences found vs existing chunks/ files
  6. Pseudogene warnings: gene names whose functionality = P in imgt_alleles.tsv.gz
  7. Unconfirmed HLA alleles: alleles present in mhc_alleles.tsv.gz with confirmed = Unconfirmed

Reference Files

FileRole
proofreading/imgt_alleles.tsv.gzPrimary IMGT V/D/J gene authority
proofreading/imgt.mdIMGT nomenclature rules
proofreading/mhc_alleles.tsv.gzPrimary HLA allele authority
proofreading/mhc.mdMHC/HLA naming rules, class I vs II, non-human
patches/nomenclature.conversionsOld → current IMGT gene name mappings
patches/IGM_nomenclature_table.tsvSecondary IMGT fallback (existing repo file)
patches/antigen_epitope_species_gene.dictKnown epitope → gene/species mappings
py_src/ScoreFactory.pyMethod vocabulary and scoring logic
py_src/ChunkQC.pyALL_COLS definition (canonical column list)
chunks/*.txtReference for consistency checks
README.mdFull VDJdb specification

Next Step

After formatting, run /proofread [path-to-formatted-tsv] to validate against py_src/ChunkQC.py and all other QC checks.