tooluniverse-variant-predictor-dms-validation

name

tooluniverse-variant-predictor-dms-validation

description

Validate a variant-effect predictor (AlphaMissense, ESM-C SAE, ESM logits, EVE, conservation scores, or any per-variant numeric score) against experimental deep mutational scanning (DMS) data. Computes per-variant predictor scores, splits variants into neutral vs disruptive groups by DMS effect, runs a Mann-Whitney U test on the predictor scores, and sweeps the stratification thresholds for robustness. Use when you need to know whether a predictor's scores track real functional disruption on a specific protein.

Variant-effect predictor benchmarking against DMS

The core user question: "I have a variant-effect predictor — does it actually correlate with experimental DMS measurements on this protein?"

The predictor can be anything that assigns a numeric score to single missense variants:

• ESM-C 6B Sparse Autoencoder (SAE) feature drops at the mutation site
• AlphaMissense pathogenicity scores
• ESM logits-based variant scoring (ESM_score_sequence)
• EVE / EVE++ scores
• Conservation scores (ConSurf, Rate4Site)
• DynaMut2 ΔΔG predictions
• A custom in-house model

This skill validates ALL of these against a DMS dataset with the same statistical framework. SAE is shown as the worked example because the surrounding skills in this collection are SAE-themed, but the procedure is predictor-agnostic.

---

When to use this skill

• You picked a variant-effect predictor and want to know if it's worth trusting on your protein of interest
• You're comparing two predictors on the same DMS dataset (run this skill twice, compare the resulting per-K Mann-Whitney U p-values + effect sizes)
• Reviewers want robustness evidence — the parameter sweep (K, neutral band, disruptive quantile) is exactly that
• You're publishing a new variant-effect method and need a benchmark figure

Not for:

• Per-position / per-feature interpretation — use tooluniverse-residue-functional-mechanism-interpretation
• Single-variant interpretation (you have one variant, no DMS) — use tooluniverse-protein-sae-variant-interpretation or tooluniverse-protein-lof-mechanism
• Building a predictor from scratch — out of scope

---

Required inputs

Input	Format	Example
DMS effect matrix	(20 amino acids × n_positions) np.array, NaN for unmeasured	from MaveDB_get_effect_matrix
Disruptive tail convention	"top" (ΔΔG positive = destabilizing) or "bottom" (fitness low = LoF)	metadata from DMS retrieval step
Per-variant predictor scores	(20 × n_positions) np.array matching DMS layout	computed from your chosen predictor — see Step 2
Aggregation K	int, mean of top-K when the predictor outputs many sub-scores per variant	only relevant for multi-feature predictors like SAE; ignore otherwise

---

Workflow

Step 1: Retrieve DMS as an effect matrix

One call returns a ready-to-analyze (20 × n_positions) matrix — HGVS parsing, single-missense filtering, score-field detection, and (optional) UniProt numbering verification are done inside the tool:

r = MaveDB_get_effect_matrix(
    urn="urn:mavedb:00000115-a-7",
    uniprot_id="P01116",     # optional but recommended — enables numbering check
)
matrix = np.array(r["data"]["matrix"], dtype=np.float32)  # (20, n_positions)
positions = r["data"]["positions"]
amino_acid_order = r["data"]["amino_acid_order"]          # always 'ACDEFGHIKLMNPQRSTVWY'
# Audit fields — surface in your report:
#   r["data"]["n_parsed_single_missense"], n_dropped, score_field_used,
#   numbering_offset, numbering_check

If numbering_offset != 0, the MaveDB position numbering differs from the UniProt canonical sequence — apply the offset before joining to any other source (PDB / SAE features / AlphaMissense).

Step 2: Compute per-variant predictor scores

Pick one of these predictor sources. The choice changes Step 2 only; Steps 3–5 are identical.

Predictor option A — ESM-C 6B SAE (the worked example)

For every variant, sum SAE activations across the residue window, compute drop = max(0, WT − mut), and aggregate to one score per variant via the top-K mean of drops:

import numpy as np

def sae_drop_per_variant(wt_pooled, variant_pooled, K=3):
    """SAE drop for one variant = mean of the K largest feature drops."""
    drops = np.maximum(0.0, wt_pooled - variant_pooled)  # (n_features,)
    sorted_desc = -np.sort(-drops)
    return float(sorted_desc[:K].mean())

Two ways to score a saturation sweep — pick based on batch size:

When	Use	Forge cost (for 19 alts × N positions)
Saturation at ≤100 variants OR you only need top-K-per-variant deltas	ESM_score_variant_sae_batch(sequence, variants=[...], top_k_features=10)	1 + 19N (1 ref + 1 per mut)
Full-protein per-feature tensor (e.g. for downstream PCA / clustering)	Loop ESM_get_sae_features(sequence=mutant), cache by (sequence, position)	2 × 19N (cached reruns free)

The batch tool is the right default — it halves Forge cost vs the per-variant disruption pattern, and the cap of 100 variants per call covers saturation mutagenesis at one position (19) or short positional sweeps (e.g. positions 10-15: 90 variants). For longer sweeps, split into multiple batch calls.

For the full per-residue × per-feature tensor needed by some predictor analyses, fall back to the loop pattern. The full library scale is well-tested: tests/integration/test_dms_pipeline_e2e_kras.py runs ~300 mutants for KRAS positions 10–25.

Predictor option B — AlphaMissense (hegelab proxy: categorical, not per-substitution numeric)

The TU AlphaMissense tools proxy a public API (hegelab.org) that returns residue-level categorical assignments, not per-(position, alt_aa) numeric scores. Three calls are available; pick the one that matches your scale:

Tool	Signature	Returns
AlphaMissense_get_variant_score	uniprot_id, variant (e.g. "p.G12V")	Residue-level data INCLUDING the alt_aa's bin (benign / ambiguous / pathogenic); also mean/mean_all
AlphaMissense_get_residue_scores	uniprot_id, position	Same residue-level data (per-position lookup, cheaper than 19 variant calls)
AlphaMissense_get_protein_scores	uniprot_id	Whole-protein dump in one call (cheapest for full-protein DMS analysis)

The response shape is the same for all three. Example for KRAS pos 12:

r = AlphaMissense_get_residue_scores(uniprot_id="P01116", position=12)
# r["data"]["scores"]:
#   {"uid":"P01116","aa":"G","resi":12,
#    "benign":"", "ambiguous":"",
#    "pathogenic":"6:A,C,D,R,S,V",                  # ← SNV-reachable subs only
#    "pathogenic_all":"19:A,C,D,E,F,...,Y",         # ← all 19 substitutions
#    "mean":0.9885,           # mean over SNV-reachable subs
#    "mean_all":0.9950}       # mean over all 19 substitutions
# r["data"]["thresholds"]:
#   {"pathogenic":"> 0.564","ambiguous":"0.34 - 0.564","benign":"< 0.34"}

To populate the (20, n_positions) predictor matrix, parse the bin strings and map each alt_aa to a numeric score (bin-midpoint is the standard imputation since the tool doesn't expose true per-substitution numerics):

BIN_MIDPOINTS = {"benign": 0.17, "ambiguous": 0.452, "pathogenic": 0.782}

def parse_bin_list(bin_str):
    """'6:A,C,D,R,S,V' → ['A','C','D','R','S','V']; '' → []."""
    if not bin_str:
        return []
    _, aas = bin_str.split(":", 1)
    return aas.split(",")

def am_per_variant_matrix(uniprot_id, positions, aa_index):
    AAS = list(aa_index)
    M = np.full((20, len(positions)), np.nan, dtype=np.float32)
    # One whole-protein call is much cheaper than n_positions calls
    p = AlphaMissense_get_protein_scores(uniprot_id=uniprot_id)
    per_res = {row["resi"]: row for row in p["data"]["scores"]}
    for pos_idx, pos in enumerate(positions):
        row = per_res.get(pos, {})
        for cat in ("benign", "ambiguous", "pathogenic"):
            for alt in parse_bin_list(row.get(f"{cat}_all", "")):
                if alt in aa_index:
                    M[aa_index[alt], pos_idx] = BIN_MIDPOINTS[cat]
    return M

Higher-resolution alternative — DeepMind bulk CSV (only if you genuinely need true per-substitution numerics rather than bin-midpoints):

# The official DeepMind release contains per-variant continuous scores
# (not just bin assignments). Not currently wrapped by a TU tool — fetch directly:
#   https://alphafold.ebi.ac.uk/files/AF-<uniprot_id>-F1-aa-substitutions.csv
# or stream-filter https://storage.googleapis.com/dm_alphamissense/AlphaMissense_aa_substitutions.tsv.gz

Use the bulk CSV when you need rank-correlation analysis (Spearman benefits from continuous values, not 3-bin midpoints). Use the TU proxy when you only need the binary "is this variant in the pathogenic bin" signal.

Both options are free, no API key required.

Predictor option C — ESM logits-based score

ESM_score_sequence(
    sequence=mutant_sequence,
    model="esmc-600m-2024-12",
)
# returns per-residue logits; compute mutant-vs-WT log-odds at the mutation site

Predictor option C2 — ESM-2 masked-marginal (keyless, no API key)

When you have no ESM_API_KEY (the option A/C tools need one), use ESM2_score_missense_variant — it runs ESM-2 over HuggingFace's free hf-inference provider and returns the masked-marginal log-likelihood ratio logP(mut) − logP(wt) (Meier et al. 2021) for one missense variant:

# one call per variant; negative LLR = mutant disfavored (candidate deleterious)
res = ESM2_score_missense_variant(
    sequence=wild_type_sequence,   # 1-letter AA string
    position=position,             # 1-based
    mutant=alt_aa,                 # e.g. "V"
)
score = res["data"]["log_likelihood_ratio"]   # use directly as the predictor score

It is one HTTP call per variant (no batch endpoint), so for a saturation sweep it is slower than the key-based ESM-C batch tools — prefer option A/C when you have a key, and reach for this as the zero-setup fallback. Sequences over ~1022 residues are auto-windowed around the variant (see metadata.windowed). The LLR is a ranking score, not a calibrated probability — Steps 3–5 handle the thresholding, so feed the raw LLR straight into the (20, n_positions) matrix.

Predictor option D — any external score

Bring your own. Just produce a (20, n_positions) np.ndarray aligned to the DMS matrix.

Step 3: Stratify DMS into neutral vs disruptive

def categorize(dms_matrix, disruptive_tail, neutral_abs=0.1, disruptive_quantile=0.05):
    """Split variants into neutral and disruptive masks.

    disruptive_tail: 'top' (positive = destabilizing, e.g. folding ΔΔG)
                     'bottom' (low = LoF, e.g. fitness)
    """
    flat = dms_matrix[~np.isnan(dms_matrix)]
    if disruptive_tail == "top":
        cut = np.quantile(flat, 1 - disruptive_quantile)
        disruptive = dms_matrix >= cut
    elif disruptive_tail == "bottom":
        cut = np.quantile(flat, disruptive_quantile)
        disruptive = dms_matrix <= cut
    else:
        raise ValueError("disruptive_tail must be 'top' or 'bottom'")
    neutral = np.abs(dms_matrix) <= neutral_abs
    disruptive = disruptive & ~np.isnan(dms_matrix)
    neutral = neutral & ~np.isnan(dms_matrix) & ~disruptive
    return neutral, disruptive

Keep the neutral band tight (|effect| ≤ 0.1). A loose neutral band leaks weakly-disruptive variants into the "neutral" group and erodes the contrast. Sign matters — get disruptive_tail from the DMS-retrieval skill's metadata; a flipped sign silently inverts every conclusion.

Step 3.5 (MANDATORY): Pre-MWU sanity gate — catch silent NaN failures

Before running any statistical test, verify the predictor scores actually populated. Silent NaN matrices are the most common failure mode in this workflow — a batch SAE compute that errored midway, an AlphaMissense fetch that skipped variants, an ESM forge call that timed out — and they produce "successful" runs that report meaningless statistics.

neutral, disruptive = categorize(dms_matrix, disruptive_tail)
s_neutral_all = predictor_scores[neutral]
s_disruptive_all = predictor_scores[disruptive]
s_neutral_finite = s_neutral_all[~np.isnan(s_neutral_all)]
s_disruptive_finite = s_disruptive_all[~np.isnan(s_disruptive_all)]

# Hard gate: NaN coverage check
coverage_n = len(s_neutral_finite) / max(len(s_neutral_all), 1)
coverage_d = len(s_disruptive_finite) / max(len(s_disruptive_all), 1)
if len(s_neutral_finite) < 5 or len(s_disruptive_finite) < 5:
    raise ValueError(
        f"Insufficient predictor scores: only {len(s_neutral_finite)} neutral "
        f"and {len(s_disruptive_finite)} disruptive non-NaN values. "
        f"Coverage = {coverage_n:.0%} / {coverage_d:.0%}. "
        f"Predictor matrix may be empty / failed to populate. "
        f"INVESTIGATE THE PREDICTOR COMPUTATION STEP before continuing."
    )
if coverage_n < 0.5 or coverage_d < 0.5:
    print(f"WARNING: predictor coverage only {coverage_n:.0%} (neutral) / "
          f"{coverage_d:.0%} (disruptive). Results may be biased toward the "
          f"non-NaN subset.")

If you hit the ValueError: do not paper over with "predictor X wins by default". The right response is to debug the predictor computation step (re-run, check API keys, check log files) and report what failed.

Sign-convention double-check (also mandatory if the dataset is new): verify disruptive_tail against the data using an internal landmark. The metadata field can be misleading on subsets (e.g. a window of TP53 DBD might run the opposite direction from the full TP53 abundance assay). The cheapest check is Spearman correlation between DMS effect and a predictor known to align in a fixed direction (AlphaMissense pathogenicity score is always positive=more-damaging):

from scipy.stats import spearmanr
flat_dms = dms_matrix.ravel()
flat_pred = predictor_scores.ravel()
mask = ~(np.isnan(flat_dms) | np.isnan(flat_pred))
rho, p_corr = spearmanr(flat_dms[mask], flat_pred[mask])
expected_sign = "+" if disruptive_tail == "top" else "-"
got_sign = "+" if rho > 0 else "-"
if got_sign != expected_sign and abs(rho) > 0.1:
    print(f"WARNING: Spearman rho = {rho:.3f} (sign={got_sign}) but "
          f"disruptive_tail='{disruptive_tail}' expects sign={expected_sign}. "
          f"Sign convention may be inverted for THIS subset. Verify before "
          f"interpreting MWU.")

Step 4: One-sided Mann-Whitney U test

from scipy.stats import mannwhitneyu

u, p = mannwhitneyu(s_disruptive_finite, s_neutral_finite, alternative="greater")
print(f"disruptive median = {np.median(s_disruptive_finite):.4f}, "
      f"neutral median = {np.median(s_neutral_finite):.4f}, p = {p:.3g}")

For SAE-style multi-feature predictors with a top-K parameter, run this for K ∈ {1, 3, 10} and report all three — the best K is usually different across predictors and you want the comparison transparent, not tuned.

MWU is the discrimination test, but it's not the only valid analysis. Consider also reporting (one or both):

• Spearman rank correlation between predictor and DMS effect — captures graded calibration the binary neutral/disruptive split discards. Best for "is this predictor calibrated?" questions, not just "does it discriminate?"
• AUROC at a clinically-meaningful disruption threshold (e.g. ΔΔG > 1 kcal/mol) — gives a 0-1 number practitioners recognize and lets you compare to literature predictors directly.

The eval that motivated this skill (KRAS folding AlphaMissense benchmark) got qualitatively similar answers from MWU (p=0.20, "not reliable") and Spearman (ρ=0.23, p<1e-30, "weakly calibrated") — but Spearman's reading was richer. If the user just asks "is X reliable?", give both unless one is clearly inappropriate for the data shape.

Step 5: Robustness sweep

sweep = []
for neutral_abs in (0.05, 0.1, 0.2):
    for q in (0.05, 0.1):
        neut, disr = categorize(dms_matrix, disruptive_tail,
                                neutral_abs=neutral_abs,
                                disruptive_quantile=q)
        s_n = predictor_scores[neut][~np.isnan(predictor_scores[neut])]
        s_d = predictor_scores[disr][~np.isnan(predictor_scores[disr])]
        if len(s_n) < 5 or len(s_d) < 5:
            continue
        _u, p = mannwhitneyu(s_d, s_n, alternative="greater")
        sweep.append({"neutral_abs": neutral_abs, "disruptive_q": q, "p": p,
                      "n_n": len(s_n), "n_d": len(s_d)})

A predictor that passes only at one (neutral_abs, q) point is suspect. A predictor that passes across the grid is robust.

Step 6: Visualize + interpret

import matplotlib.pyplot as plt

fig, ax = plt.subplots(figsize=(4, 4))
ax.boxplot(
    [s_neutral, s_disruptive],
    labels=[f"neutral (n={len(s_neutral)})", f"disruptive (n={len(s_disruptive)})"]
)
ax.set_ylabel("Predictor score")
ax.set_title(f"p = {p:.3g}")
plt.tight_layout()
plt.savefig("predictor_vs_dms.png", dpi=150)

---

Interpretation

Result	What it means
p < 0.01 AND robust across sweep	Predictor reliably distinguishes disruptive from neutral on this protein. Safe to use for prioritization (not classification — see limits)
p < 0.05 but flips signs in sweep	Borderline. Effect exists but is sensitive to stratification — needs more data or tighter neutral band
p > 0.05	Predictor is not informative on this DMS assay. Possible causes: wrong disruptive_tail, predictor mis-calibrated for this protein family, DMS measures something the predictor wasn't trained for
Significant at K=1 but not K=10 (multi-feature predictors only)	Disruption is concentrated in a few features (K=1 best) vs distributed across many (K=10)

---

Comparing two predictors

Run this skill twice on the same DMS dataset (e.g. SAE drops AND AlphaMissense), keep the same stratification (disruptive_tail, neutral_abs, disruptive_quantile), and compare:

Metric	Better predictor has
Lower p-value	More confidence of discrimination
Larger median gap (disruptive − neutral)	Larger effect size
Fewer NaNs in coverage	Predicts more variants
Robust across sweep	More reliable in different conditions

---

Honest limitations

1. Per-protein test only. Generalizing "predictor X is good" requires running this on multiple proteins from different families.
2. Per-assay only. A predictor calibrated for stability might fail on binding-fitness assays — same protein, different DMS, different result.
3. Coarse signal. This says "predictor responds to mutational disruptiveness." It does NOT say "predictor identifies the right residues" — for that, run tooluniverse-residue-functional-mechanism-interpretation.
4. MWU assumes independence. DMS variants at the same position are mildly correlated (shared structural context); the p-values are slightly optimistic.
5. Tail definitions are arbitrary. 5% disruptive cutoff and 0.1 neutral band are reasonable defaults; the right thresholds depend on the assay's signal-to-noise. The sweep is what gives you robustness, not any single choice.

---

Cross-references

Step	Tool / Skill
DMS retrieval	MaveDB_get_effect_matrix
Per-variant SAE scoring (≤100 variants)	ESM_score_variant_sae_batch (preferred — N+1 calls)
Per-variant SAE scoring (full tensor / unlimited)	ESM_get_sae_features (loop + cache), ESM_score_variant_sae_disruption (single variant)
Per-variant AlphaMissense (single lookup)	AlphaMissense_get_variant_score(uniprot_id, variant)
Per-position AlphaMissense (saturation)	AlphaMissense_get_residue_scores(uniprot_id, position)
Whole-protein AlphaMissense (cheapest for DMS)	AlphaMissense_get_protein_scores(uniprot_id)
Per-variant ESM logits	ESM_score_sequence
Structural prior (for predictor analysis)	Structure_annotate_per_residue
Next step: per-hotspot mechanism	tooluniverse-residue-functional-mechanism-interpretation
Final visualization	Step 7 of tooluniverse-residue-functional-mechanism-interpretation (annotated heatmap + callouts)