生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
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Rank and prioritize neoantigen/epitope candidates by likely T-cell response using NeoFox feature annotation, PRIME2.0, BigMHC-IM, the Łuksza/Balachandran fitness model (agretopicity + foreignness), and pVACtools tiering. Encodes the field's hard truths that immunogenicity is the least-solved layer (dedicated scores ~AUROC 0.6-0.7, modest PPV), that scores are valid only for RANKING within one patient (never absolute go/no-go or cross-patient), that DAI has anchor-inflation and WT-denominator traps, and that stacking weak correlated scores into one number is a red flag. Use when ordering a candidate list for a vaccine. Binding lives in mhc-binding-prediction; calling in neoantigen-prediction.
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Reference examples tested with: NeoFox 1.0+, pVACtools 4.1+, pandas 2.2+, numpy 1.26+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signatures<tool> --version then <tool> --help to confirm flagsIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
Notes specific to this skill: NeoFox annotates ~16 published features (it does not rank candidates automatically); PRIME 2.x requires MixMHCpred v3.0+ on PATH; BigMHC has separate -m el and -m im heads. ImmunoBERT is a PRESENTATION model, not an immunogenicity predictor — do not use it here. PRIME2.0 is the Cell Systems 2023 paper (the Cell Reports Medicine 2021 paper is PRIME v1). Re-verify tool versions and the supported-allele lists before scoring.
"Rank my neoantigen candidates by how likely a T cell responds" -> Annotate presentation + recognition features and order candidates within a patient; never assign an absolute immunogenicity verdict.
NeoFox to compute the published feature panel; PRIME / BigMHC -m im for recognition scoresBinding/presentation is genuinely good (AUROC high-0.9s); immunogenicity is not close. Predicting whether a displayed peptide provokes a T-cell response requires knowing whether a cognate TCR exists in this patient's repertoire, whether that clone survived thymic negative selection (escaped tolerance), and whether it activates in a suppressive tumor microenvironment — none observable from sequence. Dedicated immunogenicity tools land around AUROC 0.6-0.7 on their own test sets and worse on independent data; in TESLA the dedicated in-silico immunogenicity scores correlated poorly with validated immunogenicity, while presentation strength, binding stability, abundance/expression, agretopicity, and foreignness carried the signal. Two operational rules follow. First, immunogenicity scores are calibrated within a context (a tool, an allele, often a patient's HLA), so they are legitimate for ordering one patient's candidate list and illegitimate for absolute go/no-go or cross-patient/cross-allele comparison. Second, a confident single composite number is a red flag: stacking weak, correlated, IEDB-bias-trained scores into one value launders the bias at higher apparent precision. The honest deliverable is an ordered, feature-annotated shortlist with its uncertainty stated out loud.
The best-binder heuristic fails on a tolerance argument: a peptide that binds MHC superbly but closely resembles a self-peptide the thymus presented has had its cognate T cells deleted, so display does not help. A moderate binder that looks strikingly un-self may have a full, un-tolerized repertoire. The modern requirement is conjunctive — a useful neoantigen must be both PRESENTED (binding) AND FOREIGN enough (different from self) to have escaped tolerance. The Łuksza/Balachandran fitness model formalizes this: quality = amplitude (how much better the mutant is presented than its WT, a DAI-like term) x recognition potential R (resemblance to known immunogenic foreign epitopes). This is why agretopicity and foreignness, not raw affinity, recur in every validated analysis.
| Tool | Citation | What it scores | Note |
|---|---|---|---|
| NeoFox | Lang 2021 | ~16 features at once (DAI, foreignness, dissimilarity, PRIME, PHBR, ...) | Annotates, does NOT rank — the right division of labor |
| pVACtools tiering | Hundal 2020 | Rule-based tiers + within-tier sort | Auditable default; quarantines anchor/subclonal traps |
| PRIME2.0 | Gfeller 2023 | Class I immunogenicity (presentation x TCR-recognition) | Strong; needs MixMHCpred v3.0+ |
| BigMHC-IM | Albert 2023 | Class I immunogenicity (transfer-learned) | High precision; pan-allelic |
| IEDB immunogenicity | Calis 2013 | Class I (AA + position) | Weak, allele-pooled, no self-comparison; one feature only |
| DeepImmuno | Li 2021 | Class I CNN | 9/10mer only; limited alleles |
| fitness model (foreignness) | Łuksza 2017; Balachandran 2017 | Quality = amplitude x recognition | The conceptual backbone |
| Scenario | Recommended | Why |
|---|---|---|
| Default: rank a patient's candidates | NeoFox features -> pVACtools tiering -> human curation | Transparent features + auditable tiers, not a black-box score |
| Need a single recognition score | PRIME2.0 or BigMHC-IM | Best-validated class I; report alongside features, not alone |
| "Is this one immunogenic, yes/no?" | Reframe to ranking | No honest tool gives an absolute verdict |
| CD4 / class II immunogenicity | Flag as a frontier (TLimmuno2 etc.) | Class II immunogenicity is even less solved |
| Final shortlist for synthesis | Feature-annotated table + expression/clonality filters | Presentation + abundance carry most real signal (TESLA) |
Goal: Order one patient's candidates without collapsing fragile features into a single over-trusted number.
Approach: Compute the feature panel (NeoFox), apply the non-negotiable expression/clonality filters first, then sort by presentation + abundance + quality features, keeping the features visible side by side for human curation. Cross-patient comparison is invalid.
import pandas as pd
def rank_within_patient(df, expr_col='gene_expression', vaf_col='rna_vaf'):
'''Filter (not score) on expression/clonality first, then order by presentation,
abundance, and quality. Returns a feature-annotated table for human curation, not
a verdict. Scores are within-patient only - never compare across patients/alleles.'''
keep = df[(df[expr_col] >= 1.0) & (df[vaf_col] >= 0.25)].copy()
sort_cols = ['presentation_rank', 'gene_expression', 'agretopicity', 'foreignness']
ascending = [True, False, False, False]
cols = [c for c in sort_cols if c in keep.columns]
asc = [a for c, a in zip(sort_cols, ascending) if c in keep.columns]
return keep.sort_values(cols, ascending=asc)
Goal: Use the mutant-vs-WT binding gain without falling into its two traps.
Approach: Agretopicity (ratio, IC50_WT / IC50_MT; the DAI family — Duan 2014 uses the difference form) rewards a mutant that binds while WT does not. Trap 1: an anchor-position mutation inflates it without changing the TCR-facing surface (quarantine via the Anchor tier). Trap 2: when WT binds very poorly, the denominator explodes and the ratio is dominated by prediction noise — a value of 200 on a barely-estimable WT is not 100x more meaningful than a value of 2.
def defensive_dai(df, wt='wt_ic50', mt='mt_ic50', anchor='mutation_at_anchor', wt_cap=5000):
'''Flag anchor-inflated and denominator-unstable DAI rather than trusting the number.'''
out = df.copy()
out['dai'] = out[wt] / out[mt]
out['dai_anchor_artifact'] = out[anchor] # surface unchanged -> DAI is artifact
out['dai_unstable'] = out[wt] > wt_cap # WT barely presented -> ratio is noise
out['dai_trustworthy'] = ~out['dai_anchor_artifact'] & ~out['dai_unstable']
return out
Trigger: "score > X means immunogenic" or comparing scores across patients. Mechanism: scores are calibrated within tool/allele/patient. Symptom: false confidence; cross-patient mis-ranking. Fix: rank within a patient; state uncertainty; never threshold absolutely.
Trigger: summing/modeling DAI + foreignness + dissimilarity + hydrophobicity + PRIME into one number. Mechanism: components are weak, correlated (several measure "un-selfness"), and trained on ill-defined negatives. Symptom: an authoritative-looking 3-decimal number hiding fragile assumptions. Fix: keep features side by side; use auditable tiers; let a human weigh axes.
Trigger: trusting a high DAI. Mechanism: anchor mutation changes binding not TCR surface; tiny WT binding blows up the ratio. Symptom: top-ranked candidates that are anchor artifacts or noise. Fix: inspect mutation position and actual WT binding; quarantine via Anchor tier.
Trigger: trusting a new tool's headline AUROC. Mechanism: IEDB "negatives" conflate proven-non-immunogenic with untested; redrawing realistic negatives collapses performance. Symptom: great benchmark, poor real-world PPV. Fix: ask how negatives were defined before reading the number.
Trigger: optimizing a vaccine purely on class I immunogenicity. Mechanism: CD4 help drives durable efficacy but class II immunogenicity is a frontier. Symptom: optimizing the better-measured half of a two-armed problem. Fix: flag class II as unproven; include CD4 epitopes via mhc-class-ii-prediction.
| Threshold | Source | Rationale |
|---|---|---|
| Dedicated immunogenicity AUROC ~0.6-0.7 | TESLA; tool benchmarks | The honest performance ceiling; weak prior, not verdict |
| Gene TPM >= 1, RNA VAF >= 0.25 | pVACtools defaults | Unexpressed/low-VAF peptides are not displayed (filter first) |
| Subclonal at DNA VAF <= purity/4 | pVACtools | Clonal targets beat subclonal (McGranahan 2016) |
| Presentation + abundance carry the signal | Wells 2020 (TESLA) | Most predictive power is upstream of recognition scores |
| Rank within patient only | Score calibration | Cross-patient/allele comparison is invalid |
| Agretopicity ratio (amplitude); DAI difference | Łuksza 2017; Duan 2014 | Inspect position + WT binding; anchor inflation and denominator instability |
| Error / symptom | Cause | Solution |
|---|---|---|
| Absolute "immunogenic: yes/no" claim | Thresholded a within-context score | Reframe as within-patient ranking |
| Over-trusted single composite | Stacked weak correlated scores | Keep features visible; audit with tiers |
| High-DAI artifacts at top | Anchor mutation / unstable WT denominator | Defensive DAI; Anchor tier |
| Used ImmunoBERT as immunogenicity | It is a presentation model | Use PRIME/BigMHC-IM/Calis for recognition |
| Great AUROC, poor validation | Ill-defined negative set | Interrogate negatives; demand functional validation |
| Class II candidates over-trusted | CD4 immunogenicity is a frontier | Flag uncertainty; treat as unproven |
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概要と使いどころ
生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
日本語の概要は準備中です。原文の説明を表示しています。
Predicts ADMET properties using ADMETlab 3.0 (119 endpoints with uncertainty), ADMET-AI, DeepChem MolNet, and chemprop D-MPNN with explicit handling of OECD QSAR principles, applicability domain assessment, calibration, hERG/CYP/AMES gold-standard endpoints, and PAINS / Lipinski / Ro5 / Veber / BBB druglikeness filters. Use when filtering compounds for drug-likeness, prioritizing leads by predicted safety, or building an in-house ADMET QSAR model.
日本語の概要は準備中です。原文の説明を表示しています。
Trim PCR primers from aligned reads in amplicon-panel BAMs using samtools ampliconclip. Use when processing SARS-CoV-2 ARTIC, hereditary cancer panels, ctDNA hot-spot panels, or any amplicon assay where primer-derived bases would falsely confirm reference at primer footprints.
日本語の概要は準備中です。原文の説明を表示しています。
Filter alignments by flags, mapping quality, and regions using samtools view and pysam. Use when extracting specific reads, removing low-quality alignments, or subsetting to target regions.
日本語の概要は準備中です。原文の説明を表示しています。
Create and use BAI/CSI indices for BAM/CRAM files using samtools and pysam. Use when enabling random access to alignment files or fetching specific genomic regions.
日本語の概要は準備中です。原文の説明を表示しています。
Read, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.
日本語の概要は準備中です。原文の説明を表示しています。