Skip to content
v0.1.3latest release121 skills4 categories6 sub-categories247 tested scripts397 reference docsContact us

minitab-analysis-interpreter

Interpret Minitab output for quality and Six Sigma work: read pasted Session window or report text and extract the key numbers from Process Capability reports (Cp, Cpk, Pp, Ppk, observed vs expected PPM), Gage R&R ANOVA (%Study Var, %Tolerance, ndc, Part*Operator interaction, dominant component), regression (coefficients, P-values, VIF, S, R-sq, R-sq(adj), R-sq(pred)), one-way ANOVA, two-sample and paired t-tests (P-value, confidence interval), Anderson-Darling normality tests and DOE coded coefficients; flag what needs attention (Cpk below 1.33, Ppk well below Cpk, PPM far above prediction, GRR above 10 or 30 percent, ndc below 5, over-fitted models, insignificant terms, multicollinearity) and state the conclusion in plain words. Covers how to read each output and the most common misreadings. Use when someone pastes Minitab results and asks what they mean, before presenting results at a tollgate, or when checking a Green Belt's analysis.

Minitab prints everything; the skill is knowing which numbers decide the question and which warnings are hiding in the output. scripts/parse_minitab.py recognises the common analyses in pasted text, extracts the deciding numbers and marks problems (WARN) and conclusions (RESULT).

Trigger Conditions

Activate this skill when the user:

  • Pastes Minitab output and asks "what does this mean?" or "is this good?"
  • Is preparing a DMAIC tollgate or report from Minitab results
  • Needs a Green Belt or supplier analysis checked for mistakes
  • Asks about R-sq(pred), VIF, %Study Var, ndc, Ppk vs Cpk or a p-value

Running the tests without Minitab: hypothesis-test-selector, manufacturing-cpk-capability-calculator, gage-rr-msa-analyzer.

Workflow

text
1. PASTE    -> save the Session window text (or copy from the report) to output.txt
2. PARSE    -> python scripts/parse_minitab.py output.txt
3. CONTEXT  -> what question was the analysis meant to answer? what data, how collected?
4. INTERPRET-> deciding numbers, warnings, conclusion in plain words (reading-minitab-output.md)
5. CHECK    -> graphs Minitab also produced: control chart, residual plots, normal probability plot
6. NEXT     -> what to do: collect more data, reduce the model, fix the gauge, act on the finding

Example

text
Recognised: regression
        Regression: S 0.08812, R-sq 87.4%, R-sq(adj) 84.1%, R-sq(pred) 71.2%
WARN    R-sq(pred) 71.2% is 16 points below R-sq: the model is over-fitted; remove weak terms
WARN    term Speed: VIF 6.8 > 5: correlated with other predictors; coefficients unstable

Per-analysis guide (capability, Gage R&R, regression, t-tests, ANOVA, DOE) with criteria: reading-minitab-output.md. Misreadings to correct: common-misreadings.md.

Output Format

Deliver:

  1. What was analysed and the question it answers.
  2. Key numbers (from parse_minitab.py).
  3. Interpretation in plain words, including what the warnings mean.
  4. Validity checks still needed (graphs, assumptions, data collection).
  5. Recommended next step.

Scripts

bash
python scripts/parse_minitab.py output.txt [--alpha 0.05]
pbpaste | python scripts/parse_minitab.py -

Exit codes: 0 parsed with no warnings, 1 parsed with warnings, 2 nothing recognised or read error.

Additional Resources

FileContent
reading-minitab-output.mdCapability, Gage R&R, regression, t-test, ANOVA and DOE outputs and criteria
common-misreadings.mdTen common misreadings and the correct reading
More in Quality Management & ISO 9001

8d-problem-solving-report-writer

Write and review 8D problem-solving reports for customer complaints and serious nonconformities (automotive and aerospace practice: Ford Global 8D, VDA, GM, Stellantis formats): D0 emergency response, D1 cross-functional team and champion, D2 problem description with 5W2H and is / is-not and no cause in the statement, D3 interim containment within 24 hours with verification and clean point, D4 verified occurrence and escape (non-detection) root causes plus systemic cause, D5 permanent corrective actions for each cause verified before implementation, D6 implementation, validation with production data and removal of containment, D7 PFMEA, control plan and read-across to similar products, D8 closure and recognition. Checks an 8D discipline by discipline for missing content, human-error root causes, missing escape cause or action, late containment and dates out of order.

acceptance-sampling-plan-selector

Select and evaluate acceptance sampling plans for incoming, in-process and final inspection: ANSI/ASQ Z1.4 / ISO 2859-1 single sampling under normal inspection (code letter from lot size and inspection level I, II, III, S-1 to S-4; sample size, Ac and Re from AQL, following the table's arrows to the correct plan; 100% when n reaches the lot size; AQLs above 10 per 100 units), operating characteristic curves (Pa at any quality, producer's quality level, indifference point, LTPD, AOQ and AOQL, binomial or hypergeometric), plans designed from producer and consumer risk, and c = 0 zero-acceptance plans. Covers AQL choice by defect class, switching rules between normal, tightened and reduced inspection, when sampling is not appropriate, and random sampling.

approved-supplier-list-manager

Manage and audit an approved supplier list (ASL) / external provider register for ISO 9001 8.4.1, IATF 16949 8.4 and AS9100 8.4.1: supplier status (approved, conditional, probation, pending, disqualified), scope of approval by commodity and process, risk class, certification and expiry, re-evaluation intervals by risk, conditions with end dates, single-source contingency, approver and customer-directed sources. Audits the list for expired or expiring certificates, overdue re-evaluations, conditional or probation status past its decision date, high-risk suppliers without the required certification, single-source suppliers without backup and missing approvers, and checks purchase orders for suppliers that are off-list, disqualified or pending, or buying outside the approved scope. Covers ERP blocks, PO requirements, off-list and emergency purchases.

apqp-phase-planner

Plan and track Advanced Product Quality Planning (AIAG APQP 3rd edition, IATF 16949) for a new or changed automotive part: back-schedule the five phases (plan and define, product design, process design, product and process validation, launch and feedback) from the start-of-production date by program complexity, with overlap, PPAP lead and safe-launch period; list the deliverables and gate for each phase (DFMEA, DVP&R, feasibility, process flow, PFMEA, control plans, MSA, Ppk, run at rate, PPAP, safe launch, lessons learned); adjust for build-to-print suppliers; flag compressed timelines and late or untracked deliverables against a status list. Covers gate reviews, red/yellow/green status reporting, run at rate and safe-launch exit criteria.

as9100-gap-analyzer

Run an AS9100D / EN 9100:2018 gap analysis for aviation, space and defence suppliers on the requirements added to ISO 9001: on-time delivery and conformity focus, management representative, ethics and human-factors awareness, operational planning and operational risk management, configuration management, product safety, counterfeit-part prevention, special requirements, critical items and key characteristics, external provider register and flow-down, FOD prevention, tooling and NC program control, special process validation, first article inspection (AS9102), traceability, in-service data and nonconforming product control. Generates and scores a worksheet, grades missing core controls as major, and checks invalid n/a claims. Covers AS9101/AS9104, OASIS, AS9102 FAI forms, counterfeit standards (AS5553, AS6174, AS6081), NADCAP and the planned IA9100 transition.

audit-report-writer

Write internal, supplier and pre-certification audit reports with the content ISO 19011:2018 6.5 expects: audit objectives, scope, criteria with revisions, dates, team and auditees, method and sampling statement, specific strengths, findings table and three-part finding details (requirement, evidence, statement), conclusion on the degree of fulfilment of criteria, diverging opinions, follow-up deadlines and distribution. Builds a Markdown report from a JSON audit record, generates the conclusion from the findings (major / minor / none) and flags reports missing required content or findings without clause or evidence. Covers conclusion wording, closing meetings, response expectations and verifying corrective actions.