What problem does it solve? Writing medical, biological, or clinical research papers requires strict adherence to discipline-specific reporting guidelines (CONSORT, STROBE, PRISMA), ethics declarations, and statistical reporting conventions that differ from general scientific writing. This Skill provides the specialized structure and checklists needed to produce compliant medical manuscripts. ## Core Features & Use Cases - Reporting Guideline Selection: Maps study types (RCT, cohort, case-control, systematic review, diagnostic accuracy, case report) to the correct reporting standard such as CONSORT, STROBE, PRISMA, STARD, CARE, or ARRIVE. - Ethics and Registration Templates: Provides ready-to-use statements for ethics committee approval, informed consent, and clinical trial registration (ChiCTR, ClinicalTrials.gov). - Statistical Reporting Conventions: Supplies standard phrasing for statistical methods, P-value formatting rules, confidence interval presentation, and baseline characteristics table layouts. - Use Case: A researcher finishing a randomized controlled trial can use this Skill to structure the manuscript in IMRaD format, insert the CONSORT flow requirements, and verify every item on the ethics and statistics checklist before submission. ## Quick Start Help me write the methods and results sections of my randomized controlled trial paper following CONSORT guidelines.
