Condense an academic paper into a structured abstract of up to 250 words, organized by background, objective, methods, results, and conclusion. It aims to retain key quantitative findings and supports papers from several research fields; figures and charts are not interpreted.
- Creating a concise abstract from a research paper
- Summarizing empirical studies while retaining key statistics
- Preparing structured summaries across multiple papers
aipoch/medical-research-skills☆ 2KUpdated Sep 17, 2026
Trim English academic abstracts to a target word count while preserving key findings, statistics, and the background-to-conclusion structure. Choose conservative, balanced, or aggressive compression, check word counts, and review the edited text for readability and accuracy.
- Cutting an abstract to meet a journal word limit
- Preparing a conference abstract with a strict word count
- Checking an abstract's word count before submission
aipoch/medical-research-skills☆ 2KUpdated Sep 17, 2026
Creates three to five concise English Highlights for journal submission from manuscript text or supported files. It adapts bullets to the article type, keeps each within 85 characters, and grounds every claim in the supplied source without inventing results.
- Draft journal Highlights from an abstract or manuscript
- Summarize a meta-analysis or review for submission
- Extract key findings from a supported PDF or DOCX
aipoch/medical-research-skills☆ 2KUpdated Sep 17, 2026
Design comparative drug safety studies using FAERS, the FDA’s adverse event reporting database, within one defined safety area. The plan compares drugs or classes, lays out workload options and analysis steps, and distinguishes detected signals from conclusions the data cannot support.
- Comparing drug classes within one adverse event area
- Planning a FAERS study with active comparators
- Adding declared subgroup or onset characterization
aipoch/medical-research-skills☆ 2KUpdated Sep 17, 2026
Predicts absorption, distribution, metabolism, and excretion properties for small molecules from their structures. Use the results to compare compounds, screen libraries, and review drug-likeness scores in structured outputs. Predictions support prioritization and need experimental validation.
- Compare predicted ADME profiles for small-molecule candidates
- Screen a compound library for drug-likeness
- Rank candidates against target property ranges
aipoch/medical-research-skills☆ 2KUpdated Sep 17, 2026
Turn adverse event case details into structured safety narratives for regulatory reporting. The skill checks required fields, organizes the event timeline, supports MedDRA coding and causality assessment, and formats drafts for CIOMS I, ICH E2B R3, or FDA MedWatch.
- Drafting an ICSR narrative from an adverse event case
- Checking a case for missing CIOMS I fields
- Organizing drug and event dates into a timeline
aipoch/medical-research-skills☆ 2KUpdated Sep 17, 2026