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Design healthcare staff training programs. TRIGGERS - Use when user needs help with staff-training-health related tasks.
Prepare ethics applications, develop informed consent protocols, and navigate institutional review processes for human subjects research
Systematic literature-review workflow for academic, biomedical, technical, and scientific topics, including search planning, source screening, synthesis, citation checks, and evidence logging.
Checks biomedical manuscripts against reporting guidelines such as CONSORT, STROBE, PRISMA, and TRIPOD to identify missing or weak reporting elements before submission or revision.
Organizes biomedical figures, analyses, and result blocks into a clear Results section structure with disciplined narrative ordering and evidence-aware presentation.
Writes the full Results section of a biomedical manuscript from a sufficiently clear result structure, figure inventory, or analysis summary while preserving evidence boundaries and result hierarchy.
Write and revise the Methods section of research papers to ensure reproducibility; use when preparing an IMRAD manuscript or responding to journal/reporting-guideline requirements (e.g., CONSORT/STROBE/PRISMA).
Acknowledges limitations in sample, design, measurement, and validation in a professional way that improves credibility without undermining the whole paper. Use when writing the limitations paragraph of a Discussion section, preparing a grant risk assessment, responding to reviewers about study w...
Evaluate research rigor. Assess methodology, experimental design, statistical validity, biases, confounding, evidence quality (GRADE, Cochrane ROB), for critical analysis of scientific claims.
Converts LabArchives notebook data, entry metadata, and authorized ELN exports into manuscript-ready academic writing outputs such as Methods sections, data-availability statements, reproducibility appendices, experiment timelines, and submission support notes. Optional bundled scripts can be use...
Use when interpreting scientific graphs and charts, explaining data visualizations for research presentations, writing figure captions for publications, or analyzing trends in clinical research data. Converts complex visual data into clear, accurate explanations for academic papers, clinical repo...
Refines broad, vague, or aspirational biomedical research objectives into clear, bounded, measurable, executable, and downstream-ready study objective statements. Always use this skill when a user has a general aim such as “explore a mechanism,” “study prognosis,” “investigate biomarkers,” or “lo...
Draft IACUC protocol applications with focus on the 3Rs principles justification.
Automated abstract screening tool for systematic literature reviews with PRISMA workflow support.
Write a structured research protocol or study design document. Use when asked to write a research protocol, study protocol, research plan, methodology section, or research proposal. Produces a complete protocol with objectives, methodology, ethical considerations, and analysis plan.
Generates the Methods section for a meta-analysis paper, including search strategy, screening, quality assessment, data extraction, and statistical analysis.
Generate ethical, compliant, and patient-friendly recruitment advertisements for clinical trials.
Guides research ethics compliance including IRB protocol preparation, informed consent document drafting, research integrity standards, data management plans, and ethical considerations for human/animal subjects; trigger when users discuss IRB, ethical approval, consent forms, or responsible cond...
Read, summarize, and critically analyze scientific papers. Extract key findings, methodology, limitations, and contributions. Use when user shares a paper (PDF/URL/DOI), asks to summarize a paper, critique methodology, extract data from a paper, compare papers, or do a critical review. Triggers o...
Conduct comprehensive literature searches, quality assessments, evidence synthesis, and meta-analyses
Navigate institutional review board processes, informed consent, confidentiality, and ethical considerations in human subjects research
Praeregistrierung und Replikationsstudien im DFG-Antrag: Hypothesen ex ante festlegen, registered reports, OSF-Praeregistrierung, Replikationsplaene als eigenstaendiges Vorhaben. DFG-Statement to scientific integrity. Vorteile für Reviewer-Akzeptanz, typische Stolpersteine bei der Formulierung.
Generate concise (3-4 page), focused medical treatment plans in LaTeX/PDF format for all clinical specialties. Supports general medical treatment, rehabilitation therapy, mental health care, chronic disease management, perioperative care, and pain management. Includes SMART goal frameworks, evide...
Structures NIH/foundation grant applications with specific aims, significance, and innovation sections. Use when writing research grants, preparing NIH applications, or structuring grant proposals.
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