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Cancer Cell Ethics & Data Availability

brycewang-stanfordbybrycewang-stanford
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Learning & Documentation

Validates and structures ethics approvals, consent declarations, biosafety compliance, and data and code availability statements for Cancer Cell submissions.

The cc-ethics-registration skill ensures Cancer Cell (Cell Press) manuscripts meet strict regulatory, ethical, and open-science compliance standards prior to submission. It guides authors through drafting and auditing animal IACUC protocols, human subject IRB approvals, informed consent documentation, Declaration of Helsinki affirmations, and clinical trial registrations. Furthermore, it enforces Cell Press data and code availability mandates—verifying public repository accessions (GEO, PRIDE, PDB), controlled-access plans for patient genomics (dbGaP, EGA), and citable DOIs for custom code to prevent desk rejections.

Key Features

01Validates IACUC animal research approvals with institutional protocol numbers
02Verifies human IRB approvals, informed consent statements, and Declaration of Helsinki compliance
03Audits controlled-access plans for patient-identifiable genomic and multi-omic data
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05Generates Cell Press-compliant Data and Code Availability statements with repository accessions and DOIs
06Checks biosafety protocols, clinical trial registrations, and author disclosure statements

Use Cases

01Formatting public data accessions and custom code DOIs for Cell Press Key Resources Tables
02Auditing human translational cancer studies for patient consent and controlled-access repository compliance
03Preparing compliance and ethics declarations for a Cancer Cell manuscript submission