--- name: molcell-data description: Use to build Molecular Cell's data and code deposition plan and the Data and Code Availability statement inside STAR Methods Resource Availability — approved repositories (GEO, PDB/EMDB, PRIDE), accessions/DOIs at submission, and Cell Press's standardized availability format with Mendeley Data as Elsevier's default. --- # Data & Code Availability (molcell-data) ## When to trigger - There is no Data and Code Availability statement, or it says "available on request." - Sequencing / structures / proteomics / datasets are not deposited or lack accessions. - Custom analysis code is not in a public, archived repository. - You need to draft the standardized statement for STAR Methods Resource Availability. ## Where the statement lives Molecular Cell's **Data and Code Availability** statement is a required subsection of **Resource Availability** inside **STAR Methods** (see `molcell-star-methods`) — not a free-floating paragraph. Datasets deposited for *this paper* must also appear in the **Key Resources Table** under "Deposited Data." ## Deposit in approved repositories (with accession/DOI) | Data type | Deposit in (examples) | |-----------|------------------------| | High-throughput sequencing (ChIP/RNA/ATAC/CLIP-seq) | **GEO** / **SRA** | | Nucleotide / genome sequences | GenBank / ENA / DDBJ | | Macromolecular structures | **PDB** | | Cryo-EM maps (and half-maps) | **EMDB** (map) + **PDB** (model) | | Crystallography | PDB (coordinates + structure factors) | | Proteomics / mass spec / cross-linking MS | **PRIDE** / **ProteomeXchange** (+ **jPOST** where used) | | NMR | **BMRB** + PDB | | Imaging / general structured datasets | **BioStudies** / BioImage Archive | | Generic datasets (Elsevier default) | **Mendeley Data**, or Zenodo / Dryad | | Plasmids / unique reagents | **Addgene** | | Code (archive a release for a DOI) | GitHub/GitLab **+ Zenodo** (citable DOI) | > **Mendeley Data is Elsevier's default repository** for datasets without a dedicated community repository. Prefer a community repository (GEO, PDB/EMDB, PRIDE) when one exists for the data type — Molecular Cell's molecular focus means most primary data have one. - Obtain **accession numbers / DOIs before submission**; reviewers and editors expect them in hand, and for structures they will check map-model fit against the deposited entry. - Code that reproduces the analysis must be **public and archived** (a citable DOI via Zenodo) — a bare GitHub link is not durable. ## Cell Press Data and Code Availability format Cell Press uses a standardized statement. Provide a sentence for each item: ``` Data and Code Availability • [DATA] The [datatype] data generated in this study have been deposited at [GEO / PDB+EMDB / PRIDE] and are publicly available as of the date of publication. Accession numbers are listed in the Key Resources Table. / This paper analyzes existing, publicly available data [accessions in KRT]. • [CODE] All original code has been deposited at [Zenodo/Mendeley Data] and is publicly available as of the date of publication. DOIs are listed in the Key Resources Table. / This paper does not report original code. • [ADDITIONAL] Any additional information required to reanalyze the data reported in this paper is available from the Lead Contact upon request. ``` Each item must be addressed even if the answer is "this paper does not report…". Restricted human/clinical data must state the controlled-access procedure and the controlling body. ## Structure-specific deposition (Molecular Cell-heavy) - **Cryo-EM**: deposit the map (and typically half-maps and mask) at **EMDB** and the model at **PDB**; report the resolution and the FSC threshold used. - **X-ray**: deposit coordinates **and structure factors** at PDB. - Validation reports should be generatable from the deposited entries — reviewers may request them. ## Materials & ethics cross-links - Unique materials sharing belongs in **Materials Availability** (`molcell-star-methods`); use Addgene/MTA and state how. - Ethics approvals (IRB/IACUC, consent, permits) belong in **Experimental Model and Subject Details**. - Identify key reagents with **RRIDs** in the Key Resources Table. ## Output format ``` 【Data deposited】 type → repository → accession/DOI (list each) | gaps 【Structures】 EMDB/PDB (map+model) or PDB (coords+SF)? resolution/FSC stated? 【Code public + archived DOI】 yes/no (repo + Zenodo/Mendeley DOI) 【Statement】 DATA ☐ / CODE ☐ / ADDITIONAL ☐ — all drafted? 【In KRT "Deposited Data"】 accessions listed? yes/no 【Restricted data】 controlled-access procedure stated where needed? 【Next】 molcell-summary ``` ## Anti-patterns - **Do not** write "available on request" for the primary data behind the figures. - **Do not** deposit a structure model without its map/structure factors. - **Do not** link only to a personal/lab website — use an archival repository with a DOI. - **Do not** forget to mirror accessions into the Key Resources Table. - **Do not** submit without accession numbers/DOIs in hand. > Confirm repository requirements and the exact availability wording against current Cell Press / STAR Methods guidelines.