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Protocol Preparation Guidelines for Authors
The condensed methodologies typically published in the Methods sections of original research articles or other types of publications (e.g., book chapters) can be hard to reproduce. Bio-protocol helps to fill this gap by providing a platform for clearly written, step-by-step, peer-reviewed, and validated protocols that contain sufficient detail to ensure their reproducibility. The goal of our published protocols is to provide enough information for a novice to perform the experiment successfully with appropriate advice or supervision. We welcome submissions of both newly developed protocols as well as classic methods lacking detailed descriptions elsewhere in the literature. Our peer review process emphasizes feasibility, not novelty. Most reviewer-requested changes involve text edits for clarity and detail, which most authors can easily address.
Authors can submit their manuscript via the Bio-protocol website here. For any questions about protocol preparation or submission, contact our Managing Editor, Marisa Rosa (marisa.rosa@ed.bio-protocol.org). Please see the general guidelines below describing the main components of Bio-protocol articles.
General Guidelines
Authors must follow the provided template for manuscript preparation and ensure that all information they choose to include is relevant to the protocol described. Bio-protocol requires authors to submit all text and figures as a single Microsoft Word file, while videos must be submitted as separate files. The manuscript should contain the elements described below in the "Protocol format" section below. Abbreviations should only be used if necessary and defined upon first use in the Abstract and in the main text. Click here to see an example of an article in the standard Bio-protocol format.
Protocol Format
Submitting authors must follow the standard Bio-protocol format, described below. For more details about each element, please see the manuscript template.
1. Protocol title
The Title should indicate the goal of the protocol and provide enough detail to help a prospective researcher determine whether the protocol is of interest to them. Keep in mind that your protocol could be useful for researchers from a completely different field; as such, the title should be clear to a broad range of scientists.
2. Author information
Please provide complete affiliation information (department, research institution, city, country) for each author.
3. Abstract
The Abstract should briefly introduce the research field and provide a summary of the protocol, highlighting its goal and advantages over other methods.
4. Key features
Key features are bullet points that convey important elements of the protocol. These should not simply repeat or condense ideas conveyed in the Abstract; instead, they should highlight characteristics that will allow readers to determine whether the protocol is relevant to their work.
5. Keywords
Include technical or method-related keywords to help readers easily find your protocol using Google or other search engines. Repeat the relevant keywords used in your original research paper (if applicable).
6. Graphical overview
The graphical overview could be a flowchart of the method/procedures or a graphical highlight of key steps; it should not be a simple copy of other images in the manuscript. See an example here. Please provide the graphical overview in figure format. This section is highly recommended but not mandatory.
7. Background
Briefly introduce the research area(s) that your protocol can be used to advance, providing the rationale for developing the protocol. Place the protocol in the context of existing technology of the research field, discussing previously used related methodologies, and summarizing the advantages, limitations, and applications of your approach.
8. Materials and reagents
This section should provide a detailed list of all biological materials, reagents, solutions (with recipes), and laboratory supplies required for the successful execution of the protocol, including manufacturer catalog numbers, instructions on how to acquire/produce items that are not commercially available, and storage conditions/shelf-life for critical reagents. Be precise about the ingredients used, as a lack of clarity on minor details might lead to the failure of the experiment. Authors should indicate whether any materials are subject to Material Transfer Agreements (MTAs) or if any data are subject to Data Use Agreements (DUAs).
9. Equipment
List the equipment used in the experiments, including specific catalog/model numbers.
10. Software and datasets
List individual software or datasets used in the experiments, including version. Provide references for items that are not commercially available.
11. Procedure
List all steps of the procedure chronologically, as it makes the protocol easier to follow. Be specific in your instructions. Include details for material and reagents used (e.g., volume added, specific container/tube, and incubation time) and the conditions in which the step is performed (e.g., temperature, agitation speed, and equipment settings); avoid using vague terms such as "several" or "enough."
At crucial steps, make sure to include labels ("Caution," "Pause point," or "Critical," as appropriate) and notes (see General Notes and Troubleshooting below), especially if it would increase the likelihood of successfully repeating the experiment. As needed, include images and videos to clarify key steps and representative data to illustrate the type of results obtained.
For formatting details for text, figures, tables, and videos, see the manuscript template.
12. Data analysis
Provide a detailed description of data processing and analyses, including statistical tests, criteria for data inclusion/exclusion, and details on the recommended number of biological and technical replicates in each experiment. Highlight any specific skills necessary to perform the analyses (e.g., expertise using Linux, R, or other specific data analysis software).
When a detailed description of the data analysis method already appears in a published or posted research article, summarize the analysis method and cite the publication or preprint. Please indicate clearly where the description of the analysis can be found (e.g., Supplemental information or Figure X).
13. Validation of protocol
This section aims to ensure readers that the protocol has been tested and can produce reliable results. You may provide evidence that the protocol is robust and reproducible by:
Note: We highly encourage authors to provide validation data directly in this section while also citing data published elsewhere, particularly if the original research work is not open access.
14. General notes and troubleshooting
Include comments that apply broadly to the protocol and are not fundamental to completing individual steps. For example, address limitations of the protocol, its applicability to other experimental systems or model organisms, or variability.
If stating common problems that might occur, please describe ways to address them.
15. Supplementary information
Include source or extended data and any relevant supporting materials in this section.
16. Acknowledgments
Specify the individual contributions of each author of the manuscript; you may use the example provided in our manuscript template or any other format you deem appropriate. Additionally, acknowledge funding sources that have supported the work. If the protocol was adapted or modified from previous work, acknowledge the relevant publications as well. If your original research was published in one of our partner journals, cite it here and add its DOI.
17. Competing interests
Provide a statement of financial and non-financial competing interests on behalf of all authors. At Bio-protocol, one typical type of financial competing interest is the receipt of funding or free products from the vendors of reagents/equipment or other advertisers. For more information, see our guidelines for disclaiming competing interests here.
18. Ethical considerations
All protocols that have used human and/or animal subjects must mention the specific ethics committee that approved the described experiment. Protocols including human subjects should also indicate that informed consent was obtained from all subjects. Protocols including clinical trials should clearly state the name of the trial registry and the clinical trial registration number in the manuscript. For animal research, we recommend following the guidelines established in Animal Research: Reporting of In Vivo Experiments (ARRIVE). For more information, see our publishing ethics notes.
19. References
Cite journal articles that are accepted, published, or posted as preprints. For in press accepted articles, add the expected date of publication. Add the relevant citations for all datasets, program code, and other resources used in the protocol.