Overview¶
This document provides guidelines for making a contribution to the Distribution. Since technical contributions are made by submitting a Developer Note, these contribution guidelines include both minimal requirements for submitting a DevNote and suggestions for increasing the likelihood that your contribution will be onboarded into the Distribution.
To clarify this distinction, we define several phrases:
Must. This word means that something is an absolute requirement when submitting a Developer Note.
Should. This word means that including something will make it more likely that the submission will be onboarded into the Distribution by the Core Development Team.
Where possible. This phrase means that including something may prove technically challenging and situation dependent. Use good judgment, and post on the Forum if you need guidance on feasibility.
Note: Before reading the following guidelines, we highly recommend reading the document titled From Zero to DevNote which describes how to prepare your first Developer Note for inclusion into the Distribution. It provides a concrete description of the key components of a submission.
General Consideration¶
General¶
Must include Author(s) orcid ID
Should include a schematic of the contribution
Bill of Materials¶
Must have a section titled “Critical Reagents” that contains a table describing reagents that are critical for the experiment. The table Must have the following form:
| Reagent | Product Name | Manufacturer | Part # | Price | Storage Conditions | Link |
|---|---|---|---|---|---|---|
| Amino Acids | L-Amino acids, analytical standard | Sigma-Aldrich | LAA21-1KT | $558 | 1C to 4C | link |
Should have a complete reagent list. In most circumstances, submissions will be modifying Processes with existing reagent lists. You are encouraged to reuse and modify these lists as appropriate and exercise good judgement when reagent substitutions should be regarded as “Critical”
DNA Sequence Maps¶
Must include linear or plasmid DNA sequence maps.
Must include a statement attesting to sequence validity.
Must include a table containing names of sequences used and links to files in the project. The table should have the following form:
Should be in pOpen backbone
Should include sequence verification data.
Should follow DNA Distribution design guidelines
Lab Notebook Entry¶
Must include a document (format as .pdf or .txt) that describes reaction preparation in sufficient detail to allow for their reproduction. At a minimum this includes the composition of stock solutions and master mixes.
Should include notes on handling or preparation that are non-obvious. For example, “preparing an aqueous stock solution of FITC requires first suspending in DMSO at 100 mM concentration” or “use of modified amino acid mixture requires EXTENSIVE vortexing, do not use until solution is completely transparent”.
Should include appropriate QC data on intermediate products like DNA, proteins, and so on...
Considerations for Cytosols¶
Testing and Experimental Design¶
Must be tested in reference to the PURE system, either from a commercial vendor or self-prepared.
If using a self-prepared PURE system results Must be tested across at least 2 batches.
Data involving other systems such as lysates can be included but Must be done in reference to the PURE system.
Must include at least >3 technical replicates for each reaction condition.
Must include an Appropriately Designed positive and negative control.
Should be tested in reference to version-specified Cytosol, the open-formulation flavor of PURE described on the Distribution.
Where Possible measurements are made as timeseries, not just endpoints.
Data¶
Must include raw data in a format that can be ingested by the Nucleus CDK
Must include a platemap in format that can be ingested by the Nucleus CDK
Where possible data is analyzed using Nucleus CDK tools
Considerations for Cells¶
Testing and Experimental Design¶
Must include appropriately designed controls
Must include >2 biological replicates to support each result
Data¶
Must be possible to determine the size of liposomes
Must analyze >100 liposomes to support conclusions
Where Possible, raw files of all images included in the DevNote should be included
Where Possible, raw data files for all graphs in the DevNote should be included