User:Macowell/Part Documentation Guidelines

From 2007.igem.org

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== Part Main page ==
== Part Main page ==
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The main page should offer Registry users a "part-at-a-glance" summary to help decide whether or not a particular part interests them or meets a specific need.
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* '''1''' Part title
* '''1''' Part title
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* '''2''' Abstract
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* '''2''' Part Description
** '''2.1''' What is it needed for? Function.
** '''2.1''' What is it needed for? Function.
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** '''2.2''' How does it work
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** '''2.2''' How does it work?
** '''2.3''' How do you use it?
** '''2.3''' How do you use it?
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* '''3''' Dependencies (other parts, chemicals, strains) (explicitly stated)
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* '''3''' Dependencies on other parts, chemicals, strains, etc. -- (state explicitly)
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* '''4''' Subparts figure
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* '''4''' Subparts figure for ''all composite parts."  (use icons)
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* '''5''' Diagram is encouraged
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* '''5''' Diagram showing part features, ''e.g.,'' predicted RNA secondary structures, a protein 3D structure illustration, a complete biochemical circuit containing the part, etc.
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** '''5.1''' Inputs and outputs should be clearly labelled
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** '''5.1''' Inputs and outputs should be clearly labelled for all circuits.
== Part Design page ==
== Part Design page ==
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This page functions somewhat like a "Materials and Methods" section and should include enough detail for users to understand how the part was constructed and what its special features are.
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* '''6''' How did you build it?  What you would need to know if you wanted to re-create the part?  For instance, include as warranted info about:
* '''6''' How did you build it?  What you would need to know if you wanted to re-create the part?  For instance, include as warranted info about:
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** Primers used if DNA was PCRed out of a natural system
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** Primers used if DNA was extracted from a natural system using PCR.
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** Mutagenesis performed (i.e. for standards compliance)
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** Mutagenesis performed (''e.g.,'' for standards compliance or manipulation of RNA secondary structure)
** Codon optimization
** Codon optimization
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** Removal or addition Biobrick cloning sites
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** Removal or addition BioBrick cloning sites
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** Synthesis details, if DNA synthesized
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** Synthesis details, if DNA synthesized (method used and vendor -- if purchased)
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* '''7''' Source of part material - i.e. where did the provided sequence in Hard Info come from?  If in online database, provide accession no. else provide pertinent info about the sequencing run (perhaps links to sequence read files, uploaded to registry?)
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* '''7''' Source of original sequence - ''i.e.'' where did the sequence provided in Hard Information come from?  If from an online database, provide the relevant accession number, otherwise provide pertinent information about the sequencing run.
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** '''7.1''' Species, Strain
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** '''7.1''' Biological species, strain
** '''7.2''' Sequence: accession number & database used for sequence, or details about sequencing run.
** '''7.2''' Sequence: accession number & database used for sequence, or details about sequencing run.
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** '''7.3''' What lab is the strain from / what company supplied it, what is the order number?
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** '''7.3''' What lab did the strain from / or what company supplied it [what is the order number?]
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* '''8''' References (at least 2 – if not, justify it and provide links to the other resources used - i.e. online open-access textbook, OWW page, etc.)
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* '''8''' References (at least 2 – if none, provide links to the other resources used - ''e.g.'' online open-access textbook, OWW page, etc.)
* '''9''' Pitfalls – designs that didn't work, revisions necessary, or an explicit statement that everything worked as planned
* '''9''' Pitfalls – designs that didn't work, revisions necessary, or an explicit statement that everything worked as planned
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* '''10''' <strike>MTAs, patents - Significant IP? Do we want an explicit answer?  Really? (we should make the heading automatically link to the disclaimer page about IP & iGEM issues)</strike>  Attribution - who worked on this part?  (whole team, certain members of the team if they divided into subteams,etc.) Acknowledgement - who worked on parts that went into this part?  Sponsorship - who provided funding for the development of this part?
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* '''10''' Provide complete attribution to everyone who worked on/is affiliated with the part.
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**'''10.1''' Attribution - who worked on this part?  (whole team, certain members of the team if they divided into subteams,etc.)  
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**'''10.2''' Acknowledgement - who worked on parts that went into this part?   
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**'''10.3''' Sponsorship - who provided funding for the development of this part?
== User Experience Page ==
== User Experience Page ==
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* '''11''' Experience - explicitly state how the part worked in your lab; provide any available experimental details generated from testing the part (including uploading data files to the registry wiki)
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The creators of the part should provide as much information as possible here so that other users can benefit from their successes (and failures!).  This kind of information will weigh heavily in the decision someone else will make about whether or not to use your part.
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 +
 
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* '''11''' Experience - explicitly state how the part worked in your lab; provide any available experimental details generated from testing the part (including uploading data files to the Registry wiki).
== Hard Info ==
== Hard Info ==
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This page includes data that belongs permanently with the part and its details should be carefully checked for accuracy.
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* '''12.1''' Sequence
* '''12.1''' Sequence
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* '''12.2''' Significant features - If any of the features from the features list is mentioned/talked about in your part description, make sure that it is part of the sequence and features
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* '''12.2''' Significant features - If any of the features from the features list is mentioned/talked about in your part description, make sure that it is part of the sequence and features.
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= Best Documentation Candidates =
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* <partinfo>J45200</partinfo>

Latest revision as of 14:54, 12 October 2007

This is a draft of the part documentation guidelines used to evaluate parts Submitted for Acceptance. We want every part to have a paragraph or more of text on the main page, preferably with a diagram (but not necessarily), that clearly answers the questions posed in 2.1, 2.2, and 2.3 of the guidelines.

Contents

Part Main page

The main page should offer Registry users a "part-at-a-glance" summary to help decide whether or not a particular part interests them or meets a specific need.

  • 1 Part title
  • 2 Part Description
    • 2.1 What is it needed for? Function.
    • 2.2 How does it work?
    • 2.3 How do you use it?
  • 3 Dependencies on other parts, chemicals, strains, etc. -- (state explicitly)
  • 4 Subparts figure for all composite parts." (use icons)
  • 5 Diagram showing part features, e.g., predicted RNA secondary structures, a protein 3D structure illustration, a complete biochemical circuit containing the part, etc.
    • 5.1 Inputs and outputs should be clearly labelled for all circuits.

Part Design page

This page functions somewhat like a "Materials and Methods" section and should include enough detail for users to understand how the part was constructed and what its special features are.

  • 6 How did you build it? What you would need to know if you wanted to re-create the part? For instance, include as warranted info about:
    • Primers used if DNA was extracted from a natural system using PCR.
    • Mutagenesis performed (e.g., for standards compliance or manipulation of RNA secondary structure)
    • Codon optimization
    • Removal or addition BioBrick cloning sites
    • Synthesis details, if DNA synthesized (method used and vendor -- if purchased)
  • 7 Source of original sequence - i.e. where did the sequence provided in Hard Information come from? If from an online database, provide the relevant accession number, otherwise provide pertinent information about the sequencing run.
    • 7.1 Biological species, strain
    • 7.2 Sequence: accession number & database used for sequence, or details about sequencing run.
    • 7.3 What lab did the strain from / or what company supplied it [what is the order number?]
  • 8 References (at least 2 – if none, provide links to the other resources used - e.g. online open-access textbook, OWW page, etc.)
  • 9 Pitfalls – designs that didn't work, revisions necessary, or an explicit statement that everything worked as planned
  • 10 Provide complete attribution to everyone who worked on/is affiliated with the part.
    • 10.1 Attribution - who worked on this part? (whole team, certain members of the team if they divided into subteams,etc.)
    • 10.2 Acknowledgement - who worked on parts that went into this part?
    • 10.3 Sponsorship - who provided funding for the development of this part?

User Experience Page

The creators of the part should provide as much information as possible here so that other users can benefit from their successes (and failures!). This kind of information will weigh heavily in the decision someone else will make about whether or not to use your part.


  • 11 Experience - explicitly state how the part worked in your lab; provide any available experimental details generated from testing the part (including uploading data files to the Registry wiki).

Hard Info

This page includes data that belongs permanently with the part and its details should be carefully checked for accuracy.

  • 12.1 Sequence
  • 12.2 Significant features - If any of the features from the features list is mentioned/talked about in your part description, make sure that it is part of the sequence and features.

Best Documentation Candidates