Targeted Development of Registries of Biological Parts
2008

Creating a Database of Biological Parts

Sample size: 995 publication Evidence: moderate

Author Information

Author(s): Peccoud Jean, Blauvelt Megan F., Cai Yizhi, Cooper Kristal L., Crasta Oswald, DeLalla Emily C., Evans Clive, Folkerts Otto, Lyons Blair M., Mane Shrinivasrao P., Shelton Rebecca, Sweede Matthew A., Waldon Sally A.

Primary Institution: Virginia Bioinformatics Institute, Blacksburg, Virginia, United States of America

Hypothesis

How can we effectively design and manage a registry of biological parts for synthetic biology?

Conclusion

The study suggests that careful management and curation of biological parts are essential to maintain the quality and usability of the registry.

Supporting Evidence

  • The Registry of Standard Biological Parts is the largest publicly available library of genetic parts.
  • The study identified 1383 relationships among 995 entries in the Registry.
  • Only 162 out of 789 sequenced clones confirmed their published sequences.

Takeaway

This study is about making a big library of tiny building blocks for making new biological things, and it shows how to keep that library organized and useful.

Methodology

The study analyzed the relationships between sequences in a database of biological parts and examined the physical clones associated with these entries.

Potential Biases

Potential biases may arise from the lack of unique identifiers for clones, making quality control difficult.

Limitations

The study is limited to a specific distribution of the DNA repository and does not account for variations in other distributions.

Digital Object Identifier (DOI)

10.1371/journal.pone.0002671

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