Evidence map›Paper›PMID 36035514›Full record

ArticleSynthetic biology (Oxford, England)2022

A toolkit for enhanced reproducibility of RNASeq analysis for synthetic biologists.

Benjamin J Garcia, Joshua Urrutia, George Zheng, Diveena Becker, Carolyn Corbet, Paul Maschhoff, Alexander Cristofaro, Niall Gaffney, Matthew Vaughn, Uma Saxena and 3 more

Abstract read
In one paragraph

Article in Synthetic biology (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Special issue: reproducibility in synthetic biology.Synthetic biology (Oxford, England) · 2023
    Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Benjamin J GarciaDepartment of Biological Engineering, Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, MA, USA.
Joshua UrrutiaTexas Advanced Computing Center, University of Texas at Austin, Austin, TX, USA.
George ZhengNetrias LLC, Annapolis, MD, USA.
Diveena BeckerGinkgo Bioworks, Boston, MA, USA.
Carolyn CorbetGinkgo Bioworks, Boston, MA, USA.
Paul MaschhoffGinkgo Bioworks, Boston, MA, USA.
Alexander CristofaroDepartment of Biological Engineering, Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID https://orcid.org/0000-0001-7905-9264
Niall GaffneyTexas Advanced Computing Center, University of Texas at Austin, Austin, TX, USA.
Matthew VaughnTexas Advanced Computing Center, University of Texas at Austin, Austin, TX, USA.
Uma SaxenaDepartment of Biological Engineering, Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, MA, USA.
Yi-Pei ChenNetrias LLC, Annapolis, MD, USA.ORCID https://orcid.org/0000-0002-5703-0310
D Benjamin GordonDepartment of Biological Engineering, Synthetic Biology Center, Massachusetts Institute of Technology, Cambridge, MA, USA.
Mohammed EslamiNetrias LLC, Annapolis, MD, USA.ORCID https://orcid.org/0000-0001-5488-1542

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequencing technologies, in particular RNASeq, have become critical tools in the design, build, test and learn cycle of synthetic biology. They provide a better understanding of synthetic designs, and they help identify ways to improve and select designs. While these data are beneficial to design, their collection and analysis is a complex, multistep process that has implications on both discovery and reproducibility of experiments. Additionally, tool parameters, experimental metadata, normalization of data and standardization of file formats present challenges that are computationally intensive. This calls for high-throughput pipelines expressly designed to handle the combinatorial and longitudinal nature of synthetic biology. In this paper, we present a pipeline to maximize the analytical reproducibility of RNASeq for synthetic biologists. We also explore the impact of reproducibility on the validation of machine learning models. We present the design of a pipeline that combines traditional RNASeq data processing tools with structured metadata tracking to allow for the exploration of the combinatorial design in a high-throughput and reproducible manner. We then demonstrate utility via two different experiments: a control comparison experiment and a machine learning model experiment. The first experiment compares datasets collected from identical biological controls across multiple days for two different organisms. It shows that a reproducible experimental protocol for one organism does not guarantee reproducibility in another. The second experiment quantifies the differences in experimental runs from multiple perspectives. It shows that the lack of reproducibility from these different perspectives can place an upper bound on the validation of machine learning models trained on RNASeq data. Graphical Abstract.

Indexed as

automationmachine learningstandardizationtranscriptomics

Identifiers

PMID36035514
PMCPMC9408027

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.