| Literature DB >> 27135536 |
Graham Heimberg1,2,3, Rajat Bhatnagar1,3, Hana El-Samad1,3, Matt Thomson3.
Abstract
A tradeoff between precision and throughput constrains all biological measurements, including sequencing-based technologies. Here, we develop a mathematical framework that defines this tradeoff between mRNA-sequencing depth and error in the extraction of biological information. We find that transcriptional programs can be reproducibly identified at 1% of conventional read depths. We demonstrate that this resilience to noise of "shallow" sequencing derives from a natural property, low dimensionality, which is a fundamental feature of gene expression data. Accordingly, our conclusions hold for ∼350 single-cell and bulk gene expression datasets across yeast, mouse, and human. In total, our approach provides quantitative guidelines for the choice of sequencing depth necessary to achieve a desired level of analytical resolution. We codify these guidelines in an open-source read depth calculator. This work demonstrates that the structure inherent in biological networks can be productively exploited to increase measurement throughput, an idea that is now common in many branches of science, such as image processing.Entities:
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Year: 2016 PMID: 27135536 PMCID: PMC4856162 DOI: 10.1016/j.cels.2016.04.001
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304