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Related Concept Videos

Cis-regulatory Sequences02:02

Cis-regulatory Sequences

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Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
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Combinatorial gene control is the synergistic action of several transcriptional factors to regulate the expression of a single gene. The absence of one or more of these factors may lead to a significant difference in the level of gene expression or repression.
The expression of more than 30,000 genes is controlled by approximately 2000-3000 transcription factors. This is possible because a single transcription factor can recognize more than one regulatory sequence. The specificity in gene...
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Updated: Jun 3, 2025

Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues
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Droplet Barcoding-Based Single Cell Transcriptomics of Adult Mammalian Tissues

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Deterministic patterns in single-cell transcriptomic data.

Zhixing Cao1,2, Yiling Wang3, Ramon Grima4

  • 1State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China. z.cao@queensu.ca.

NPJ Systems Biology and Applications
|January 11, 2025
PubMed
Summary
This summary is machine-generated.

Deterministic patterns in single-cell transcriptomic data arise from finite sample size effects, not artifacts or biology. Our theory precisely predicts these patterns across various single-cell measurement platforms.

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Last Updated: Jun 3, 2025

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Area of Science:

  • Genomics
  • Computational Biology
  • Biophysics

Background:

  • Single-cell transcriptomic data analysis often reveals unexpected patterns.
  • Distinguishing true biological signals from technical artifacts is crucial for accurate interpretation.

Purpose of the Study:

  • To identify the origin of deterministic patterns observed in single-cell transcriptomic data.
  • To develop a theoretical framework explaining these patterns.
  • To validate the theory across diverse single-cell measurement technologies.

Main Methods:

  • Statistical analysis of single-cell transcriptomic datasets.
  • Development of a theoretical model based on finite sample size effects.
  • Validation using data from multiplexed error-robust fluorescence in situ hybridization (MERFISH) and five sequencing platforms.

Main Results:

  • Deterministic patterns were confirmed in statistical plots of single-cell transcriptomic data.
  • A novel theory attributes these patterns to finite sample size effects.
  • The theory accurately predicts observed patterns across MERFISH and various sequencing data.

Conclusions:

  • The observed deterministic patterns are an inherent emergent property of finite sampling in transcriptomics.
  • These patterns are not indicative of measurement artifacts or specific biological mechanisms.
  • The developed theory provides a robust framework for understanding data characteristics across multiple single-cell technologies.