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Allele Specific Expression Quality Control Fills Critical Gap in Transcriptome Assisted Rare Variant Interpretation.

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A new tool, aseQC, assesses allele-specific expression (ASE) quality, identifying noisy samples that can skew genetic variation analysis. This improves the reliability of transcriptome data for rare variant interpretation.

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Area of Science:

  • Genomics
  • Transcriptomics
  • Bioinformatics

Background:

  • Allele-specific expression (ASE) reveals genetic variation's impact on transcription but is susceptible to artifacts.
  • High-quality data is crucial for accurate cis-regulatory effect analysis.

Purpose of the Study:

  • Introduce aseQC, a statistical framework to quantify sample-level ASE quality.
  • Improve the robustness of downstream transcriptome analyses by excluding noisy samples.

Main Methods:

  • Developed a statistical framework (aseQC) to measure extra-binomial variation in ASE data.
  • Applied aseQC to datasets including rare Mendelian muscular disorders and GTEx project data.
  • Evaluated the impact of low-quality samples on rare and common variant analyses.

Main Results:

  • aseQC identified low-quality samples in rare disease cohorts, demonstrating clinical utility.
  • Discovered 563 low-quality samples in GTEx data, linked to processing dates and exhibiting excessive allelic imbalance.
  • Low-quality samples significantly increased ASE and splicing outliers, degrading rare variant interpretation but not affecting common variant analysis.

Conclusions:

  • aseQC provides a reliable method for assessing sample quality in transcriptome data.
  • Excluding low-quality samples is critical for accurate rare variant analysis.
  • aseQC enhances the reliability of genomic studies utilizing allele-specific expression data.