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The Utility of Ultra-Deep RNA sequencing in Mendelian Disorder Diagnostics

2025-01-29

Abstract excerpt

Clinical RNA-seq has become an essential tool for resolving variants of uncertain significance (VUS), particularly those affecting gene expression and splicing. However, most reference data and diagnostic protocols employ relatively modest sequencing depths (∼50-150 million reads), which may fail to capture low-abundance transcripts and rare splicing events critical for accurate diagnoses. We evaluated the diagnos...

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Literature Corpus work
5f5dcddd-a772-5e39-9747-32ebf3f993a0
DOI
10.1101/2025.01.28.25321295
Open publication

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The Utility of Ultra-Deep RNA sequencing in Mendelian Disorder DiagnosticsDOI 10.1101/2025.01.28.25321295
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