medRxivGenetic & Genomic MedicinePreprint
Enriching for Answers in Rare Diseases
Yilei FuiD, Adam C. EnglishiD, Luis F. PauliniD, Shalini N. JhangianiiD, George WeissenbergeriD, Vanessa Vee, Yi HaniD, Heer Hemant MehtaiD, Donna Marie MuznyiD, Richard A. GibbsiD, Jennifer E. PoseyiD, Daniel G. CalameiD, Fritz Joachim SedlazeckiD
Abstract
We present Trio-barcoded ONT Adaptive Sampling (TBAS), a cost-efficient long-read sequencing strategy combining sample barcoding and adaptive enrichment to sequence rare-disease trios on a single PromethION flow cell. TBAS achieved near-complete variant phasing and detection of small variants, structural variants, and tandem repeats with high accuracy and 77% potential solve rate. This scalable approach retains methylation data and enables clinically relevant, phenotype-guided long-read diagnostics at a fraction of current costs.
- organism: human
- assay: whole-genome sequencing
- research focus: variant calling
- approach: experimental assay
- Citations
- 1
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Constellation illuminates rare disease genetics
Siyuan Cheng, Qing Zhang, … Fritz Joachim Sedlazeck·medRxiv·Oct 15, 2025
- Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detection
Shloka Negi, Sarah L. Stenton, … Benedict Paten·The American Journal of Human GeneticsPeer-reviewed·Jan 24, 2025
- HiFi long-read genomes for difficult-to-detect clinically relevant variants
Wolfram Höps, Marjan M. Weiss, … Lisenka E.L.M. Vissers·The American Journal of Human GeneticsPeer-reviewed·Jan 13, 2025
- Targeted long-read sequencing resolves complex structural variants and identifies missing disease-causing variants
Danny E. Miller, Arvis Sulovari, … Evan E. Eichler·bioRxiv·Nov 3, 2020
- Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencing
Alba Sanchis‐Juan, Yulia Mostovoy, … Michael E. Talkowski·medRxiv·Jun 24, 2026
- Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders
Susan M. Hiatt, James M.J. Lawlor, … Gregory M. Cooper·Genome ResearchPeer-reviewed·Nov 1, 2024