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Cancer Genetics|December 17, 2018
Validation of a next-generation sequencing oncology panel optimized for low input DNARobyn T Sussman, Sydney Shaffer, Elizabeth M Azzato, et al.
Neuro-Oncology Advances|January 4, 2021
Near haploidization is a genomic hallmark which defines a molecular subgroup of giant cell glioblastomaTiffany G Baker, Jay Alden, Adrian M Dubuc, et al.
Clinical Chemistry|July 23, 2022
Clinical Validation of Genome Reference Consortium Human Build 38 in a Laboratory Utilizing Next-Generation Sequencing TechnologiesLisa A Lansdon, Maxime Cadieux-Dion, John C Herriges, et al.
Cancers|December 11, 2025
MicroRNA Profiling Identifies Diagnostic and Prognostic Markers in Pediatric SarcomaTerrie G Flatt, Leonid M Yermakov, Shreeram Akilesh, et al.
The Journal of Molecular Diagnostics : JMD|February 25, 2021
Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation SequencingLisa A Lansdon, Maxime Cadieux-Dion, Byunggil Yoo, et al.
The Journal of Molecular Diagnostics : JMD|May 8, 2016
Multi-Institutional FASTQ File Exchange as a Means of Proficiency Testing for Next-Generation Sequencing Bioinformatics and Variant InterpretationKurtis D Davies, Midhat S Farooqi, Mike Gruidl, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Successful classification of clinical pediatric leukemia genetic subtypes via structural variant detection using HiFi long-read sequencingLisa A Lansdon, Byunggil Yoo, Ayse Keskus, et al.
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