Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Cancer Genetics|March 14, 2023
Integrated genetic profiling of archival pediatric high-grade glial tumors and reassessment with 2021 WHO classification of paediatric CNS tumoursLinda D Cooley, Lisa A Lansdon, Kris Laurence, et al.
Genetics|November 23, 2017
Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in HumansLisa A Lansdon, Benjamin W Darbro, Aline L Petrin, 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.
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.
American Journal of Human Genetics|December 9, 2022
Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genesLisa A Lansdon, Amanda Dickinson, Sydney Arlis, 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.
NPJ Genomic Medicine|April 9, 2026
Proof-of-concept study for the detection of somatic structural variant driver alterations using HiFi long-read sequencing in a pediatric leukemia cohortLisa A Lansdon, Byunggil Yoo, Ayse Keskus, et al.
Biorxiv : the Preprint Server for Biology|September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologiesJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Nature Biotechnology|October 16, 2025
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomaticJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Severus: accurate detection and characterization of somatic structural variation in tumor genomes using long readsAyse Keskus, Asher Bryant, Tanveer Ahmad, et al.
Pageof 3