P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples

P585: Amplification-based nanopore sequencing accurately detects HBA and HBB SNVs, indels, and structural variants in clinical thalassemia samples

Bibliographic Details
Main Authors: Jaime Lopes, Marcus Cannon, Jonathan Turner, Monica Roberts, Theodore Markulin, Christopher Fraher, Bryan Killinger, Stela Filipovic-Sadic, Bradley Hall
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Genetics in Medicine Open
Online Access:http://www.sciencedirect.com/science/article/pii/S294977442400637X
Description
ISSN:2949-7744

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