| Literature DB >> 30039375 |
Saki Chan1, Ernest Lam1, Michael Saghbini1, Sven Bocklandt1, Alex Hastie1, Han Cao1, Erik Holmlin1, Mark Borodkin2.
Abstract
The need to accurately identify the complete structural variation profile of genomes is becoming increasingly evident. In contrast to reference-based methods like sequencing or comparative methods like aCGH, optical mapping is a de novo assembly-based method that enables better realization of true genomic structure. It allows for independently detecting balanced and unbalanced structural variants (SVs) from separate alleles and for discovering de novo events. Here we show how Bionano Genome Mapping creates de novo assemblies from native and intact, megabase-scale DNA molecules and uses those assemblies to detect a wide range of structural variants.Keywords: Deletion; Genome structure; Genomics; Insertion; Inversion; Long reads; Optical mapping; Structural Variation; Translocation
Mesh:
Year: 2018 PMID: 30039375 DOI: 10.1007/978-1-4939-8666-8_16
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745