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A Comparison of Structural Variant Calling from Short-Read and Nanopore-Based Whole-Genome Sequencing Using Optical Genome Mapping as a Benchmark. (2024)

First Author: Pei Y

Attributed to: Uncovering new mechanisms of craniosynostosis associated with structural and copy number variation, using mouse modelling and human neural crest cells funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3390/genes15070925

PubMed Identifier: 39062704

Publication URI: http://europepmc.org/abstract/MED/39062704

Type: Journal Article/Review

Volume: 15

Parent Publication: Genes

Issue: 7

ISSN: 2073-4425