Author

Henry C. M. Leung

University of Hong Kong

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Bioinformatics· 3

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:database / resource· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ho‐Ming LukiD· 3 shared Ivan F. M. LoiD· 3 shared Ruibang LuoiD· 3 shared Tak‐Wah LamiD· 3 shared Amy Wing-Sze LeungiD· 2 shared Chak-Lim Wong· 2 shared Wai-Chun Law· 2 shared Bin YaniD· 1 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersBioinformatics

Ho‐Ming LukORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BioinformaticsScientific ReportsPeer-reviewedMar 16, 2022

SENSV: Detecting Structural Variations with Precise Breakpoints using Low-Depth WGS Data from a Single Oxford Nanopore MinION Flowcell

Henry C. M. Leung, Huijing Yu, Yifan Zhang…·Tak‐Wah Lam

SENSV detects structural variations with high sensitivity and precise breakpoints using low-depth Oxford Nanopore WGS data from a single MinION flowcell, outperforming existing tools in pathogenic SV detection.

11 citations

humanwhole-genome sequencing

𝕏 PostBluesky

BioinformaticsNAR Genomics and BioinformaticsPeer-reviewedJan 13, 2022

HKG: An open genetic variant database of 205 Hong Kong Cantonese exomes

Min Ou, Henry C. M. Leung, Amy Wing-Sze Leung…·Ruibang Luo

HKG is a variant database of 205 Hong Kong Cantonese exomes that fills a gap in southern Chinese genetics, showing unique variants and improving variant imputation.

4 citations

humanwhole-exome sequencing

𝕏 PostBluesky

BioinformaticsbioRxivPreprintApr 5, 2021

ECNano: A Cost-Effective Workflow for Target Enrichment Sequencing and Accurate Variant Calling on 4,800 Clinically Significant Genes Using a Single MinION Flowcell

Amy Wing-Sze Leung, Henry C. M. Leung, Chak-Lim Wong…·Tak‐Wah Lam

DOI 10.1101/2021.04.05.438455

humanwhole-exome sequencing

𝕏 PostBluesky