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Chun H. Au, Ph.D.

Affiliations: 
2011 The Chinese University of Hong Kong, Hong Kong, Hong Kong 
Area:
Genetics
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"Chun Au"
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Hoi S. Kwan grad student 2011 Chinese University of Hong Kong
 (Genome Sequence of Shiitake Mushroom Lentinula edodes and Comparative Mushroom Genomics with Platform Construction.)

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Publications

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Chan WS, Au CH, Leung SM, et al. (2020) Potential utility of targeted Nanopore sequencing for improving etiologic diagnosis of bacterial and fungal respiratory infection. Diagnostic Pathology. 15: 41
Kwong A, Shin VY, Chen J, et al. (2020) Germline mutation in 1,338 BRCA-negative Chinese hereditary breast and/or ovarian cancer patients: clinical testing with a multigene test panel. The Journal of Molecular Diagnostics : Jmd
Chan WS, Au CH, Leung HC, et al. (2019) Potential utility of metagenomic sequencing for improving etiologic diagnosis of infective endocarditis. Future Cardiology
Au CH, Ho DN, Ip BBK, et al. (2019) Rapid detection of chromosomal translocation and precise breakpoint characterization in acute myeloid leukemia by nanopore long-read sequencing. Cancer Genetics. 239: 22-25
Ma ESK, Wan TSK, Au CH, et al. (2017) Next-generation sequencing and molecular cytogenetic characterization of ETV6-LYN fusion due to chromosomes 1, 8 and 12 rearrangement in acute myeloid leukemia. Cancer Genetics. 218: 15-19
Au CH, Ho DN, Kwong A, et al. (2017) BAMClipper: removing primers from alignments to minimize false-negative mutations in amplicon next-generation sequencing. Scientific Reports. 7: 1567
Au CH, Leung AY, Kwong A, et al. (2017) INDELseek: detection of complex insertions and deletions from next-generation sequencing data. Bmc Genomics. 18: 16
Au CH, Wa A, Ho DN, et al. (2016) Clinical evaluation of panel testing by next-generation sequencing (NGS) for gene mutations in myeloid neoplasms. Diagnostic Pathology. 11: 11
Ou M, Ma R, Cheung J, et al. (2015) database.bio: a web application for interpreting human variations. Bioinformatics (Oxford, England)
Kwong A, Chen J, Shin VY, et al. (2015) The importance of analysis of long-range rearrangement of BRCA1 and BRCA2 in genetic diagnosis of familial breast cancer. Cancer Genetics
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