Chan TL - Search Results

1

BAMClipper: removing primers from alignments to minimize false-negative mutations in amplicon next-generation sequencing.

Au CH, Ho DN, Kwong A, Chan TL, Ma ESK. Au CH, et al. Among authors: chan tl. Sci Rep. 2017 May 8;7(1):1567. doi: 10.1038/s41598-017-01703-6. Sci Rep. 2017. PMID: 28484262 Free PMC article.

2

Clinical evaluation of panel testing by next-generation sequencing (NGS) for gene mutations in myeloid neoplasms.

Au CH, Wa A, Ho DN, Chan TL, Ma ES. Au CH, et al. Among authors: chan tl. Diagn Pathol. 2016 Jan 22;11:11. doi: 10.1186/s13000-016-0456-8. Diagn Pathol. 2016. PMID: 26796102 Free PMC article.

3

INDELseek: detection of complex insertions and deletions from next-generation sequencing data.

Au CH, Leung AY, Kwong A, Chan TL, Ma ES. Au CH, et al. Among authors: chan tl. BMC Genomics. 2017 Jan 5;18(1):16. doi: 10.1186/s12864-016-3449-9. BMC Genomics. 2017. PMID: 28056804 Free PMC article.

4

Next-generation sequencing and molecular cytogenetic characterization of ETV6-LYN fusion due to chromosomes 1, 8 and 12 rearrangement in acute myeloid leukemia.

Ma ESK, Wan TSK, Au CH, Ho DN, Ma SY, Ng MHL, Chan TL. Ma ESK, et al. Among authors: chan tl. Cancer Genet. 2017 Dec;218-219:15-19. doi: 10.1016/j.cancergen.2017.09.001. Epub 2017 Sep 13. Cancer Genet. 2017. PMID: 29153093 Free article.

5

Detection of Germline Mutation in Hereditary Breast and/or Ovarian Cancers by Next-Generation Sequencing on a Four-Gene Panel.

Kwong A, Shin VY, Au CH, Law FB, Ho DN, Ip BK, Wong AT, Lau SS, To RM, Choy G, Ford JM, Ma ES, Chan TL. Kwong A, et al. Among authors: chan tl. J Mol Diagn. 2016 Jul;18(4):580-94. doi: 10.1016/j.jmoldx.2016.03.005. Epub 2016 May 5. J Mol Diagn. 2016. PMID: 27157322 Free article.

6

The importance of analysis of long-range rearrangement of BRCA1 and BRCA2 in genetic diagnosis of familial breast cancer.

Kwong A, Chen J, Shin VY, Ho JC, Law FB, Au CH, Chan TL, Ma ES, Ford JM. Kwong A, et al. Among authors: chan tl. Cancer Genet. 2015 Sep;208(9):448-54. doi: 10.1016/j.cancergen.2015.05.031. Epub 2015 Jun 9. Cancer Genet. 2015. PMID: 26271414

7

Mutation screening of germline TP53 mutations in high-risk Chinese breast cancer patients.

Kwong A, Shin VY, Ho CYS, Au CH, Slavin TP, Weitzel JN, Chan TL, Ma ESK. Kwong A, et al. Among authors: chan tl. BMC Cancer. 2020 Nov 2;20(1):1053. doi: 10.1186/s12885-020-07476-y. BMC Cancer. 2020. PMID: 33138793 Free PMC article.

8

Rapid detection of chromosomal translocation and precise breakpoint characterization in acute myeloid leukemia by nanopore long-read sequencing.

Au CH, Ho DN, Ip BBK, Wan TSK, Ng MHL, Chiu EKW, Chan TL, Ma ESK. Au CH, et al. Among authors: chan tl. Cancer Genet. 2019 Nov;239:22-25. doi: 10.1016/j.cancergen.2019.08.005. Epub 2019 Aug 23. Cancer Genet. 2019. PMID: 31473470 Free article.

9

Potential utility of targeted Nanopore sequencing for improving etiologic diagnosis of bacterial and fungal respiratory infection.

Chan WS, Au CH, Leung SM, Ho DN, Wong EYL, To MY, Ng MK, Chan TL, Ma ESK, Tang BSF. Chan WS, et al. Among authors: chan tl. Diagn Pathol. 2020 Apr 27;15(1):41. doi: 10.1186/s13000-020-00960-w. Diagn Pathol. 2020. PMID: 32340617 Free PMC article.

10

Rapid and economical drug resistance profiling with Nanopore MinION for clinical specimens with low bacillary burden of Mycobacterium tuberculosis.

Chan WS, Au CH, Chung Y, Leung HCM, Ho DN, Wong EYL, Lam TW, Chan TL, Ma ESK, Tang BSF. Chan WS, et al. Among authors: chan tl. BMC Res Notes. 2020 Sep 18;13(1):444. doi: 10.1186/s13104-020-05287-9. BMC Res Notes. 2020. PMID: 32948225 Free PMC article.

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