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  1. Article ; Online: In silico analysis of BRCA1 and BRCA2 missense variants and the relevance in molecular genetic testing.

    Poon, Kok-Siong

    Scientific reports

    2021  Volume 11, Issue 1, Page(s) 11114

    Abstract: Over the years since the genetic testing of BRCA1 and BRCA2 has been conducted for research and later introduced into clinical practice, a high number of missense variants have been reported in the literature and deposited in public databases. ... ...

    Abstract Over the years since the genetic testing of BRCA1 and BRCA2 has been conducted for research and later introduced into clinical practice, a high number of missense variants have been reported in the literature and deposited in public databases. Polymorphism Phenotyping v2 (PolyPhen-2) and Sorting Intolerant from Tolerant (SIFT) are two widely applied bioinformatics tools used to assess the functional impacts of missense variants. A total of 2605 BRCA1 and 4763 BRCA2 variants from the ClinVar database were analysed with PolyPhen2 and SIFT. When SIFT was evaluated alongside PolyPhen-2 HumDiv and HumVar, it had shown top performance in terms of negative predictive value (NPV) (100%) and sensitivity (100%) for ClinVar classified benign and pathogenic BRCA1 variants. Both SIFT and PolyPhen-2 HumDiv achieved 100% NPV and 100% sensitivity in prediction of pathogenicity of the BRCA2 variants. Agreement was achieved in prediction outcomes from the three tested approaches in 55.04% and 68.97% of the variants of unknown significance (VUS) for BRCA1 and BRCA2, respectively. The performances of PolyPhen-2 and SIFT in predicting functional impacts varied across the two genes. Due to lack of high concordance in prediction outcomes among the two tested algorithms, their usefulness in classifying the pathogenicity of VUS identified through molecular testing of BRCA1 and BRCA2 is hence limited in the clinical setting.
    MeSH term(s) BRCA1 Protein/genetics ; BRCA2 Protein/genetics ; Computational Biology ; Computer Simulation ; Female ; Genetic Predisposition to Disease ; Humans ; Molecular Diagnostic Techniques ; Mutation, Missense ; Polymorphism, Single Nucleotide
    Chemical Substances BRCA1 Protein ; BRCA2 Protein
    Language English
    Publishing date 2021-05-27
    Publishing country England
    Document type Journal Article
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-021-88586-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: In silico analysis of BRCA1 and BRCA2 missense variants and the relevance in molecular genetic testing

    Kok-Siong Poon

    Scientific Reports, Vol 11, Iss 1, Pp 1-

    2021  Volume 8

    Abstract: Abstract Over the years since the genetic testing of BRCA1 and BRCA2 has been conducted for research and later introduced into clinical practice, a high number of missense variants have been reported in the literature and deposited in public databases. ... ...

    Abstract Abstract Over the years since the genetic testing of BRCA1 and BRCA2 has been conducted for research and later introduced into clinical practice, a high number of missense variants have been reported in the literature and deposited in public databases. Polymorphism Phenotyping v2 (PolyPhen-2) and Sorting Intolerant from Tolerant (SIFT) are two widely applied bioinformatics tools used to assess the functional impacts of missense variants. A total of 2605 BRCA1 and 4763 BRCA2 variants from the ClinVar database were analysed with PolyPhen2 and SIFT. When SIFT was evaluated alongside PolyPhen-2 HumDiv and HumVar, it had shown top performance in terms of negative predictive value (NPV) (100%) and sensitivity (100%) for ClinVar classified benign and pathogenic BRCA1 variants. Both SIFT and PolyPhen-2 HumDiv achieved 100% NPV and 100% sensitivity in prediction of pathogenicity of the BRCA2 variants. Agreement was achieved in prediction outcomes from the three tested approaches in 55.04% and 68.97% of the variants of unknown significance (VUS) for BRCA1 and BRCA2, respectively. The performances of PolyPhen-2 and SIFT in predicting functional impacts varied across the two genes. Due to lack of high concordance in prediction outcomes among the two tested algorithms, their usefulness in classifying the pathogenicity of VUS identified through molecular testing of BRCA1 and BRCA2 is hence limited in the clinical setting.
    Keywords Medicine ; R ; Science ; Q
    Language English
    Publishing date 2021-05-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Obesity-Associated GNAS Mutations and the Melanocortin Pathway.

    Poon, Kok-Siong / Tan, Karen M

    The New England journal of medicine

    2022  Volume 387, Issue 3, Page(s) 284

    MeSH term(s) Chromogranins/genetics ; GTP-Binding Protein alpha Subunits, Gs/genetics ; Humans ; Melanocortins/genetics ; Melanocortins/metabolism ; Mutation ; Obesity/genetics ; Obesity/metabolism
    Chemical Substances Chromogranins ; Melanocortins ; GNAS protein, human (EC 3.6.1.-) ; GTP-Binding Protein alpha Subunits, Gs (EC 3.6.5.1)
    Language English
    Publishing date 2022-07-20
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 207154-x
    ISSN 1533-4406 ; 0028-4793
    ISSN (online) 1533-4406
    ISSN 0028-4793
    DOI 10.1056/NEJMc2119110
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Pitfalls of PCR-RFLP in Detecting SARS-CoV-2 D614G Mutation.

    Poon, Kok-Siong / Tan, Karen Mei-Ling

    Global medical genetics

    2022  Volume 9, Issue 2, Page(s) 189–190

    Language English
    Publishing date 2022-06-13
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 3009997-3
    ISSN 2699-9404 ; 2699-9404
    ISSN (online) 2699-9404
    ISSN 2699-9404
    DOI 10.1055/s-0041-1735556
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Laboratory Verification of a

    Poon, Kok-Siong / Chiu, Lily / Tan, Karen Mei-Ling

    Global medical genetics

    2021  Volume 8, Issue 2, Page(s) 62–68

    Abstract: ... ...

    Abstract Introduction
    Language English
    Publishing date 2021-03-16
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 3009997-3
    ISSN 2699-9404 ; 2699-9404
    ISSN (online) 2699-9404
    ISSN 2699-9404
    DOI 10.1055/s-0041-1726338
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Reclassification of Whole Exome Sequencing-derived Genetic Variants in Pendred Syndrome with ACMG/AMP Standards.

    Poon, Kok-Siong / Tan, Karen Mei-Ling

    Global medical genetics

    2021  Volume 8, Issue 3, Page(s) 129–131

    Language English
    Publishing date 2021-03-10
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 3009997-3
    ISSN 2699-9404 ; 2699-9404
    ISSN (online) 2699-9404
    ISSN 2699-9404
    DOI 10.1055/s-0041-1725072
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Variant Curation is Crucial to Claim Digenic Inheritance in Juvenile Open Angle Glaucoma.

    Poon, Kok-Siong / Tan, Karen Mei-Ling

    Global medical genetics

    2021  Volume 9, Issue 1, Page(s) 54–55

    Language English
    Publishing date 2021-08-19
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 3009997-3
    ISSN 2699-9404 ; 2699-9404
    ISSN (online) 2699-9404
    ISSN 2699-9404
    DOI 10.1055/s-0041-1733963
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Realistic considerations for comparison between SARS-CoV-2 molecular diagnostic assays.

    Poon, Kok-Siong / Tee, Nancy Wen-Sim

    Biomedical journal

    2021  Volume 44, Issue 3, Page(s) 373–374

    MeSH term(s) COVID-19 ; COVID-19 Testing ; Humans ; Pathology, Molecular ; SARS-CoV-2
    Language English
    Publishing date 2021-03-31
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 2698541-X
    ISSN 2320-2890 ; 2320-2890
    ISSN (online) 2320-2890
    ISSN 2320-2890
    DOI 10.1016/j.bj.2021.03.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Diagnostic genomic laboratories should share their data.

    Poon, Kok-Siong / Koay, Evelyn Siew-Chuan

    Nature

    2021  Volume 594, Issue 7862, Page(s) 177

    MeSH term(s) Databases, Genetic ; Genetic Variation ; Genome, Human/genetics ; Genomics ; Humans ; Information Dissemination/ethics ; Informed Consent ; Laboratories ; Open Access Publishing ; Phenotype ; Research Personnel
    Language English
    Publishing date 2021-06-08
    Publishing country England
    Document type Letter
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/d41586-021-01523-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Detecting SARS-CoV-2 RNA in fecal specimens: The practical challenges.

    Poon, Kok-Siong / Tee, Nancy Wen-Sim

    Journal of medical virology

    2021  Volume 93, Issue 9, Page(s) 5241–5242

    MeSH term(s) COVID-19 ; Feces ; Humans ; RNA, Viral/genetics ; SARS-CoV-2
    Chemical Substances RNA, Viral
    Language English
    Publishing date 2021-06-08
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 752392-0
    ISSN 1096-9071 ; 0146-6615
    ISSN (online) 1096-9071
    ISSN 0146-6615
    DOI 10.1002/jmv.27071
    Database MEDical Literature Analysis and Retrieval System OnLINE

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