Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Aaron Wing Cheung Kwok"'
Autor:
Aaron Wing Cheung Kwok, Chen Qiao, Rongting Huang, Mai-Har Sham, Joshua W. K. Ho, Yuanhua Huang
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-10 (2022)
Mitochondrial variants are informative endogenous barcodes for clonal substructure. Here, the authors developed a computational method MQuad to effectively detect these clonal informed mtDNA variants from single-cell RNA, DNA or ATAC sequencing data.
Externí odkaz:
https://doaj.org/article/cd44ae84c32f4f68b35945be525d6186
Autor:
Jeffrey Fong Ting Chau, Mullin Ho Chung Yu, Martin Man Chun Chui, Cyrus Chun Wing Yeung, Aaron Wing Cheung Kwok, Xuehan Zhuang, Ryan Lee, Jasmine Lee Fong Fung, Mianne Lee, Christopher Chun Yu Mak, Nicole Ying Ting Ng, Claudia Ching Yan Chung, Marcus Chun Yin Chan, Mandy Ho Yin Tsang, Joshua Chun Ki Chan, Kelvin Yuen Kwong Chan, Anita Sik Yau Kan, Patrick Ho Yu Chung, Wanling Yang, So Lun Lee, Godfrey Chi Fung Chan, Paul Kwong Hang Tam, Yu Lung Lau, Kit San Yeung, Brian Hon Yin Chung, Clara Sze Man Tang
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-9 (2022)
Abstract Traditional carrier screening has been utilized for the detection of carriers of genetic disorders. Since a comprehensive assessment of the carrier frequencies of recessive conditions in the Southern Chinese population is not yet available,
Externí odkaz:
https://doaj.org/article/a4439854ca474791ac85c6eeb89fbddb
Autor:
Jeffrey Fong Ting Chau, Mullin Ho Chung Yu, Martin Man Chun Chui, Cyrus Chun Wing Yeung, Aaron Wing Cheung Kwok, Xuehan Zhuang, Ryan Lee, Jasmine Lee Fong Fung, Mianne Lee, Christopher Chun Yu Mak, Nicole Ying Ting Ng, Claudia Ching Yan Chung, Marcus Chun Yin Chan, Mandy Ho Yin Tsang, Joshua Chun Ki Chan, Kelvin Yuen Kwong Chan, Anita Sik Yau Kan, Patrick Ho Yu Chung, Wanling Yang, So Lun Lee, Godfrey Chi Fung Chan, Paul Kwong Hang Tam, Yu Lung Lau, Kit San Yeung, Brian Hon Yin Chung, Clara Sze Man Tang
Publikováno v:
NPJ genomic medicine. 7(1)
Traditional carrier screening has been utilized for the detection of carriers of genetic disorders. Since a comprehensive assessment of the carrier frequencies of recessive conditions in the Southern Chinese population is not yet available, we perfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d237aecededd7fce66cf66494f604fb
https://pubmed.ncbi.nlm.nih.gov/35314707
https://pubmed.ncbi.nlm.nih.gov/35314707
Autor:
Chen Qiao, Joshua W. K. Ho, Mai Har Sham, Aaron Wing Cheung Kwok, Yuanhua Huang, Rongting Huang
Mitochondrial mutations are increasingly recognised as informative endogenous genetic markers that can be used to reconstruct cellular clonal structure using single-cell RNA or DNA sequencing data. However, there is a lack of effective computational
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42bb4d8e65598f5e70335e2d87905785
https://doi.org/10.1101/2021.03.27.437331
https://doi.org/10.1101/2021.03.27.437331
