检索结果 - Sarah Ng

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  1. 1
    How to Codeliver Translational Health Service Research Education With Clinicians Through Effective Governance

    How to Codeliver Translational Health Service Research Education With Clinicians Through Effective Governance 由 Robyn Taylor, Nazlee Siddiqui, Bridget Farrell, Dr Sarah Ng

    出版 2025
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  2. 2
    <i>cis</i>- and <i>trans</i>-Acting Determinants of Transcription Termination by Yeast RNA Polymerase II

    <i>cis</i>- and <i>trans</i>-Acting Determinants of Transcription Termination by Yeast RNA Polymerase II 由 Eric J. Steinmetz, Sarah Ng, Joseph P. Cloute, David A. Brow

    出版 2006
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  3. 3
    Massively parallel exon capture and library-free resequencing across 16 genomes

    Massively parallel exon capture and library-free resequencing across 16 genomes 由 Emily H. Turner, Choli Lee, Sarah Ng, Deborah A. Nickerson, Jay Shendure

    出版 2009
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  4. 4
    Next generation sequence analysis for mitochondrial disorders

    Next generation sequence analysis for mitochondrial disorders 由 Valeria Vasta, Sarah Ng, Emily H. Turner, Jay Shendure, Si Houn Hahn

    出版 2009
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  5. 5
    Exome-wide DNA capture and next generation sequencing in domestic and wild species

    Exome-wide DNA capture and next generation sequencing in domestic and wild species 由 Ted Cosart, Albano Beja‐Pereira, Shanyuan Chen, Sarah Ng, Jay Shendure, Gordon Luikart

    出版 2011
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  6. 6
    The perceived impact of Covid-19 on periodontal practice in the United Kingdom: A questionnaire study

    The perceived impact of Covid-19 on periodontal practice in the United Kingdom: A questionnaire study 由 Luigi Nibali, Mark Ide, Dr Sarah Ng, Zoe Buontempo, Y.M. CLAYTON, Koula Asimakopoulou

    出版 2020
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  7. 7
    A Non-Active-Site SET Domain Surface Crucial for the Interaction of MLL1 and the RbBP5/Ash2L Heterodimer within MLL Family Core Complexes

    A Non-Active-Site SET Domain Surface Crucial for the Interaction of MLL1 and the RbBP5/Ash2L Heterodimer within MLL Family Core Complexes 由 Stephen A. Shinsky, Michael S. Hu, Valarie E. Vought, Sarah Ng, Michael J. Bamshad, Jay Shendure, Michael S. Cosgrove

    出版 2014
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  8. 8
    Single-nucleotide evolutionary constraint scores highlight disease-causing mutations

    Single-nucleotide evolutionary constraint scores highlight disease-causing mutations 由 Gregory M. Cooper, David L. Goode, Sarah Ng, Arend Sidow, Michael J. Bamshad, Jay Shendure, Deborah A. Nickerson

    出版 2010
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  9. 9
    <i>Trans</i> genomic capture and sequencing of primate exomes reveals new targets of positive selection

    <i>Trans</i> genomic capture and sequencing of primate exomes reveals new targets of positive selection 由 Renee D. George, Graham McVicker, Rachel Diederich, Sarah Ng, Alexandra P MacKenzie, Willie J. Swanson, Jay Shendure, James H. Thomas

    出版 2011
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  10. 10
    Haplotype-resolved genome sequencing of a Gujarati Indian individual

    Haplotype-resolved genome sequencing of a Gujarati Indian individual 由 Jacob O. Kitzman, Alexandra P MacKenzie, Andrew Adey, Joseph B. Hiatt, Rupali P Patwardhan, Peter H. Sudmant, Sarah Ng, Can Alkan, Ruolan Qiu, Evan E. Eichler, Jay Shendure

    出版 2010
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  11. 11
    Single-nucleotide-resolution sequencing of human<i>N</i>6-methyldeoxyadenosine reveals strand-asymmetric clusters associated with SSBP1 on the mitochondrial genome

    Single-nucleotide-resolution sequencing of human<i>N</i>6-methyldeoxyadenosine reveals strand-asymmetric clusters associated with SSBP1 on the mitochondrial genome 由 Casslynn W.Q. Koh, Yeek Teck Goh, Joel D. W. Toh, Suat Peng Neo, Sarah Ng, Jayantha Gunaratne, Yong‐Gui Gao, Stephen R. Quake, William F. Burkholder, W.S. Sho Goh

    出版 2018
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  12. 12
    Targeted capture and massively parallel sequencing of 12 human exomes

    Targeted capture and massively parallel sequencing of 12 human exomes 由 Sarah Ng, Emily H. Turner, Peggy D. Robertson, Steven Flygare, Abigail W. Bigham, Choli Lee, Tristan Shaffer, Michelle Wong, Arindam Bhattacharjee, Evan E. Eichler, Michael J. Bamshad, Deborah A. Nickerson, Jay Shendure

    出版 2009
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  13. 13
    Exome sequencing identifies the cause of a mendelian disorder

    Exome sequencing identifies the cause of a mendelian disorder 由 Sarah Ng, Kati J. Buckingham, Choli Lee, Abigail W. Bigham, Holly K. Tabor, Karin M. Dent, Chad D. Huff, Paul Shannon, Ethylin Wang Jabs, Deborah A. Nickerson, Jay Shendure, Michael J. Bamshad

    出版 2009
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  14. 14
    A Genome-Wide Association Study Identifies Novel and Functionally Related Susceptibility Loci for Kawasaki Disease

    A Genome-Wide Association Study Identifies Novel and Functionally Related Susceptibility Loci for Kawasaki Disease 由 David Burgner, Sonia Dávila, Willemijn B. Breunis, Sarah Ng, Yi Li, Carine Bonnard, Ling Ling, Victoria Wright, Anbupalam Thalamuthu, Miranda Odam, Chisato Shimizu, Jane C. Burns, Michael Levin, Taco W. Kuijpers, Martin L. Hibberd

    出版 2009
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  15. 15
    Spatial profiling of gastric cancer patient-matched primary and locoregional metastases reveals principles of tumour dissemination

    Spatial profiling of gastric cancer patient-matched primary and locoregional metastases reveals principles of tumour dissemination 由 Raghav Sundar, Drolaiz Hw Liu, Gordon G.A. Hutchins, Hayley Slaney, Arnaldo N. S. Silva, Jan Oosting, Jeremy D. Hayden, Lindsay C. Hewitt, Cedric Chuan Young Ng, Amrita Mangalvedhekar, Sarah Ng, Iain Tan, Patrick Tan, Heike I. Grabsch

    出版 2020
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  16. 16
    Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

    Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations 由 Brian J. O’Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J. Schwartz, Santhosh Girirajan, Emre Karakoç, Alexandra P MacKenzie, Sarah Ng, Carl Baker, Mark J. Rieder, Deborah A. Nickerson, Raphael Bernier, Simon E. Fisher, Jay Shendure, Evan E. Eichler

    出版 2011
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  17. 17
    Identification of differential RNA modifications from nanopore direct RNA sequencing with xPore

    Identification of differential RNA modifications from nanopore direct RNA sequencing with xPore 由 Ploy N. Pratanwanich, Fei Yao, Ying Chen, Casslynn W.Q. Koh, Yuk Kei Wan, Christopher Hendra, Polly Poon, Yeek Teck Goh, Phoebe M. L. Yap, Jing Yuan Chooi, Wee Joo Chng, Sarah Ng, Alexandre H. Thiéry, W.S. Sho Goh, Jonathan Göke

    出版 2021
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  18. 18
    Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers

    Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers 由 Akash Kumar, Thomas A. White, Alexandra P MacKenzie, Nigel Clegg, Choli Lee, Ruth F. Dumpit, Ilsa M. Coleman, Sarah Ng, Stephen J. Salipante, Mark J. Rieder, Deborah A. Nickerson, Eva Corey, Paul H. Lange, Colm Morrissey, Robert L. Vessella, Peter S. Nelson, Jay Shendure

    出版 2011
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  19. 19
    Tissue-specific cell-free DNA degradation quantifies circulating tumor DNA burden

    Tissue-specific cell-free DNA degradation quantifies circulating tumor DNA burden 由 Guanhua Zhu, Yu Amanda Guo, Danliang Ho, Polly Poon, Zhong Wee Poh, Pui‐Mun Wong, Anna Gan, Mei Mei Chang, Dimitrios Kleftogiannis, Yi Ting Lau, Brenda Tay, Wan Jun Lim, Clarinda Chua, Tira J. Tan, Si‐Lin Koo, Dawn Q. Chong, Yoon Sim Yap, Iain Beehuat Tan, Sarah Ng, Anders J. Skanderup

    出版 2021
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  20. 20
    Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

    Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome 由 Sarah Ng, Abigail W. Bigham, Kati J. Buckingham, Mark C. Hannibal, Margaret J. McMillin, Heidi Gildersleeve, Anita Beck, Holly K. Tabor, Gregory M. Cooper, Heather C Mefford, Choli Lee, Emily H. Turner, Joshua D. Smith, Mark J. Rieder, Koh-ichiro Yoshiura, Naomichi Matsumoto, Tohru Ohta, Norio Niikawa, Deborah A. Nickerson, Michael J. Bamshad, Jay Shendure

    出版 2010
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