Canlyniadau Chwilio - Fiona Cunningham

Mireinio'r Canlyniadau
  1. 1
    Paralogous annotation of disease-causing variants in long QT syndrome genes

    Paralogous annotation of disease-causing variants in long QT syndrome genes gan James S. Ware, Roddy Walsh, Fiona Cunningham, Ewan Birney, Stuart A. Cook

    Cyhoeddwyd 2012
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  2. 2
    Contrasting <i>in vitro</i> lymphocyte chemotactic activity of the hydroxyl enantiomers of 12‐hydroxy‐5,8,10,14‐eicosatetraenoic acid

    Contrasting <i>in vitro</i> lymphocyte chemotactic activity of the hydroxyl enantiomers of 12‐hydroxy‐5,8,10,14‐eicosatetraenoic acid gan Kevin B. Bacon, R.D.R. Camp, Fiona Cunningham, P.M. Woollard

    Cyhoeddwyd 1988
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  3. 3
    Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

    Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor gan William McLaren, Bethan Pritchard, Daniel Ríos, Yuan Chen, Paul Flicek, Fiona Cunningham

    Cyhoeddwyd 2010
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  4. 4
    A Combined Functional Annotation Score for Non-Synonymous Variants

    A Combined Functional Annotation Score for Non-Synonymous Variants gan Margarida C. Lopes, Christopher Joyce, Graham R. S. Ritchie, Sally John, Fiona Cunningham, Jennifer L. Asimit, Eleftheria Zeggini

    Cyhoeddwyd 2012
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  5. 5
    Leukotriene B<sub>4</sub>‐like material in scale of psoriatic skin lesions

    Leukotriene B<sub>4</sub>‐like material in scale of psoriatic skin lesions gan Susan D. Brain, R.D.R. Camp, Fiona Cunningham, P.M. Dowd, Malcolm W. Greaves, A. Kobza Black

    Cyhoeddwyd 1984
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  6. 6
    The Ensembl Variant Effect Predictor

    The Ensembl Variant Effect Predictor gan William McLaren, Laurent Gil, Sarah Hunt, Harpreet Singh Riat, Graham R. S. Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham

    Cyhoeddwyd 2016
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  7. 7
    The Ensembl Variant Effect Predictor

    The Ensembl Variant Effect Predictor gan William McLaren, Laurent Gil, Sarah Hunt, Harpreet Singh Riat, Graham R. S. Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham

    Cyhoeddwyd 2016
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  8. 8
    A standard variation file format for human genome sequences

    A standard variation file format for human genome sequences gan Martin G. Reese, Barry Moore, Colin Batchelor, Fidel Salas, Fiona Cunningham, Gábor Marth, Lincoln Stein, Paul Flicek, Mark Yandell, Karen Eilbeck

    Cyhoeddwyd 2010
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  9. 9
    Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants

    Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants gan Jacqueline MacArthur, Joannella Morales, Ray Tully, Alex Astashyn, Laurent Gil, Elspeth A. Bruford, Pontus Larsson, Paul Flicek, Raymond Dalgleish, Donna Maglott, Fiona Cunningham

    Cyhoeddwyd 2013
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  10. 10
    Ensembl variation resources

    Ensembl variation resources gan Sarah Hunt, William McLaren, Laurent Gil, Anja Thormann, Helen Schuilenburg, Dan Sheppard, Andrew Parton, Irina M. Armean, Stephen J. Trevanion, Paul Flicek, Fiona Cunningham

    Cyhoeddwyd 2018
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  11. 11
    Scaling up data curation using deep learning: An application to literature triage in genomic variation resources

    Scaling up data curation using deep learning: An application to literature triage in genomic variation resources gan Kyubum Lee, Maria Livia Famiglietti, Aoife McMahon, Chih-Hsuan Wei, Jacqueline MacArthur, Sylvain Poux, Lionel Breuza, Alan Bridge, Fiona Cunningham, Ioannis Xénarios, Zhiyong Lu

    Cyhoeddwyd 2018
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  12. 12
    The European Variation Archive: a FAIR resource of genomic variation for all species

    The European Variation Archive: a FAIR resource of genomic variation for all species gan Timothée Cezard, Fiona Cunningham, Sarah Hunt, Baron Koylass, Nitin Kumar, Gary Saunders, April Shen, Andres F Silva, Kirill Tsukanov, Sundararaman Venkataraman, Paul Flicek, Helen Parkinson, Thomas Keane

    Cyhoeddwyd 2021
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  13. 13
    Ensembl variation resources

    Ensembl variation resources gan Yuan Chen, Fiona Cunningham, Daniel Ríos, William McLaren, James Smith, Bethan Pritchard, Giulietta Spudich, Simon Brent, Eugene Kulesha, Pablo Marín-García, Damian Smedley, Ewan Birney, Paul Flicek

    Cyhoeddwyd 2010
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  14. 14
    Annotating and prioritizing genomic variants using the Ensembl Variant Effect Predictor—A tutorial

    Annotating and prioritizing genomic variants using the Ensembl Variant Effect Predictor—A tutorial gan Sarah Hunt, Benjamin Moore, Ridwan Amode, Irina M. Armean, Diana Lemos, Aleena Mushtaq, Andrew Parton, Helen Schuilenburg, Michał Szpak, Anja Thormann, Emily Perry, Stephen J. Trevanion, Paul Flicek, Andrew Yates, Fiona Cunningham

    Cyhoeddwyd 2021
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  15. 15
    Phenotypic and functional characterization of a CD4+ CD25high FOXP3high regulatory T-cell population in the dog

    Phenotypic and functional characterization of a CD4+ CD25high FOXP3high regulatory T-cell population in the dog gan Damilola Pinheiro, Yogesh Singh, Charlotte R. Grant, Richard C. Appleton, Flavio Sacchini, Kate R. L. Walker, Alden H. Chadbourne, Charlotte A. Palmer, Elizabeth Armitage‐Chan, Ian M. Thompson, Lina Williamson, Fiona Cunningham, Oliver A. Garden

    Cyhoeddwyd 2010
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  16. 16
    Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP

    Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP gan Anja Thormann, Mihail Halachev, William McLaren, David Moore, Victoria Svinti, Archie Campbell, Shona M. Kerr, Marc Tischkowitz, Sarah Hunt, Malcolm G. Dunlop, Matthew E. Hurles, Caroline F. Wright, Helen V. Firth, Fiona Cunningham, David Fitzpatrick

    Cyhoeddwyd 2019
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  17. 17
    The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)

    The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog) gan Jacqueline MacArthur, Emily Bowler-Barnett, María Cerezo, Laurent Gil, Peggy Hall, Emma Hastings, Heather Junkins, Aoife McMahon, Annalisa Milano, Joannella Morales, Zoë May Pendlington, Danielle Welter, Tony Burdett, Lucia A. Hindorff, Paul Flicek, Fiona Cunningham, Helen Parkinson

    Cyhoeddwyd 2016
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  18. 18
    A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog

    A standardized framework for representation of ancestry data in genomics studies, with application to the NHGRI-EBI GWAS Catalog gan Joannella Morales, Danielle Welter, Emily Bowler-Barnett, María Cerezo, Laura W. Harris, Aoife McMahon, Peggy Hall, Heather Junkins, Annalisa Milano, Emma Hastings, Claudio Malangone, Annalisa Buniello, Tony Burdett, Paul Flicek, Helen Parkinson, Fiona Cunningham, Lucia A. Hindorff, Jacqueline MacArthur

    Cyhoeddwyd 2018
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  19. 19
    Locus Reference Genomic sequences: an improved basis for describing human DNA variants

    Locus Reference Genomic sequences: an improved basis for describing human DNA variants gan Raymond Dalgleish, Paul Flicek, Fiona Cunningham, Alex Astashyn, Raymond E. Tully, Glenn Proctor, Yuan Chen, William McLaren, Pontus Larsson, Brendan Vaughan, Christophe Béroud, Glen Dobson, Heikki Lehväslaiho, Peter E.M. Taschner, Johan T. den Dunnen, A. Devereau, Ewan Birney, Anthony J. Brookes, Donna Maglott

    Cyhoeddwyd 2010
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  20. 20
    The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019

    The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019 gan Annalisa Buniello, Jacqueline MacArthur, María Cerezo, Laura W. Harris, James Hayhurst, Claudio Malangone, Aoife McMahon, Joannella Morales, Edward Mountjoy, Elliot Sollis, Dániel Süveges, Olga Vrousgou, Patricia L. Whetzel, Ridwan Amode, José Ángel Guillén, Harpreet Singh Riat, Stephen J. Trevanion, Peggy Hall, Heather Junkins, Paul Flicek, Tony Burdett, Lucia A. Hindorff, Fiona Cunningham, Helen Parkinson

    Cyhoeddwyd 2018
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