Search Results - Plagnol, Vincent

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  1. 1
    Association tests and software for copy number variant data

    Association tests and software for copy number variant data by Plagnol, Vincent

    Published 2009
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  2. 2
    Bayesian mixture analysis for metagenomic community profiling

    Bayesian mixture analysis for metagenomic community profiling by Morfopoulou, Sofia, Plagnol, Vincent

    Published 2015
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  3. 3
    Possible Ancestral Structure in Human Populations

    Possible Ancestral Structure in Human Populations by Plagnol, Vincent, Wall, Jeffrey D

    Published 2006
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  4. 4
    Detecting Ancient Admixture and Estimating Demographic Parameters in Multiple Human Populations

    Detecting Ancient Admixture and Estimating Demographic Parameters in Multiple Human Populations by Wall, Jeffrey D., Lohmueller, Kirk E., Plagnol, Vincent

    Published 2009
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  5. 5
    Markov chain Monte Carlo without likelihoods

    Markov chain Monte Carlo without likelihoods by Marjoram, Paul, Molitor, John, Plagnol, Vincent, Tavaré, Simon

    Published 2003
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  6. 6
    RAPIDR: an analysis package for non-invasive prenatal testing of aneuploidy

    RAPIDR: an analysis package for non-invasive prenatal testing of aneuploidy by Lo, Kitty K., Boustred, Christopher, Chitty, Lyn S., Plagnol, Vincent

    Published 2014
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  7. 7
    A Comparison of Low Read Depth QuantSeq 3′ Sequencing to Total RNA-Seq in FUS Mutant Mice

    A Comparison of Low Read Depth QuantSeq 3′ Sequencing to Total RNA-Seq in FUS Mutant Mice by Jarvis, Seth, Birsa, Nicol, Secrier, Maria, Fratta, Pietro, Plagnol, Vincent

    Published 2020
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  8. 8
    Relative Influences of Crossing Over and Gene Conversion on the Pattern of Linkage Disequilibrium in Arabidopsis thaliana

    Relative Influences of Crossing Over and Gene Conversion on the Pattern of Linkage Disequilibrium in Arabidopsis thaliana by Plagnol, Vincent, Padhukasahasram, Badri, Wall, Jeffrey D., Marjoram, Paul, Nordborg, Magnus

    Published 2006
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  9. 9
    A Method to Address Differential Bias in Genotyping in Large-Scale Association Studies

    A Method to Address Differential Bias in Genotyping in Large-Scale Association Studies by Plagnol, Vincent, Cooper, Jason. D, Todd, John A, Clayton, David G

    Published 2007
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  10. 10
    Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13

    Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13 by Plagnol, Vincent, Smyth, Deborah J., Todd, John A., Clayton, David G.

    Published 2009
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  11. 11
    Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita

    Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita by Walne, Amanda J., Vulliamy, Tom, Kirwan, Michael, Plagnol, Vincent, Dokal, Inderjeet

    Published 2013
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  12. 12
    Quantitative analysis of cryptic splicing associated with TDP-43 depletion

    Quantitative analysis of cryptic splicing associated with TDP-43 depletion by Humphrey, Jack, Emmett, Warren, Fratta, Pietro, Isaacs, Adrian M., Plagnol, Vincent

    Published 2017
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  13. 13
    Fluorescence Intensity Normalisation: Correcting for Time Effects in Large-Scale Flow Cytometric Analysis

    Fluorescence Intensity Normalisation: Correcting for Time Effects in Large-Scale Flow Cytometric Analysis by Dendrou, Calliope A., Fung, Erik, Esposito, Laura, Todd, John A., Wicker, Linda S., Plagnol, Vincent

    Published 2009
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  14. 14
    Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia

    Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia by Futema, Marta, Plagnol, Vincent, Whittall, Ros A, Neil, H Andrew W, Humphries, Steve Eric

    Published 2012
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  15. 15
    Study of the genetic variability in a Parkinson's Disease gene: EIF4G1

    Study of the genetic variability in a Parkinson's Disease gene: EIF4G1 by Tucci, Arianna, Charlesworth, Gavin, Sheerin, Una-Marie, Plagnol, Vincent, Wood, Nicholas W., Hardy, John

    Published 2012
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  16. 16
    Extreme Clonality in Lymphoblastoid Cell Lines with Implications for Allele Specific Expression Analyses

    Extreme Clonality in Lymphoblastoid Cell Lines with Implications for Allele Specific Expression Analyses by Plagnol, Vincent, Uz, Elif, Wallace, Chris, Stevens, Helen, Clayton, David, Ozcelik, Tayfun, Todd, John A.

    Published 2008
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  17. 17
    A robust statistical method for case-control association testing with copy number variation

    A robust statistical method for case-control association testing with copy number variation by Barnes, Chris, Plagnol, Vincent, Fitzgerald, Tomas, Redon, Richard, Marchini, Jonathan, Clayton, David, Hurles, Matthew E

    Published 2008
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  18. 18
    Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics

    Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics by Giambartolomei, Claudia, Vukcevic, Damjan, Schadt, Eric E., Franke, Lude, Hingorani, Aroon D., Wallace, Chris, Plagnol, Vincent

    Published 2014
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  19. 19
    Tubular aggregates caused by serine active site containing 1 (SERAC1) mutations in a patient with a mitochondrial encephalopathy

    Tubular aggregates caused by serine active site containing 1 (SERAC1) mutations in a patient with a mitochondrial encephalopathy by Wedatilake, Yehani, Plagnol, Vincent, Anderson, Glenn, Paine, Simon M. L., Clayton, Peter T., Jacques, Thomas S., Rahman, Shamima

    Published 2015
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  20. 20
    Exome Sequencing Identifies Autosomal-Dominant SRP72 Mutations Associated with Familial Aplasia and Myelodysplasia

    Exome Sequencing Identifies Autosomal-Dominant SRP72 Mutations Associated with Familial Aplasia and Myelodysplasia by Kirwan, Michael, Walne, Amanda J., Plagnol, Vincent, Velangi, Mark, Ho, Aloysius, Hossain, Upal, Vulliamy, Tom, Dokal, Inderjeet

    Published 2012
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