Resultados de búsqueda - Melanie Bahlo

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  1. 1
    Generating linkage mapping files from Affymetrix SNP chip data

    Generating linkage mapping files from Affymetrix SNP chip data por Melanie Bahlo, C.J. Bromhead

    Publicado 2009
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  2. 2
    High-resolution characterization of sequence signatures due to non-random cleavage of cell-free DNA

    High-resolution characterization of sequence signatures due to non-random cleavage of cell-free DNA por Dineika Chandrananda, Natalie Thorne, Melanie Bahlo

    Publicado 2015
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  3. 3
    The Genetics of Epilepsy

    The Genetics of Epilepsy por Piero Perucca, Melanie Bahlo, Samuel F. Berkovic

    Publicado 2020
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  4. 4
    Dating Rare Mutations from Small Samples with Dense Marker Data

    Dating Rare Mutations from Small Samples with Dense Marker Data por Luke C. Gandolfo, Melanie Bahlo, Terence P. Speed

    Publicado 2014
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  5. 5
    Comparison of clustering tools in R for medium-sized 10x Genomics single-cell RNA-sequencing data

    Comparison of clustering tools in R for medium-sized 10x Genomics single-cell RNA-sequencing data por Saskia Freytag, Luyi Tian, Ingrid Lönnstedt, Milica Ng, Melanie Bahlo

    Publicado 2018
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  6. 6
    Comparison of clustering tools in R for medium-sized 10x Genomics single-cell RNA-sequencing data

    Comparison of clustering tools in R for medium-sized 10x Genomics single-cell RNA-sequencing data por Saskia Freytag, Luyi Tian, Ingrid Lönnstedt, Milica Ng, Melanie Bahlo

    Publicado 2018
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  7. 7
    Systematic noise degrades gene co-expression signals but can be corrected

    Systematic noise degrades gene co-expression signals but can be corrected por Saskia Freytag, Johann A. Gagnon-Bartsch, Terence P. Speed, Melanie Bahlo

    Publicado 2015
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  8. 8
    Identity-by-descent analyses for measuring population dynamics and selection in recombining pathogens

    Identity-by-descent analyses for measuring population dynamics and selection in recombining pathogens por Lyndal Henden, Stuart Lee, Ivo Müeller, Alyssa E. Barry, Melanie Bahlo

    Publicado 2018
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  9. 9
    dtangle: accurate and robust cell type deconvolution

    dtangle: accurate and robust cell type deconvolution por Gregory J. Hunt, Saskia Freytag, Melanie Bahlo, Johann A. Gagnon-Bartsch

    Publicado 2018
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  10. 10
    Mitochondrial Genome Sequence of the Scabies Mite Provides Insight into the Genetic Diversity of Individual Scabies Infections

    Mitochondrial Genome Sequence of the Scabies Mite Provides Insight into the Genetic Diversity of Individual Scabies Infections por Ehtesham Mofiz, Torsten Seemann, Melanie Bahlo, Deborah C. Holt, Bart J. Currie, Katja Fischer, Anthony T. Papenfuss

    Publicado 2016
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  11. 11
    Recent advances in the detection of repeat expansions with short-read next-generation sequencing

    Recent advances in the detection of repeat expansions with short-read next-generation sequencing por Melanie Bahlo, Mark F. Bennett, Peter Degorski, Rick M. Tankard, Martin B. Delatycki, Paul J. Lockhart

    Publicado 2018
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  12. 12
    Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing Data

    Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing Data por Rick M. Tankard, Mark F. Bennett, Peter Degorski, Martin B. Delatycki, Paul J. Lockhart, Melanie Bahlo

    Publicado 2018
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  13. 13
    <scp>Genes4Epilepsy</scp>: An epilepsy gene resource

    <scp>Genes4Epilepsy</scp>: An epilepsy gene resource por Karen Oliver, Ingrid E. Scheffer, Mark F. Bennett, Bronwyn E. Grinton, Melanie Bahlo, Samuel F. Berkovic

    Publicado 2023
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  14. 14
    Identification and Analysis of Error Types in High-Throughput Genotyping

    Identification and Analysis of Error Types in High-Throughput Genotyping por Kelly R. Ewen, Melanie Bahlo, Susan A. Treloar, Douglas F. Levinson, Bryan Mowry, John Barlow, Simon J. Foote

    Publicado 2000
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  15. 15
    Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20

    Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20 por Melanie A. Knight, R. J McKinlay Gardner, Melanie Bahlo, Tohru Matsuura, Judith A. Dixon, Susan M. Forrest, Elsdon Storey

    Publicado 2004
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  16. 16
    Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

    Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies por Melanie Bahlo, Jim Stankovich, Patrick Danoy, Peter F. Hickey, Bruce Taylor, Sharon R. Browning, Matthew A. Brown, Justin P. Rubio

    Publicado 2010
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  17. 17
    Plasmodium vivax Populations Are More Genetically Diverse and Less Structured than Sympatric Plasmodium falciparum Populations

    Plasmodium vivax Populations Are More Genetically Diverse and Less Structured than Sympatric Plasmodium falciparum Populations por Charlie Jennison, Alicia Arnott, Natacha Tessier, Livingstone Tavul, Cristian Koepfli, Ingrid Felger, Peter M. Siba, John C. Reeder, Melanie Bahlo, Ivo Müeller, Alyssa E. Barry

    Publicado 2015
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  18. 18
    Mutations in Contactin-1, a Neural Adhesion and Neuromuscular Junction Protein, Cause a Familial Form of Lethal Congenital Myopathy

    Mutations in Contactin-1, a Neural Adhesion and Neuromuscular Junction Protein, Cause a Familial Form of Lethal Congenital Myopathy por Alison G. Compton, Douglas E. Albrecht, Jane T. Seto, Sandra T. Cooper, Biljana Ilkovski, Kristi Jones, Daniel Challis, David Mowat, Barbara Ranscht, Melanie Bahlo, Stanley C. Froehner, Kathryn N. North

    Publicado 2008
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  19. 19
    GFI1B mutation causes a bleeding disorder with abnormal platelet function

    GFI1B mutation causes a bleeding disorder with abnormal platelet function por William Stevenson, Marie‐Christine Morel‐Kopp, Q. Chen, Hai-Yi Liang, C.J. Bromhead, Stephen Wright, Р. И. Туракулов, Ashley P. Ng, Andrew W. Roberts, Melanie Bahlo, Christopher Wård

    Publicado 2013
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  20. 20
    Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes

    Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes por Katherine R. Smith, Catherine J. Bromhead, Michael S. Hildebrand, A. Eliot Shearer, Paul J. Lockhart, Hossein Najmabadi, Richard J. Leventer, George McGillivray, David J. Amor, Richard J. Smith, Melanie Bahlo

    Publicado 2011
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