Search Results - O'Fallon, Brendan D

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  1. 1
    Native Americans experienced a strong population bottleneck coincident with European contact

    Native Americans experienced a strong population bottleneck coincident with European contact by O'Fallon, Brendan D., Fehren-Schmitz, Lars

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  2. 2
    ACG: rapid inference of population history from recombining nucleotide sequences

    ACG: rapid inference of population history from recombining nucleotide sequences by O'Fallon, Brendan D

    Published in BMC bioinformatics
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  3. 3
    A support vector machine for identification of single-nucleotide polymorphisms from next-generation sequencing data

    A support vector machine for identification of single-nucleotide polymorphisms from next-generation sequencing data by O'Fallon, Brendan D, Wooderchak-Donahue, Whitney, Crockett, David K

    Published in Bioinformatics
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  4. 4
    Quasi-species evolution in subdivided populations favours maximally deleterious mutations

    Quasi-species evolution in subdivided populations favours maximally deleterious mutations by O'Fallon, Brendan D, Adler, Frederick R, Proulx, Stephen R

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  5. 5
    A method to correct for the effects of purifying selection on genealogical inference

    A method to correct for the effects of purifying selection on genealogical inference by O'Fallon, Brendan D

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  6. 6
    A continuous-state coalescent and the impact of weak selection on the structure of gene genealogies

    A continuous-state coalescent and the impact of weak selection on the structure of gene genealogies by O'Fallon, Brendan D, Seger, Jon, Adler, Frederick R

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  7. 7
    A Method for Accurate Inference of Population Size from Serially Sampled Genealogies Distorted by Selection

    A Method for Accurate Inference of Population Size from Serially Sampled Genealogies Distorted by Selection by O'Fallon, Brendan D.

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  8. 8
    VarRanker: rapid prioritization of sequence variations associated with human disease

    VarRanker: rapid prioritization of sequence variations associated with human disease by O'Fallon, Brendan D, Wooderchak-Donahue, Whitney, Bayrak-Toydemir, Pinar, Crockett, David

    Published in BMC bioinformatics
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  9. 9
    Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) files

    Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) files by Ebbert, Mark T W, Wadsworth, Mark E, Boehme, Kevin L, Hoyt, Kaitlyn L, Sharp, Aaron R, O'Fallon, Brendan D, Kauwe, John S K, Ridge, Perry G

    Published in BMC bioinformatics
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  10. 10
    BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia

    BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia by Wooderchak-Donahue, Whitney L., McDonald, Jamie, O’Fallon, Brendan, Upton, Paul D., Li, Wei, Roman, Beth L., Young, Sarah, Plant, Parker, Fülöp, Gyula T., Langa, Carmen, Morrell, Nicholas W., Botella, Luisa M., Bernabeu, Carmelo, Stevenson, David A., Runo, James R., Bayrak-Toydemir, Pinar

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  11. 11
    A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspective

    A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspective by Wooderchak-Donahue, Whitney L, O'Fallon, Brendan, Furtado, Larissa V, Durtschi, Jacob D, Plant, Parker, Ridge, Perry G, Rope, Alan F, Yetman, Angela T, Bayrak-Toydemir, Pinar

    Published in BMC medical genomics
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