Ingo Ruczinski

  1. Title:
    Inferring rare disease risk variants based on exact probabilities of sharing among multiple affected relatives.

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  2. Title:
    Detection of de novo copy number deletions from targeted sequencing of trios

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  3. Title:
    Sharing of rare nucleotide and copy number variants in extended multiplex families

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  4. Title:
    A brief note about genetic variation

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  5. Title:
    Sequencing family members to detect disease risk variants

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  6. Title:
    "Detecting And Quantifying Antibody Reactivity In Phip-Seq Data"

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