Daniel G MacArthur

Summary

Affiliation: Wellcome Trust Genome Campus
Country: UK

Publications

  1. ncbi Biology of Genomes: making sense of sequence
    Daniel G MacArthur
    Human Evolution, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK
    Genome Med 1:61. 2009
  2. ncbi Loss-of-function variants in the genomes of healthy humans
    Daniel G MacArthur
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK
    Hum Mol Genet 19:R125-30. 2010
  3. ncbi Human Y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree
    Yali Xue
    The Wellcome Trust Sanger Institute, Hinxton, Cambs CB10 1SA, UK
    Curr Biol 19:1453-7. 2009
  4. ncbi Dindel: accurate indel calls from short-read data
    Cornelis A Albers
    Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire CB10 1HH, United Kingdom
    Genome Res 21:961-73. 2011
  5. ncbi A map of human genome variation from population-scale sequencing
    Richard M Durbin
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge CB10 1SA, UK
    Nature 467:1061-73. 2010
  6. ncbi Origins and functional impact of copy number variation in the human genome
    Donald F Conrad
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA UK
    Nature 464:704-12. 2010
  7. ncbi The promise and reality of personal genomics
    Bryndis Yngvadottir
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1SA, UK
    Genome Biol 10:237. 2009

Detail Information

Publications7

  1. ncbi Biology of Genomes: making sense of sequence
    Daniel G MacArthur
    Human Evolution, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SA, UK
    Genome Med 1:61. 2009
    ..ABSTRACT : A report on the Biology of Genomes meeting held at Cold Spring Harbor Laboratory, NY, USA, 5-9 May 2009...
  2. ncbi Loss-of-function variants in the genomes of healthy humans
    Daniel G MacArthur
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK
    Hum Mol Genet 19:R125-30. 2010
    ....
  3. ncbi Human Y chromosome base-substitution mutation rate measured by direct sequencing in a deep-rooting pedigree
    Yali Xue
    The Wellcome Trust Sanger Institute, Hinxton, Cambs CB10 1SA, UK
    Curr Biol 19:1453-7. 2009
    ..0 x 10(-8)), consistent with estimates of 2.3 x 10(-8)-6.3 x 10(-8) mutations/nucleotide/generation for the same Y-chromosomal region from published human-chimpanzee comparisons depending on the generation and split times assumed...
  4. ncbi Dindel: accurate indel calls from short-read data
    Cornelis A Albers
    Wellcome Trust Sanger Institute, Hinxton, Cambridgeshire CB10 1HH, United Kingdom
    Genome Res 21:961-73. 2011
    ..The algorithm is implemented in the program Dindel, which has been used in the 1000 Genomes Project call sets...
  5. ncbi A map of human genome variation from population-scale sequencing
    Richard M Durbin
    Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge CB10 1SA, UK
    Nature 467:1061-73. 2010
    ..These methods and public data will support the next phase of human genetic research...
  6. ncbi Origins and functional impact of copy number variation in the human genome
    Donald F Conrad
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA UK
    Nature 464:704-12. 2010
    ....
  7. ncbi The promise and reality of personal genomics
    Bryndis Yngvadottir
    The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1SA, UK
    Genome Biol 10:237. 2009
    ..The publication of the highest-quality and best-annotated personal genome yet tells us much about sequencing technology, something about genetic ancestry, but still little of medical relevance...