Martin O. Pollard

Employment

• Wellcome Sanger Institute Technical Innovator
  2020 - Present
• Wellcome Sanger Institute Senior Software Engineer
  2012 - 2019

Education

• University of Cambridge PhD
  2020 - Present
• University of Cambridge PhD
  2015 - 2016

Projects & Funding

Projects & funding information is unavailable.

Publications (16)

• High-resolution African HLA resource uncovers HLA-DRB1 expression effects underlying vaccine response
  Alexander J. Mentzer, Alexander Dilthey, Martin Pollard +43 more
  Nature Medicine 2024 DOI: 10.1038/s41591-024-02944-5
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• Twelve years of SAMtools and BCFtools
  GigaScience 2021 DOI: 10.1093/gigascience/giab008
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• Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections
  Nature Communications 2020 DOI: 10.1038/s41467-020-17696-2
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• Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits
  Nature Communications 2018 DOI: 10.1038/s41467-018-07730-9
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• Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits
  Nature Communications 2018 DOI: 10.1038/s41467-018-07070-8
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• Long Reads: their Purpose and Place.
  Human molecular genetics 2018 DOI: 10.1093/hmg/ddy177
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• Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits
  2018 DOI: 10.1101/283481
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• Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot.
  Global health, epidemiology and genomics 2017 DOI: 10.1017/gheg.2017.16
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• Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype.
  Lynette Grant Sadleir, Emily I. Mountier, Deepak S. Gill +97 more
  Neurology 2017 DOI: 10.1212/wnl.0000000000004331
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• Very low depth whole genome sequencing in complex trait association studies
  2017 DOI: 10.1101/169789
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• Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.
  Yang Luo, Katrina M. de Lange, Luke Jostins +27 more
  Nature Genetics 2017 DOI: 10.1038/ng.3761
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• Prevalence and architecture of de novo mutations in developmental disorders.
  Deciphering Developmental Disorders Study
  Nature 2017 DOI: 10.1038/nature21062
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• Deep Roots for Aboriginal Australian Y Chromosomes.
  Current Biology 2016 DOI: 10.1016/j.cub.2016.01.028
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• Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
  the INTERVAL Study, Alejandro Sifrim, the Deciphering Developmental Disorders Study +71 more
  Nat Genet 2016 DOI: 10.1038/ng.3627
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• The African Genome Variation Project shapes medical genetics in Africa
  Nature 2014 DOI: 10.1038/nature13997
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• Using haploid human DNA to design and evaluate the HiSeq X data processing strategy
  2014
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