Dissertation/ Thesis

Quantitative trait variation and adaptation in contemporary humans

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Quantitative trait variation and adaptation in contemporary humans
Συγγραφείς: Mostafavi, Hakhamanesh
Έτος έκδοσης: 2019
Συλλογή: Columbia University: Academic Commons
Θεματικοί όροι: Biology, Genetics, Human evolution, Genomes--Data processing, Human genetics--Variation, Mortality
Περιγραφή: Human genomic data sets are now reaching sample sizes on the order of hundreds of thousands and soon exceeding millions, providing unprecedented opportunities to understand human evolution. Most studies of human adaptation so far have focused on selection that has acted over the past million to few thousand years. However, powered by large data sets, it is now feasible to study allele frequency changes that occur within the short timescale of a few generations, directly observing selection acting in contemporary humans. I take this approach in the work presented in Chapter 1 of this thesis, where we performed a genome-wide scan to identify a set of genetic variants that influence age-specific mortality in present-day samples. Our findings include two variants in the APOE and CHRNA3 loci, as well as sets of variants contributing to a number of traits, including coronary artery disease and cholesterol levels, and intriguingly, to timing of puberty and child birth. New research directions have also opened up with the advent of large-scale genome-wide association studies (GWAS), which have begun to uncover genetic variants underlying a number of human traits, ranging from disease susceptibility to social and behavioral traits such as educational attainment and neuroticism. One such direction is the use of polygenic scores (PGS), which aggregate GWAS findings into one score as a measure of genetic propensity for traits, for phenotypic prediction. A major obstacle to this application is that the prediction accuracy of PGS drops in samples that have a different genetic ancestry than the GWAS sample. Our work, presented in Chapter 2, demonstrates that PGS prediction accuracy is also variable within genetic ancestries depending on factors such as age, sex, and socioeconomic status, as well as GWAS study design. These findings have important implications for the increasing use of these measures in diverse disciplines such as social sciences and human genetics.
Τύπος εγγράφου: thesis
Γλώσσα: English
DOI: 10.7916/d8-41g8-bd32
Διαθεσιμότητα: https://doi.org/10.7916/d8-41g8-bd32
Αριθμός Καταχώρησης: edsbas.C8A9623D
Βάση Δεδομένων: BASE
FullText Text:
  Availability: 0
CustomLinks:
  – Url: https://doi.org/10.7916/d8-41g8-bd32#
    Name: EDS - BASE (ns324271)
    Category: fullText
    Text: View record from BASE
Header DbId: edsbas
DbLabel: BASE
An: edsbas.C8A9623D
RelevancyScore: 805
AccessLevel: 3
PubType: Dissertation/ Thesis
PubTypeId: dissertation
PreciseRelevancyScore: 805.215454101563
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Quantitative trait variation and adaptation in contemporary humans
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Mostafavi%2C+Hakhamanesh%22">Mostafavi, Hakhamanesh</searchLink>
– Name: DatePubCY
  Label: Publication Year
  Group: Date
  Data: 2019
– Name: Subset
  Label: Collection
  Group: HoldingsInfo
  Data: Columbia University: Academic Commons
– Name: Subject
  Label: Subject Terms
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Biology%22">Biology</searchLink><br /><searchLink fieldCode="DE" term="%22Genetics%22">Genetics</searchLink><br /><searchLink fieldCode="DE" term="%22Human+evolution%22">Human evolution</searchLink><br /><searchLink fieldCode="DE" term="%22Genomes--Data+processing%22">Genomes--Data processing</searchLink><br /><searchLink fieldCode="DE" term="%22Human+genetics--Variation%22">Human genetics--Variation</searchLink><br /><searchLink fieldCode="DE" term="%22Mortality%22">Mortality</searchLink>
– Name: Abstract
  Label: Description
  Group: Ab
  Data: Human genomic data sets are now reaching sample sizes on the order of hundreds of thousands and soon exceeding millions, providing unprecedented opportunities to understand human evolution. Most studies of human adaptation so far have focused on selection that has acted over the past million to few thousand years. However, powered by large data sets, it is now feasible to study allele frequency changes that occur within the short timescale of a few generations, directly observing selection acting in contemporary humans. I take this approach in the work presented in Chapter 1 of this thesis, where we performed a genome-wide scan to identify a set of genetic variants that influence age-specific mortality in present-day samples. Our findings include two variants in the APOE and CHRNA3 loci, as well as sets of variants contributing to a number of traits, including coronary artery disease and cholesterol levels, and intriguingly, to timing of puberty and child birth. New research directions have also opened up with the advent of large-scale genome-wide association studies (GWAS), which have begun to uncover genetic variants underlying a number of human traits, ranging from disease susceptibility to social and behavioral traits such as educational attainment and neuroticism. One such direction is the use of polygenic scores (PGS), which aggregate GWAS findings into one score as a measure of genetic propensity for traits, for phenotypic prediction. A major obstacle to this application is that the prediction accuracy of PGS drops in samples that have a different genetic ancestry than the GWAS sample. Our work, presented in Chapter 2, demonstrates that PGS prediction accuracy is also variable within genetic ancestries depending on factors such as age, sex, and socioeconomic status, as well as GWAS study design. These findings have important implications for the increasing use of these measures in diverse disciplines such as social sciences and human genetics.
– Name: TypeDocument
  Label: Document Type
  Group: TypDoc
  Data: thesis
– Name: Language
  Label: Language
  Group: Lang
  Data: English
– Name: DOI
  Label: DOI
  Group: ID
  Data: 10.7916/d8-41g8-bd32
– Name: URL
  Label: Availability
  Group: URL
  Data: https://doi.org/10.7916/d8-41g8-bd32
– Name: AN
  Label: Accession Number
  Group: ID
  Data: edsbas.C8A9623D
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=edsbas&AN=edsbas.C8A9623D
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.7916/d8-41g8-bd32
    Languages:
      – Text: English
    Subjects:
      – SubjectFull: Biology
        Type: general
      – SubjectFull: Genetics
        Type: general
      – SubjectFull: Human evolution
        Type: general
      – SubjectFull: Genomes--Data processing
        Type: general
      – SubjectFull: Human genetics--Variation
        Type: general
      – SubjectFull: Mortality
        Type: general
    Titles:
      – TitleFull: Quantitative trait variation and adaptation in contemporary humans
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Mostafavi, Hakhamanesh
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 01
              Type: published
              Y: 2019
          Identifiers:
            – Type: issn-locals
              Value: edsbas
            – Type: issn-locals
              Value: edsbas.oa
ResultId 1