Deyana Lewis

Research Fellow, National Institutes of Health (NIH)

9 active projects

Duplicate of PCa_test_V7_Hail

To identify prostate cancer risk variants and genes in African American men. The reason for exploring this data is that prostate cancer develops more often in men of African ancestry than in men of other races. However, so far, prostate…

Scientific Questions Being Studied

To identify prostate cancer risk variants and genes in African American men. The reason for exploring this data is that prostate cancer develops more often in men of African ancestry than in men of other races. However, so far, prostate cancer genetic studies are based on the available data that mostly come from white men. This racial disparity has biased the discovery of genetic risk factors and therapeutic approaches, leading disparity in mortality rates

Project Purpose(s)

  • Disease Focused Research (prostate carcinoma)
  • Social / Behavioral
  • Ancestry

Scientific Approaches

I will design a two matched case-control studies black and white men. Thereafter, conduct a GWAS to identify variants and genes with higher mutation frequency. Next, I will identify genes mutated with larger functional impact through functional annotation analyses. Will repeat analysis using rare variants which will include rare variant association tests

Anticipated Findings

I anticipate finding novel variants and confirming prostate cancer risk variants that are specific to men of African ancestry. Doing so will increase the representation of African American men in prostate cancer genomic studies and increase African American awareness of early detection screening protocols.

Demographic Categories of Interest

  • Race / Ethnicity

Data Set Used

Controlled Tier

Research Team

Owner:

  • Deyana Lewis - Research Fellow, National Institutes of Health (NIH)

Duplicate of GWAS_EXAMPLE

Hypertension is one of the most common diseases in the US. Here, we will be determining what genetic variants contribute to higher systolic blood pressure, diastolic blood pressure, and pulse pressure in participants of African ancestry.

Scientific Questions Being Studied

Hypertension is one of the most common diseases in the US. Here, we will be determining what genetic variants contribute to higher systolic blood pressure, diastolic blood pressure, and pulse pressure in participants of African ancestry.

Project Purpose(s)

  • Disease Focused Research (hypertension)
  • Ancestry

Scientific Approaches

I plan to use median measurement values to determine median SBP, DBP, and PP. Then I plan to use the genetic data available and a GWAS run with Plink to determine which associations exist. This GWAS will be using quantitative data and thus will use linear regression.

Anticipated Findings

We anticipate replicating previously reported hypertension GWAS findings. In addition, since most hypertension GWAS are done in European ancestry, we expect to identify new variants associated with participants of African ancestry

Demographic Categories of Interest

  • Race / Ethnicity

Data Set Used

Controlled Tier

Research Team

Owner:

  • Deyana Lewis - Research Fellow, National Institutes of Health (NIH)

PCa_test_V7

To identify prostate cancer risk variants and genes in African American men. The reason for exploring this data is that prostate cancer develops more often in men of African ancestry than in men of other races. However, so far, prostate…

Scientific Questions Being Studied

To identify prostate cancer risk variants and genes in African American men. The reason for exploring this data is that prostate cancer develops more often in men of African ancestry than in men of other races. However, so far, prostate cancer genetic studies are based on the available data that mostly come from white men. This racial disparity has biased the discovery of genetic risk factors and therapeutic approaches, leading disparity in mortality rates

Project Purpose(s)

  • Disease Focused Research (prostate carcinoma)
  • Social / Behavioral
  • Ancestry

Scientific Approaches

I will design a two matched case-control studies black and white men. Thereafter, conduct a GWAS to identify variants and genes with higher mutation frequency. Next, I will identify genes mutated with larger functional impact through functional annotation analyses. Will repeat analysis using rare variants which will include rare variant association tests

Anticipated Findings

I anticipate finding novel variants and confirming prostate cancer risk variants that are specific to men of African ancestry. Doing so will increase the representation of African American men in prostate cancer genomic studies and increase African American awareness of early detection screening protocols.

Demographic Categories of Interest

  • Race / Ethnicity

Data Set Used

Controlled Tier

Research Team

Owner:

  • Deyana Lewis - Research Fellow, National Institutes of Health (NIH)

PCa_v7

Prostate Adenocarcinoma (PRAD) is associated with 1 in 25 African American men deaths, compared to 1 in 45 White American men deaths. Genetic and societal factors may contribute to this racial disparity and our project aims to shed light in…

Scientific Questions Being Studied

Prostate Adenocarcinoma (PRAD) is associated with 1 in 25 African American men deaths, compared to 1 in 45 White American men deaths. Genetic and societal factors may contribute to this racial disparity and our project aims to shed light in both factors. Our goals are to find ethnic specific risk factors using survey-based features and genetic risk factors using the genetic variants data.

Project Purpose(s)

  • Disease Focused Research (prostate cancer)
  • Population Health
  • Educational
  • Methods Development
  • Ancestry

Scientific Approaches

To achieve our goals we will use statistical tests and state-of-the-art tools to compare case and control genomes in order to identify variants that appear disproportionally in cases and genes with heavy variant load in cases. Such tools include the Evolutionary Action method and the software packages EMMAX and ACAT, amongst others.

Anticipated Findings

We anticipate obtaining lists of candidate genes and their variants that drive PRAD in African American men and in White American men, which we will contrast and compare with the current knowledge (e.g. BRCA1, BRCA2, and HOXB13 genes). This work may provide new genetic targets that affect the development and progression of PRAD, especially amongst the African American men and reduce the racial disparity in genetic risk diagnosis.

Demographic Categories of Interest

  • Race / Ethnicity

Data Set Used

Controlled Tier

Research Team

Owner:

Collaborators:

  • Jun Qian - Other, All of Us Program Operational Use

Dream_Team

Prostate Adenocarcinoma (PRAD) is associated with 1 in 25 African American men deaths, compared to 1 in 45 White American men deaths. Genetic and societal factors may contribute to this racial disparity and our project aims to shed light in…

Scientific Questions Being Studied

Prostate Adenocarcinoma (PRAD) is associated with 1 in 25 African American men deaths, compared to 1 in 45 White American men deaths. Genetic and societal factors may contribute to this racial disparity and our project aims to shed light in both factors. Our goals are to find ethnic specific risk factors using survey-based features and genetic risk factors using the genetic variants data.

Project Purpose(s)

  • Disease Focused Research (prostate cancer)
  • Population Health
  • Educational
  • Methods Development
  • Ancestry

Scientific Approaches

To achieve our goals we will use statistical tests and state-of-the-art tools to compare case and control genomes in order to identify variants that appear disproportionally in cases and genes with heavy variant load in cases. Such tools include the Evolutionary Action method and the software packages EMMAX and ACAT, amongst others.

Anticipated Findings

We anticipate obtaining lists of candidate genes and their variants that drive PRAD in African American men and in White American men, which we will contrast and compare with the current knowledge (e.g. BRCA1, BRCA2, and HOXB13 genes). This work may provide new genetic targets that affect the development and progression of PRAD, especially amongst the African American men and reduce the racial disparity in genetic risk diagnosis.

Demographic Categories of Interest

  • Race / Ethnicity

Data Set Used

Controlled Tier

Research Team

Owner:

Collaborators:

  • Jun Qian - Other, All of Us Program Operational Use

Duplicate of Introductory example of GWAS with type 2 diabetes phenotype

Not applicable - this workspace is intended to be an introductory example of how to do a genome-wide association study on the All of Us genomic data that individuals can easily click through and understand.

Scientific Questions Being Studied

Not applicable - this workspace is intended to be an introductory example of how to do a genome-wide association study on the All of Us genomic data that individuals can easily click through and understand.

Project Purpose(s)

  • Educational

Scientific Approaches

Not applicable - this workspace is intended to be an introductory example of how to do a genome-wide association study on the All of Us genomic data that individuals can easily click through and understand.

Anticipated Findings

Not applicable - this workspace is intended to be an introductory example of how to do a genome-wide association study on the All of Us genomic data that individuals can easily click through and understand.

Demographic Categories of Interest

This study will not center on underrepresented populations.

Data Set Used

Controlled Tier

Research Team

Owner:

  • Deyana Lewis - Research Fellow, National Institutes of Health (NIH)

Duplicate of How to Work with All of Us Genomic Data (Hail - Plink)(v6)

Not applicable - these notebooks demonstrate example analysis how to use Hail and PLINK to perform genome-wide association studies using the All of Us genomic data and phenotypic data.

Scientific Questions Being Studied

Not applicable - these notebooks demonstrate example analysis how to use Hail and PLINK to perform genome-wide association studies using the All of Us genomic data and phenotypic data.

Project Purpose(s)

  • Other Purpose (Demonstrate to the All of Us Researcher Workbench users how to get started with the All of Us genomic data and tools. It includes an overview of all the All of Us genomic data and shows some simple examples on how to use these data.)

Scientific Approaches

Not applicable - these notebooks demonstrate example analysis how to use Hail and PLINK to perform genome-wide association studies using the All of Us genomic data and phenotypic data.

Anticipated Findings

Not applicable - these notebooks demonstrate example analysis how to use Hail and PLINK to perform genome-wide association studies using the All of Us genomic data and phenotypic data.

Demographic Categories of Interest

This study will not center on underrepresented populations.

Data Set Used

Controlled Tier

Research Team

Owner:

  • Deyana Lewis - Research Fellow, National Institutes of Health (NIH)

Exploring Hypertension Data Types

Not applicable-this Workspace is intended for educational purposes at the 2022 UBR Faculty Summit to learn how to use the Researcher Workbench by analyzing a data type for hypertension.

Scientific Questions Being Studied

Not applicable-this Workspace is intended for educational purposes at the 2022 UBR Faculty Summit to learn how to use the Researcher Workbench by analyzing a data type for hypertension.

Project Purpose(s)

  • Educational

Scientific Approaches

Not applicable-this Workspace is intended for educational purposes at the 2022 UBR Faculty Summit to learn how to use the Researcher Workbench by analyzing a data type for hypertension.

Anticipated Findings

Not applicable-this Workspace is intended for educational purposes at the 2022 UBR Faculty Summit to learn how to use the Researcher Workbench by analyzing a data type for hypertension.

Demographic Categories of Interest

This study will not center on underrepresented populations.

Data Set Used

Registered Tier

Research Team

Owner:

  • Deyana Lewis - Research Fellow, National Institutes of Health (NIH)

Duplicate of Introductory example of GWAS with type 2 diabetes phenotype

Not applicable - this workspace is intended to be an introductory example of how to do a genome-wide association study on the All of Us genomic data that individuals can easily click through and understand.

Scientific Questions Being Studied

Not applicable - this workspace is intended to be an introductory example of how to do a genome-wide association study on the All of Us genomic data that individuals can easily click through and understand.

Project Purpose(s)

  • Educational

Scientific Approaches

Not applicable - this workspace is intended to be an introductory example of how to do a genome-wide association study on the All of Us genomic data that individuals can easily click through and understand.

Anticipated Findings

Not applicable - this workspace is intended to be an introductory example of how to do a genome-wide association study on the All of Us genomic data that individuals can easily click through and understand.

Demographic Categories of Interest

This study will not center on underrepresented populations.

Data Set Used

Controlled Tier

Research Team

Owner:

  • Deyana Lewis - Research Fellow, National Institutes of Health (NIH)
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