Nandita Mukhopadhyay

Project Personnel, University of Pittsburgh

4 active projects

Cleft_regions_stomach_cancer_Aug10_2023

The goal of this research is to test whether variants in orofacial cleft risk genes are associated with risk of cancer.

Scientific Questions Being Studied

The goal of this research is to test whether variants in orofacial cleft risk genes are associated with risk of cancer.

Project Purpose(s)

  • Ancestry

Scientific Approaches

Subjects with a known cancer status will be extracted and analyzed using logistic regression to their array genotypes in selected regions. HAIL and/or PLINK will be used. Following single variant association on common variants, we will also run rare-variant association and gene-set analysis.

Anticipated Findings

Prior studies have reported increased risk of certain types of cancer in individuals born with an orofacial cleft defect, as well as higher rates of cancer in the relatives of affected subjects. This indicates that the two phenotypes may share a common genetic etilogy We intend to study if this is true in the All of Us research subjects.

Demographic Categories of Interest

This study will not center on underrepresented populations.

Data Set Used

Controlled Tier

Research Team

Owner:

Cleft_regions_stomach_cancer

The goal of this research is to test whether variants in orofacial cleft rish genes are associated with risk of cancer.

Scientific Questions Being Studied

The goal of this research is to test whether variants in orofacial cleft rish genes are associated with risk of cancer.

Project Purpose(s)

  • Ancestry

Scientific Approaches

Subjects with a known cancer status will be extracted and analyzed using logistic regression to their array genotypes in selected regions. HAIL and/or PLINK will be used. Following single variant association on common variants, we will also run rare-variant association and gene-set analysis.

Anticipated Findings

Prior studies have reported increased risk of certain types of cancer in individuals born with an orofacial cleft defect, as well as higher rates of cancer in the relatives of affected subjects. This indicates that the two phenotypes may share a common genetic etilogy We intend to study if this is true in the All of Us research subjects.

Demographic Categories of Interest

This study will not center on underrepresented populations.

Data Set Used

Controlled Tier

Research Team

Owner:

Genomic Data (Hail - Plink)(v7) copy

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)

  • Ancestry
  • 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:

Extraction of Stomach tumor Data (Hail - Plink)

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)

  • Ancestry
  • 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:

Collaborators:

  • Henry Condon - Project Personnel, All of Us Program Operational Use
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