Cancer Genomics Postdoc: Polygenic Risk Scores

The University of Manchester

Manchester

Presencial

GBP 35.000 - 50.000

Jornada completa

Hace 6 días
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Ventajas ofrecidas por este puesto de trabajo

Pension scheme
29 days annual leave + bank holidays
Ride to work scheme
EV car scheme

Descripción de la vacante

The University of Manchester invites applications for a post-doctoral research associate/fellow with cancer genomics experience to join the GP-TEST-Pro study. You will analyse genomic data and calculate prostate cancer polygenic risk scores within a multidisciplinary team spanning several institutions.

Responsibilities include secure data handling, genotype QC, using PLINK/PLINK2, imputation outputs and exploring additional genomic markers.

Formación

  • PhD in a relevant field such as genetic epidemiology, statistical genetics, bioinformatics or cancer genomics.
  • Hands-on analysis of genetic/genomic datasets in cancer research.
  • Experience with quality control of genotype/imputed data and population structure.

Responsabilidades

  • Analyse genomic data and calculate polygenic risk scores for prostate cancer.
  • securely store and manage data under governance requirements.
  • perform QC at sample and variant levels and assess population structure.
  • use PLINK/PLINK2 and imputation outputs to clean and analyse data.
  • evaluate additional genomic markers or PRS methods relevant to detection.

Conocimientos

PhD in genetics
Cancer genomics experience
Genotype QC
PRS calculation
Genetic epidemiology concepts

Educación

PhD in relevant field

Herramientas

PLINK/PLINK2
Imputation server outputs

Descripción del empleo

The University of Manchester invites applications for a post-doctoral research associate/fellow with cancer genomics experience to join the GP-TEST-Pro study. You will analyse genomic data and calculate prostate cancer polygenic risk scores within a multidisciplinary team spanning several institutions.

Responsibilities include secure data handling, genotype QC, using PLINK/PLINK2, imputation outputs and exploring additional genomic markers.

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