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opportunities [2014/11/11 19:03]
dvuzman
opportunities [2018/10/16 14:53] (current)
cassa [Position available: Postdoctoral Fellow in Statistical Genetics]
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-We are currently looking for a postdoctoral fellow interested in identifying the roles of non-coding variants using whole genome sequencing of patients with rare Mendelian phenotypes. This position is in collaboration with Merck Research Labs. Interested candidates should contact Shamil with a CV and statement of research interests and background.  ​+=====Job Opportunities=====
  
-We have an opportunity ​for a postdoctoral fellow ​interested in a computational project on the functional effects ​of coding variantsGenerallypostdoctoral candidates ​with a strong background in computational biology, population genetics, protein ​structure or molecular evolution ​and interested ​in applications to human genetics ​are encouraged ​to contact Shamil.+Specific opportunities for postdoctoral fellows and staff scientists are posted on this page when available. Irrespectively of specific openings, we always encourage qualified candidates to contact us.  
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 +====Position available: Postdoctoral Fellow in Statistical Genetics==== 
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 +We have an opening ​for a statistical geneticist ​interested ​both in theory/​method development and analysis of large-scale sequencing, genotyping and epigenomics datasets. Potential projects include ​the analysis ​of regulatory variation; unresolved issues of allelic architecture and phenotype prediction; development of new methods for the analysis of large-scale sequencing datasetsExperience in statistical genetics will be considered as a significant plusand an understanding of evolutionary and/or human genetics is also helpful. However, we will consider all applicants ​with a strong ​quantitative ​background ​willing to learn and work at the forefront of this rapidly expanding field. ​  
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 +====Position available: Postdoctoral Fellow in Mendelian Human Genetics==== 
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 +We have an opening for a human geneticist with an interest in method development for variant prediction ​in Mendelian disorders using large-scale sequencinggenotyping and epigenomics datasets. Potential projects include the estimation of penetrance for disease variants; integration of protein ​structural information ​and relevant domains ​in functional predictions;​ development of new methods for the analysis of large-scale case and control sequencing datasets. Experience in Mendelian ​human genetics ​will be considered as a significant plus, and an understanding of statistical genetics and sequencing is also helpful. However, we will consider all applicants with a strong quantitative background willing ​to learn and work at the forefront of this rapidly expanding field