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  • ChrisMaher
    Junior Member
    • Aug 2011
    • 9

    Postdoctoral Scholar in Cancer Genetics/Bioinformatics

    A Postdoctoral Scholar position in the area of Cancer Genomics and Bioinformatics is available in the laboratory of Dr. Christopher Maher (www.maherlab.com) at The McDonnell Genome Institute at the Washington University School of Medicine in St. Louis. Our lab focuses on developing computational methods for analyzing large-scale cancer genomics data collections from solid tumors to improve our understanding of non-coding RNA biology, identify novel diagnostic/prognostic biomarkers, and develop novel treatment strategies to improve patient care. The candidate will also work closely with cancer biologists to test/validate their computational analyses.

    Preferred Qualifications

    --Recent Ph.D. in Bioinformatics, Computational Biology, Computer Science, Engineering or a related field

    -- Expertise in programming and statistics is required. Candidates should be comfortable working on UNIX/Linux operating system, program with Perl and/or Python, and familiar with statistical analysis packages (SAS, R, or Bioconductor).

    -- Experience with bioinformatics tools and analysis of omics datasets is required. Experience with machine learning / data mining is preferred. Previous experience in cancer genomics would be an advantage but is not mandatory.

    -- The successful candidate will be self-motivated, eager to acquire new knowledge and skills on a regular basis, and must demonstrate independent and critical thinking skills.

    -- Must be able to analyze and interpret results, communicate results with an inter-disciplinary team, and have scientific writing experience (i.e., solid track record of scientific publications).

    Benefits

    This opportunity is eligible for full-time benefits. Please visit our website at http://hr.wustl.edu to view a summary of benefits.

    Review of applications will begin immediately and will continue until the position is filled. Please send a CV to Dr. Christopher Maher ([email protected])

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  • SEQadmin2
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    I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

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