Job ID:
Job date: 2014-10-01
End Date:
Company : Regeneron Pharmaceuticals Country : Role : Research Scientist
Job date: 2014-10-01
End Date:
Company : Regeneron Pharmaceuticals Country : Role : Research Scientist
Job Description:
Job Location: Tarrytown, NY Auto req ID: 2360BR Job Posting Title: Bioinformatics R&D Developer Person Type: Regular Posting Category: Regeneron Genetics Center Location: Tarrytown Job Summary And Essential Functions The Regeneron Genetics Center is a wholly-owned subsidiary of the Company organized to collaborate with health systems and research groups to elucidate, on a large scale, genetic factors that cause or influence a range of human diseases. Building upon Regeneron's strengths in mouse genetics and genetics-driven drug discovery and development, the Center will specialize in ultra-high-throughput exome sequencing and computational biology; discovery of genotype-phenotype associations through linkage to well-annotated de-identified patient electronic medical records; and validation of discoveries using Regeneron’s VelociGene® technology. Our interests encompass a breadth of different areas such as Mendelian and family frameworks, large-scale population genetics (both common and rare variants), and gene-gene interactions. Program goals include target discovery, indication discovery, and patient-disease stratification. Objectives include advancing basic science around the world through public sharing of discoveries, providing clinically-valuable insights to physicians and patients of collaborating health-care systems, and identifying novel targets for drug development. We Are Looking For a Bioinformatics Scientist To Analyze Proprietary Human Genetic Variation Data And Associated Medical Information To Uncover Gene-disease Links And New Targets, New Indications For Existing Drug Targets, And New Ways To Stratify Disease-bearing Populations. Implement And Develop Analysis Pipeline Using Cutting-edge Algorithms And Statistically Sound Methodologies. This Scientist Will
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Job Location: Tarrytown, NY Auto req ID: 2360BR Job Posting Title: Bioinformatics R&D Developer Person Type: Regular Posting Category: Regeneron Genetics Center Location: Tarrytown Job Summary And Essential Functions The Regeneron Genetics Center is a wholly-owned subsidiary of the Company organized to collaborate with health systems and research groups to elucidate, on a large scale, genetic factors that cause or influence a range of human diseases. Building upon Regeneron's strengths in mouse genetics and genetics-driven drug discovery and development, the Center will specialize in ultra-high-throughput exome sequencing and computational biology; discovery of genotype-phenotype associations through linkage to well-annotated de-identified patient electronic medical records; and validation of discoveries using Regeneron’s VelociGene® technology. Our interests encompass a breadth of different areas such as Mendelian and family frameworks, large-scale population genetics (both common and rare variants), and gene-gene interactions. Program goals include target discovery, indication discovery, and patient-disease stratification. Objectives include advancing basic science around the world through public sharing of discoveries, providing clinically-valuable insights to physicians and patients of collaborating health-care systems, and identifying novel targets for drug development. We Are Looking For a Bioinformatics Scientist To Analyze Proprietary Human Genetic Variation Data And Associated Medical Information To Uncover Gene-disease Links And New Targets, New Indications For Existing Drug Targets, And New Ways To Stratify Disease-bearing Populations. Implement And Develop Analysis Pipeline Using Cutting-edge Algorithms And Statistically Sound Methodologies. This Scientist Will
- Collaborate with scientists from Human Genetics, Pre-clinical, and Clinical departments to design experiments linking variation to medical information. Communicate results with scientists, refine analysis based on feedback, and plan/prioritize follow-up experiments. Prepare clear, concise and easy-to-understand presentations and documentation for collaborators, senior management and regulatory agencies.
- Have responsibility for variant calling and filtering as part of DNA analysis pipelines and subsequent association analyses.
- Analyze proprietary and public genetics data to support identification of new drug targets.
- Analyze proprietary and public genetics data to suggest new indications for existing drug therapeutics.
- Analyze proprietary and public genetics data to support Clinical studies
- Analyze proprietary and public genetics data to suggest new disease stratification strategies.
- Participate in team effort of organizing and integrating proprietary and public genetics data to enable data sharing and visualization for bench scientists.
- Contribute to team effort of developing genetics analytical strategies and establishing data analysis best practices.
- Expertise in analysis of human next-generation sequencing data and knowledge of best practices.
- Expertise in assessment of genetic variation and deleterious effects.
- Experience in analysis genetic sequencing data in the public domain.
- Familiarity with modeling (e.g., machine learning) and network building (e.g. gene regulation networks), as well as a keen interest and determination to be at the cutting-edge of algorithms and model building.
- Experience with relevant Sequencing Analysis tools; such as BWA, GATK, SAMtools or related.
- Experience with NGS HLA sequence analysis and/or HLA typing a plus
- Understanding of the complexities of genomic analysis work in highly variable and difficult to sequence genomic regions a must
- Familiarity with bioinformatics tools and software such as R, Linux, Perl, Python, Ruby, Java, Ruby on Rails, MatLab, SQL, and web development tools.
- Ability to work both independently and collaboratively with commitment to share data across the organization.
- Excellent communication and presentation skills required.
- Experience with Cloud-based analytical tools and parallel processing is strongly preferred, but not required
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