13 data-"https:" "https:" "https:" "https:" "Paris Saclay university" positions at Centre for Genomic Regulation
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was established in October 2018 and is part of the “Computational Biology and Health Genomics” program at the CRG. Further information can be found at https://weghornlab.org/ and at www.crg.eu/en/programmes-groups
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3 Mar 2026 Job Information Organisation/Company Centre for Genomic Regulation Research Field Other Researcher Profile First Stage Researcher (R1) Positions Postdoc Positions Application Deadline 18
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26 Feb 2026 Job Information Organisation/Company Centre for Genomic Regulation Research Field Computer science » Other Researcher Profile First Stage Researcher (R1) Positions Bachelor Positions
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organizational skills to manage high-throughput experimental workflows and data and capable of working at agile paces Strong problem-solving abilities, with a proactive and innovative mindset. Effective
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18 Feb 2026 Job Information Organisation/Company Centre for Genomic Regulation Research Field Other Researcher Profile First Stage Researcher (R1) Positions Master Positions Application Deadline 19
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contact details. Contact details of two referees. All applications must be addressed to Dr. Lars Velten and be submitted online on the CRG Career site - http://www.crg.eu/en/content/careers/job
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23 Dec 2025 Job Information Organisation/Company Centre for Genomic Regulation Research Field Other Researcher Profile First Stage Researcher (R1) Recognised Researcher (R2) Positions Master
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Outbred Rats (https://ratgenes.org/ ). Whom would we like to hire? Professional experience Must Have You have proven experience reconstructing MAGs from deep shotun sequencing data and, ideally, long read
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). The candidate will design and apply integrative data analysis (computational/statistical/causal) and visualization techniques for multi-omic (transcriptomics, mirnomic and proteomics) data to address research
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for the analysis of DNA sequencing data derived from a unique cohort of animal tumors. Responsibilities will include aligning DNA sequencing reads to reference genome scaffolds, calling mutations and conducting