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innovation proposals for European and national funding programmes (e.g., Horizon Europe, Erasmus, AEI calls, etc.), ensuring alignment with call requirements and institutional priorities. - Budget Preparation
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and operability of encoding techniques for scientific data such as those generated by synchrotrons, DNA sequencing and space. Synchrotrons, DNA sequencing, satellites and Earth observatories produce
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diverse environments in suitable vectors; (iii) adapt existing enzyme assays to droplet format; (iv) screen libraries from metagenomes; v) sequence and structure determination, biochemical and
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in Nursing. b) EXPERIENCE • Training in Multiple Sclerosis of at least 5 years. c) OTHER REQUIREMENTS • Master’s Degree in Multiple Sclerosis. • Experience in handling electronic case report forms
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businesses) · Establishing and supervising work protocols for each project (extraction, sequencing, assembly, analysis, etc.) · Fostering the platform’s promotion and visibility both regionally and nationally
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(1580-1750), including digital scores (MusicXML, MIDI, MuseScore), harmonic annotations, text, and audio. To develop an optimized sequencing format for training Large Language Models (LLMs) on symbolic
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Institut de Recerca Biomèdica de Lleida, Fundació Dr. Pifarré (IRBLleida) | Spain | about 2 months ago
with miRNA, including extraction, detection, and inhibition assays, as well as basic bioinformatic analysis of sequencing data -Proficiency in cell culture techniques, including transfection and
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of the work and experimental work: Cell Sorting Flow cytometry: cell marking and analysis. Cell cultures Molecular biology techniques: massive sequencing techniques; processing of biological samples DNA, RNA
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, RT-PCR). Data and Bioinformatics: Genomic and transcriptomic analysis. Comparative genomics of pathogens and hosts. Phylogenetic analysis and sequence databases. Statistical analysis of biological
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applying innovative technologies, such as genome sequencing and optical genome mapping, in patients with a high suspicion of genetic etiology after routine genetic testing methods have been non-conclusive