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- Anyone interested in bioinformatics1
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- The course is aimed at research scientists with a minimum of a degree in a biological discipline, including laboratory and clinical staff, as well as specialists in related fields.1
- This webinar is aimed at scientists with an interest in learning more about the Europe PMC and optimising their literature searches.1
- This workshop is aimed at PhD students within the PhD programme "Genetics, Molecular and Cellular Biology" (University of Pavia) and the PhD programmme "Biomolecular Sciences and Biotechnology" (IUSS, University School for Advanced Studies Pavia.1
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- posit-conf-202321
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- Input datasets34
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- 2nd PaN EOSC Symposium6
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- Assembly slides3
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- Part 33
- Part 43
- ChIP-Seq data analysis dataset2
- Epigenetics dataset2
- Galaxy Server administration slides2
- Genome Annotation dataset2
- McStas2
- Metagenomics dataset2
- Part 22
- Part 52
- Part 62
- Part 72
- Part 82
- Part 92
- Sequence analysis slides2
- Assessing the FAIRness of a prototypical PaN instrument at BESSY II Talk (slides)1
- Beacon v2: a discovery tool for genomic and pheno-clinical data1
- Booklet of presentations1
- Browse the PaNET ontology in BioPortal1
- COBRA Toolbox1
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- Contributing to the Galaxy Training Material slides1
- DCAT V21
- DMPortal1
- Data Stewardship Wizard1
- Demeter github1
- Demeter github.io1
- DisGeNET: a discovery platform designed to address a variety of questions concerning the genetic underpinning of human diseases1
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- EGA Submitter Portal Tutorial1
- ELIXIR's Impact Toolkit1
- EOSC Symposium 2022 plenary1
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- GPAP: the RD-Connect Genome-Phenome Analysis Platform for diagnosis and gene discovery in rare disease research1
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- Genome Annotation slides1
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- Introduction to Galaxy Analyses dataset1
- Introduction to Galaxy dataset1
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- Part 101
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- Part 2b1
- Part 3/31
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- Slides | Beacon v2: a discovery tool for genomic and pheno-clinical data1
- Slides | DisGeNET: a discovery platform designed to address a variety of questions concerning the genetic underpinning of human diseases1
- Slides | GPAP: the RD-Connect Genome-Phenome Analysis Platform for diagnosis and gene discovery in rare disease research1
- Slides | Introduction to the EGA and sharing sensitive data1
- Statistics dataset1
- TELBE workflow1
- Transcriptomics slides1
- UmbrellaID Workshop : 3rd of May, github1
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- VEIS webinar: The essentials of DUO codes | Presentation1
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- PHENotyping and EnviroTyping (PHENET training collection)19
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