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Content provider
- IFB French Institute of Bioinformatics2
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Scientific topic
- Bioinformatics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Exomes2
- Genetic variation2
- Genome annotation2
- Genome sequencing2
- Genomes2
- Genomic variation2
- Genomics2
- High throughput sequencing2
- High-throughput sequencing2
- MicroRNA sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Personal genomics2
- Polymorphism2
- Primer walking2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sanger sequencing2
- Sequencing2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Synthetic genomics2
- Targeted next-generation sequencing panels2
- Transcriptome profiling2
- Viral genomics2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole genomes2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
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Operation
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- Expression analysis2
- Expression data analysis2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Metagenomic inference2
- Microarray data analysis2
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Plotting2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Rendering2
- Sequence alignment2
- Sequence alignment (constrained)2
- Sequence alignment construction2
- Sequence alignment generation2
- Sequence read pre-processing2
- Sequence variation analysis2
- Short oligonucleotide alignment2
- Short read alignment2
- Short read mapping2
- Short sequence read mapping2
- Transcript variant analysis2
- Variant analysis2
- Visualisation2
- Allele calling1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses2
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Country
- France2
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Target audience
- Cette formation est destinée aux biologistes (i...
- PhD students10
- post-docs7
- Academics5
- Researchers5
- Industry4
- Life Science Researchers3
- Medical Device2
- PhD2
- PhD Students2
- bioinformaticians2
- postgrad2
- R&D engineers1
- Bench biologists1
- Biologists1
- Biologists, Genomicists, Computer Scientists1
- Biotech1
- Compliance Engineering1
- Data Managers1
- Data stewards1
- Early Career Researchers (ECRs)1
- Master students1
- Modeller1
- Molecular Biologists1
- Pathologists1
- PhD candidates1
- Pharmaceutical1
- Postdoctoral Researchers1
- Postdoctoral students1
- Principal Investigators (PIs)1
- Professors1
- Quality Assurance & Control1
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- Researcher in life sciences1
- Students1
- Technicians1
- Wet-lab Researchers1
- auditors1
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- engineers1
- laboratory professionals1
- life scientists1
- postdocs1
- postdoctoral researchers1
- product-development professionals1
- quality/production managers1
- regulatory/quality professionals1
- researchers1
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Eligibility
- Registration of interest2
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