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Content provider
- IFB French Institute of Bioinformatics1
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Scientific topic
- Bioinformatics1
- ChIP-exo1
- ChIP-seq1
- ChIP-sequencing1
- Chip Seq1
- Chip sequencing1
- Chip-sequencing1
- Chromosome walking1
- Clone verification1
- DNA variation1
- DNA-Seq1
- DNase-Seq1
- De novo genome sequencing1
- Exomes1
- Genetic variation1
- Genome annotation1
- Genome sequencing1
- Genomes1
- Genomic variation1
- Genomics1
- High throughput sequencing1
- High-throughput sequencing1
- MicroRNA sequencing1
- Mutation1
- NGS1
- NGS data analysis1
- Next gen sequencing1
- Next generation sequencing1
- Panels1
- Personal genomics1
- Polymorphism1
- Primer walking1
- RNA sequencing1
- RNA-Seq1
- RNA-Seq analysis1
- Sanger sequencing1
- Sequencing1
- Small RNA sequencing1
- Small RNA-Seq1
- Small-Seq1
- Somatic mutations1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Transcriptome profiling1
- Viral genomics1
- WGS1
- WTSS1
- Whole genome resequencing1
- Whole genome sequencing1
- Whole genomes1
- Whole transcriptome shotgun sequencing1
- miRNA-seq1
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Operation
- Mutation detection
- 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
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Event type
- Workshops and courses1
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Country
- France1
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Eligibility
- Registration of interest1
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