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Content provider
- IFB French Institute of Bioinformatics2
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Scientific topic
- RNA-Seq
- Bioinformatics60
- Exomes11
- Genome annotation11
- Genomes11
- Genomics11
- Personal genomics11
- Synthetic genomics11
- Viral genomics11
- Whole genomes11
- Bottom-up proteomics7
- Computational pharmacology7
- Discovery proteomics7
- MS-based targeted proteomics7
- MS-based untargeted proteomics7
- Metaproteomics7
- Peptide identification7
- Pharmacoinformatics7
- Pharmacology7
- Protein and peptide identification7
- Proteomics7
- Quantitative proteomics7
- Targeted proteomics7
- Top-down proteomics7
- Comparative transcriptomics3
- Transcriptome3
- Transcriptomics3
- Bayesian methods2
- Biological modelling2
- Biological system modelling2
- Biomedical research2
- Biostatistics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clinical medicine2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Descriptive statistics2
- Experimental medicine2
- Gaussian processes2
- General medicine2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- High throughput sequencing2
- High-throughput sequencing2
- Inferential statistics2
- Internal medicine2
- Markov processes2
- Medicine2
- MicroRNA sequencing2
- Multivariate statistics2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Polymorphism2
- Primer walking2
- Probabilistic graphical model2
- Probability2
- RNA sequencing2
- RNA-Seq analysis2
- Sanger sequencing2
- Sequencing2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Statistics2
- Statistics and probability2
- Systems biology2
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- Targeted next-generation sequencing panels2
- Transcriptome profiling2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Biome sequencing1
- Metagenomics1
- Protein databases1
- Protein expression1
- Shotgun metagenomics1
- Translation1
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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 courses
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- France2
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- Registration of interest2
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