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- IFB French Institute of Bioinformatics2
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Scientific topic
- ChIP-seq
- Bioinformatics49
- Biological modelling16
- Biological system modelling16
- Systems biology16
- Systems modelling16
- Exomes15
- Genome annotation15
- Genomes15
- Genomics15
- Personal genomics15
- Synthetic genomics15
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- Biomedical research11
- Clinical medicine11
- Experimental medicine11
- General medicine11
- Internal medicine11
- Medicine11
- Bottom-up proteomics10
- Discovery proteomics10
- MS-based targeted proteomics10
- MS-based untargeted proteomics10
- Metaproteomics10
- Peptide identification10
- Protein and peptide identification10
- Proteomics10
- Quantitative proteomics10
- Targeted proteomics10
- Top-down proteomics10
- Computational pharmacology7
- Pharmacoinformatics7
- Pharmacology7
- Immunology5
- Bayesian methods4
- Biostatistics4
- Descriptive statistics4
- Gaussian processes4
- Inferential statistics4
- Markov processes4
- Multivariate statistics4
- Probabilistic graphical model4
- Probability4
- Statistics4
- Statistics and probability4
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Data management3
- High throughput sequencing3
- High-throughput sequencing3
- Metadata management3
- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Primer walking3
- Sanger sequencing3
- Sequencing3
- Targeted next-generation sequencing panels3
- Biomathematics2
- ChIP-exo2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Comparative transcriptomics2
- Computational biology2
- DNA variation2
- De novo genome sequencing2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- Mathematical biology2
- MicroRNA sequencing2
- Mutation2
- Polymorphism2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Theoretical biology2
- Transcriptome2
- Transcriptome profiling2
- Transcriptomics2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Active learning1
- Biological sequences1
- Biome sequencing1
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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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- France2
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- Registration of interest2
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