- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Scientific topic
- DNA-Seq
- DNA variation4
- Genetic variation4
- Genomic variation4
- Mutation4
- Polymorphism4
- Somatic mutations4
- Bioinformatics3
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- Personal genomics3
- Synthetic genomics3
- Viral genomics3
- Whole genomes3
- Chromosome walking2
- Clone verification2
- DNase-Seq2
- De novo genome sequencing2
- Genome sequencing2
- High throughput sequencing2
- High-throughput sequencing2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Primer walking2
- Sanger sequencing2
- Sequencing2
- Targeted next-generation sequencing panels2
- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Biomarkers1
- Biotherapeutics1
- Cancer1
- Cancer biology1
- ChIP-exo1
- ChIP-seq1
- ChIP-sequencing1
- Chip Seq1
- Chip sequencing1
- Chip-sequencing1
- Diagnostic markers1
- MicroRNA sequencing1
- Neoplasm1
- Neoplasms1
- Oncology1
- Pipelines1
- RNA sequencing1
- RNA-Seq1
- RNA-Seq analysis1
- Small RNA sequencing1
- Small RNA-Seq1
- Small-Seq1
- Software integration1
- Tool integration1
- Tool interoperability1
- Transcriptome profiling1
- WTSS1
- Whole transcriptome shotgun sequencing1
- Workflows1
- miRNA-seq1
- Show N_FILTERS more
-
-
-
Operation
- Allele calling
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- Exome variant detection2
- Expression analysis2
- Expression data analysis2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Genome variant detection2
- Germ line variant calling2
- Metagenomic inference2
- Microarray data analysis2
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Mutation detection2
- 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
- Somatic variant calling2
- Transcript variant analysis2
- Variant analysis2
- Variant calling2
- Variant mapping2
- Visualisation2
- de novo mutation detection2
- Alternative splicing analysis1
- Alternative splicing detection1
- Alternative splicing prediction1
- Cartography1
- Differential expression analysis1
- Differential gene analysis1
- Differential gene expression analysis1
- Differential gene expression profiling1
- Differential splicing analysis1
- Differentially expressed gene identification1
- Mapping1
- Optimisation and refinement1
- Sequencing QC1
- Sequencing quality assessment1
- Sequencing quality control1
- Splice transcript prediction1
- Split read mapping1
- Split-read mapping1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses2
- Show N_FILTERS more
-
-
-
Country
- France1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events