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Scientific topic
- Sequencing
- Bioinformatics19
- Exomes10
- Genome annotation10
- Genomes10
- Genomics10
- Personal genomics10
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- Bayesian methods3
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- Chromosome walking3
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- DNase-Seq3
- Descriptive statistics3
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- NGS3
- NGS data analysis3
- Next gen sequencing3
- Next generation sequencing3
- Panels3
- Primer walking3
- Probabilistic graphical model3
- Probability3
- RNA sequencing3
- RNA-Seq3
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- Sanger sequencing3
- Small RNA sequencing3
- Small RNA-Seq3
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- Statistics3
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- Targeted next-generation sequencing panels3
- Transcriptome profiling3
- WTSS3
- Whole transcriptome shotgun sequencing3
- miRNA-seq3
- Biological modelling2
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- ChIP-exo2
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- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- DNA variation2
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- Genetic variation2
- Genome sequencing2
- Genomic variation2
- Mutation2
- Polymorphism2
- Somatic mutations2
- Systems biology2
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- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Biodiversity1
- Bottom-up proteomics1
- Comparative genomics1
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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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