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- IFB French Institute of Bioinformatics2
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Scientific topic
- RNA-Seq
- Bioinformatics13
- Exomes5
- Genome annotation5
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- Personal genomics5
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- MicroRNA sequencing4
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- Biomedical research3
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- Algorithms2
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- ChIP-exo2
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- Chip Seq2
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- Chromosome walking2
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- Data structures2
- De novo genome sequencing2
- Descriptive statistics2
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- High throughput sequencing2
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- LC-MS-based metabolomics2
- MS-based metabolomics2
- MS-based targeted metabolomics2
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- Metabolites2
- Metabolome2
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- Sanger sequencing2
- Sequencing2
- Software development2
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- Somatic mutations2
- Statistics2
- Statistics and probability2
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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 courses4
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