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- IFB French Institute of Bioinformatics2
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Scientific topic
- ChIP-seq
- Bioinformatics28
- Exomes20
- Genome annotation20
- Genomes20
- Genomics20
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- Bottom-up proteomics3
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Discovery proteomics3
- High throughput sequencing3
- High-throughput sequencing3
- MS-based targeted proteomics3
- MS-based untargeted proteomics3
- Metaproteomics3
- MicroRNA sequencing3
- NGS3
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- Next gen sequencing3
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- Panels3
- Peptide identification3
- Primer walking3
- Protein and peptide identification3
- Proteomics3
- Quantitative proteomics3
- RNA sequencing3
- RNA-Seq3
- RNA-Seq analysis3
- Sanger sequencing3
- Sequencing3
- Small RNA sequencing3
- Small RNA-Seq3
- Small-Seq3
- Targeted next-generation sequencing panels3
- Targeted proteomics3
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- Transcriptome profiling3
- WTSS3
- Whole transcriptome shotgun sequencing3
- miRNA-seq3
- Antimicrobial stewardship2
- Applied ontology2
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- Biological sequences2
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- ChIP-exo2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Computational chemistry2
- DNA variation2
- Data curation2
- Data provenance2
- Data submission, annotation, and curation2
- Database curation2
- De novo genome sequencing2
- Descriptive statistics2
- Epidemiology2
- Gaussian processes2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- Inferential statistics2
- Markov processes2
- Medical microbiology2
- Microbial genetics2
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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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