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Keyword
- NGS
- Gene expression (gene-expression)5
- Expression Atlas4
- HDRUK4
- ArrayExpress Archive of Functional Genomics Data3
- Bioinformatics2
- Gene Expression2
- Advances in spatial omics1
- DNA & RNA (dna-rna)1
- Data Integration1
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- High Throughput Sequencing Analysis1
- Introduction to single cell expression atlas1
- Life cell by cell1
- Nextflow1
- Pathway analysis1
- RNA-Seq1
- RNA-seq1
- SCEA1
- Sequence Analysis1
- Single Cell Expression Atlas1
- Single cell RNA-seq1
- Spatial transcriptomics1
- Workflows1
- Workshop1
- machine learning1
- nf-core1
- omics data1
- single-cells1
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Scientific topic
- DNA microarrays
- High-throughput sequencing6
- Chromosome walking5
- Clone verification5
- DNA-Seq5
- DNase-Seq5
- Exomes5
- Genome annotation5
- Genomes5
- Genomics5
- High throughput sequencing5
- NGS5
- NGS data analysis5
- Next gen sequencing5
- Next generation sequencing5
- Panels5
- Personal genomics5
- Primer walking5
- Sanger sequencing5
- Sequencing5
- Synthetic genomics5
- Targeted next-generation sequencing panels5
- Viral genomics5
- Whole genomes5
- Bioinformatics3
- Antimicrobial stewardship2
- Assembly2
- Biological sequences2
- Cancer2
- Cancer biology2
- Communicable disease2
- DNA polymorphism2
- DNA variation2
- Epidemiology2
- Genetic variation2
- Genomic variation2
- Infectious disease2
- Medical microbiology2
- Microbial genetics2
- Microbial physiology2
- Microbial surveillance2
- Microbiological surveillance2
- Microbiology2
- Microsatellites2
- Molecular infection biology2
- Molecular microbiology2
- Mutation2
- Neoplasm2
- Neoplasms2
- Oncology2
- Phylogenetic clocks2
- Phylogenetic dating2
- Phylogenetic simulation2
- Phylogenetic stratigraphy2
- Phylogeny2
- Phylogeny reconstruction2
- Polymorphism2
- Public health2
- Public health and epidemiology2
- RFLP2
- SNP2
- Sequence analysis2
- Sequence assembly2
- Sequence databases2
- Single nucleotide polymorphism2
- Somatic mutations2
- Transmissible disease2
- VNTR2
- Variable number of tandem repeat polymorphism2
- snps2
- Allele calling1
- Alternative splicing1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Codon usage1
- Comparative transcriptomics1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- DNA chips1
- De novo genome sequencing1
- Exome variant detection1
- Expression1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Genome sequencing1
- Genome variant detection1
- Germ line variant calling1
- MicroRNA sequencing1
- Mutation detection1
- Pipelines1
- RNA sequencing1
- RNA splicing1
- RNA-Seq1
- RNA-Seq analysis1
- SNP calling1
- SNP detection1
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- Workshops and courses1
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- Italy1
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- ELIXIR Italy1
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