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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
- Data analysis1
- Data integration1
- Ensembl1
- Functional analysis1
- Gene regulation1
- Genome1
- Genomic data1
- 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
- Codon usage
- High-throughput sequencing7
- Chromosome walking6
- Clone verification6
- DNA-Seq6
- DNase-Seq6
- High throughput sequencing6
- NGS6
- NGS data analysis6
- Next gen sequencing6
- Next generation sequencing6
- Panels6
- Primer walking6
- Sanger sequencing6
- Sequencing6
- Targeted next-generation sequencing panels6
- Bioinformatics4
- Exomes4
- Genome annotation4
- Genomes4
- Genomics4
- Personal genomics4
- Synthetic genomics4
- Viral genomics4
- Whole genomes4
- Biological sequences2
- Cancer2
- Cancer biology2
- MicroRNA sequencing2
- Neoplasm2
- Neoplasms2
- Oncology2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sequence analysis2
- Sequence databases2
- Sequences2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Transcriptome profiling2
- WTSS2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Allele calling1
- Alternative splicing1
- Antimicrobial stewardship1
- Assembly1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Communicable disease1
- Comparative transcriptomics1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- DNA chips1
- DNA microarrays1
- DNA polymorphism1
- DNA variation1
- De novo genome sequencing1
- Epidemiology1
- Exome variant detection1
- Expression1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Genetic variation1
- Genome sequencing1
- Genome variant detection1
- Genomic variation1
- Germ line variant calling1
- Infectious disease1
- Medical microbiology1
- Microbial genetics1
- Microbial physiology1
- Microbial surveillance1
- Microbiological surveillance1
- Microbiology1
- Microsatellites1
- Molecular infection biology1
- Molecular microbiology1
- Mutation1
- Mutation detection1
- Phylogenetic clocks1
- Phylogenetic dating1
- Phylogenetic simulation1
- Phylogenetic stratigraphy1
- Phylogeny1
- Phylogeny reconstruction1
- Pipelines1
- Polymorphism1
- Public health1
- Public health and epidemiology1
- RFLP1
- RNA splicing1
- SNP1
- SNP calling1
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Event type
- Workshops and courses1
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Country
- Italy1
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Organizer
- Anna Marabotti (University of Salerno and ELIXIR-IIB Training Team, Italy), Roberto Tagliaferri (University of Salerno, Italy), Alessandro Weisz (University of Salerno, Italy), Loredana Le Pera (ELIXIR-IIB Training Team and IIT, Italy), Allegra Via (ELIXIR-IIB Training Coordinator, CNR-IBPM, Italy) 1
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Sponsor
- ELIXIR Italy1
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