- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- iAnn1
- Show N_FILTERS more
-
-
-
Keyword
- NGS
- HDRUK284
- bioinformatics130
- ISCB122
- OtherEvents98
- Galaxy64
- Bioinformatics57
- Ensembl29
- DNA & RNA (dna-rna)28
- ABR27
- RNA-Seq26
- Ensembl Variant Effect Predictor23
- Ensembl Genomes22
- ISCBCo-SponsoredorAffiliatedEvent17
- life sciences17
- Nextflow13
- Workflows11
- metagenomics11
- ISCBEvent10
- Python9
- Snakemake9
- R-programming8
- Data analysis8
- Docker8
- HPC8
- lifescience8
- ISCBEvents7
- VLSCI7
- Cross domain (cross-domain)6
- Programming6
- RNA-Seq6
- SoftwareCarpentry6
- Unix6
- microscopy6
- toxicogenomics6
- Computer Programming5
- Genomics5
- Metabolomics5
- Project management5
- Proteomics5
- Team building5
- data management5
- genome browsing5
- Budgeting4
- ComputationalBiology4
- Containers4
- Core facility services4
- Data management plan4
- Git4
- Introductory4
- Linux4
- Principal investigators4
- Variant calling4
- genomics4
- machine learning4
- supercomputer4
- toxicology4
- Linux3
- CWL3
- Cloud computing3
- Computational Biology3
- DNA-seq3
- Diseases3
- EMBnet3
- EeLP3
- Gene expression (gene-expression)3
- H3Africa genotyping array3
- High performance computing3
- Introduction to bioinformatics3
- NGS bioinformatics3
- Population Genomics3
- Protein Data Bank in Europe3
- Python for Biologists3
- Reproducibility3
- Transcriptomics3
- eLearning3
- genes3
- linux3
- metadata3
- nf-core3
- python3
- transcriptomics3
- workflows3
- Statistics2
- African populations2
- Artificial Intelligence2
- Big Data2
- BioModels database2
- Biological databases2
- COMBINE2
- Clinical Bioinformatics2
- Command line2
- Diagnosis2
- European Nucleotide Archive2
- Expression Atlas2
- GWAS workflow2
- Gene Expression2
- Genome Assembly2
- Genome Wide Association Studies2
- Genotype calling2
- Show N_FILTERS more
-
-
-
Scientific topic
- Bioinformatics
- 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
- 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
- Codon usage1
- 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
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses4
- Show N_FILTERS more
-
-
-
Country
- Italy1
- United Kingdom1
- Show N_FILTERS more
-
-
-
Organizer
- ecSeq Bioinformatics GmbH2
- 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
- University of Leicester1
- Show N_FILTERS more
-
-
-
Sponsor
- ELIXIR Italy1
- Show N_FILTERS more
-
-
-
Target audience
- Biologists2
- Biologists, Genomicists, Computer Scientists2
- Molecular Biologists2
- Pathologists2
- bioinformaticians2
- post-docs2
- PhD Students1
- PhD students1
- PhD students and young researchers in the life science and computational biology field who are planning to use RNA-seq data and are looking for the best practices to analyze these types of data1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events