- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- European Bioinformatics Institute (EBI)4
- Show N_FILTERS more
-
-
-
Keyword
- HDRUK1511
- training202
- bioinformatics198
- ISCB160
- OtherEvents131
- online116
- omics109
- programming105
- communication skills91
- ELIXIR84
- statistics83
- Bioinformatics81
- Proteins (proteins)78
- personal effectiveness72
- software70
- Galaxy69
- DNA & RNA (dna-rna)65
- advanced bioinformatics65
- Ensembl60
- ABR59
- data management59
- career development56
- genes and genomes53
- R52
- data visualisation49
- hands-on49
- next generation sequencing46
- research data management46
- torsten schwede & thierry sengstag group45
- UniProt: The Universal Protein Resource43
- DMP42
- NGS42
- basic bioinformatics41
- mark ibberson group40
- biostatistics38
- functional genomics38
- reproducibility38
- transcriptomics36
- Data management34
- ELIXIR-CONVERGE34
- FAIR34
- experimental biology33
- RNA-seq31
- high-performance computing30
- HPC29
- eLearning29
- leadership & management29
- life sciences29
- EeLP28
- Ensembl Variant Effect Predictor28
- data analysis28
- grant writing28
- rémy bruggmann group28
- tess28
- microscopy27
- API26
- CONVERGE26
- Ensembl Genomes26
- Genomics24
- Python23
- RNA-Seq22
- Data management plan22
- Protein Data Bank in Europe22
- Workflows22
- machine learning22
- medicine and health22
- Nextflow21
- Data analysis20
- imaging20
- metadata20
- R-programming19
- Europe PubMed Central19
- biomarkers19
- environmental science19
- services and resources19
- Cross domain (cross-domain)18
- Gene expression (gene-expression)18
- ISCBCo-SponsoredorAffiliatedEvent18
- TESS18
- population genomics18
- single-cell biology18
- wellbeing18
- Expression Atlas17
- Open Targets17
- Programmatic access17
- biochemistry17
- data FAIRness17
- IntAct Molecular Interaction Database16
- raphael gottardo group16
- Data visualisation15
- Literature (literature)15
- Metabolomics15
- SoftwareCarpentry15
- data publication15
- Git14
- InterPro14
- Reactome pathways database14
- genomics14
- storage14
- BioExcel13
- Show N_FILTERS more
-
-
-
Scientific topic
- Cancer3
- Cancer biology3
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- High throughput sequencing3
- High-throughput sequencing3
- NGS3
- NGS data analysis3
- Neoplasm3
- Neoplasms3
- Next gen sequencing3
- Next generation sequencing3
- Oncology3
- Panels3
- Personal genomics3
- Primer walking3
- Sanger sequencing3
- Sequencing3
- Synthetic genomics3
- Targeted next-generation sequencing panels3
- Viral genomics3
- Whole genomes3
- Allele calling1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- SNP calling1
- SNP detection1
- SNP discovery1
- Single nucleotide polymorphism detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses4
- Show N_FILTERS more
-
-
-
Country
- United Kingdom4
- Show N_FILTERS more
-
-
-
Target audience
- This course is aimed at PhD students and post-doctoral researchers who are applying or planning to apply high throughput sequencing technologies in cancer research and wish to familiarise themselves with bioinformatics tools and data analysis methodologies specific to cancer data. Familiarity with the technology and biological use cases of high throughput sequencing (HTS) is required, as is some experience with R/Bioconductor (basic understanding of the R syntax and ability to manipulate R objects) and the Unix/Linux operating system.1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events