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Content provider
- European Bioinformatics Institute (EBI)3
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Keyword
- SNV analysis
- DNA & RNA (dna-rna)9
- NGS6
- European Nucleotide Archive4
- HDRUK4
- bioinformatics4
- next-generation sequencing4
- CNV analysis3
- CRISPR-Cas93
- Long-read RNA-seq3
- NGS bioinformatics3
- RNA-Seq3
- Bioinformatics2
- ChIP-seq2
- DNA-seq2
- Ensembl2
- European Variation Archive2
- Long reads2
- RNA-seq2
- Raw sequencing data2
- Sequencing2
- Single Cell Genomics2
- Spatial transcriptomics2
- Variant calling2
- Variant detection2
- analysis pipeline2
- genome graph2
- read mapping2
- sequence alignment and mapping (SAM)2
- transcriptomics2
- RNA-Seq1
- Alzheimers Clinical Trials And StudiesAlzheimers DiseaseAmnesiaAnimal Models In DementiaAnxiety Autoimmune Disorders & Multiple SclerosisBehavioral IssuesBiopsychiatry Blood-Brain BarrierBrain DiagnosisBrain Disease & FailureBrain InjuryBrain TumourCentral Nervous SystemCerebrovascular DiseaseChild NeurologyClinical NeurophysiologyCNS TumorsCognitive DisordersDementiaDementia CareDemyelinationDiagnosis And TherapyEpilepsyGenetics Genetics And Epigenetics Geriatric NeurologyGut- Brain AxisHeadacheIntervention NeuroradiologyMeningitisMental HealthMental Health NursingMetastatisMovement DisordersMultiple SclerosisMultiple Sclerosis DiagnosisNervous SystemNeural EngineeringNeural EnhancementNeuro-Oncology NeuroanaatomyNeuroanatomyNeurocritical CareNeurodegenerationNeurodegenerative DisorderNeurodegenerative DisordersNeurogeneticsNeuroimagingNeuroimmunologyNeurological DisordersNeurological Disorders And StrokeNeurological InfectionsNeurological SurgeryNeurologistNeurologyNeuromedicinesNeuromuscular MedicineNeuronal AutoantibodiesNeuropathyNeuropeptidesNeuropharmacologyNeuroscienceNeurosurgeryNeurotoxicologyNeurotoxinsNeurotransmissionNeurotransmittersParkinsonParkinsons DiseasePediatric NeurologyPharmacology Psychiatry Psychology PsychoneuroimmunologyRecent Research And Case StudiesRehabilitation TherapyStem Cell Treatment For Neurological DisordersStrokesTraumatic Brain Injury1
- Bisulfite-Seq1
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- Genome sequence analysis1
- Genomics1
- High Throughput Sequencing Analysis1
- Hyb-Seq method1
- Mapping1
- Metagenomics1
- Molecular building blocks of life1
- Next generation sequencing data analysis1
- Next-generation sequencing1
- Open-access data archive1
- Plant webinar series1
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- Symbiotes1
- Transcriptomics1
- cell diversity1
- clinical sequencing1
- disease research1
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- omics1
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- • New developments in technology 1
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Scientific topic
- NGS
- Cancer3
- Cancer biology3
- Chromosome walking3
- Clone verification3
- DNA-Seq3
- DNase-Seq3
- Exomes3
- Genome annotation3
- Genomes3
- Genomics3
- High throughput sequencing3
- High-throughput sequencing3
- 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
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Event type
- Workshops and courses3
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Country
- United Kingdom3
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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
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