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Content provider
- ELIXIR Portugal1
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Scientific topic
- Oncology
- DNA variation4
- Genetic variation4
- Genomic variation4
- Mutation4
- Polymorphism4
- Somatic mutations4
- Bioinformatics3
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- Chromosome walking2
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- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Genome sequencing2
- High throughput sequencing2
- High-throughput sequencing2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Primer walking2
- Sanger sequencing2
- Sequencing2
- Targeted next-generation sequencing panels2
- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Biomarkers1
- Biotherapeutics1
- Cancer1
- Cancer biology1
- ChIP-exo1
- ChIP-seq1
- ChIP-sequencing1
- Chip Seq1
- Chip sequencing1
- Chip-sequencing1
- Diagnostic markers1
- MicroRNA sequencing1
- Neoplasm1
- Neoplasms1
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- RNA sequencing1
- RNA-Seq1
- RNA-Seq analysis1
- Small RNA sequencing1
- Small RNA-Seq1
- Small-Seq1
- Software integration1
- Tool integration1
- Tool interoperability1
- Transcriptome profiling1
- WTSS1
- Whole transcriptome shotgun sequencing1
- Workflows1
- miRNA-seq1
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Event type
- Workshops and courses1
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Country
- Portugal1
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Organizer
- Pedro Fernandes1
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