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Scientific topic
- Bioinformatics1
- Biological sequences1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- DNase-Seq1
- High throughput sequencing1
- High-throughput sequencing1
- NGS1
- NGS data analysis1
- Next gen sequencing1
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- Targeted next-generation sequencing panels1
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Operation
- Sequencing QC
- Allele calling3
- Exome variant detection3
- Genome variant detection3
- Germ line variant calling3
- Mutation detection3
- Somatic variant calling3
- Variant calling3
- Variant mapping3
- de novo mutation detection3
- Data handling2
- File handling2
- File processing2
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- Utility operation2
- Alternative splicing analysis1
- Alternative splicing detection1
- Alternative splicing prediction1
- Cartography1
- Data visualisation1
- Differential splicing analysis1
- Mapping1
- Molecular visualisation1
- Plotting1
- Rendering1
- Sequencing quality assessment1
- Sequencing quality control1
- Splice transcript prediction1
- Split read mapping1
- Split-read mapping1
- Visualisation1
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- Workshops and courses1
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- Germany1
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