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To better assist you with your request, please choose a research area provided by Leiden University Medical Center - Leiden Genome Technology Center. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.
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RNA Sequencing
Use Next Generation Sequencing techniques to Identify RNA transcripts, examine differential expression patterns and analyze splice variants.
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Whole Genome Sequencing
Determine the entire genetic make-up of an organism.
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Targeted Sequencing/Resequencing
Detect variations in a genome subset.
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RNA Sequencing/Resequencing
Identify RNA transcripts, examine differential expression patterns and analyze splice variants.
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Single Cell RNA Sequencing
Quantify mRNA variants in a single cell.
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De Novo Genome Sequencing
Determine the DNA sequence of uncharacterized genomes.
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Single Cell Transcriptome Sequencing
Detect distinct, rare or abnomal cell types in a heterogenous population.
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Single Cell DNA Sequencing
Examine genetic variations in a single cell.
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Whole Transcriptome Amplification
Amplify total RNA from a single cell.
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De Novo Transcriptome Sequencing
Identify new genes without the need for a reference genome sequence.
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