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To better assist you with your request, please choose a research area provided by Deep Biotech Solutions Ltd.. 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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NGS: Next Generation Sequencing
Sequence millions of template DNA molecules in parallel.
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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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Machine Learning/ AI
Predict and model an outcome (e.g. disease progression) based on input variables (i.e. features.)
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Data and Text Mining
Derive structured data from free text in order to become accessible for data-mining algorithms.
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Targeted Sequencing/Resequencing
Detect variations in a genome subset.
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CRISPR
Using advanced CRISPR technology, add or delete base pairs at a specifically targeted DNA loci.
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RNA Sequencing/Resequencing
Identify RNA transcripts, examine differential expression patterns and analyze splice variants.
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Genome Editing
Use CRISPR, ZFN, TALEN or AAV gene targeting for targeted gene mutations and creation of transgenics.
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Exome Sequencing
Determine protein-coding nucleotide sequences in a DNA sample.
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