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EXOME SEQUENCING

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The exome and untranslated regulatory regions (UTRs) comprise only 1-2% of the human genome, yet house as many as 85% of disease-related mutations. As a research tool, exome sequencing is a powerful way to investigate common and rare genetic variations that play an important role in complex human diseases.

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GENEWIZ provides complete solutions for exome sequencing projects from experimental design through advanced bioinformatics analysis.