Exome Sequencing


The exome represents less than 2% of the human genome, but contains ~85% of known disease-causing variants, making whole-exome sequencing a cost-effective alternative to whole-genome sequencing. With exome sequencing, you can investigate the protein coding regions of the genome when sequencing an entire genome is not practical or necessary. It can efficiently identify variants across a wide range of applications, including population genetics, genetic disease, and cancer studies.

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Using Illumina sequencing technology, MCLAB offers comprehensive exome sequencing solutions, from library preparation to data generation. MCLAB provides exceptional flexibility in study design, enables projects from one to hundreds of exomes per run, and delivers high enrichment rates, coverage uniformity and reproducibility.

Sample Requirements:

Miminal 0.5ug gDNA at high quality and purity, without contaminants of ssDNA, RNA, oligos, organic contaminants such as phenol and ethanol, does not contain more than 1 mM EDTA

Shipping Conditionx:

On dry ice through FedEx overnight

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Exome Sequencing, Exome Sequencing

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