The sequencing of amplified regions of DNA or RNA for the purpose of analyzing genetic variation.
CD Genomics provides amplicon sequencing services by using Illumina platforms. We can offer multiple options for ultra-deep sequencing of amplicons and highest-quality data analysis applications at low cost.
Amplicon sequencing is based on NGS technology or PacBio SMRT sequencing. The ultra-deep sequencing of amplicons (PCR products) allows efficient variant identification and characterization. This technique has a wide range of applications, including 16S/18S/ITS gene sequencing, SNP genotyping, CRISPR sequencing, somatic/complex variant discovery, antibody screening sequencing, immune repertoire sequencing, et al.
Whether you would like to detect the diversity of microbial communities or discover rare somatic mutations in complex samples. CD Genomics could provide professional, cost-efficient and high-speed amplicon sequencing services to meet your project requirements.
The sequencing of amplified regions of DNA or RNA for the purpose of analyzing genetic variation.