The sequencing of amplified regions of DNA or RNA for the purpose of analyzing genetic variation.
The sequencing of amplified regions of DNA or RNA for the purpose of analyzing genetic variation.
The sequencing of amplified regions of DNA or RNA for the purpose of analyzing genetic variation.
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.
Amplicon sequencing is when a DNA or RNA sequence is amplified, or copied many times, using PCR. The amplified sequences are converted to libraries, pooled and sequenced. Amplicon sequencing has been used for biomonitoring, diet analysis and microbial metagenomics. Amplicons commonly targeted for sequencing include 16s ribosomal RNA (rRNA), 18s rRNA and ITS (internal transcribed spacer). The ITS sequence is a nonfunctional RNA located between structural rRNA of a common precursor transcript. 16s, 18s and ITS sequencing are used for taxonomy and identifying the relationships between species and genera in bacteria and fungi because these regions are highly variable in sequence.
Amplicon sequencing is based on Next Generation Sequencing (NGS) technology or PacBio SMRT sequencing. 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, and immune repertoire sequencing.
The sequencing of amplified regions of DNA or RNA for the purpose of analyzing genetic variation.
The sequencing of amplified regions of DNA or RNA for the purpose of analyzing genetic variation.
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, CRISPRCRISPR sequencing, somatic/complex variant discovery, antibody screening sequencing, immune repertoire sequencing, et al.
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 sequencingAmplicon 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.
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.