CD Genomics
Shirley, NY 11967
New TCR-Seq Service for Analyzing T-Cell Clone Diversity and Clonality
Extracts DNA or RNA and uses Illumina platform for high-throughput sequencing. Utilizes multiple bioinformatics tools, including VDJtools and tcR, to accurately genotype TCR sequences and identify clones. Ideal for R&D of immunotherapy drugs, cancer immunology and viral infection research.
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New Mitochondrial Diseases Panel Sequencing Service Detects Genetic Mutations
Allows researchers to identify mitochondrial DNA and nuclear DNA mutations accurately. Provides high accuracy, sensitivity and specificity, ensuring the reliable results. Contains over 200 genes associated with mitochondrial function and metabolism.
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New RNA-Solutions for Understanding Human Diseases Mechanisms
Provides quality assessment for purified exosomal RNAs utilizing real-time PCR and electrophoresis. Supports exoLR characterization and the development of companion diagnostics and other applications. Ideal for analysis of mRNA, circRNA and lncRNA in exosomes.
Read More »
New HLA Typing Service for Assessing Immune Compatibility
Products can be expressed on different cell surfaces in antigen presentation and immune signaling. Suitable for research of immune-related diseases, the screening of vaccine and organ transplantations. Application including susceptible gene detection, hematopoietic stem cell transplantation and drug allergy testing.
Read More »New Cancer Hotspot Panel Sequencing Covers 248 Genes
Accelerate research on disease pathogenesis, disease identification, biomarker discovery and targeted drug development. Provides efficient method for discovering rare somatic mutations. Can detect SNVs, indels and structural rearrangement.
Read More »
New Plasmid Identification Service for Microbial Genomics and Bioinformatics Analysis
Provides advanced genomics solutions and genome-based analysis. Available with next-generation sequencing and long-read sequencing platforms. Identifies antibiotic resistance genes, mobile genetic elements and any other genetic information of interest.
Read More »
New Long Amplicon Analysis Tool Analyzes Single Molecule Real-Time Sequencing (SMRT) Data
Generates highly accurate, phased and full-length consensus sequences for multiple genes in a single sequencing run. Provides complete, uniform and unbiased coverage across long amplicons. Applications include full-length 16S, 18S and ITS rRNA gene sequencing.
Read More »
New Microbial Transcriptomics for Predicting Resistance to Specific Antibiotics
Contains all RNAs encoded by a group of organisms in a complex sample. Cellular RNA is extracted and converted to cDNA for sequencing library preparation. Identification of high and low expression in a single bacterial, viral, or other microbial RNA-Seq experiment.
Read More »
New RNA-Seq Service Uses Illumina Sequencing Techniques
Designed for input amounts down to 2 pg, applicable for good quality RNA from challenging samples. Offers a powerful tool for analyzing the gene expression in cancer research and studies. Allows to detect splice junctions and significant changes in gene expression for low abundant transcripts.
Read More »New TCR-Seq Service for Analyzing T-Cell Clone Diversity and Clonality
Extracts DNA or RNA and uses Illumina platform for high-throughput sequencing. Utilizes multiple bioinformatics tools, including VDJtools and tcR, to accurately genotype TCR sequences and identify clones. Ideal for R&D of immunotherapy drugs, cancer immunology and viral infection research.
Read More »
New Mitochondrial Diseases Panel Sequencing Service Detects Genetic Mutations
Allows researchers to identify mitochondrial DNA and nuclear DNA mutations accurately. Provides high accuracy, sensitivity and specificity, ensuring the reliable results. Contains over 200 genes associated with mitochondrial function and metabolism.
Read More »
New RNA-Solutions for Understanding Human Diseases Mechanisms
Provides quality assessment for purified exosomal RNAs utilizing real-time PCR and electrophoresis. Supports exoLR characterization and the development of companion diagnostics and other applications. Ideal for analysis of mRNA, circRNA and lncRNA in exosomes.
Read More »
New HLA Typing Service for Assessing Immune Compatibility
Products can be expressed on different cell surfaces in antigen presentation and immune signaling. Suitable for research of immune-related diseases, the screening of vaccine and organ transplantations. Application including susceptible gene detection, hematopoietic stem cell transplantation and drug allergy testing.
Read More »New Cancer Hotspot Panel Sequencing Covers 248 Genes
Accelerate research on disease pathogenesis, disease identification, biomarker discovery and targeted drug development. Provides efficient method for discovering rare somatic mutations. Can detect SNVs, indels and structural rearrangement.
Read More »
New Plasmid Identification Service for Microbial Genomics and Bioinformatics Analysis
Provides advanced genomics solutions and genome-based analysis. Available with next-generation sequencing and long-read sequencing platforms. Identifies antibiotic resistance genes, mobile genetic elements and any other genetic information of interest.
Read More »
New Long Amplicon Analysis Tool Analyzes Single Molecule Real-Time Sequencing (SMRT) Data
Generates highly accurate, phased and full-length consensus sequences for multiple genes in a single sequencing run. Provides complete, uniform and unbiased coverage across long amplicons. Applications include full-length 16S, 18S and ITS rRNA gene sequencing.
Read More »
New Microbial Transcriptomics for Predicting Resistance to Specific Antibiotics
Contains all RNAs encoded by a group of organisms in a complex sample. Cellular RNA is extracted and converted to cDNA for sequencing library preparation. Identification of high and low expression in a single bacterial, viral, or other microbial RNA-Seq experiment.
Read More »
New RNA-Seq Service Uses Illumina Sequencing Techniques
Designed for input amounts down to 2 pg, applicable for good quality RNA from challenging samples. Offers a powerful tool for analyzing the gene expression in cancer research and studies. Allows to detect splice junctions and significant changes in gene expression for low abundant transcripts.
Read More »