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Genomics and Computational Bioinformatics Services

CD Genomics offers various solutions, from genome-wide association studies on tens of thousands of samples to single SNP interrogations of several hundred individuals. Our experts and technicians are knowledgeable and have years of experience providing Genomics and Computational Bioinformatics Services.

Name of the Instrument/Technicial Service

Genomics and Computational Bioinformatics Services

Introduction

To provide expert consultation on experimental designs and analysis approaches of large-scale microarray and NGS datasets.
To generate microarray and high-throughput sequence data in a cost-effective efficient manner with rapid-turn around.
To perform intermediate analysis of high-throughput sequence data including, DNA variant calling, mRNA isoform calling, miRNA analysis and DNA methylation analysis using established pipelines.
To analyze genomic data including tumor profiling for DNA somatic mutations, differential expression analysis, as well as network and systems analysis.

Our Services

Illumina sequencing
PacBio Sequencing
10x Genomics Single Cell RNA Sequencing
Library Preparation (DNA / RNA / small RNA)
Sample QC
Agilent 2100 Bioanalyzer / TapeStation
Genotyping Arrays
Methylation Arrays
Covaris Shearing
Roche 454 Sequencing
Fluidigm Access Array System
Affymetrix Microarrays / Nimblegen Arrays
Agilent 2100 Bioanalyzer / Nanodrop

CD Genomics has already updated its technology platforms to mainstream NGS, long-read sequencing, and microarray instruments. We continue to strive to offer the same reliable services to pharmaceutical and biotechnology companies, as well as academia and government agencies, for all your sequencing or array needs. If you are interested, please contact us directly for assistance.

For research use only, not intended for any clinical use.

Online Inquiry

Please fill out the form below and we will get back to you as soon as possible with a quotation for the item you are interested in.