CD Genomics CD Genomics is a leading genomic service provider in United States. We provide   snp genotyping , library construction, bioinformatics, aptamers, microarray,  mutagenesis analyses and others for the genomics industry.   Whole Genome Sequencing .  Comprehensive genome re-sequencing solutions for samples from human and other species, ensure high coverage and great accuracy. Microbial Whole Genome Sequencing .  Individual bacterial and fungal whole genome shotgun sequencing, sequenced with both Illumina HiSeq and PacBio SMRT technologies. Whole Exome Sequencing .  Powerful and cost-effective alternative to Whole Genome Sequencing. Enrichment of exome with panels provided by Agilent, Illumina or Nimblegen. Targeted Region Sequencing .  Comprehensive services from strategy design and custom data analysis. More samples can be sequenced within a sequencing run. Whole Genome SNP Genotyping   CD Genomics provides whole-genome SNP genotyping for the overview of the entire genome by using both microarray technologies and high-throughput next-generation sequencing (NGS), enabling genome-wide discoveries and screening of the SNP loci. Genome-wide association studies with SNP markers are expected to allow identification of genetic variation that underlie complex disorders. Bioinformatics Services  CD Genomics provides statistical and bioinformatic data analysis services that help explain the large amounts of data commonly generated by next generation sequencing and genotyping experiments. Transcriptomics Microarray   MicroRNA Expression Profiling Microarray Service Gene Expression Profiling Microarray Service LncRNA Microarray Service Genomics Microarray SNP Microarray Service CGH Microarray Service Epigenetics Microarray ChIP-on-chip Service DNA Methylation Microarray Service