Whole Genome Resequencing: Using the Known to Find the Unknown

SHIRLEY, NY - Oct 26, 2014 - Whole genome resequencing is a laboratory process that determines the complete DNA sequence of an organism's genome which is already known. With next generation sequencing technology, whole genome resequencing across multiple samples in a population provides an unprecedented opportunity for comprehensively characterizing the polymorphic variants in the population. With this technology, we can find endless unknown, such as, SNP, Insertion/Deletion, and Structure Variation, by using the already known genome sequences.

Whole Genome Resequencing Service of CD Genomics Inc. includes data filtering, alignment report, SNPs and indel calling, CNV detection and breakpoint determinations with single nucleotide precision, determination of structural variations, annotations and data mapping, and other customized analysis. In addition, CD Genomics proprietary GenSeqTM Technology provides whole genome resequencing to your human, plant, animal, and microbe samples in order to understand genetic differences and implications.

The major benefits of Whole Genome Resequencing include rapid and standardized delivery of high standards of accuracy, complete solutions from sample prep to bioinformatics, advanced technical capabilities, as well as cost effective. In one word, CD Genomics Inc. can provide the best Whole Genome Resequencing service with the highest quality and the most favorable price.

About CD Genomics

CD Genomics Inc. is a leading global biotech company, providing health services, sequencing services, microarray, custom libraries, bioinformatics, and genotyping, etc. With near ten years’ experience, CD Genomics takes it its commission to contribute to accelerating scientific discovery. Today all CD Genomics members are committed to offering state-of-the-art services and products and will stay active all the time!

For more detailed information, you can visit CD Genomics website http://www.cd-genomics.com.