Whole Genome Resequencing

Whole Genome Resequencing

Whole genome resequencing is widely used as a purposeful sequencing method in human disease and plant and animal breeding research. CD Genomics, a sequencing company representing international standards, provides researchers with a highly accurate whole genome resequencing (WGR) service.

What Is Whole Genome Resequencing?

Whole-genome resequencing is the process of sequencing the genomes of different individuals of species with known genome sequences and based on this, individual or population variability analysis is performed to determine the best match position of specific reads in the genome. Whole genome resequencing can detect a large amount of variation information through sequence alignment, including SNP, InDel, SV, and CNV.

Sequencing Methods

WGR is based on high-throughput parallel sequencing technology and is capable of retrieving enough DNA fragments to cover the entire genome span. Depending on the size of the genome and the type of mutations identified, different sequencing technologies can be used, including Illumina, PacBio, Oxford Nanopore, and Bionano.

Customers Need to Provide

Samples

We accept a wide variety of samples, including colonies, frozen cell precipitates (mammalian or bacterial), etc.

• For routine samples, the total amount of intact genomic DNA is 1 μg.
• For low input samples, the total amount of intact genomic DNA should be ≥ 200 ng.

Please note that all samples are shipped on an adequate amount of dry ice.

Sample Information

Please provide the specific concentration, volume, preparation time, and species origin for each sample. And inform about the specific information as well as the control and experimental samples (if there are groupings, describe in detail the grouping analysis information).

Deliverables

• Sequencing raw data
• Data analysis report
• Experimental results type files
• Graphs required for publication
• Descriptions of some of the methods used in the published article

Applications

• In-depth exploration of the mysteries of disease genomes.
• Genetic evolutionary analysis and candidate gene prediction for important traits.
• Genotyping and classification of eukaryotic and/or prokaryotic cell lines
• Efficient identification of trait-linked regions in plants and animals, providing the scientific basis and technical support for genetic breeding.

Our Advantages

• Helps to analyze genomic variation information.
• Capable of amplifying individual reference genomic information into genetic characteristics of a population of organisms.

Our Workflow

CD Genomics offers whole genome resequencing that can help you analyze the genome of any species you are interested in and can help you scan and detect gene sequence differences and structural variants associated with important traits. If you are interested in this service, please feel free to contact us.

For research use only, not for any clinical use.