CD Genomics: Bioinformatics-Analysis Division Provides Genotyping Analysis Service for Studying Genetic Variations

The Bioinformatics-analysis division is a new division of CD Genomics that provides reliable next-generation and third-generation high-throughput sequencing data analysis, comprehensive technology services, database construction, and other related data analysis services. CD Genomics recently launched various types of genotyping analysis services, including analysis of data generated by different classification techniques, such as whole-genome sequencing, whole-exome sequencing, whole-genome SNP chips, and mass spectrometry.

Researchers are able to use genotyping to study genetic variation, such as single nucleotide polymorphisms (SNPs) and larger DNA structural changes. High-throughput genomic technologies such as next-generation sequencing (NGS) and microarrays allow researchers to gain a deeper understanding of disease etiology at the molecular level.

Since there may be many genomic targets that can cause disease, analysis requires flexibility and accuracy. Genotyping analysis using bioinformatics methods, such as SNP genotyping and copy number variation (CNV) analysis, can analyze the results of millions of markers and probes, detect sample outliers, and predict the functional consequences of genetic variation. The commonly used genotyping methods include whole-genome sequencing, whole-exome sequencing, whole-genome SNP chip, mass spectrometry, etc.

“Genotyping is the process of examining the DNA sequence of an individual through the use of biological tests. It is also a process of comparing the target sequence with the sequence of another individual or a reference sequence to determine differences in the genetic makeup (genotype) of an individual. CD Genomics aims to help researchers effectively identify coding variants in a wide range of applications including population genetics, genetic disease and cancer research,” commented Senior Scientist of CD Genomics.

CD Genomics provides customers with different types of genotyping analysis services according to your experimental data and data analysis needs. The services it provides include but are not limited to:

• Whole Exome Genotyping Analysis
• GWAS Analysis
• TWAS Analysis
• Whole Genome SNP Genotyping
• CNV Analysis
• SV Analysis
• InDel Analysis
• Whole Genome Multilocus Sequence Typing

“As one of the providers of genotyping analysis, CD Genomics uses bioinformatics to help you quickly locate mutations and explore genetic variations. Our unique data analysis skills and appropriate software can meet customers' personalized laboratory data analysis needs and provide easy-to-interpret data analysis reports,” said CD Genomics’s Project Manager.

About CD Genomics

CD Genomics is one of the reliable providers of bioinformatics analysis services, with a high-performance computing platform and a bioinformatics analysis team dominated by Ph.D. and Master's degrees. CD Genomics uses cutting-edge bioinformatics analysis technology to carry out the main business of genomics, transcriptomics, microorganisms, epigenetics, proteomics, metabolomics, single-cell omics, and so on.

Contact

Address: Shirley, NY 11967, USA

Email: contact@cd-genomics.com