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Genotyping Services

Whole Genome Mapping 
Whole genome mapping is a de novo process that generates whole genome, ordered, restriction maps with no requirement for previous sequence information and provides a comprehensive view of genomic architecture. Resembling a barcode, the whole genome map is unique to the organism and provides a complete, structural view of the genome that reveals its architecture in a single, easy-to-interpret image.

Whole Genome Mapping Features and Benefits:

A more accurate approach – enables detection and correction of assembly errors for higher accuracy sequence assembly.
Without references – independent of sequence information, and do not require amplification or PCR steps.
High resolution – accelerate whole genome sequencing.
Whole Genome Mapping Applications:

Estimate the absolute length of a genome
Assemble Whole Genome Sequencing
Quickly detect differences between two genomes
Strain Typing
CD Genomics Whole Genome Mapping Service includes:

Enzyme digestion result
Assembly and analysis
Scaffold placement

Genome-Wide Association Studies (GWAS)
Genome-wide association studies (GWAS), thousands or up to millions of genetic markers are genotyped in groups of individuals that either carries a certain trait (cases) or not (controls). Differences in the allele and genotype frequencies between the different groups lead to the detection of genomic regions that are associated with the certain trait. GWAS typically focus on associations between single-nucleotide polymorphisms (SNPs) and traits like major diseases in humans or breeding traits in animals and plants. Equipped with Affymetrix GeneChip® Scanner 3000 7G and Illumina’s iScan System, We offers researchers the flexibility to profile samples with millions of markers in high-throughput format, and deliver dense genome wide coverage with the most up-to-date content available from the scientific community.

Service Range

Multi-stage Design and Analysis
Replication Analysis
Linkage Analysis
SNP Positioning and Search
Disease Associated Study
Odds Ratio, Relative Risk Calculation
dbSNP Annotation
Hapmap Comparison
Linkage Disequilibrium (LD) Analysis
Why Choose Sunomix Biosciences?

Cost-effective analysis using custom arrays
Exceptional study design, data analysis options and support
Peace of mind with complete sample tracking and quality assurance
Rapid and standardized delivery of high-quality results using automated, high-throughput sample processing.

CNV Analysis Service
Agilent aCGH Technology

Agilent’s oligonucleotide aCGH platform offers genome-wide as well as customized profiling on 60-mer oligo CGH microarrays for human, mouse and rat. Agilent’s CGH end-to-end solution consists of flexible microarray formats, optimized and easy-to-use protocol, high resolution microarray scanning and powerful analytics software.

Features:

High-resolution
Supports a variety of formats, probes, and species
Custom arrays with user-defined content
Commercial arrays with standard content
Genome-wide studies
Focused-content studies
SNP Arrays

Both Affymetrix and Illumina offer solutions for CNV analysis using SNP arrays. We provides wet lab and data analysis services for each platform.

Features:

Analyze SNP and CNV data across millions of markers
Estimate Log R ratio and B-allele frequency for copy number analysis
Call genotypes, normalize and cluster data, and generate SNP statistics
Export genotype data to various third party applications; access multiple CNV algorithms and CNV analysis tools
Generate a chromosomal heat map for examining copy number aberrations across the entire genome for multiple samples
Your Benefits

Free advice on experimental design
Peace of mind of using a laboratory with extensive experience of running small, medium and large-scale projects
Excellent data quality
Lowest costs

To find out more details about this custom service, Please request a quote today.