Service Description:
Whole genome sequencing (WGS) is a comprehensive method for analyzing entire genomes which can identify DNA biomarkers such as single nucleotide polymorphism (SNPs), insertions and deletions (indels), structure variations (SVs), copy number variations (CNVs) and other genetic changes of the sequenced species with high accuracy. It is also an indispensable part of genome-wide association study (GWAS), where common genetic variants indifferent individuals are assessed to determine if a variant is associated with a particular phenotype. GWAS can be broadly used in food safety, agriculture, pharmacy and personalized medicine. What抯 more, it provides an unprecedented opportunity for characterizing the polymorphicvariants in a population, which comprehensively unravels the underlying mechanisms of species origin, development, growth, and evolution.
Omics Drive provides both illumina and Nanopore platforms to provide a fast and accurate whole genome resequencing and bioinformatics analysis for any species. Our highly experienced expert team executes quality management, following every procedure to ensure reliable results.
Advantages of Whole Genome Resequencing:
Single base-pair resolution
genome-wide mutation characterization
Population evolution and phylogenetic studies
Sequencing Platforms:
HiSeq 4000/ HiSeq X Ten/NovaSeq 6000/Pabio Sequel/Nanopore
Bioinformatics Analysis:
Data quality control
Alignment to reference genome
Variant (SNP, CNV, InDel and SV) calling,annotation and statistics
...
(More analysis upon request)
Analysis Flow:
