Human Whole Genome Sequencing
DESCRIPTION
SPECIFICATION
RESOURCES
Service Description

Whole genome sequencing detects the complete human genome sequence at one time and provides the most comprehensive collection of an individual's genetic variation based on the human reference genome. The microarray-based genotyping studies have gradually moved to whole genome sequencing with the falling costs of sequencing technology.

Whole genome sequencing can be applied to human genetics and evolution studies to detect genome-wide genetic variations, pathogenic and susceptibility genes, and to enable the genetic diversity and evolution analysis. It can also be applied to translational research to provide information on cancer and disease associated mutations and is one of the most important approaches of precision medicine.

Project workflow

We care for your samples from the start through to the result reporting. Highly experienced laboratory professionals follow strict quality procedures to ensure the integrity of your results.

Sample QC
Library QC
Data QC
Sample
preparation
Library
construction
Sequencing
Raw data
output
Bioinformatics
Analysis
Sequencing Services
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