---
title: "Whole Genome Sequencing"
lang: en
url: https://www.gereallife.com/en/services/wgs.html
canonical: https://www.gereallife.com/en/services/wgs.html
entity: Shanghai Gereallife Biotech Co., Ltd
updated: 2026-11-02
---
WHOLE GENOME 
 

# Whole Genome Sequencing

 

Whole Genome Sequencing (WGS)

 

High-throughput whole-genome sequencing of samples, covering SNP, InDel and CNV detection and annotation to resolve genotype–phenotype associations at the genomic level. Suited to plant and animal breeding, population genetics, disease-associated variant discovery and microbial-genome research.

 
 
 Whole genome unbiased, genome-wide coverage GENOME-WIDE COVERAGE Multi-variant SNP / InDel / CNV detection VARIANT CALLING High depth depth tailored to the study FLEXIBLE DEPTH 

## Technical Specifications

 TECHNICAL SPECIFICATIONS 

| Sequencing Platform | Illumina high-throughput sequencing platform (PE150) |
| --- | --- |
| Analysis Content | Variant detection and annotation, population-genetics analysis, functional-gene mining |
| Sequencing depth | Tailored to the study objective (typically 10–30×) |
| Deliverables | raw data + standard analysis report |

 
 

## Sample Requirements

 SAMPLE REQUIREMENTS Genomic DNA ≥ 1 μg（OD260/280 1.8–2.0） Tissue ≥ 100 mg Whole Blood ≥ 1 mL (anticoagulated) Quality requirements: intact, non-degraded DNA free of RNA and protein contamination; agarose-gel electrophoresis confirmation recommended. Submission notes: ship DNA samples on dry ice or ice packs; specify species, reference-genome version and sample origin. 
 

## Workflow

 WORKFLOW 1 Consultation species / research objective 2 Proposal & Quote Depth / timeline / agreement 3 Sample QC concentration / purity / integrity 4 Library & Sequencing library QC / sequencing 5 Analysis delivery variant annotation + analysis report 
 

## FAQ

 FAQ 
 How long does a Whole Genome Sequencing project take? From sample QC approval, standard timelines are 3-6 weeks (library prep, sequencing and bioinformatics included); large cohorts or deep custom analyses follow the confirmed study plan. What if my samples fail QC? Failed QC is reported immediately with reasons, and we discuss resampling or plan adjustments with you — sequencing never proceeds without qualification. What bioinformatics is included? Can I add custom analyses? Standard delivery covers QC, mapping/assembly, quantification, differential and functional enrichment analyses. Custom deep-dive and multi-omics integrative analyses are supported on request. What samples do you need for Whole Genome Sequencing? Total RNA ≥1 μg with RIN ≥7 (snap-frozen, dry ice); microbial and faecal samples ≥200 mg (sterile, −80 °C); whole blood for WGS ≥500 μL (EDTA only, never heparin). RNA integrity matters more than concentration. See Technical Resources → Sample Guide . 
 
 

## Related Services

 RELATED SERVICES 
 

### Eukaryotic RNA-seq

Eukaryotic RNA-seq

 

### Amplicon Sequencing

Amplicon Sequencing

 

### Metagenomics

Metagenomics

 
 
 

Delivery timing: sample shipping, customs declaration and similar steps may extend turnaround; actual project timelines prevail.

 
 
 
 

## Request a Quote or Study Design

Tell us about your project — we reply within one business day (free assessment)

 
 
 
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 Sample type, number of samples and aims (optional) 
 
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## Start Your Multi-omics Project

 

Free study design · Interactive execution · In-depth data interpretation

 
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