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Whole genome resequencing of animals and plants

Service Advantages

Simple technology, good stability, and high-quality (Q30) sequencing data

Rich detection of variant types: can detect multiple variant types such as SNP, InDel, SV, and CNV, and can be used as molecular markers

High density markers: capable of detecting SNP information across the entire genome, while also detecting low-frequency SNPs

High cost-effectiveness: Compared with whole genome de novo sequencing, it takes less time and costs less
Service Period
| Sample type | Conventional DNA small fragment library | PCR free library |
| DNA sample | DNA≥ 1 μ g | DNA≥ 3 μ g |
| Fresh cultured cells (number of cells) | ≥ 5× 106 cell | ≥ 1× 107 cell |
| Animal tissue | ≥ 300mg | ≥ 500mg |
| Plant tissue | ≥ 1g | ≥ 2g |
| Whole blood | ≥ 1 mL | ≥ 2 mL |
Service Process

experimental design

nucleic acid extraction

library construction

High throughput sequencing

Bioinformatics analysis
Delivery Results
If you have any other requirements, please send an email to marketing@gentlegen.com,We will serve you as soon as possible.
raw data
analysis report

Service&Support
Inquiry and ordering
Directly log in to GentleGen GBS Online Ordering System,Automatically obtain quotes and place orders; stay“Data Download”Download the corresponding service subscription form and send an email. We will provide you with a quotation as soon as possible.
Sample Preparation

DNA≥ 1 μg

Fresh cultured cells (number of cells) ≥ 5 × 106 cells

Animal tissue ≥ 300mg

If you have any questions, please contact us
