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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 order@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