Các dịch vụ đa dạng phù hợp với mọi nhu cầu của khách hàng. Khách hàng có thể lựa chọn nhiều gói dịch vụ khác nhau.

Cung cấp đầy đủ dịch vụ từ chuẩn bị thư viện cho đến phân tích tin sinh học

- Không ghép chung mẫu, mỗi khách hàng được dành 1 lane riêng giúp tránh nhầm lẫn và nhiễu kết quả

- Tiền chuẩn bị thư viện tính riêng khách hàng có thể tùy chọn tự chuẩn bị thư viện

- Đơn giá ước tính 300 - 500 usd/mẫu phụ thuộc vào số mẫu gửi.

Các dịch vụ:

EXOME SEQUENCING

The exome and untranslated regulatory regions (UTRs) comprise only 1-2% of the human genome, yet house as many as 85% of disease-related mutations. As a research tool, exome sequencing is a powerful way to investigate common and rare genetic variations that play an important role in complex human diseases. Providing complete solutions for exome sequencing projects from experimental design through advanced bioinformatics analysis.

WHOLE GENOME SEQUENCING

Whole genome sequencing (WGS) provides unprecedented access to genomic information and promises to deliver breakthroughs in personalized medicine, pharmacogenomics, agrigenomics, oncogenomics, phylogenetics, and biomarker discovery.

Now with the PacBio Sequel and Illumina® HiSeq™ X Ten!

At GENEWIZ, we are using next generation sequencing platforms like the powerful Illumina® HiSeq™ X Ten and the long-read PacBio Sequel to support researchers all over the world with their genome sequencing needs.  Our capabilities include;

Germline variant detection

Somatic variant detection

de novo genome assembly

Whole genome re-sequencing

Structural variant discovery

Copy number variation

While the greatest interest for whole genome sequencing tends to be related to human genomes, GENEWIZ supports whole genome analysis of any species including plants, animals, bacteria, and viruses.

TARGETED RESEQUENCING
Targeted resequencing is an effective method for analyzing your selected gene(s) of interest by next generation sequencing. Whether you are interested in a few genes, or a few hundred genes, targeted resequencing panels offer high sensitivity and specificity, providing in-depth coverage, resulting in high-quality data.

With targeted resequencing gene panels, you can discover point mutations, insertions/deletions (INDELS), copy number variations (CNVs), and gene rearrangements.

16S METAVX™ METAGENOMICS SEQUENCING

Metagenomic sequencing is an important tool that often uses next generation amplicon sequencing to target specific hypervariable regions of the microbial 16S rRNA gene. This is used to identify any relative abundance calculation of bacteria and archaea present in heterogeneous samples, such as soil, marine, or gut microbiome.

16S MetaVx™ is a proprietary, patent-pending assay that improves upon current 16S metagenomics techniques with significant sensitivity and specificity. Compared side-by-side with the most commonly used 16S metagenomics assays, 16S MetaVx™ has the ability to detect more bacterial and archaeal genera with a lower limit of detection.

AMPLICON SEQUENCING

GENEWIZ accepts pre-made amplicons or DNA fragments for next generation sequencing.  GENEWIZ commonly adds sequencing adapters directly to your amplicons for contiguous sequencing.  Alternatively, if your amplicons are large, we can fragment then perform standard DNA library preparation and sequencing.  Applications for this service include antibody library screening, natural antibody repertoire profiling, disease genotyping, CRISPR mutation analysis, screening of molecular clones, and analysis of plasmid stocks.

BIOINFORMATICS SOLUTIONS

GENEWIZ bioinformatics solutions provide researchers with the tools required to effectively analyze and manage vast quantities of data. Bioinformatics solutions are available as standalone services for bioinformatics projects, as well as in conjunction with our Next Generation Sequencing Services. With flexible and customizable service options, GENEWIZ offers complete and effective solutions for your projects.