Location:Home / Application

STR&SNP sequencing

Forensic laboratories currently use PCR and capillary electrophoresis (CE) methods to analyze short tandem repeat (STR) markers and other polymorphic markers. Due to the limitations of fluorescent color and length, multiple polymorphic markers are usually required multiple rounds of detection. Next-generation sequencing (NGS) can perform analysis of whole-chromosomal STR markers and a large number of single nucleotide polymorphisms (SNPs) and mitochondrial hypervariable regions by a single test. MGI's DNBSEQTM sequencing technology features high accuracy, low duplicate rate, and low index hopping, enabling you to get more information from DNA and help you solve problems efficiently.
Workflow

Sample Prep

Sequencing Bioinformatic analysis

MGIEasy Signature Identification Library Prep Kit (Coming soon) Detect over 360 markers in one tube and it includes all reagents required to prepare a sequencing library for forensic DNA samples

DNBSEQ-G400RS,A fully validated next-generation sequencing system for forensic genomics

Zlims
Automated Sample Prep System MGISP-960, MGISP-100 DNBSEQ-G400RS High-throughput Sequencing Set (SE400) Bioinformatics accelerator MegaBOLT
>
  • Hotline (Global)
    +86-4000-688-114
  • Email
    MGI-service@mgi-tech.com
  • Special Recommendations
  • *For research use only.

    Not for use in diagnostic procedures (except as specifically noted).
Copyright © 2024 All Rights Reserved MGI Tech Co., Ltd. Guangdong ICP 16117185Privacy PolicyLegal NoticesCookie Policy
Our use of cookies
We would like to use necessary cookies to improve your browsing experience and the quality of our website. We would also like to set analytics cookies and advertisement cookies that help us make improvements by measuring how you use our website. Detailed information about the use of cookies on this website and how you can control your consent can be found in our Cookie Policy and Privacy Policy.
Accept only strictly necessary cookiesAccept all cookies