Log in
Enquire now
‌

US Patent 7838647 Non-invasive detection of fetal genetic traits

Patent 7838647 was granted and assigned to Sequenom on November, 2010 by the United States Patent and Trademark Office.

OverviewStructured DataIssuesContributors

Contents

Is a
Patent
Patent
0

Patent attributes

Current Assignee
Sequenom
Sequenom
0
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
0
Patent Number
78386470
Patent Inventor Names
Sinuhe Hahn0
Bernhard Zimmermann0
Wolfgang Holzgreve0
Ying Li0
Date of Patent
November 23, 2010
0
Patent Application Number
118555580
Date Filed
September 14, 2007
0
Patent Citations Received
‌
US Patent 12116624 Systems and methods to detect rare mutations and copy number variation
0
0
‌
US Patent 12060614 Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing
0
‌
US Patent 12065703 System and method for cleaning noisy genetic data and determining chromosome copy number
0
‌
US Patent 12084720 Assessing graft suitability for transplantation
0
‌
US Patent 12094573 Methods for multi-resolution analysis of cell-free nucleic acids
0
‌
US Patent 12110552 Methods for simultaneous amplification of target loci
0
‌
US Patent 12110560 Methods for monitoring residual disease
0
...
Patent Primary Examiner
‌
Stephen Kapushoc
0
Patent abstract

Blood plasma of pregnant women contains fetal and (generally>90%) maternal circulatory extracellular DNA. Most of said fetal DNA contains .Itoreq.500 base pairs, said maternal DNA having a greater size. Separation of circulatory extracellular DNA of .Itoreq.500 base pairs results in separation of fetal from maternal DNA. A fraction of a blood plasma or serum sample of a pregnant woman containing, due to size separation (e.g. by chromatography, density gradient centrifugation or nanotechnological methods), extracellular DNA substantially comprising .Itoreq.500 base pairs is useful for non-invasive detection of fetal genetic traits (including the fetal RhD gene in pregnancies at risk for HDN; fetal Y chromosome-specific sequences in pregnancies at risk for X chromosome-linked disorders; chromosomal aberrations; hereditary Mendelian genetic disorders and corresponding genetic markers; and traits decisive for paternity determination) by e.g. PCR, ligand chain reaction or probe hybridization techniques, or nucleic acid arrays.

Timeline

No Timeline data yet.

Further Resources

Title
Author
Link
Type
Date
No Further Resources data yet.

References

Find more entities like US Patent 7838647 Non-invasive detection of fetal genetic traits

Use the Golden Query Tool to find similar entities by any field in the Knowledge Graph, including industry, location, and more.
Open Query Tool
Access by API
Golden Query Tool
Golden logo

Company

  • Home
  • Press & Media
  • Blog
  • Careers
  • WE'RE HIRING

Products

  • Knowledge Graph
  • Query Tool
  • Data Requests
  • Knowledge Storage
  • API
  • Pricing
  • Enterprise
  • ChatGPT Plugin

Legal

  • Terms of Service
  • Enterprise Terms of Service
  • Privacy Policy

Help

  • Help center
  • API Documentation
  • Contact Us
By using this site, you agree to our Terms of Service.