US2011003293A1PendingUtilityA1
Fetal aneuploidy detection by sequencing
Est. expiryJun 14, 2026(expired)· nominal 20-yr term from priority
C12Q 1/6883C12Q 2600/156C12Q 1/6874
62
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention provides apparatus and methods for enriching components or cells from a sample and conducting genetic analysis, such as SNP genotyping to provide diagnostic results for fetal disorders or conditions.
Claims
exact text as granted — not AI-modified1 . A method for detecting fetal abnormality comprising: determining a ratio of abundance of maternal allele(s) to abundance of paternal allele(s) in genomic DNA from fetal cells enriched from a maternal blood sample using size-based separation.
Join the waitlist — get patent alerts
Track US2011003293A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.