IP Library Granted Patent US 12668843
Granted Patent B2
US 12668843 · App. 18/620,822 · Granted Jun 30, 2026

Methods for simultaneous amplification of target loci

Inventors: Matthew Rabinowitz (San Francisco, CA); Matthew Micah Hill (Belmont, CA); Bernhard Zimmermann (Manteca, CA); Johan Baner (San Francisco, CA); George Gemelos (Portland, OR); Milena Banjevic (Los Altos Hills, CA); Allison Ryan (Belmont, CA); Styrmir Sigurjonsson (San Jose, CA); Zachary Demko (San Francisco, CA)
Assignee: Natera, Inc.
C12Q1/6883C12Q1/6809C12Q1/6811C12Q1/6844C12Q1/6848C12Q1/6851C12Q1/6855C12Q1/6869C12Q1/6874C12Q2600/156
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Quick Facts
Patent No.
US 12668843
App. No.
18/620,822
Granted
Jun 30, 2026
Kind
B2
Abstract

The invention provides methods for simultaneously amplifying multiple nucleic acid regions of interest in one reaction volume as well as methods for selecting a library of primers for use in such amplification methods. The invention also provides library of primers with desirable characteristics, such as minimal formation of amplified primer dimers or other non-target amplicons.

Claims (16)

1 . A method for preparing tagged amplified products useful for analyzing a plurality of polymorphic loci associated with cancer, comprising

performing targeted multiplex amplification on cell-free DNA extracted from a plasma sample of a human subject to obtain a plurality of amplicons, wherein the targeted multiplex amplification amplifies 20-2,000 polymorphic loci associated with cancer in a single reaction volume;

ligating the plurality of amplicons with one or more universal adaptors and a plurality of different molecular barcodes to obtain tagged amplicons;

amplifying the tagged amplicons using the universal adaptors to generate tagged amplified products each containing at least one polymorphic locus associated with cancer, a molecular barcode, and one or more sequencing tags; and

conducting massively parallel sequencing on the tagged amplified products to produce sequence reads.

2 . The method of claim 1 wherein the polymorphic loci comprise single nucleotide polymorphisms or single nucleotide variants or both.

3 . The method of claim 1 , wherein the one or more universal tail adaptors each comprise a first strand and a second strand, wherein a first end of each of the universal tail adaptors comprises a double-stranded section comprising the 5′ portion of the first strand and the 3′ portion of the second strand, wherein the first end is ligated to the nucleic acids.

4 . The method of claim 3 , wherein the targeted multiplex amplification comprises a first amplifying step and a second amplifying step, wherein the first amplifying step comprises using a first target-specific primer that anneals to a specific target sequence and a first adaptor primer having a nucleotide sequence identical to a first portion of the first strand to generate a first amplification product.

5 . The method of claim 4 , wherein the second amplifying step comprises using a second target-specific primer that anneals to the first amplification product and a second adaptor primer having a nucleotide sequence identical to a second portion of the first strand to generate the final amplification product.

6 . The method of claim 5 , wherein the second adaptor primer is nested relative to the first adaptor primer.

7 . The method of claim 6 , wherein the second target-specific primer comprises an index tag.

8 . The method of claim 7 , wherein the second amplifying step further comprises using an index primer comprising a sequence complementary to the index tag.

9 . The method of claim 1 , wherein the one or more universal tail adaptors comprise a second sequencing tag.

10 . The method of claim 1 , wherein the one or more universal tail adaptors comprise a first universal tail adaptor and a second universal tail adaptor.

11 . The method of claim 1 , wherein the targeted multiplex amplification comprises a single amplifying step.

12 . The method of claim 11 , wherein the targeted multiplex amplification comprises using a third primer and a fourth primer, wherein the third primer comprises a first sequencing tag and wherein the fourth primer comprises a second sequencing tag.