IP Library › Patent Application 16121555
Patent Application
App. No. 16/121,555

COMPOSITIONS AND METHODS FOR ACCURATELY IDENTIFYING MUTATIONS

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
16/121,555
Abstract

The present disclosure provides compositions and methods for accurately detecting mutations by uniquely tagging double stranded nucleic acid molecules with dual cyphers such that sequence data obtained from a sense strand can be linked to sequence data obtained from an anti-sense strand when sequenced, for example, by massively parallel sequencing methods.

Claims (14)

1 .- 38 . (canceled)

39 . A method of determining an error-corrected sequence of a double-stranded target nucleic acid molecule, comprising:

(a) ligating the double-stranded target nucleic acid molecule to at least one cypher polynucleotide, to form a cypher-target nucleic acid complex, wherein the at least one cypher polynucleotide comprises:

(i) a random or partially-random identifier sequence that alone or in combination with an end of the target nucleic acid molecule uniquely labels the double-stranded target nucleic acid molecule; and

(ii) a nucleotide sequence that tags each strand of the cypher-target nucleic acid complex such that each strand of the cypher-target nucleic acid complex has a distinct nucleotide sequence relative to its complementary strand;

(b) amplifying each strand of the cypher-target nucleic acid complex to produce a plurality of cypher-target amplification products from each of a first strand and a complementary second strand of the cypher-target nucleic acid complex;

(c) sequencing the cypher-target amplification products to produce a plurality of first-strand sequencing reads and a plurality of second-strand sequencing reads; and

(d) comparing the first-strand sequencing reads with the second-strand sequencing reads, and generating an error-corrected sequence of the double-stranded target nucleic acid molecule by distinguishing erroneous nucleotides in one strand that lack a matched base change in the complementary strand.

40 . The method of claim 39 , wherein the double-stranded target nucleic acid molecule comprises (i) a DNA molecule, or (ii) an RNA molecule.

41 . The method of claim 39 , wherein the cypher-target nucleic acid complex comprises at least two nucleic acid molecule priming sites.

42 . The method of claim 39 , wherein the cypher-target nucleic acid complex comprises an identifier sequence on both strands.

43 . The method of claim 39 , wherein the cypher-target nucleic acid complex comprises an identifier sequence at each end.

44 . The method of claim 42 , wherein the random or partially-random identifier sequence is double-stranded.

45 . The method of claim 44 , wherein the random or partially-random identifier sequence comprises about 5 to about 20 nucleotides.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2019
From: BIELAS, JASON H.; BERTOUT, JESSICA A.
To: FRED HUTCHINSON CANCER RESEARCH CENTER
Reel/Frame 050923/0670 →