IP Library › Patent Application 17412105
Patent Application
App. No. 17/412,105

COMPOSITIONS AND METHODS FOR ACCURATELY IDENTIFYING MUTATIONS

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Patent No.
US None
App. No.
17/412,105
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 (42)

1 .- 38 . (canceled)

39 . A method comprising:

(a) providing a sample comprising a set of double-stranded polynucleotide molecules, each double-stranded polynucleotide molecule including first and second complementary strands;

(b) tagging said double-stranded polynucleotide molecules with a set of double-stranded cypher polynucleotides to form double-stranded cypher-target nucleic acid complexes, wherein the cypher polynucleotides comprise double-stranded bar codes;

(c) sequencing the cypher-target nucleic acid complexes to produce a plurality of first-strand sequencing reads and a plurality of second-strand sequencing reads;

(d) grouping sequencing reads based on the bar codes, wherein a group comprises sequencing reads for a first tagged strand and a second differently-tagged complementary strand derived from an original double-stranded polynucleotide molecule in said set; and

(e) quantifying said groups of sequencing reads and the read depth of said groups of sequencing reads.

40 . The method of claim 39 , further comprising quantifying one or more mutations in the sample based on said quantification of said groups of said sequencing reads that map to one or more genetic loci.

41 . The method of claim 39 , wherein said cypher polynucleotides are not sequencing adapters.

42 . The method of claim 39 , wherein for a plurality of cypher-target nucleic acid complexes, the method further comprises comparing first-strand sequencing reads with second-strand sequencing reads produced from amplified products of one of the cypher-target nucleic acid complexes to form an error-corrected sequence of the original double-stranded polynucleotide molecule.

43 . The method of claim 42 , further comprising identifying double-stranded polynucleotide molecules comprising a sequence variant at one or more genetic loci.

44 . The method of claim 42 , further comprising quantifying a mutation by mapping error-corrected sequences to a reference sequence, and quantifying the error-corrected sequences corresponding to one or more genetic loci of the reference sequence.

45 . The method of claim 39 , further comprising quantifying said groups of sequencing reads that map to a genetic locus, wherein the reads for the first and second strand of a group comprise a sequence variant.

46 . The method of claim 39 , wherein said set of double-stranded polynucleotide molecules comprises double-stranded circulating nucleic acid molecules obtained from a patient sample.

47 . The method of claim 46 , wherein said double-stranded circulating nucleic acid molecules comprise a mutation present at a frequency of 2.1×10 −6 or lower.

48 . The method of claim 47 , wherein said mutation: (i) is a single nucleotide mutation, (ii) is a cancer biomarker, and (iii) maps to a cancer-associated genetic locus in a reference genome.

49 . The method of claim 48 , further comprising quantifying the single nucleotide mutation cancer biomarker.

50 . The method of claim 49 , wherein quantifying the single nucleotide mutation cancer biomarker comprises quantifying groups of sequencing reads having the single nucleotide mutation cancer biomarker that maps to the cancer-associated genetic locus.

51 . The method of claim 46 , wherein the circulating nucleic acid molecules comprise genomic DNA originating from one or more of a healthy cell, a tumor cell, and a cancer cell.

52 . The method of claim 51 , wherein the circulating nucleic acid molecules comprise plasma DNA biomarkers.

53 . The method of claim 51 , wherein the patient sample comprises a blood sample.

54 . The method of claim 51 , wherein the circulating nucleic acid molecules are obtained from plasma.

55 . The method of claim 39 , wherein the set of double-stranded polynucleotide molecules were generated by nuclease cleavage.

56 . The method of claim 55 , wherein the nuclease is a restriction endonuclease.

57 . The method of claim 55 , wherein the double-stranded polynucleotide molecules comprise overhangs or blunt ends.

58 . The method of claim 39 , wherein

(i) the bar codes are selected from a plurality of distinct bar code sequences;

(ii) at least two of the bar codes are identical in sequence and are ligated to different double-stranded polynucleotide molecules, thereby non-uniquely tagging the different double-stranded polynucleotide molecules; and

(iii) the different double-stranded polynucleotide molecules that are non-uniquely tagged comprise distinguishable end sequences.

59 . The method of claim 58 , wherein the bar code sequences comprise known oligonucleotide sequences.

60 . The method of claim 58 , wherein the bar code sequences comprise random or partially random sequences.

61 . The method of claim 39 , wherein the tagging step comprises attaching double-stranded cypher polynucleotides to both ends of each of the double-stranded polynucleotide molecules, and wherein individual cypher-target nucleic acid complexes can be distinguished by different pairs of bar codes.

62 . The method of claim 39 , wherein:

(a) the tagging step comprises attaching double-stranded cypher polynucleotides to both ends of each of the double-stranded polynucleotide molecules;

(b) at least two of the bar codes are identical in sequence and are ligated to different double-stranded polynucleotide molecules, thereby non-uniquely tagging the different double-stranded polynucleotide molecules; and

(c) said cypher-target nucleic acid complexes can be differentiated from other cypher-target nucleic acid complexes using:

(i) a combination of a bar code and sequence information derived from the original double-stranded polynucleotide molecule,

(ii) a combination of a first bar code at a first end of the double-stranded polynucleotide molecule and a second bar code at a second end of the double-stranded polynucleotide molecule, or

(iii) a combination of (i) and (ii).

63 . The method of claim 62 , wherein in (c) (i) the bar code is a non-unique bar code, and in (c) (ii) the first bar code is a first non-unique bar code and the second bar code is a second non-unique bar code.

64 . The method of claim 39 , wherein prior to sequencing, the method further comprises purifying a plurality of cypher-target nucleic acid complexes comprising double-stranded polynucleotide molecules from specific genomic regions.

65 . The method of claim 39 , further comprising determining a total number of original double-stranded polynucleotide molecules in the sample based on the quantification of said groups of sequencing reads.

Assignments (2)
MERGER AND CHANGE OF NAME Recorded Jun 1, 2022
From: FRED HUTCHINSON CANCER RESEARCH CENTER; SEATTLE CANCER CARE ALLIANCE
To: FRED HUTCHINSON CANCER CENTER
Reel/Frame 060254/0115 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 27, 2022
From: BIELAS, JASON H.; BERTOUT, JESSICA A.
To: FRED HUTCHINSON CANCER RESEARCH CENTER
Reel/Frame 060042/0776 →