Methods and systems for generation and error-correction of unique molecular index sets with heterogeneous molecular lengths

Patent metadata

Field	Value
Publication number	US-10844429-B2
Application number	US-201815863737-A
Country	US
Kind code	B2
Filing date	Jan 5, 2018
Priority date	Jan 18, 2017
Publication date	Nov 24, 2020
Grant date	Nov 24, 2020

Abstract

The disclosed embodiments concern methods, apparatus, systems and computer program products for determining sequences of interest using unique molecular index sequences that are uniquely associable with individual polynucleotide fragments, including sequences with low allele frequencies and long sequence length. In some implementations, the unique molecular index sequences include variable-length nonrandom sequences. In some implementations, the unique molecular index sequences are associated with the individual polynucleotide fragments based on alignment scores indicating similarity between the unique molecular index sequences and subsequences of sequence reads obtained from the individual polynucleotide fragments. System, apparatus, and computer program products are also provided for determining a sequence of interest implementing the methods disclosed.

First claim

What is claimed is:

1. A method for sequencing nucleic acid molecules from a sample, comprising
(a) applying adapters to DNA fragments in the sample to obtain DNA-adapter products,
wherein each adapter comprises a nonrandom unique molecular index,
wherein nonrandom unique molecular indices of the adapters have at least two different molecular lengths and form a set of variable-length, nonrandom unique molecular indices (vNRUMIs), and
wherein the adapters are obtained by:
(i) providing a set of oligonucleotide sequences having at least two different molecular lengths,
(ii) selecting a subset of oligonucleotide sequences from the set of oligonucleotide sequences, all edit distances between oligonucleotide sequences of the subset of oligonucleotide sequences meeting a threshold value, the subset of oligonucleotide sequences forming the set of vNRUMIs, and
(iii) synthesizing the adapters each comprising a double-stranded hybridized region, a single-stranded 5′ arm, a single-stranded 3′ arm, and at least one vNRUMI of the set of vNRUMIs;

(b) amplifying the DNA-adapter products to obtain a plurality of amplified polynucleotides;
(c) sequencing the plurality of amplified polynucleotides, thereby obtaining a plurality of reads associated with the set of vNRUMIs;
(d) identifying, among the plurality of reads, reads associated with a same variable-length, nonrandom unique molecular index (vNRUMI); and
(e) determining a sequence of a DNA fragment in the sample using the reads associated with the same vNRUMI.

2. The method of claim 1 , wherein the threshold value is 3.

3. The method of claim 1 , wherein the set of vNRUMIs comprise vNRUMIs of 6 nucleotides and vNRUMIs of 7 nucleotides.

4. The method of claim 1 , wherein (e) comprises collapsing reads associated with the same vNRUMI into a group to obtain a consensus nucleotide sequence for the sequence of the DNA fragment in the sample.

5. The method of claim 4 , the consensus nucleotide sequence is obtained based partly on quality scores of the reads.

6. The method of claim 1 , wherein (e) comprises:
identifying, among the reads associated with the same vNRUMI, reads having a same read position or similar read positions in a reference sequence, and
determining the sequence of the DNA fragment using reads that (i) are associated with the same vNRUMI and (ii) have the same read position or similar read positions in the reference sequence.

7. The method of claim 1 , wherein the set of vNRUMIs includes no more than about 10,000 different vNRUMIs.

8. The method of claim 7 , wherein the set of vNRUMIs includes no more than about 1,000 different vNRUMIs.

9. The method of claim 8 , wherein the set of vNRUMIs includes no more than about 200 different vNRUMIs.

10. The method of claim 1 , applying adapters to the DNA fragments in the sample comprises applying adapters to both ends of the DNA fragments in the sample.

Assignees

• Illumina Inc

Inventors

• Wu Kevin
• Zhao Chen
• Chuang Han-Yu
• So Alex
• Tanner Stephen
• Gross Stephen M

Classifications

• C12Q2525/204

  specific length of the oligonucleotides · CPC title

• C12Q2525/191

  incorporating an adaptor · CPC title

• C12Q2535/122

  Massive parallel sequencing · CPC title

• G16B25/20

  Polymerase chain reaction [PCR]; Primer or probe design; Probe optimisation · CPC title

• G16B30/10 Primary

  Sequence alignment; Homology search · CPC title