# US 12,110,537 B2 · Capture reactions

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- Number: US 12,110,537 B2
- Document ID: US12110537B2
- Status: Granted
- Kind: B2
- Application number: 16/901,467
- Filed: 2020-06-15
- Published: 2021-04-29
- Granted: 2024-10-08
- Earliest claimed: 2012-04-16
- Assignees: Molecular Loop Biosciences, Inc.
- Applicants: Molecular Loop Biosciences, Inc.
- Inventors: Mark Umbarger; Gregory Porreca; Charles Towne; George Church
- Web page: https://patentgrep.com/patent/US12110537B2

## CPC

- C12Q 1/6816: characterised by the detection means (C12Q1/6804 takes precedence)
- C12Q 1/6806: Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence)
- C12Q 1/6813: Hybridisation assays
- C12Q 1/6869: Methods for sequencing
- C12Q: MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS (immunoassay G01N33/53); COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES

## Abstract

The invention generally relates to methods of performing a capture reaction. In certain embodiments, the method involves obtaining a nucleic acid, fragmenting the nucleic acid, and capturing a target sequence on the nucleic acid fragment using a capture moiety, such as a molecular inversion probe.

## Claims

### Claim 1

A method of improving performance of molecular inversion probe capture reactions, the method comprising:
fragmenting nucleic acid into a plurality of fragments by heating a buffer comprising the nucleic acid to about 65 degrees C. for at least about 16 hours to shift pH of the buffer to between about 6 and about 6.5 to hereby initiate acid hydrolysis;
introducing a plurality of molecular inversion probes (MIPs) to the plurality of fragments, wherein each of the plurality of MIPs hybridize to the fragments and captures a different one of a plurality of overlapping subregions of the same strand of a fragment, wherein the fragmenting step promotes hybridization of the MIPs to the fragments;
circularizing the hybridized MIPs;
amplifying the circularized MIPs to generate amplicons; and
sequencing the amplicons.

### Claim 2 (depends on 1)

The method of claim 1, further comprising the step of denaturing the nucleic acid or at least one of the plurality of fragments prior to the introducing step.

### Claim 3 (depends on 1)

The method of claim 1, wherein the plurality of fragments are from about 10 kb to about 20 kb in length.

### Claim 4 (depends on 1)

The method of claim 1, wherein the plurality of fragments are from about 1 kb to about 10 kb in length.

### Claim 5 (depends on 1)

The method of claim 1, wherein the nucleic acid is genomic DNA, wherein the plurality of MIPs includes thousands of probes, and wherein the introducing step includes capturing thousands of the subregions using the thousands of probes in a single reaction.

### Claim 6 (depends on 2)

The method of claim 2, wherein the genomic nucleic acid is genomic DNA and the method comprises: obtaining a sample comprising the genomic DNA; determining a concentration of the genomic DNA in the sample; and performing the introducing step at a predetermined ratio of the plurality of MIPs to the genomic DNA.

### Claim 7 (depends on 1)

The method of claim 1, wherein a greater number of the MIPs hybridize to the fragments than would hybridize to un-fragmented genomic nucleic acid.

### Claim 8 (depends on 1)

The method of claim 1, wherein the MIPs capture the subregions with a distribution that is more uniform than if the MIPs were exposed to the un-fragmented genomic nucleic acid.

### Claim 9

A method of improving performance of molecular inversion probe capture reactions, the method comprising:
fragmenting genomic nucleic acid suspended in a buffer into a plurality of fragments wherein the fragmenting is performed by heating the buffer to about 65 degrees C. for at least about 16 hours to thereby lower pH and initiate acid hydrolysis;
introducing a plurality of molecular inversion probes (MIPs) to the plurality of fragments, wherein each of the plurality of MIPs hybridize to the fragments and captures a different one of a plurality of overlapping subregions of the same strand of a fragment, wherein the fragmenting step promotes hybridization of the MIPs to the plurality of fragments;
circularizing the hybridized MIPs;
amplifying the circularized MIPs to generate amplicons; and
sequencing the amplicons.

### Claim 10 (depends on 9)

The method of claim 9, wherein the plurality of MIPs hybridize to the fragment in a staggered probe layout.

### Claim 11 (depends on 9)

The method of claim 9 wherein the plurality of MIPs hybridize to the fragment in an alternating staggered probe layout.

### Claim 12 (depends on 9)

The method of claim 9, wherein the plurality of MIPs hybridize to the fragment in a tile probe layout.

### Claim 13 (depends on 9)

The method of claim 9, wherein the plurality of fragments are from about 5 kb to about 100 kb in length.

### Claim 14 (depends on 9)

The method of claim 9, wherein the plurality of fragments are from about 1 kb to about 10 kb in length.

### Claim 15 (depends on 9)

The method of claim 9, wherein the nucleic acid is selected from the group of genomic DNA, RNA, whole or partial genome amplification product, high molecular weight DNA, and high molecular weight RNA.

### Claim 16 (depends on 9)

The method of claim 9, wherein a greater number of the MIPs hybridize to the fragments than would hybridize to un-fragmented genomic nucleic acid and wherein the MIPs capture the subregions with a distribution that is more uniform than if the MIPs were exposed to the un-fragmented genomic nucleic acid.