IP Library Granted Patent US 12,545,950
Granted Patent B2
US 12,545,950 · App. 17/311,521 · Granted Feb 10, 2026

Methods for preparing CDNA samples for RNA sequencing, and CDNA samples and uses thereof

Inventors: Yexun Wang (Ellicott City, MD); Marcus Lewis (Clarksburg, MD)
Assignee: QIAGEN Sciences, LLC
C12Q1/6853C12Q1/6848
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Quick Facts
Patent No.
US 12,545,950
App. No.
17/311,521
Granted
Feb 10, 2026
Kind
B2
Abstract

The invention relates to methods for preparing cDNA samples for RNA sequencing using random priming oligonucleotides comprising a cell barcode (cID), a unique molecular index (UMI), and a random sequence region, and performing a reverse transcription reaction (RT). The invention also relates to cDNA samples prepared by the methods and uses thereof.

Claims (11)

1 . A method of generating a cDNA sample, comprising

adding to an RNA sample, a plurality of random priming oligonucleotides, each random priming oligonucleotide comprising a cell barcode (cID), a unique molecular index (UMI), and a random sequence region of 5 to 8 nucleotides, and

performing a reverse transcription reaction (RT),

wherein the random sequence region consists of (a) random nucleotides selected from A, C, and T bases; (b) 5 random nucleotides selected from A, C, G, and T bases and 3 G bases; (c) 5 random nucleotides selected from A, C, G, and T bases and 3 G bases in a 5′ to 3′ direction; (d) 5 random nucleotides selected from A, C, G, and T bases and 3 T bases; or (e) 5 random nucleotides selected from A, C, G, and T bases and 3 T bases in a 5′ to 3′ direction.

2 . The method of claim 1 , wherein the random priming oligonucleotides further comprise a universal PCR handle.

3 . The method of claim 2 , further comprising adding a template switching oligonucleotide (TSO) comprising a 5′ universal PCR handle and performing a template switching reaction (TS) to generate a cDNA sample comprising a universal PCR handle at the 5′ end and at the 3′ end.

4 . The method of claim 3 , wherein the TS is decoupled from the RT.

5 . The method of claim 2 , further comprising adding a homopolymer oligonucleotide tail to a first strand cDNA by adding a terminal transferase (TdT) and then performing a primer extension reaction using a template switching oligonucleotide (TSO) comprising a 5′ universal PCR handle, wherein the TSO hybridizes to the homopolymer oligonucleotide tail and the primer extension reaction generates a second strand cDNA comprising a universal PCR handle at the 5′ end and at the 3′ end.

6 . The method of claim 1 , wherein two or more of the random priming oligonucleotides bind to a single RNA molecule.

7 . The method of claim 1 , further comprising performing an amplification reaction to generate a cDNA sample.

8 . The method of claim 7 , further comprising sequencing the cDNA sample.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2021
From: WANG, YEXUN; LEWIS, MARCUS
To: QIAGEN SCIENCES, LLC
Reel/Frame 058390/0747 →
Continuity (2)
Provisional Application 62776697 · Dec 7, 2018
Related Publication 20220017954A1 · Jan 20, 2022
References Cited (46)
US 4683195A · Mullis et al. · 1987 [cited by applicant]
US 4683202A · Mullis · 1987 [cited by applicant]
US 4965188A · Mullis et al. · 1990 [cited by applicant]
US 6432360B1 · Church · 2002 [cited by applicant]
US 6485944B1 · Church et al. · 2002 [cited by applicant]
US 6511803B1 · Church et al. · 2003 [cited by applicant]
US 7425431B2 · Church et al. · 2008 [cited by applicant]
US 10131958B1 · Fan et al. · 2018 [cited by applicant]
US 20060014167A1 · Church · 2006 [cited by examiner]
US 20090018024A1 · Church et al. · 2009 [cited by applicant]
US 20110013845A1 · Tu et al. · 2011 [cited by applicant]
US 20120010091A1 · Linnarson · 2012 [cited by examiner]
US 20140357500A1 · Vigneault et al. · 2014 [cited by applicant]
US 20160053253A1 · Salathia et al. · 2016 [cited by applicant]
US 20170268056A1 · Vigneault et al. · 2017 [cited by applicant]
US 20180002764A1 · Fan · 2018 [cited by examiner]
US 20180163201A1 · Larson · 2018 [cited by applicant]
US 20180208975A1 · Peterson et al. · 2018 [cited by applicant]
WO 2005082098A2 · 2005 [cited by applicant]
WO 2006073504A2 · 2006 [cited by applicant]
WO 2010107416A1 · 2010 [cited by applicant]
WO 2015103339A1 · 2015 [cited by applicant]
WO 2017040306A1 · 2017 [cited by applicant]
WO 2017053905A1 · 2017 [cited by applicant]
WO 2018144813A1 · 2018 [cited by applicant]
Frohman et al. Proceedings of the National Academy of Sciences, USA 1988; 85: 8998-9002 (Year: 1988). [cited by examiner]
Blanco et al., “Highly Efficient DNA Synthesis by the Phage o29 BNA Polymerase,” The Journal of Biological Chemistry, 1989, vol. 264(15), pp. 8935-8940, Elsevier, Amsterdam, Netherlands. [cited by applicant]
International Preliminary Report on Patentability dated Jun. 17, 2021, issued in International Application No. PCT/US2019/064977. [cited by applicant]
International Search Report and Written Opinion of the International Searching Authority dated Mar. 9, 2020 in International Application No. PCT/US2019/064977. [cited by applicant]
Islam et al., “Characterization of the single-cell transcriptional landscape by highly multiplex RNA-seq,” Genome Research, 2011, vol. 21, pp. 1160-1167, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York. [cited by applicant]
Jaitin et al., “Massively parallel single cell RNA-Seq for marker-free decomposition of tissues into cell types,” Science, 2014, vol. 343(6172), pp. 776-779, American Association for the Advancement of Science, Washingt… [cited by applicant]
Kivioja et al., “Counting absolute numbers of molecules using unique molecular identifiers,” Nature Methods, 2012, vol. 9(1), pp. 72-76, Nature Portfolio, Berlin, Germany. [cited by applicant]
Kwok, “High-throughput genotyping assay approaches,” Pharmacogenomics, 2000, vol. 1(1), pp. 1-5, Ashley Publications Ltd., London, United Kingdom. [cited by applicant]
Landegren et al., “Reading Bits of Genetic Information: Methods for Single-Nucleotide Polymorphism Analysis,” Genome Research, 1998, vol. 8, pp. 769-776, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York. [cited by applicant]
Notomi et al., “Loop-mediated isothermal amplification of DNA,” Nucleic Acids Research, 2000, vol. 28(12), pp. i-vii, Oxford University Press, Oxford, United Kingdom. [cited by applicant]
Porreca et al., “Multiplex amplification of large sets of human exons,” Nature Methods, 2007, vol. 4, pp. 931-936, Nature Portfolio, Berlin, Germany. [cited by applicant]
Shendure et al., “Accurate Multiplex Polony Sequencing of an Evolved Bacterial Genome,” Science, 2005, vol. 309, pp. 1728-1732, American Association for the Advancement of Science, Washington, DC. [cited by applicant]
Shi, “Enabling Large-Scale Pharmacogenetic Studies by High-Throughput Mutation Detection and Genotyping Technologies,” Clinical Chemistry, 2001, vol. 47(20), pp. 164-0172, Oxford University Press, Oxford, United Kingdom. [cited by applicant]
Xiong, et al., “A Comparison of mRNA Sequencing with Random Primed and 3′-Directed Libraries,” Scientific Reports, Nov. 2017, vol. 7:14626, Nature Research, Springer Nature. [cited by applicant]
Zhu et al., “Reverse Transcriptase Template Switching: A Smart Approach for Full-Length cDNA Library Construction,” BioTechniques, 2001, vol. 30(4), pp. 892-897, London, England. [cited by applicant]
Ziegenhain et al., “Comparative Analysis of Single-Cell RNA Sequencing Methods,” Molecular Cell Article, 2017, vol. 65, pp. 631-673, Elsevier, Amsterdam, Netherlands. [cited by applicant]
Lizardi et al., “Mutation detection and single-molecule counting using isothermal rolling-circle amplification,” Nature Genetics, 1998, vol. 19, pp. 225-232, Nature Portfolio, Berlin, Germany. [cited by applicant]
Wu et al., “The Ligation Amplification Reaction (LAR)—Amplification of Specific DNA Sequences Using Sequential Rounds of Template-Dependent Ligation,” Genome, 1989, vol. 4(4), pp. 560-569, Elsevier, Amsterdam, Netherlan… [cited by applicant]
Fan et al., Single-cell RNA-seq transcriptome analysis of linear and circular RNAs in mouse preimplantation embryos, Genome Biology, vol. 16, No. 1, 2015. [cited by applicant]
Islam et al., Highly multiplexed and strand-specific single-cell RNA 5′ end sequencing, Nature Protocols, vol. 7, No. 5., 2012. [cited by applicant]
The extended European Search Report completed Aug. 3, 2022 for European Application No. 19893636.1. [cited by applicant]