Granted Patent B2

US 12,331,353 · App. 18/592,843 · Granted Jun 17, 2025

Inventors: Radoje Drmanac (Los Altos Hills, CA); Matthew J. Callow (Redwood City, CA); Snezana Drmanac (Los Altos Hills, CA); Brian K. Hauser (Campbell, CA); George Yeung (Mountain View, CA)

Assignee: Complete Genomics, Inc.

C12Q1/6874C07H21/04C07K1/047C12Q1/6806C12Q1/682C12Q1/6837C12Q1/6869G01N15/1404G01N15/1434C12Q2525/151C12Q2525/313C12Q2531/125C12Q2565/513Y10S977/778Y10S977/789Y10S977/792Y10S977/88Y10S977/882

Abstract

Claims (32)

1. A method of characterizing polynucleotide molecules, said method comprising the steps of:

(a) providing a solid support comprising a surface;

(b) providing a plurality of polynucleotide molecules attached to the surface, wherein each polynucleotide molecule has a random coil state and comprises a concatemer of multiple copies of one or more target sequences,

wherein each polynucleotide molecule is attached to the surface within a binding region substantially equivalent to a projection of the random coil on the surface,

wherein the polynucleotide molecules are arranged on the surface such that the polynucleotide molecules can be resolved by optics of an imaging system; and then

(c) detecting complete or partial nucleotide sequences of said one or more target sequences from said polynucleotide molecules from images of said plurality of polynucleotide molecules obtained using said imaging system;

wherein the solid support is not a bead.

2. The method of claim 1 , wherein density of said polynucleotide molecules on the surface is at least 10 million per mm 2 .

3. The method of claim 1 , wherein said concatemers have a diameter of from 100 to 300 nm.

4. The method of claim 1 , wherein said concatemers are generated by rolling circle replication.

5. The method of claim 1 , wherein each of said concatemers contains at least 10 copies of its respective target sequences.

6. The method of claim 1 , wherein said nucleotide sequences are detected by probe hybridization, probe-probe ligation, or sequencing by synthesis.

7. The method of claim 6 , wherein said nucleotide sequences are detected by scanning electron microscopy, near field scanning optical microscopy (NSOM), or total internal reflection fluorescence microscopy (TIRFM).

8. The method of claim 1 , wherein said imaging system is a 10 megapixel camera that has a 20× lens with a 1.25 mm field of view.

9. The method of claim 1 , wherein at least 90% of the binding regions on the surface have a single species of said polynucleotide molecules per region.

10. The method of claim 9 , wherein 80% to 99% of the binding regions on the surface are occupied.

11. A method of characterizing polynucleotide molecules, said method comprising the steps of:

(a) providing a solid support comprising a surface;

(b) providing a plurality of polynucleotide molecules attached to the surface, wherein each polynucleotide molecule has a random coil state and comprises a concatemer of multiple copies of one or more target sequences,

wherein each polynucleotide molecule is attached to the surface within a region substantially equivalent to a projection of the random coil on the surface;

wherein the polynucleotide molecules are arranged on the surface at a density of at least 10 million per mm 2 ; and then

(c) detecting complete or partial nucleotide sequences of said one or more target sequences from said polynucleotide molecules;

wherein the solid support is not a bead.

12. A method of characterizing polynucleotide molecules, said method comprising the steps of:

(a) providing a solid support comprising a surface;

(b) providing a plurality of polynucleotide molecules attached to the surface, wherein each polynucleotide molecule has a random coil state and comprises a concatemer of multiple copies of one or more target sequences,

wherein each polynucleotide molecule is attached to the surface within a binding region substantially equivalent to a projection of the random coil on the surface;

wherein the polynucleotide molecules are arranged on the surface such that at least 90% of said binding regions on the surface have a single species of said polynucleotide molecules per region; then

(c) detecting complete or partial nucleotide sequences of said one or more target sequences from said polynucleotide molecules;

wherein the solid support is not a bead.

13. The method of claim 12 , wherein 80% to 99% of the binding regions on the surface are occupied.

14. The method of claim 1 , wherein said one or more target sequences are each a sequence of a cDNA molecule.

Assignments (2)

Continuity (11)

References Cited (400)