초록 ▼

The invention relates to methods and devices for analyzing single molecules, i.e. nucleic acids. Such single molecules may be derived from natural samples, such as cells, tissues, soil, air and water without separating or enriching individual components. In certain aspects of the invention, the meth

The invention relates to methods and devices for analyzing single molecules, i.e. nucleic acids. Such single molecules may be derived from natural samples, such as cells, tissues, soil, air and water without separating or enriching individual components. In certain aspects of the invention, the methods and devices are useful in performing nucleic acid sequence analysis by probe hybridization.

대표청구항 ▼

1. A method for determining all or part of the sequence of a plurality of target nucleic acid sequences comprising: (a) providing an array comprising a plurality of different target nucleic acid sequences randomly distributed on a surface of said array, wherein each target nucleic acid comprises a f

1. A method for determining all or part of the sequence of a plurality of target nucleic acid sequences comprising: (a) providing an array comprising a plurality of different target nucleic acid sequences randomly distributed on a surface of said array, wherein each target nucleic acid comprises a first target domain and an adjacent second target domain, wherein said first and second target domains each comprise multiple nucleotides;(b) contacting said array with: (i) a first probe set comprising: 1. a first probe pool comprising probes complementary to said first target domains;2. a second probe pool comprising probes complementary to said second target domains; wherein at least one of said first and second probe pools comprises a label; (c) ligating probes from said first probe pool and probes from said second probe pool when hybridized to said first and second target domains to form first ligated probes;(d) detecting said first ligated probes to determine at least one nucleotide of said first target domain;(e) removing said first ligated probes;(f) repeating steps (b)-(d) to determine all nucleotides of said first target domain, wherein each nucleotide of said first target domain is determined multiple times. 2. A method according to claim 1 wherein said label is selected from the group consisting of fluorophores, radioisotopes, chromophores, and chemiluminescent moieties. 3. A method according to claim 1 wherein each of said first and second probe pools comprises a label. 4. A method according to claim 3 wherein the label on said first probe pool and the label on said second probe pool are FRET pairs. 5. A method according to claim 3, wherein said label is attached to the terminus of each of said first and second probe pools. 6. A method according to claim 5, wherein said probes of said first probe pool have free 3′ hydroxyl groups and wherein said probes of said second probe pool have free 5′ phosphate groups. 7. A method according to claim 1, wherein said plurality of target nucleic acid sequences comprise genomic DNA. 8. A method according to claim 1, wherein said first and second probe pools comprise probes of 8 to 10 bases in length. 9. A method according to claim 1, wherein said plurality of target nucleic acids comprises at least about 100, 1000, 10,000, 100,000, 1 million, or 10 million target nucleic acids. 10. A method according to claim 1, wherein said plurality of target nucleic acids are treated with a phosphatase such that said target nucleic acids are unable to ligate to each other. 11. A method according to claim 1, wherein said plurality of target nucleic acids are prepared so that they cannot be ligated to each other through amplification with random primers that have no phosphate at their 5′ ends. 12. A method according to claim 1, wherein said plurality of target nucleic acids is immobilized to said surface. 13. A method according to claim 12, wherein said plurality of target nucleic acids is immobilized to said surface at a density of a single target nucleic acid per pixel. 14. A method according to claim 12, wherein said plurality of target nucleic acids is immobilized to said surface by a member selected from: passive adsorption, UV light, covalent binding, and formation of an amide bond between said target nucleic acids and said surface. 15. A method according to claim 12, wherein said plurality of target nucleic acids is immobilized to said surface through a reactive group, wherein said reactive group is a member selected from a hydroxyl group, a carboxyl group, and an amino group. 16. A method according to claim 12, wherein each of said plurality of target nucleic acids comprises an adapter, wherein said surface comprises capture oligonucleotides, and wherein said plurality of target nucleic acids are immobilized to said surface through hybridization of said adapters to said capture oligonucleotides. 17. A method according to claim 1, wherein probes within the same pool cannot ligate to each other. 18. A method according to claim 1, wherein said label is attached to said at least one of said first and second probe pools using a method that is a member selected from: direct chemical labeling, kinasing and nick-translation. 19. A method according to claim 1, wherein prior to said detecting step (d), unligated probes are removed from said array. 20. A method according to claim 1, wherein at least one of said first and second probe pools is a universal probe pool comprising probes of 10 bases in length. 21. A method according to claim 1, wherein prior to said contacting step (b), said target nucleic acid sequences undergo in situ amplification. 22. A method according to claim 21, wherein said target nucleic acid sequences are amplified at least 10-, 100-, 1000-, or 10,000-fold. 23. A method according to claim 1, wherein all of said probes in said first probe pool comprise an identical sequence. 24. A method according to claim 1, wherein said plurality of target nucleic acids comprises one or more genomes. 25. A method according to claim 1, wherein said plurality of target nucleic acids comprises a member selected from entire genes, mixtures of genes, mixtures of mRNAs, segments of chromosomes, entire chromosomes, and mixtures of chromosomes. 26. A method for determining all or part of the sequence of a plurality of target nucleic acid sequences comprising: (a) providing an array comprising a plurality of different target nucleic acid sequences randomly distributed on a surface of said array, wherein each target nucleic acid comprises a first target domain and an adjacent second target domain, wherein said first and second target domains each comprise multiple nucleotides;(b) contacting said array with: (i) a first probe set comprising: 1. a first probe pool comprising probes complementary to said first target domains;2. a second probe pool comprising probes complementary to said second target domains; wherein at least one of said first and second probe pools comprises a label; (c) ligating probes from said first probe pool and probes from said second probe pool when hybridized to said first and second target domains to form first ligated probes;(d) detecting said first ligated probes to determine at least one nucleotide of said first target domain;(e) removing said first ligated probes;(f) contacting said array with: (i) a second probe set comprising: 1. a third probe pool comprising probes complementary to said first target domains;2. a fourth probe pool comprising probes complementary to said second target domains; wherein at least one of said third and fourth probe pools comprises a label; (g) ligating probes from said third probe pool and probes from said fourth probe pool when hybridized to said first and second target domains to form second ligated probes;(h) detecting said second ligated probes to determine at least one nucleotide of said first target domain, wherein at least one nucleotide of said first target domain is determined by both said detecting of said first ligated probes and said detecting of said second ligated probes.