High Density Sequence Detection Methods
A method for performing PCR on a liquid sample comprising a plurality of polynucleotide targets, wherein each polynucleotide target is present at very low concentration within the sample. The method comprises applying PCR reactants to the surface of a substrate to produce a plurality of reaction spots on the surface of the substrate; loading the liquid sample and a PCR reagent mixture onto the reaction spots; forming a sealed reaction chamber, having a volume of less than about 20 nanoliters, over each of the reaction spots; and amplifying the sample.
1 . A method for performing PCR on a liquid sample comprising a plurality of polynucleotide targets, each polynucleotide target being present at very low concentration within the sample, comprising:
applying PCR reactants to the surface of a substrate to produce a plurality of reaction spots on the surface of the substrate;
loading the liquid sample and a PCR reagent mixture onto the reaction spots;
forming a sealed reaction chamber, having a volume of less than about 20 nanoliters, over each of the reaction spots; and
amplifying the sample.
2 . A method according to claim 1 , wherein said surface of the substrate comprises a plurality of reaction spots, wherein each spot comprises PCR reactants comprising at least one probe and set of primers for one or more targets among said polynucleotide targets.
3 . A method according to claim 1 further comprising loading said liquid sample and said reagent mixtures in separate steps.
4 . A method according to claim 3 further comprising removing said liquid sample from said surface prior to said applying of said PCR reagent mixture.
5 . A method according to claim 3 , comprising the additional sub-step of removing said PCR reagent mixture from the surface of said substrate adjacent to said reaction spots, after applying of said PCR reagent mixture.
6 . A method according to claim 1 , wherein the applying said PCR reactants comprises spraying said reactants on said surface of the substrate.
7 . A method according to claim 1 , wherein said forming comprises loading a sealing fluid on said surface of the substrate so as to substantially cover the reaction spots.
8 . A method according to claim 1 , wherein said reaction chamber has a volume of from about 1 to about 5 nanoliters.
9 . A method according to claim 1 further comprising providing said substrate comprising hydrophobic regions and hydrophilic reaction spots.
10 . A method according to claim 1 further comprising depositing a hydrophilic material to said reaction spots on said substrate before the applying PCR reactants.
11 . A method according to claim 1 further comprising producing at least about 10,000 reaction spots.
12 . A method according to claim 1 further comprising detecting an amplification of the sample.
13 . A method for simultaneously quantitatively detecting a plurality of polynucleotide targets in a liquid sample comprising a genomic mixture of polynucleotides present at very low concentration, comprising:
(a) distributing the liquid sample into an array of reaction chambers on a planar substrate, wherein
(i) each chamber has a volume of less than about 100 nanoliters, and
(ii) each chamber comprises (1) at least one amplification primer for one of the polynucleotide targets, and (2) a probe associated with the primer which emits a concentration dependent signal if the amplification primer binds with a polynucleotide, and
(iii) the array comprises at least one chamber comprising at least one amplification primer for each of the polynucleotide targets;
(b) performing amplification on the samples in the array so as to increase the concentration of polynucleotide in each of the chambers in which the polynucleotide binds to a amplification primer; and
(c) identifying which of the reaction chambers contains a polynucleotide that has been bound to a amplification primer, by detecting the presence of the probe associated with the amplification primer.
14 . A method according to claim 13 further comprising preamplifying the sample prior to the distributing step, by (1) mixing the portion with reactants comprising a plurality of amplification primers corresponding to the amplification primers in a subset of the chambers of the substrate; (2) thermal cycling the mixture so as to produce a pre-amplified sample; and (3) distributing the preamplified sample to the subset of chambers.
15 . A method according to claim 13 further comprising affixing an amplification reagent to each reaction spot of said surface of said substrate.
16 . A method according to claim 14 , wherein said surface of the substrate comprises a plurality of reaction spots, wherein each spot comprises at least one probe and at least one set of primers for one or more targets among said polynucleotide targets.
17 . A method according to claim 13 further comprising loading said liquid sample and said reagent mixtures in separate steps.
18 . A method according to claim 17 further comprising removing said liquid sample from said surface prior to said applying of said PCR reagent mixture.
19 . A method according to claim 17 , comprising the additional sub-step of removing said PCR reagent mixture from the surface of said substrate adjacent to said reaction spots, after applying of said PCR reagent mixture.
20 . A method according to claim 13 further comprising loading a sealing fluid on said surface of the substrate so as to substantially cover the reaction spots.