摘要 |
A composition for analyzing a target nucleic acid sequence obtained or derived from a patient genomic sample and for identifying the patient providing the sample. The composition comprises: a first set of oligonucleotide for identifying the target nucleic acid sequence obtained or derived from the patient sample; a second set of oligonucleotide for identifying marker sequences, wherein the marker sequences are derived from subsequences in the patient genomic sample, the subsequences each including at least one polymorphic marker, the identification of the marker providing for identification of the patient, wherein the oligonucleotides of the first and the second set are attached to beads that are associated with a chemically or physically distinguishable characteristic that identifies the oligonucleotides attached to the beads. Also described is a method for analyzing a target nucleic sequence obtained or derived from a patient genomic sample and for identifying the patient providing the sample, comprising the steps: (a) providing a first set of oligonucleotides for identifying the target nucleic acid sequence obtained or derived from the patient sample; (b) a second set of oligonucleotides for identifying marker sequences that are derived from subsequences each including at least one polymorphic marker, the identification of the marker sequences providing for the identification of the patient, wherein the first and second set of oligonucleotides are attached to beads that are associated with a chemical or physically distinguishable characteristic that identifies the oligonucleotides attached to the beads; (c) contacting the target sequence
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