US2003059791A1PendingUtilityA1

Method for evaluating DNA probes position on substrate

Priority: Feb 28, 2001Filed: Feb 27, 2002Published: Mar 27, 2003
Est. expiryFeb 28, 2021(expired)· nominal 20-yr term from priority
G16B 25/20G16B 25/30C12Q 1/6883G16B 25/00C12Q 2600/158C12Q 2565/513C12Q 2600/166
52
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Claims

Abstract

An oligonucleotide array comprising an array of multiple oligonucleotides with different base sequences fixed onto known and separate positions on a support substrate, wherein said oligonucleotides are biological stress related genes or complementary sequence chains to the said genes, and the said oligonucleotides are classified according to their gene functions, wherein the fixation region on the support substrate is divided into the said classification.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . An oligonucleotide array comprising an array of multiple oligonucleotides with different base sequences fixed onto known and separate positions on a support substrate, wherein said oligonucleotides are biological stress related genes or complementary sequence chains to the said genes, and the said oligonucleotides are classified according to their gene functions, wherein the fixation region on the support substrate is divided into the said classification.  
     
     
         2 . An oligonucleotide array comprising multiple subblock regions and oligonucleotides with different base sequences positioned to each of said multiple subblock regions, wherein said oligonucleotides are positioned according to an arrangement pattern wherein oligonucleotides with a first correlation degree are positioned closer to each other than oligonucleotides that have a lower correlation degree.  
     
     
         3 . The oligonucleotide array according to  claim 2  wherein said oligonucleotides are oligonucleotides related to a particular phenotype.  
     
     
         4 . The oligonucleotide array according to  claim 2  wherein said phenotype is related to stress response.  
     
     
         5 . The oligonucleotide array according to  claim 4  wherein said oligonucleotides are one of the following: internal or external standard genes for calibration, stress tolerance or survival related genes and hormonal genes, cytokine genes, apoptosis inducing genes, glucocorticoid and other anti-inflammation related genes and growth repressor genes, immune response related transcription factors and signaling molecules, cell disorder triggering cytokine inductive transcription factors and signaling molecules, growth inhibition related transcription factors and signaling molecules, stress tolerance related transcription factors and signaling molecules.  
     
     
         6 . The oligonucleotide array according to  claim 2  wherein said correlation degrees are those determined in a database.  
     
     
         7 . The oligonucleotide array according to  claim 6  wherein said correlation degrees are determined by one or a combination of two or more of gene inter-relationship score, pairwise information of ligand and receptor, protein-protein interaction information, and gene passway information.  
     
     
         8 . The oligonucleotide array according to  claim 2  wherein said correlation degree is statistically calculated from expression amount of experimental results using samples for comparison, wherein classification algorithm used comprises either one of P value, FDD, SVM and others.  
     
     
         9 . The oligonucleotide array according to  claim 8  wherein said samples comprise samples from patients with a particular disease and samples from healthy subjects.  
     
     
         10 . A method of evaluating label detection of hybridization wherein labeled cell-derived RNA are hybridized to an oligonucleotide array comprising multiple subblock regions and oligonucleotides with different base sequences positioned to each of said multiple subblock regions, wherein said oligonucleotides are positioned according to an arrangement pattern wherein oligonucleotides with a first correlation degree are positioned closer to each other than oligonucleotides that have a lower correlation degree; and said hybridization is label detected.

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