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Methods for genomic analysis

a genomic analysis and method technology, applied in the field of genomic analysis, can solve the problems of insufficient therapeutic efficacy or unanticipated side effects, limited understanding of variations between individuals, and insufficient understanding of individual variations, etc., and achieve the complexity of the local haplotype structure of the human genome, and the distance over which individual haplotypes extend

Inactive Publication Date: 2005-12-08
GENETIC TECHNOLOGIES LIMTIED
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  • Abstract
  • Description
  • Claims
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AI Technical Summary

Benefits of technology

[0009] The present invention relates to methods for identifying variations that occur in the human genome and relating these variations to the genetic bases of phenotype such as disease resistance, disease susceptibility or drug response. “Disease” includes but is not limited to any condition, trait or characteristic of an organism that it is desirable to change. For example, the condition may be physical, physiological or psychological and may be symptomatic or asymptomatic. The methods allow for identification of variants, identification of SNPs, determination of SNP haplotype blocks, determining SNP haplotype patterns, and further, identification of informative SNPs for each pattern, which affords genetic data compression.
[0013] Also, the present invention allows for rapid scanning of genomic regions and provides a method for determining disease-related genetic loci or pharmacogenomic-related loci without a priori knowledge of the sequence or location of the disease-related genetic loci or pharmacogenomic-related loci. This can be done by determining SNP haplotype patterns from individuals in a control population, then determining SNP haplotype patterns from individuals in a experimental population, such as individuals in a diseased population or individuals that react in a particular manner when administered a drug. The frequencies of the SNP haplotype patterns of the control population are compared to the frequencies of the SNP haplotype patterns of the experimental population. Differences in these frequencies indicate locations of disease-related genetic loci or pharmacogenomic-related loci.
[0014] An additional aspect of the present invention provides a method of making associations between SNP haplotype patterns and a phenotypic trait of interest comprising: building baseline of SNP haplotype patterns of control individuals by the methods of the present invention; pooling whole genomic DNA from a clinical population having a common phenotypic trait of interest; and identifying the SNP haplotype patterns that are associated with the phenotypic trait of interest. Thus, the present invention allows for genome scanning to identify multiple haplotype blocks associated with a phenotype, which is particularly useful when studying polygenic traits.

Problems solved by technology

Additionally, knowledge of human genetics has led to a limited understanding of variations between individuals when it comes to drug response—the field of pharmocogenetics.
Even more common than toxicity issues may be cases where drugs demonstrated to be safe and / or efficacious for some individuals have been found to have either insufficient therapeutic efficacy or unanticipated side effects in other individuals.
The complexity of local haplotype structure in the human genome—and the distance over which individual haplotypes extend—is poorly defined.
Until the present invention, however, the practice and cost of genotyping over 3,000,000 SNPs across each individual of a reasonably sized population has made this endeavor impractical.

Method used

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  • Methods for genomic analysis
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Examples

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example 1

Preparation of Somatic Cell Hybrids

[0165] Standard procedures in somatic cell genetics were used to separate human DNA strands (chromosomes) from a diploid state to a haploid state. In this case, a diploid human lymphoblastoid cell line that was wildtype for the thymidine kinase gene was fused to a diploid hamster fibroblast cell line containing a mutation in the thymidine kinase gene. A sub-population of the resulting cells were hybrid cells containing human chromosomes. Hamster cell line A23 cells were pipetted into a centrifuge tube containing 10 ml DMEM in which 10% fetal bovine serum (FBS)+1× Pen / Strep+10% glutamine were added, centrifuged at 1500 rpm for 5 minutes, resuspended in 5 ml of RPMI and pipetted into a tissue culture flask containing 15 ml RPMI medium. The lymphoblastoid cells were grown at 37° C. to confluence. At the same time, human lymphoblastoid cells were pipetted into a centrifuge tube containing 10 ml RPMI in which 15% FBCS+1× Pen / Strep+10% glutamine were ad...

example 2

Selecting Haploid Hybrids

[0170] Scoring for the presence, absence and diploid / haploid state of human chromosomes in each hybrid was performed using the Affymetrix, HuSNP genechip (Affymetrix, Inc,. of Santa Clara, Calif., HuSNP Mapping Assay, reagent kit and user manual, Affymetrix Part No. 900194), which can score 1494 markers in a single chip hybridization. As controls, the hamster and human diploid lymphoblastoid cell lines were screened using the HuSNP chip hybridization assay. Any SNPs which were heterozygous in the parent lymphoblastoid diploid cell line were scored for haploidy in each fusion cell line. Assume that “A” and “B” are alternative variants at each SNP location. By comparing the markers that were present as “AB” heterozygous in the parent diploid cell line to the same markers present as “A” or “B” (hemizygous) in the hybrids, the human DNA strands which were in the haploid state in each hybrid line was determined.

[0171]FIG. 11 shows results after two human / hamste...

example 3

Long Range PCR

[0172] DNA from the hamster / human cell hybrids was used to perform long-range PCR assays. Long range PCR assays are known generally in the art and have been described, for example, in the standard long range PCR protocol from the Boehringer Mannheim Expand Long Range PCR Kit, incorporated herein by reference or all purposes.

[0173] Primers used for the amplification reactions were designed in the following way: a given sequence, for example the 23 megabase contig on chromosome 21, was entered into a software program known in the art herein called “repeat masker” which recognizes sequences that are repeated in the genome (e.g., Alu and Line elements)(see, A. F. A. Smit and P. Green, www.genome.washington.edu / uwgc / analysistools / repeatmask, incorporated herein by reference). The repeated sequences were “masked” by the program by substituting each specific nucleotide of the repeated sequence (A, T, G or C) with “N”. The sequence output after this repeat mask substitution ...

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Abstract

The present invention relates to methods for identifying variations that occur in the human genome and relating these variations to the genetic basis of disease and drug response. In particular, the present invention relates to identifying individual SNPs, determining SNP haplotype blocks and patterns, and, further, using the SNP haplotype blocks and patterns to dissect the genetic bases of disease and drug response. The methods of the present invention are useful in whole genome analysis.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS [0001] The present application claims priority to and is a continuation-in-part of U.S. provisional patent application Ser. No. 60 / 280,530, filed Mar. 30, 2001; U.S. provisional patent application Ser. No. 60 / 313,264 filed Aug. 17, 2001; U.S. provisional patent application Ser. No. 60 / 327,006, filed Oct. 5, 2001, all entitled “Identifying Human SNP Haplotypes, Informative SNPs and Uses Thereof”; and U.S. provisional patent application Ser. No. 60 / 332,550, filed Nov. 26, 2001, entitled “Methods for Genomic Analysis”; and the present application also claims priority to and is a continuation of U.S. utility patent application Ser. No. 10 / 106,097, filed Mar. 26, 2002, entitled “Methods for Genomic Analysis”, the disclosures of all of which are specifically incorporated herein by reference in their entireties for all purposes.BACKGROUND OF THE INVENTION [0002] The DNA that makes up human chromosomes provides the instructions that direct the product...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): G01N33/53G16B30/00C07H21/00C07H21/02C07H21/04C12N15/09C12P19/34G01N33/00G01N33/566G16B40/10
CPCC12Q1/6827G16B40/00G16B30/00Y10T436/143333G16B40/10C12Q1/68
Inventor PATIL, NILACOX, DAVIDBERNO, ANTHONYHINDS, DAVID
Owner GENETIC TECHNOLOGIES LIMTIED
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