Microdissection-based methods for determining genomic...

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

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C536S023100, C536S024300

Reexamination Certificate

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11084279

ABSTRACT:
The present provides a microdissection-based method for identifying a genomic feature present within a visible chromosome region. The method includes steps of: (a) micro-dissecting a single copy of a chromosome to obtain a visible chromosome region; (b) amplifying the visible chromosome region to obtain amplified single chromosome DNA; and (c) subjecting the amplified single chromosome DNA to micro-array analysis whereby such analysis identifies at least one genomic feature present within the visible chromosome region. The method is applicable to determining genomic features including, but not limited to, genomic DNA size, gene content, DNA breakpoint, or DNA polymorphism (e.g., single nucleotide polymorphisms).

REFERENCES:
patent: 6664057 (2003-12-01), Albertson et al.
patent: 2005/0112611 (2005-05-01), Helgadottir
Pastinen et al.,Minisequencing : A specific tool for DNA analysis and diagnostics on oligonucleotide arrays. Genome Research 7 : 606-614 (1997).
Wang et al. Large -scale identification, mapping , and genotyping of Single-Nucleotide polymoprphisms in the human genome. Science 280: 1077-1082 (1998).
Meltzer et al. Rapid generation of region specific probes by chromosome microdissection and their application.Nature Genetics 1(1) : 24-28 (Apr. 1992).
Cotter et al. Gene mapping by microdissection and enzymatic amplification : Heterogeneity in Leukemia associated breakpoints on chromosome 11. Gene, Chromosomes & Cancer 3 : 8-15 (1991).

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