Analysis of SNPs in artificially degraded DNA
Project/Area Number |
25893256
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Research Category |
Grant-in-Aid for Research Activity Start-up
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Allocation Type | Single-year Grants |
Research Field |
Legal medicine
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Research Institution | Tokyo Women's Medical University |
Principal Investigator |
MITSUYO Machida 東京女子医科大学, 医学部, 特任助教 (60468692)
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Project Period (FY) |
2013-08-30 – 2015-03-31
|
Project Status |
Completed (Fiscal Year 2014)
|
Budget Amount *help |
¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
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Keywords | SNP解析 / 劣化DNA / DNA損傷 / 個人識別 |
Outline of Final Research Achievements |
DNA in biological fluids at the scene is often degraded by many environmental factors. Short tandem repeats profiling, the most commonly used method for forensic DNA identification, is sometimes difficult to analyze degraded DNA samples. Here we focused on single nucleotide polymorphisms (SNPs) because the amplicon sizes are as short as those of degraded DNA in SNP analysis. To identify the SNPs that are resistant to degradation, we screened the SNPs from reported SNP lists and isolated the SNPs by amplified fragment length polymorphism analysis. Therefore six SNPs (rs891700, rs2111980, rs1360288, rs2116020, rs1636218, rs12293045) were demonstrated as detectable SNPs for degraded DNA samples.
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Report
(3 results)
Research Products
(4 results)
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[Presentation] 変性DNAのSNPs解析2014
Author(s)
町田光世、木林和彦
Organizer
第83回日本法医学会学術関東地方集会
Place of Presentation
東京女子医科大学弥生記念講堂(東京都新宿区)
Year and Date
2014-11-08
Related Report
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