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이종극
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제1부유전체분석제1장DNA-RNA-Protein/11.유전정보의전달/12.DNA/43.RNA/84.단백질(Protein)/12제2장DNA분석기술/181.DNA분리기술/182.재조합DNA클로닝기술/233.PCR증폭기술/34제3장유전체지도작성법/411.유전마커/422.유전지도의분류/453.유전체지도작성/50제4장유전체염기서열분석법/551.DNA염기서열분석법의원리/552.대용량염기서열분석법/583.인간유전체사업/614.개인유전체염기서열분석/67제5장유전체정보의해석/781.유전체염기서열해석방법/782.유전체의구성/82제6장기능유전체학/891.전사체학/902.단백질체학/963.오믹스학/103제2부유전변이분석제7장인간유전체와유전변이/1051.세포와염색체/1052.염색체와유전자/1073.유전체와유전변이형/1104.단위반복유전변이형/1155.단일염기다형성변이형/116제8장유전변이형발굴/1291.유전변이형의발굴방법/1292.염기서열정보에기초한SNP발굴/1303.SNP발굴을위한적정시료의수/1344.다형성및돌연변이표시법/1375.국제SNP발굴협의체/1396.SNP데이터베이스/140제9장유전변이형검사법/1451.전통적유전변이형검사법/1452.SNPgenotyping의원리/1473.SNPgenotyping의방법/1514.SNPgenotyping기술의응용:DNApoolinggenotyping분석/1625.Genotyping데이터에대한QC및최적의시스템선별기준/165제10장일배체형검사법/1691.단일염기다형성(SNP)과일배체형(haplotype)/1692.Haplotyping방법/1723.Haplotype-taggingSNP(htSNP)/1754.Haplotypetree분석/177제11장유전체연관구조(LD)와HapMap/1831.유전자재조합과유전자연관/1832.유전체연관(LD)의계산방법/1863.유전체연관구조(LDblocks)의조사방법/1904.유전체연관(LD)에영향을미치는요인들/1925.유전체연관구조의패턴/1956.국제일배체형지도작성사업(InternationalHapMapProject)/1997.HapMapENCODEProject/2038.1000GenomesProject/207제12장기초통계유전학/2111.유전자와유전형/2112.표현형과유전형의관계/2123.유전자빈도와유전형빈도의계산/2134.하디-와인버그법칙/2145.유전변이의측정/2196.유전적다양성에영향을미치는요인들/228제3부질병연관성분석제13장표현형(질병)의분류와질병유전자탐색전략/2311.표현형(질병)의분류/2312.표현형의다양성에관여하는요인들/2333.표현형(질병)의분류기준/2374.질병의유전학적분류와질병유전자발굴전략/2405.질병의유전적특성에따른질병유전자발굴방법/243제14장연관성연구/2561.연관성연구의의미/2562.연관성연구의개요/2573.연관성연구의방법/2604.전장유전체연관성연구/282제15장유전자-유전자및유전자-환경의상호작용/2981.유전자-유전자의상호작용/2982.유전자-성별간의상호작용/2993.유전자-환경의상호작용/3024.환경에의한유전변이의선발/3105.유전자-환경상호작용에의한선발로인종간차이를보이는표현형/314제16장유전변이형의기능연구/3201.유전변이형의기능연구에대한배경설명/3202.유전자발현을조절하는유전변이형의기능연구/3213.아미노산서열을변화시키는유전변이형의기능연구/3314.Splicingsites를변화시키는유전변이형의기능연구/3355.Non-coding유전변이형과질병연관성/3356.빈도가낮은희귀유전변이형에대한유전분석/338제17장유전자발현조절의유전분석/3451.유전자발현의유전분석필요성/3452.대립유전자발현의유형분류/3473.대립유전자발현조절분석기술/3564.통합유전체정보분석을통한유전자발현조절기전연구/362제18장유전체복제수변이형(CNV)분석/3671.유전체의구조적변이형의종류/3672.유전체의구조적변이형의분석방법/3693.유전체복제수변이형(CNV)의분석방법비교/3714.인간유전체에존재하는유전체복제수변이형(CNV)의분포/3765.유전체복제수변이형(CNV)과질병의연관성/3786.유전체복제수변이형(CNV)데이터베이스/384제4부질병유전체분석법의활용제19장엑솜염기서열분석을통한질병유전자발굴/3871.질병유전자와질병원인유전변이형의종류/3872.엑솜염기서열분석방법의개요/3893.엑솜염기서열분석방법을이용한희귀유전질병유전자발굴/3954.엑솜분석을이용한복합질병유전자발굴/404제20장암유전체정보분석/4151.유전변화에의한암발생기전/4152.암유전체정보를이용한표적항암치료/4213.혈액내암DNA정보를이용한암조기진단및치료반응성검사/426제21장비침습적산전태아유전검사/4321.CirculatingNucleicAcids(CNA)의특성/4322.CirculatingFetalDNA의특성/4343.CirculatingFetalDNA를이용한산전진단/4384.CirculatingFetalRNA를이용한산전진단/449제22장약물반응성유전자발굴/4551.약물반응성과유전/4552.약물유전체연구방법/4563.약물반응성에대한인종간차이/4624.약물유전체학의임상적용/463제23장개체식별용유전검사법/4701.개체식별용유전검사의발전과정/4702.STR마커를이용한개체식별기술/4713.SNP마커를이용한개체식별기술/4734.SNP마커를이용한표현형식별기술/4815.개체식별용SNP마커를이용한임상진단기술/488제24장유전체바이오마커발굴과미래맞춤의학/4921.유전체바이오마커발굴/4922.유전검사의원리/4953.개인유전체분석을통한유전검사/5124.미래맞춤의학/518[부록]유전체연구관련선진기술의동향및신기술소개/5251.Real-TimePCR및반도체차세대시퀀서기술(최정룡·박근준)/5272.AgilentTargetEnrichmentSystem과LibraryQC(김자은·김민주)/5343.최신GenomeMappingSystem을활용한유전체해독기술(김남일)/5414.차세대게놈해독(NextGenerationSequencing)기술기반의암패널(이승연)/5465.Bio-Rad사,QX200TMDropletDigitalTMPCRSystem(장미현)/550