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Worldwide population differentiation at
disease associated SNPs
Hong Chang Bum
Center for Genome Science, NIH, KCDC
Characterizing signals
of selection in humans
Jomon         ,     ,             (2       )
                                                     -        (       ),   (
                               )




     Seto Inland Sea
                       Yayoi
                                   2,000         ,




     Super Science High School(SSH)

48   55 (48 SSH + 7     ), 5               , 1,963
rs17822931(ABCC11)

GG Wet earwax
GA Wet earwax
AA Dry earwax




                G Ancestral allele A derived allele
My Japanese Friends
Worldwide population differentiation at
disease-associated SNPs

~1000 individuals from 53 population, 25 SNPs
6 complex human diseases
SNP                                25

individual                            952

population                 53 (7 geographic regions)


                           6 complex human diseases

                               Crohn’s disease
                               Type 1 diabetes
 disease
                                Type2 diabetes
                             Rheumatoid arthritis
                            Coronary artery disease
                                   Obesity


                               HGDP-CEPH panel
sample 1
                              KBioscience, KASPar

             empirical Fst distribution from 2,750 autosomal marker
sample 2     previously typed in 927 individuals from the CEPH-HGDP
                                       panel
ALFRED(The Allele Frequency Database)




                             HapMap



Allele frequency resources
- lactose tolerance, lactase(LCT) gene
Haplotter - iHS, detect selective sweeps


Selection resources(lactose tolerance,
lactase(LCT) gene)
 - iHS
HGDP Selection Browse




Selection Resources (thicker hair, EDAR
gene)
 - Fst, iHS, XP-EHH, allele frequency
East Asia(red haplotype under selection)   Middle East(no strong recent selection)


Selection Resources (thicker hair, EDAR
gene)
 - expanded haplotype plots
common alleles in one population, not common in
 another population

           frequency of disease-associated alleles show
           “large heterogeneity between races”

 frequency of a risk allele discovered in one
 population is not always a strong predictor of the
 frequency of that risk allele in other populations
                CAD, T2D have been targets of positive natural
                selection
local positive selection results in large allele
frequency differences between population

         positively selected alleles tend to accumulate in the
         top tail of the Fst distribution

                        allele   positive selection
                          .
replication, large
number of population
0     0.05               0.15            0.25                                                              1

   case 1.
   0 <= Fst <= 0.05
   ignore genetic differentiation
                 case 2.
                 0.05 <= Fst < 0.15
                 genetic differentiation


                                    case 3.
           within                   0.15 <= Fst
           E. Asia                  strong genetic differentiation
            0.04
                              Africa
       within
                              Europe
       Europe                                      case 4.
                               0.147
        0.02                                       0.25 <= Fst
                                                   very strong genetic differentiation
                         E. Asia.        E. Asia
             within
                         Europe          Africa
             Africa
                          0.115          0.223                                                                case 5.
  Jeju        0.05                                                                                            1 = Fst
Gyeongju               high difference Fst                                                                    perfect
 0.018               between Korea and Jeju                                                                   isolation
                             0.073


                                                                                                               1


                                                                   Source: Tishoff SA and Kidd KK.(2004). Nature Genetics Suplement
                                                                                              36:S21-27.
rs13266634, T2D
Africa: 0.941
Oceania: 0.911

rs1801281, T2D
Africa: 1
Oceania: 1

rs564398, T2D
Africa: 1
America: 0.937
Global Fst
              provides a
              rough measure
              of the
              magnitude of
              allele frequency
              differentiation
              worldwide




mean global
Fst
Thank You!
@hongiiv
http://
hongiiv.tistory.com



                      HONGII
                        V
                      Open Bioinformatics

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worldwide population

  • 1. Worldwide population differentiation at disease associated SNPs Hong Chang Bum Center for Genome Science, NIH, KCDC
  • 2.
  • 3.
  • 5. Jomon , , (2 ) - ( ), ( ) Seto Inland Sea Yayoi 2,000 , Super Science High School(SSH) 48 55 (48 SSH + 7 ), 5 , 1,963
  • 6. rs17822931(ABCC11) GG Wet earwax GA Wet earwax AA Dry earwax G Ancestral allele A derived allele
  • 8. Worldwide population differentiation at disease-associated SNPs ~1000 individuals from 53 population, 25 SNPs 6 complex human diseases
  • 9. SNP 25 individual 952 population 53 (7 geographic regions) 6 complex human diseases Crohn’s disease Type 1 diabetes disease Type2 diabetes Rheumatoid arthritis Coronary artery disease Obesity HGDP-CEPH panel sample 1 KBioscience, KASPar empirical Fst distribution from 2,750 autosomal marker sample 2 previously typed in 927 individuals from the CEPH-HGDP panel
  • 10. ALFRED(The Allele Frequency Database) HapMap Allele frequency resources - lactose tolerance, lactase(LCT) gene
  • 11. Haplotter - iHS, detect selective sweeps Selection resources(lactose tolerance, lactase(LCT) gene) - iHS
  • 12. HGDP Selection Browse Selection Resources (thicker hair, EDAR gene) - Fst, iHS, XP-EHH, allele frequency
  • 13. East Asia(red haplotype under selection) Middle East(no strong recent selection) Selection Resources (thicker hair, EDAR gene) - expanded haplotype plots
  • 14. common alleles in one population, not common in another population frequency of disease-associated alleles show “large heterogeneity between races” frequency of a risk allele discovered in one population is not always a strong predictor of the frequency of that risk allele in other populations CAD, T2D have been targets of positive natural selection local positive selection results in large allele frequency differences between population positively selected alleles tend to accumulate in the top tail of the Fst distribution allele positive selection .
  • 15.
  • 17. 0 0.05 0.15 0.25 1 case 1. 0 <= Fst <= 0.05 ignore genetic differentiation case 2. 0.05 <= Fst < 0.15 genetic differentiation case 3. within 0.15 <= Fst E. Asia strong genetic differentiation 0.04 Africa within Europe Europe case 4. 0.147 0.02 0.25 <= Fst very strong genetic differentiation E. Asia. E. Asia within Europe Africa Africa 0.115 0.223 case 5. Jeju 0.05 1 = Fst Gyeongju high difference Fst perfect 0.018 between Korea and Jeju isolation 0.073 1 Source: Tishoff SA and Kidd KK.(2004). Nature Genetics Suplement 36:S21-27.
  • 18.
  • 19.
  • 20. rs13266634, T2D Africa: 0.941 Oceania: 0.911 rs1801281, T2D Africa: 1 Oceania: 1 rs564398, T2D Africa: 1 America: 0.937
  • 21. Global Fst provides a rough measure of the magnitude of allele frequency differentiation worldwide mean global Fst
  • 22.
  • 23.
  • 24.
  • 25.
  • 26.
  • 27. Thank You! @hongiiv http:// hongiiv.tistory.com HONGII V Open Bioinformatics

Notes de l'éditeur

  1. &amp;#xB958;&amp;#xBA38;&amp;#xD2F0;&amp;#xC998;&amp;#xC131; &amp;#xAD00;&amp;#xC808;&amp;#xC5FC;, &amp;#xAD00;&amp;#xC0DD;&amp;#xB3D9;&amp;#xB9E5;&amp;#xC9C8;&amp;#xD658;,&amp;#xBE44;&amp;#xB9CC; &amp;#xACB0;&amp;#xB9D0; &amp;#xBD80;&amp;#xBD84;&amp;#xC5D0;&amp;#xC11C;&amp;#xB294; &amp;#xC9C8;&amp;#xBCD1;&amp;#xACFC; &amp;#xAD00;&amp;#xB828;&amp;#xB41C; SNP&amp;#xC740; &amp;#xC9C0;&amp;#xB188;&amp;#xC0C1;&amp;#xC758; &amp;#xB79C;&amp;#xB364;&amp;#xD55C; SNP&amp;#xACFC; &amp;#xBE44;&amp;#xAD50;&amp;#xD574;&amp;#xC11C; frequency&amp;#xC5D0; &amp;#xBCC4;&amp;#xBC18; &amp;#xCC28;&amp;#xC774;&amp;#xAC00; &amp;#xC5C6;&amp;#xB2E4;. &amp;#xC989; positive local selection&amp;#xC740; &amp;#xB9AC;&amp;#xC2A4;&amp;#xD06C; allele&amp;#xC758; frequency&amp;#xC5D0; &amp;#xAC15;&amp;#xD55C; &amp;#xC601;&amp;#xD5A5;&amp;#xC744; &amp;#xC8FC;&amp;#xC9C0; &amp;#xC54A;&amp;#xB294;&amp;#xB2E4;. &amp;#xADF8;&amp;#xB7EC;&amp;#xB098; &amp;#xBA87;&amp;#xBA87; &amp;#xC9C8;&amp;#xBCD1;&amp;#xAD00;&amp;#xB828; SNP&amp;#xC5D0;&amp;#xC11C; positive selection&amp;#xC758; &amp;#xC99D;&amp;#xAC70;&amp;#xAC00; &amp;#xAD00;&amp;#xCC30;&amp;#xB418;&amp;#xBA70;, &amp;#xC778;&amp;#xC885;&amp;#xAC04;&amp;#xC5D0; &amp;#xC9C8;&amp;#xBCD1; &amp;#xC720;&amp;#xD589;&amp;#xC758; &amp;#xCC28;&amp;#xC774;&amp;#xAC00; &amp;#xC774;&amp;#xB7EC;&amp;#xD55C; &amp;#xBCC0;&amp;#xC774;&amp;#xC5D0; &amp;#xB300;&amp;#xD55C; &amp;#xAC83;&amp;#xC774; &amp;#xD655;&amp;#xC7A5;&amp;#xD558;&amp;#xB294; &amp;#xC5F0;&amp;#xAD6C;&amp;#xAC00; &amp;#xD544;&amp;#xC694;&amp;#xD558;&amp;#xB2E4;.
  2. common disease - common variant(CDCV), &amp;#xC774; &amp;#xAC00;&amp;#xC124;&amp;#xC740; risk allele&amp;#xAC00; &amp;#xC778;&amp;#xC885; &amp;#xD2B9;&amp;#xC774;&amp;#xC801;&amp;#xC778; &amp;#xAC83;&amp;#xBCF4;&amp;#xB2E4; common &amp;#xD574;&amp;#xC57C; &amp;#xD55C;&amp;#xB2E4;. &amp;#xC9C4;&amp;#xD654;&amp;#xC801;&amp;#xC73C;&amp;#xB85C; &amp;#xBD24;&amp;#xC744;&amp;#xB54C; &amp;#xC778;&amp;#xB958;&amp;#xC9D1;&amp;#xB2E8;&amp;#xC5D0; &amp;#xAD11;&amp;#xBC94;&amp;#xC704;&amp;#xD558;&amp;#xAC8C; &amp;#xD37C;&amp;#xC838; &amp;#xC788;&amp;#xB294; &amp;#xC9C8;&amp;#xBCD1;(common disease)&amp;#xC758; &amp;#xC6D0;&amp;#xC778;&amp;#xC740;, &amp;#xB9C8;&amp;#xCC2C;&amp;#xAC00;&amp;#xC9C0;&amp;#xB85C; &amp;#xC778;&amp;#xB958; &amp;#xC9D1;&amp;#xB2E8;&amp;#xC758; &amp;#xC720;&amp;#xC804;&amp;#xC815;&amp;#xBCF4; &amp;#xC804;&amp;#xCCB4;&amp;#xC5D0;&amp;#xC11C; &amp;#xAD11;&amp;#xBC94;&amp;#xC704;&amp;#xD558;&amp;#xAC8C; &amp;#xBC1C;&amp;#xACAC;&amp;#xB418;&amp;#xB294; &amp;#xBCC0;&amp;#xC774;&amp;#xC815;&amp;#xBCF4;(common variant)&amp;#xC77C; &amp;#xAC83;&amp;#xC774;&amp;#xB77C;&amp;#xB294; &amp;#xAC00;&amp;#xC124; &amp;#xB300;&amp;#xBD80;&amp;#xBD84;&amp;#xC758; gwas&amp;#xC5F0;&amp;#xAD6C;&amp;#xAC00; &amp;#xC720;&amp;#xB7FD;&amp;#xC744; &amp;#xC911;&amp;#xC2EC;&amp;#xC73C;&amp;#xB85C; &amp;#xD55C;&amp;#xB2E4;. &amp;#xC774;&amp;#xB7EC;&amp;#xD55C; &amp;#xAC83;&amp;#xC744; &amp;#xB2E4;&amp;#xB978; &amp;#xC778;&amp;#xC885;&amp;#xC73C;&amp;#xB85C; &amp;#xD655;&amp;#xB300;&amp;#xD560;&amp;#xB54C;, &amp;#xC778;&amp;#xC885;&amp;#xAC04; &amp;#xB9AC;&amp;#xC2A4;&amp;#xD06C; &amp;#xC5BC;&amp;#xB9AC;&amp;#xC758; &amp;#xCC28;&amp;#xC774;&amp;#xAC00; &amp;#xD3EC;&amp;#xC9C0;&amp;#xD2F0;&amp;#xBE0C; &amp;#xC140;&amp;#xB809;&amp;#xC158;&amp;#xC5D0; &amp;#xC758;&amp;#xD55C; &amp;#xAC83;&amp;#xC740; &amp;#xC544;&amp;#xB2CC;&amp;#xAC00;?&amp;#xD558;&amp;#xB294;...
  3. &amp;#xC804;&amp;#xC138;&amp;#xACC4;&amp;#xC801;&amp;#xC778; &amp;#xADDC;&amp;#xBAA8;&amp;#xC758; CDCV &amp;#xBAA8;&amp;#xB378;&amp;#xC758; &amp;#xC801;&amp;#xC6A9;, &amp;#xB9AC;&amp;#xC2A4;&amp;#xD06C; &amp;#xC5BC;&amp;#xB9AC; &amp;#xD504;&amp;#xB9AC;&amp;#xD000;&amp;#xC2DC;&amp;#xC5D0;&amp;#xC11C;&amp;#xC758; &amp;#xD3EC;&amp;#xC9C0;&amp;#xD2F0;&amp;#xBE0C; &amp;#xC140;&amp;#xB809;&amp;#xC158; &amp;#xD6A8;&amp;#xACFC;&amp;#xB97C; &amp;#xAC80;&amp;#xC99D;
  4. &amp;#xB958;&amp;#xBA38;&amp;#xD2F0;&amp;#xC998;&amp;#xC131; &amp;#xAD00;&amp;#xC808;&amp;#xC5FC;, &amp;#xAD00;&amp;#xC0DD;&amp;#xB3D9;&amp;#xB9E5;&amp;#xC9C8;&amp;#xD658;,&amp;#xBE44;&amp;#xB9CC; &amp;#xC804;&amp;#xCCB4;&amp;#xC801;&amp;#xC778; Fst&amp;#xC758; &amp;#xBD84;&amp;#xD3EC;, 10% &amp;#xC548;&amp;#xC5D0; &amp;#xB4DC;&amp;#xB294; &amp;#xC989; P &amp;#xBC38;&amp;#xB958;&amp;#xAC00; 0.1 &amp;#xC774;&amp;#xD558;&amp;#xC778; &amp;#xAC83;&amp;#xB4E4;&amp;#xC774; &amp;#xAF2C;&amp;#xB9AC;&amp;#xBD80;&amp;#xBD84;&amp;#xC774;&amp;#xB77C;&amp;#xACE0; &amp;#xC0DD;&amp;#xAC01; &amp;#xC774;&amp;#xAF2C;&amp;#xB9AC;&amp;#xAC00; &amp;#xBC14;&amp;#xB85C; positive selection
  5. 25&amp;#xAC1C;&amp;#xC758; &amp;#xC9C8;&amp;#xBCD1; &amp;#xAD00;&amp;#xB828; SNP&amp;#xC758; mean global Fst&amp;#xB294; 0.1&amp;#xB85C; &amp;#xC774;&amp;#xB294; &amp;#xB300;&amp;#xB2E8;&amp;#xD788; &amp;#xB192;&amp;#xC740; &amp;#xAC12;&amp;#xC774;&amp;#xB2E4;. &amp;#xD558;&amp;#xC9C0;&amp;#xB9CC; &amp;#xC9C8;&amp;#xBCD1;&amp;#xAD00;&amp;#xB828; SNP&amp;#xC740; &amp;#xB79C;&amp;#xB364;&amp;#xD55C; SNP &amp;#xB4E4;&amp;#xACFC; &amp;#xBCC4;&amp;#xBC18; &amp;#xCC28;&amp;#xC774;&amp;#xAC00; &amp;#xC5C6;&amp;#xB2E4;. Global Fst&amp;#xAC12;&amp;#xC740; allele frequency&amp;#xC758; &amp;#xCC28;&amp;#xC774;&amp;#xB97C; &amp;#xC138;&amp;#xACC4;&amp;#xC801;&amp;#xC73C;&amp;#xB85C; &amp;#xAC1C;&amp;#xB7B5;&amp;#xC801;&amp;#xC73C;&amp;#xB85C; &amp;#xBCF4;&amp;#xC5EC;&amp;#xC8FC;&amp;#xAE30;&amp;#xB294; &amp;#xD55C;&amp;#xB2E4;. &amp;#xD3EC;&amp;#xC9C0;&amp;#xD2F0;&amp;#xBE0C; &amp;#xC140;&amp;#xB809;&amp;#xC158;&amp;#xC740; &amp;#xC880;&amp;#xB354; &amp;#xC138;&amp;#xBC00;&amp;#xD55C; &amp;#xC9C0;&amp;#xC5ED;&amp;#xC548;&amp;#xC5D0;&amp;#xC11C; &amp;#xC774;&amp;#xB8E8;&amp;#xC5B4;&amp;#xC9C0;&amp;#xAE30; &amp;#xB584;&amp;#xBB38;&amp;#xC5D0; &amp;#xAE00;&amp;#xB85C;&amp;#xBC8C; Fst&amp;#xB85C; &amp;#xCC3E;&amp;#xC744; &amp;#xC218; &amp;#xC5C6;&amp;#xC5B4;,, &amp;#xC790;&amp;#xC138;&amp;#xD788; &amp;#xB098;&amp;#xB204;&amp;#xC5B4; &amp;#xBCF4;&amp;#xAE30;&amp;#xB85C; &amp;#xD55C;&amp;#xB2E4;. 10% &amp;#xC548;&amp;#xC5D0; &amp;#xB4DC;&amp;#xB294; &amp;#xC989; P &amp;#xBC38;&amp;#xB958;&amp;#xAC00; 0.1 &amp;#xC774;&amp;#xD558;&amp;#xC778; &amp;#xAC83;&amp;#xB4E4;&amp;#xC774; &amp;#xAF2C;&amp;#xB9AC;&amp;#xBD80;&amp;#xBD84;&amp;#xC774;&amp;#xB77C;&amp;#xACE0; &amp;#xC0DD;&amp;#xAC01;
  6. &amp;#xC544;&amp;#xD504;&amp;#xB9AC;&amp;#xCE74; &amp;#xC778;&amp;#xC885;&amp;#xC774; Risk allele&amp;#xAC00; &amp;#xB0AE;&amp;#xACE0;, &amp;#xC544;&amp;#xD504;&amp;#xB9AC;&amp;#xCE74;&amp;#xC758; &amp;#xBC16;&amp;#xC73C;&amp;#xB85C; &amp;#xC99D;&amp;#xAC00;&amp;#xD558;&amp;#xB294; &amp;#xACBD;&amp;#xD5A5;&amp;#xC744; &amp;#xBCF4;&amp;#xC784; global Fst&amp;#xAC12;&amp;#xC740; empirical &amp;#xBD84;&amp;#xC0B0;&amp;#xC758; &amp;#xC0C1;&amp;#xC704; 5%&amp;#xC5D0; &amp;#xC704;&amp;#xCE58;&amp;#xD558;&amp;#xACE0; &amp;#xC788;&amp;#xC74C; &amp;#xB300;&amp;#xBD80;&amp;#xBD84; &amp;#xC778;&amp;#xC885;&amp;#xC5D0;&amp;#xC11C; &amp;#xC544;&amp;#xD504;&amp;#xB9AC;&amp;#xCE74;&amp;#xC640; &amp;#xC544;&amp;#xD504;&amp;#xB9AC;&amp;#xCE74;&amp;#xC678;&amp;#xC758; pairwise &amp;#xBE44;&amp;#xAD50;&amp;#xC5D0;&amp;#xC11C; &amp;#xB192;&amp;#xC740; &amp;#xC758;&amp;#xBBF8;(highly signification)&amp;#xB97C; &amp;#xBCF4;&amp;#xC784;
  7. &amp;#xD558;&amp;#xB098;&amp;#xC758; &amp;#xC778;&amp;#xC885;&amp;#xC5D0;&amp;#xC11C; &amp;#xD2B9;&amp;#xD788;, &amp;#xC9C8;&amp;#xBCD1;&amp;#xAD00;&amp;#xB828; SNP&amp;#xC740; &amp;#xB79C;&amp;#xB364; SNP&amp;#xACFC; freq &amp;#xBCC4;&amp;#xBC18; &amp;#xCC28;&amp;#xC774; &amp;#xC5C6;&amp;#xC74C;, &amp;#xC774;&amp;#xAC83;&amp;#xC740; &amp;#xACE7; positive local selection &amp;#xC5D0; risk allele freq&amp;#xAC00; &amp;#xC601;&amp;#xD5A5;&amp;#xC744; &amp;#xBCC4;&amp;#xB85C; &amp;#xBABB;&amp;#xC900;&amp;#xB2E4;&amp;#xB294; &amp;#xC758;&amp;#xBBF8; &amp;#xADF8;&amp;#xB7EC;&amp;#xB098; &amp;#xBA87;&amp;#xBA87; &amp;#xC9C8;&amp;#xBCD1; &amp;#xAD00;&amp;#xB828; SNP&amp;#xC5D0;&amp;#xC11C; positive local selection&amp;#xC758; &amp;#xC99D;&amp;#xAC70;&amp;#xAC00; &amp;#xBCF4;&amp;#xC784;, &amp;#xB354;&amp;#xB9CE;&amp;#xC740; &amp;#xC5F0;&amp;#xAD6C; &amp;#xD544;&amp;#xC694;,
  8. risk allele freq&amp;#xC758; &amp;#xCC28;&amp;#xC774;&amp;#xB294; &amp;#xC140;&amp;#xB809;&amp;#xC158;&amp;#xC774;&amp;#xB098;, &amp;#xC774;&amp;#xB3D9;&amp;#xACFC; &amp;#xAD00;&amp;#xACC4;&amp;#xB294; &amp;#xC5C6;&amp;#xC9C0;&amp;#xB9CC;,