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1 1 Figure S1 – Principal components analysis recapitulates geographical birth record data 2 by region. A) Labeled map of Finland, as in Figure 1A, with colors highlighting regional 3 differences. Notably, forced relocation uprooted many individuals and communities 4 following WWII for example, when Finland ceded its eastern parts (e.g. Karelia) to the 5 Soviet Union and resettled everyone living in the lost areas into the remaining parts of 6 20 24 28 32 60 62 64 66 68 70 Longitude Latitude B C A D 6 7 8 2 10 1 4 BD 11 12 5 9 X Y Z F H M E G O U AB D 22 Russia 23 27 33 28 35 21 24 25 31 26 32 Hungary 34 30 36 6 7 8 2 10 1 4 BD 11 12 5 9 X Y Z F H M E G O U AB D 22 Russia 23 27 33 28 35 21 24 25 31 26 32 Hungary 34 30 36 F ST Country Sweden Finland Estonia Russia Hungary 0 0.002 0.004 0.006 0.008 0.01

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Figure S1 – Principal components analysis recapitulates geographical birth record data 2

by region. A) Labeled map of Finland, as in Figure 1A, with colors highlighting regional 3

differences. Notably, forced relocation uprooted many individuals and communities 4

following WWII for example, when Finland ceded its eastern parts (e.g. Karelia) to the 5

Soviet Union and resettled everyone living in the lost areas into the remaining parts of 6

20 24 28 32

6062

6466

6870

Longitude

Latitude

B CA

D

6 7 8 2 10 1 4 BD 11 12 5 9 X Y Z F H M E G O U AB D 22 Russia23 27 33 28 35 21 24 25 31 26 32 Hungary34 30 36

67821014BD111259XYZFHMEGOUABD22Russia2327332835212425312632Hungary343036

FST

CountrySwedenFinlandEstoniaRussiaHungary

0

0.002

0.004

0.006

0.008

0.01

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the country 1. B) Smoothed geographical density map of all Finrisk97 samples with birth 1

record data at the centroids of municipalities (N=5,448). Regional-level birth records not 2

shown. C) PCA positions for all Finrisk97 samples with birth record data. Numbers label 3

the average PC coordinates for all individuals born in a region. Colors are as in A). D) 4

Clustered FST heat map between individuals born in different regions of Finland, 5

Sweden, Estonia, St Petersburg, Russia, and Hungary. Regions with fewer than 10 6

individuals were not included. Region labels and names are as in Table S3. 7

8

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Figure S2 – Birthplace of offspring whose parents are both born in the same region 10

(N=3,132), as indicated by panel titles. 11

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Figure S3 – Geographical distance between pairs of Finnish individuals and 4

genetic sharing. A) Pairwise genetic sharing among unrelated individuals by 5

geographical distance. B) Cumulative IBD sharing (minimum haplotype length ≥ 3 cM) 6

across the genome among unrelated individuals by geographical distance. C) Density of 7

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genetic distance between pairs of individuals by geographical distance. The distance 1

between representative city pairs are shown in blue. 2

3

Figure S4 – Effective population size change over time by region of Finland. 4

Number of individuals in each region are: 1: 1,123, 2: 1,078, 4: 378, 5: 224, 6: 304, 7: 5

1,581, 8: 1,547, 9: 225, 10: 288, 11: 1,697, 12: 184. 6

7

10 11 12

6 7 8 9

1 2 4 5

0 10 20 30 40 50 0 10 20 30 40 50 0 10 20 30 40 50

0 10 20 30 40 50

1e+04

1e+06

1e+04

1e+06

1e+04

1e+06

Time (generations)

Ne

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Figure S5 – Deme assignment for EEMS analyses in/near Finland. Black dots at 2

center of demes are proportional to sample size. A) Finland deme assignment from 3

municipality-level birth records. B) Deme assignment in Finland with municipality-level 4

birth records and for region-level birth records in neighboring countries/regions of 5

Sweden, Estonia, and St. Petersburg, Russia. 6

BA

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Figure S6 – Haplotype sharing rate genome-wide by chromosome. At each best-1

guess genotype used to call haplotypes, we quantified the number of pairs of individuals 2

who shared haplotypes. Included individuals are unrelated and have corresponding 3

exome sequencing data (N=9,363). Red line indicates the mean sharing plus 3 * 4

standard deviation. Total possible number of pairs is !" = 43,828,203. 5

6

Figure S7 – Depletion of haplotype sharing at CpG sites shows evidence of 7

mutational recurrence. A) Enrichment of haplotype sharing across all variants. B) 8

Enrichment of haplotype sharing across non-CpG variants. 9

0.001 0.010 0.100 1.000

0

5

10

15

100 10000

Allele frequency

Allele count

Het

:Ref

pai

r sha

ring

ratio

Variant classMissense

Missense (possibly)

Missense (probably)

Synonymous

CpGs includedA

0.001 0.010 0.100 1.000

0

5

10

15

100 10000

Allele frequency

Allele count

Het

:Ref

pai

r sha

ring

ratio

Variant classMissense

Missense (possibly)

Missense (probably)

Synonymous

No CpGsB

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Figure S8 – Depletion of haplotype sharing in missense and loss-of-function 2

(LoF) constrained regions. As calculated in Lek et al, missense constraint indicates 3

regions depleted of missense variation, and LoF constrained regions indicate regions 4

depleted of LoF variation 2. 5

6

Table S1 – Finnish sample genotyping summaries. Note that some FINRISK 7

samples with birth records have been included as controls for multiple different projects. 8

Population Array Project name SNPs genotyped Sample size Finland Affymetrix 6.0 MIGen 666,979 339 Finland Illumina 370k NFBC 324,674 5,363

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Finland Illumina 610k Corogene, GenMets 535,787 6,240 Finland Illumina 670k HBCS, YFS, FTC 521,500 6,492 Finland Illumina CoreExome FINRISK, CoreEX 322,929 10,641 Finland Illumina CoreExome ENGAGE 342,869 11,639 Finland Illumina OmniExpress PredictCVD, SUMMIT 606,310 2,542 Sweden Illumina OmniExpress Sw5 733,202 4,465 Sweden Illumina OmniExpress Sw6 733,202 3,873 Hungary Illumina OmniExpressExome HTB 943,987 506 Estonia Illumina OmniExpress EGCUT 710,831 6,946 Russia Illumina GlobalScreeningArray RussiaSiege 633,183 262 TOTAL 59,309 1

Table S2 – Birth record data by cohort. Municipality-level birth records were available 2

for FR97, regional-level birth records were available for FR07 for this study. 3

4

5

6

7

Table S3 – Region names by country in Finland, Sweden, and Estonia. 8

Country Code Name Finland 1 Southern Finland Finland 2 Southwestern Finland Finland 3 Åland Finland 4 Tavastia Finland 5 Southern Karelia Finland 6 Southern Savonia Finland 7 North Karelia Finland 8 Northern Savonia Finland 9 Central Finland Finland 10 Ostrobothnia Finland 11 Northern Ostrobothnia Finland 12 Lapland Sweden AB Stockholm Sweden AC Västerbotten Sweden BD Norrbotten

Project/Array FR07 FR97 ENGAGE 0 3969 FIN610K 634 458 MIGen 0 110 FINRISK, CoreEX 3065 0 PredictCVD, SUMMIT 243 911 TOTAL (N=9,390) 3942 5448

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Sweden C Uppsala Sweden D Södermanland Sweden E Östergötland Sweden F Jönköping Sweden G Kronoberg Sweden H Kalmar Sweden I Gotland Sweden K Blekinge Sweden M Skåne Sweden N Halland Sweden O Västra Götaland Sweden S Värmland Sweden T Orebro Sweden U Västmanland Sweden W Dalarna Sweden X Gävleborg Sweden Y Västernorrland Sweden Z Jämtland Estonia 21 Harju Estonia 22 Hiiu Estonia 23 Ida-Viru Estonia 24 Järva Estonia 25 Jõgeva Estonia 26 Lääne Estonia 27 Lääne-Viru Estonia 28 Pärnu Estonia 29 Peipsi Estonia 30 Põlva Estonia 31 Rapla Estonia 32 Saare Estonia 33 Tartu Estonia 34 Valga Estonia 35 Viljandi Estonia 36 Võru

1

Table S4 – Exome sequencing data included in haplotype analyses. Cohorts are 2

ordered by number of individuals contributing to this study. Full descriptions of each 3

cohort are in supplementary note. 4

Cohort name Number of individuals included FINRISK_population_cohort 7014

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IBD_FINRISK 845 NFBC 525 Health 2000 271 FINRISK_AD 238 Fusion 214 UK10K 68 Migraine 57 METSIM 45 Eufam 42 NFID 30 Twins_AD 25 ADGEN 9 IBD 4 AUTISM_ASDFI 2 AUTISM_TAMPERE 1 EPILEPSY_EPI25 1 Botnia_T2D 1

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References 2

1. Haukka J, Suvisaari J, Sarvimäki M, Martikainen P (2017) The Impact of Forced 3

Migration on Mortality. Epidemiology 28:587-593 4

2. Lek M, Karczewski KJ, Minikel EV, Samocha KE, Banks E, Fennell T, O’Donnell-5

Luria AH, Ware JS, Hill AJ, Cummings BB, Tukiainen T, Birnbaum DP, Kosmicki JA, 6

Duncan LE, Estrada K, Zhao F, Zou J, Pierce-Hoffman E, Berghout J, Cooper DN, 7

Deflaux N, DePristo M, Do R, Flannick J, Fromer M, Gauthier L, Goldstein J, Gupta N, 8

Howrigan D, Kiezun A, Kurki MI, Moonshine AL, Natarajan P, Orozco L, Peloso GM, 9

Poplin R, Rivas MA, Ruano-Rubio V, Rose SA, Ruderfer DM, Shakir K, Stenson PD, 10

Stevens C, Thomas BP, Tiao G, Tusie-Luna MT, Weisburd B, Won H, Yu D, Altshuler 11

DM, Ardissino D, Boehnke M, Danesh J, Donnelly S, Elosua R, Florez JC, Gabriel SB, 12

Getz G, Glatt SJ, Hultman CM, Kathiresan S, Laakso M, McCarroll S, McCarthy MI, 13

McGovern D, McPherson R, Neale BM, Palotie A, Purcell SM, Saleheen D, Scharf JM, 14

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Sklar P, Sullivan PF, Tuomilehto J, Tsuang MT, Watkins HC, Wilson JG, Daly MJ, 1

MacArthur DG (2016) Analysis of protein-coding genetic variation in 60,706 humans. 2

Nature 536:285-291 3