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| File | Version | Author | Date | Message |
|---|---|---|---|---|
| Rmd | 8b9cf18 | Lily Heald | 2026-03-26 | Update modern samples map |
| html | 2b2fe92 | Lily Heald | 2026-03-26 | Update introduction |
| html | 4c4faee | Lily Heald | 2026-03-26 | Build site. |
| Rmd | 9c64835 | Lily Heald | 2026-03-26 | wflow_publish("analysis/introduction.Rmd") |
| html | 68a40d3 | Lily Heald | 2026-03-26 | Build site. |
| html | a713e79 | Lily Heald | 2026-03-26 | Create summary tables |
| Rmd | 325e8b2 | Lily Heald | 2026-03-26 | wflow_publish("analysis/introduction.Rmd") |
| html | 814636a | Lily Heald | 2026-03-26 | Build site. |
| Rmd | 33e4846 | Lily Heald | 2026-03-26 | wflow_publish("analysis/introduction.Rmd") |
| html | b1060b3 | Lily Heald | 2026-03-26 | Build site. |
| Rmd | a154fb2 | Lily Heald | 2026-03-26 | wflow_publish("analysis/introduction.Rmd") |
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| Rmd | 1d15761 | Lily Heald | 2026-03-26 | wflow_publish("analysis/introduction.Rmd") |
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| Rmd | 05c4750 | Lily Heald | 2026-03-26 | stack snp distribution |
| html | 05c4750 | Lily Heald | 2026-03-26 | stack snp distribution |
| Rmd | a476f32 | Lily Heald | 2026-02-10 | Update introduction |
| html | a476f32 | Lily Heald | 2026-02-10 | Update introduction |
| html | 189b205 | Lily Heald | 2026-02-10 | Update introduction |
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| html | c555bc3 | Lily Heald | 2026-02-10 | Clean bar chart |
| html | 5cd4031 | Lily Heald | 2026-02-09 | Update introduction |
| Rmd | 4ea9339 | Lily Heald | 2026-02-09 | Update introduction |
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| html | 4a52a41 | Lily Heald | 2026-02-04 | Add distribution bar chart |
| Rmd | 289d9ed | Lily Heald | 2026-01-30 | add den3 |
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| Rmd | fe99e78 | Lily Heald | 2026-01-14 | add Denisova 25 |
| html | fe99e78 | Lily Heald | 2026-01-14 | add Denisova 25 |
| Rmd | 2cac6c9 | Lily Heald | 2026-01-14 | add vindija 87 |
| html | 2cac6c9 | Lily Heald | 2026-01-14 | add vindija 87 |
| Rmd | c6f38f2 | Lily Heald | 2026-01-14 | Add Chag8 |
| html | c6f38f2 | Lily Heald | 2026-01-14 | Add Chag8 |
| Rmd | 7bb18d4 | Lily Heald | 2025-11-20 | update sample names |
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| Rmd | 9209569 | Lily Heald | 2025-11-20 | add altai neanderthal |
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| Rmd | 1f311d9 | Lily Heald | 2025-11-18 | update figures |
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| Rmd | a1afed5 | Lily Heald | 2025-11-07 | update visibility |
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| html | 735357b | Lily Heald | 2025-11-07 | Build site. |
| Rmd | 50940c0 | Lily Heald | 2025-11-07 | Update introduction.Rmd |
| Rmd | f1b70cb | Lily Heald | 2025-11-07 | add Hstadel depth |
| Rmd | 7beeddd | Lily Heald | 2025-11-07 | add depth figure |
| Rmd | 967f438 | Lily Heald | 2025-11-07 | update callout |
| html | 967f438 | Lily Heald | 2025-11-07 | update callout |
| html | cc7d134 | Lily Heald | 2025-11-06 | updated figures |
| Rmd | b2f5585 | Lily Heald | 2025-11-06 | Update introduction.Rmd |
| html | 13755f1 | Lily Heald | 2025-11-06 | workflowr |
| Rmd | 46a0913 | Lily Heald | 2025-11-06 | start workflowr |
Ancient genome availability
DNA can persist for up to hundreds of thousands of years in skeletal remains, and can even be extracted from sediments. However, extracting such DNA poses a challenge. Ancient DNA is typically present in very small amounts, is highly fragmented, and contaminated with other endogenous organic molecules which inhibit enzymatic DNA manipulations which must be performed prior to sequencing, or exogenous DNA. There are high-quality genomic sequences available for two Denisovans and three Neanderthals. There are also low coverage sequences available spanning spatially from Gibraltar to Siberia and temporally from 39 to 120ka. A total of fourteen archaic genomic samples will be analysed in this study, including all five high coverage genomes.
| Version | Author | Date |
|---|---|---|
| 68a40d3 | Lily Heald | 2026-03-26 |
| a713e79 | Lily Heald | 2026-03-26 |
| 790813f | Lily Heald | 2026-02-09 |
| c6f38f2 | Lily Heald | 2026-01-14 |
| c8573bb | Lily Heald | 2025-11-18 |
| 08dda7e | Lily Heald | 2025-11-13 |
| 735357b | Lily Heald | 2025-11-07 |
| 967f438 | Lily Heald | 2025-11-07 |
| cc7d134 | Lily Heald | 2025-11-06 |
| 13755f1 | Lily Heald | 2025-11-06 |
High-coverage archaic nuclear genomes remain an exceptionally small record, currently including only five individuals. This narrow archaeological base limits the locus-level inference, as the archaic dataset includes a handful of individuals separated by large gaps in time rather than from a representative archaic sample.
| Specimen | Species | Location | Age |
|---|---|---|---|
| Denisova 5 | Neanderthal | Denisova cave | 122 ka |
| Chagyrskaya 8 | Neanderthal | Chagyrskaya cave | 60 ka |
| Vindija 33.19 | Neanderthal | Vindija cave | 52 ka |
| Denisova 25 | Denisovan | Denisova cave | 200 ka |
| Denisova 3 | Denisovan | Denisova cave | 72 ka |
Modern reference genomes
Modern human genomes were obtained from the Simons Genome Diversity Project (SGDP). A panel of 15 individuals representing broad global diversity (Africa, Europe, East Asia, Central Asia, and Oceania) to provide a stable reference frame for principal component analysis (PCA). Variant call files (VCFs) were downloaded as whole-genome SNP datasets aligned to the GRCh37/hg19 reference genome.
Warning: Removed 78 rows containing missing values or values outside the scale range
(`geom_point()`).
Distribution of pigmentation SNPs
In order to allow for comparison of genome-wide ancestry patterns with structure driven by a targeted functional SNP set. For pigmentation-specific analyses, a panel consisting of 395 SNPs previously associated with pigmentation phenotypes published on the NHGRI-EBI Catalog of human genome-wide association studies was used. The by-chromosome distribution of these SNPs is shown below.
The genetic architecture of human pigmentation is highly polygenic, involving many loci that contribute to variation in skin, hair, and eye color (E. Quillen et al., 2018). Genome-wide association studies have identified hundreds of single-nucleotide polymorphisms (SNPs) associated with pigmentation phenotypes. Many of these variants lie in genes involved in melanogenesis, melanosome biogenesis, melanosomal transport, or regulation of melanocyte signaling, including SLC45A2 (chr5), ADAMTS12 (chr5), TYR (chr11), SLC24A5 (chr15), OCA2 (chr15), HERC2 (chr15), and MC1R (chr16) (Sturm, 2009). The distribution of pigmentation associated SNPs across the genome is not uniform.
Current research also shows that the architecture of skin pigmentation is broader and more population-specific than earlier Eurocentric models implied (Feng et al., 2021; E. E. Quillen et al., 2019). Studies in African and admixed populations have identified additional loci, including MFSD12 and DDB1, that were not prominent in early European-focused analyses (Crawford et al., 2017; Feng et al., 2021). The number of known pigmentation SNPs is now large, effect sizes vary across populations, and older predictive panels were built on samples that only capture a fraction of the global genetic landscape (E. E. Quillen et al., 2019).
| Locus | Typical role in pigmentation biology | Evidence in modern humans |
|---|---|---|
| SLC24A5 | Melanosome associated ion transport and melanogenesis | Major contributor to lighter skin in West Eurasia and beyond |
| SLC45A2 | Melanosomal transport and pH related effects on melanogenesis | Repeatedly associated with skin color variation, especially in Europeans |
| TYR | Core melanogenic enzyme pathway | Associated with normal pigment variation and lighter pigmentation in some populations |
| OCA2/HERC2 | Pigment regulation with strong effects on eye color and broader pigment traits | Important in pigmentation architecture, especially in Eurasian datasets |
| MC1R and ASIP | Regulation of melanocytic signaling and balance of pigment outputs | Strong effects on pigment-related traits and sun sensitivity, with marked population specificity |
| ADAMTS12 | ADAMTS12 | ADAMTS12 |
sessionInfo()R version 4.4.2 (2024-10-31)
Platform: aarch64-apple-darwin20
Running under: macOS 26.3.1
Matrix products: default
BLAS: /Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/lib/libRblas.0.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/lib/libRlapack.dylib; LAPACK version 3.12.0
locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8
time zone: America/Detroit
tzcode source: internal
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] knitr_1.51 wesanderson_0.3.7 showtext_0.9-7
[4] showtextdb_3.0 sysfonts_0.8.9 reshape2_1.4.5
[7] lubridate_1.9.4 forcats_1.0.1 stringr_1.6.0
[10] dplyr_1.2.0 purrr_1.2.1 readr_2.1.6
[13] tidyr_1.3.2 tibble_3.3.1 tidyverse_2.0.0
[16] ggrepel_0.9.6 viridis_0.6.5 viridisLite_0.4.2
[19] ggspatial_1.1.10 raster_3.6-32 sp_2.2-0
[22] sf_1.0-24 rnaturalearthdata_1.0.0 rnaturalearth_1.2.0
[25] ggplot2_4.0.2 workflowr_1.7.2
loaded via a namespace (and not attached):
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[5] promises_1.5.0 digest_0.6.39 timechange_0.4.0 lifecycle_1.0.5
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[17] labeling_0.4.3 classInt_0.4-11 curl_7.0.0 plyr_1.8.9
[21] RColorBrewer_1.1-3 KernSmooth_2.23-26 withr_3.0.2 grid_4.4.2
[25] git2r_0.36.2 e1071_1.7-17 scales_1.4.0 cli_3.6.5
[29] rmarkdown_2.30 generics_0.1.4 otel_0.2.0 rstudioapi_0.18.0
[33] httr_1.4.7 tzdb_0.5.0 DBI_1.2.3 cachem_1.1.0
[37] proxy_0.4-29 vctrs_0.7.1 jsonlite_2.0.0 callr_3.7.6
[41] hms_1.1.4 jquerylib_0.1.4 units_1.0-0 glue_1.8.0
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[49] later_1.4.5 pillar_1.11.1 htmltools_0.5.9 R6_2.6.1
[53] rprojroot_2.1.1 evaluate_1.0.5 lattice_0.22-7 httpuv_1.6.16
[57] bslib_0.10.0 class_7.3-23 Rcpp_1.1.1 gridExtra_2.3
[61] whisker_0.4.1 xfun_0.56 fs_1.6.6 getPass_0.2-4
[65] pkgconfig_2.0.3