Daily Archives: March 31, 2021

DUBAI: The International Prize for Arabic Fiction has announced its six shortlisted authors who are competing to receive a $50,000 award when the winner is revealed on May 25. Read on to learn more about the writers and their novels.

Abdulatif Ould Abdullah - The Eye of Hammurabi

In the Algerian writers book The Eye of Hammurabi, he opens with the interrogation of a man in a military encampment after he fled from the angry inhabitants of Douar Sidi Majdoub.

As the story unfolds, the main character revisits his past to explore the roots of his present dilemma and tells stories which blend imagination and reality, illusion and the truth.

Jalal Bargas - Notebooks of the Bookshop Keeper

Notebooks of the Bookshop Keeper is by Jordanian poet and novelist Jalal Bargas. Set between 1947 and 2019, this novel is based on several notebooks of stories about people facing different hardships, such as losing their homes or not knowing who their family are.

The main character is Ibrahim, a bookshop keeper, a cultured man and voracious reader of novels. However, due to his isolation, loneliness and maltreatment by a cruel world, he suffers mental illness and descends into full schizophrenia. He attempts suicide, before meeting the woman who will change his life.

Amira Ghenim- The Calamity of the Nobility

The Tunisian writer and academics book The Calamity of the Nobility relates an untold story from Tunisias contemporary history about renowned author, scholar and reformer El-Taher El-Haddad.

Although historical references do not mention anything about his relationship with women, except for his desperate defense of them, the author adds an imaginary love affair with a woman called Lella Zubaida to her fictional retelling of his life.

The novel gives prominence to the voices of female narrators, as custodians of memory who contradict a distorted, patriarchal version of history.

Dunya Mikhail- The Bird Tattoo'

The Iraqi authors The Bird Tattoo is a painful novel about the sale of Yazidi women in Iraq by Daesh.

It focuses on Helen and Elias, who fall in love and marry, and their experiences with the group. Alongside this tragedy, the novel sheds light on aspects of Yazidi folklore, rich in customs and legends.

Abdelmajid Sebbata - File 42

File 42, by Moroccan author Abdelmajid Sebbata, follows two parallel storylines. In the first, Christine Macmillan, a successful American novelist, and Rasheed Benaser, a young Moroccan researcher and doctoral student, embark on an investigation to find the unknown author of a forgotten Moroccan novel from 1989, in which Christines father, Steve, appears as one of the characters.

The second plot line is narrated by Zuheir Belqasem, a rich and delinquent Moroccan teenager who assaults Al-Ghalia, an underaged maid. His mother uses her influence as a prominent lawyer to close the case and send him to Russia to pursue his university studies. However, horrors await him there which no-one had foreseen.

Habib Selmi- Longing for the Woman Next Door

The Tunisian authors book tells the story of two neighbors who have nothing in common, apart from both being Tunisian and living in the same apartment building.

He is in his sixties, educated and married to a Frenchwoman. She is several years younger and from a lower social stratum, and married to an eccentric man. At first, he is cautious and patronizing. But later, the rules of the game change. The novel explores a rich, turbulent and extraordinary relationship, which celebrates life in its simplest and most beautiful manifestations but is also tinged with darkness and tragedy.

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What We Are Reading Today: The Genome Odyssey by Euan Angus Ashley - Arab News

Technological developments in next-generation sequencing (NGS) approaches and mass spectrometry (MS)-based methods have advanced the landscape of molecular biology research. Scientists are now able to identify and characterize various constituents of a cell, tissue or organism and analyze them in their totality their "ome" be it the entire expression of genes (genome), proteins (proteome) or metabolites (metabolome), at any given time.Piecing together this information helps us to understand the molecular journey from genotype to phenotype and where it can go wrong, in the case of disease phenotypes. As an increasing quantity of omics information becomes accessible to researchers, it has become clear that working with the data sets in segregation can limit their utility. Connectivity between the omics "worlds" is fundamental, but it has been challenging until now.

In January, theEuropean Molecular Biology Laboratorys European Bioinformatics Institute (EMBL-EBI) announced that it had launched the Genome Integrations with Function and Sequence, or GIFTS, platform. This novel platform enables scientists that are using Ensembl and UniProt to access all of the up-to-date genomic and protein data for human and mouse genomes. Technology Networks spoke with Beth Flint, Ensembl applications project leader at EMBL-EBI, Maria Martin, team leader in protein function development at EMBL-EBI and Daniel Zerbino, team leader in genome analysis at EMBL-EBI, to learn more about GIFTS and how it will be used to help the research community.

Molly Campbell (MC): Please can you talk to us about the rationale behind the Genome Integrations with Function and Sequence (GIFTS)?Daniel Zerbino (DZ): GIFTS aims to provide a clear and unambiguous bridge between two flagship data resources at the EMBLs European Bioinformatics Institute (www.ebi.ac.uk), namely Ensembl and UniProt. Together, they offer a wealth of information on protein synthesis: Ensembl describes the upstream sequences of nucleotides that encode protein-coding genes, whose transcripts are transcribed into downstream protein isoforms, documented in UniProt. Each resource already points to the other, thus connecting genes to proteins and vice-versa, but because of differences in release cycle calendars these links were not 100% consistent. GIFTS now details our shared understanding of which gene maps to which protein.

MC: Who is behind the development of GIFTS?Beth Flint (BF): GIFTS has been developed at EMBL-EBI as a collaboration between Ensembl and UniProt. The project brought together the expertise from these two groups and allowed us to build a tool that will allow people to easily explore the relationships between the data these groups produce. Collaborative projects of this nature take full advantage of the breadth of knowledge and diverse range of skills at EMBL-EBI. The GIFTS project was possible due to the input of curators, annotators, database and API experts, user interface developers and pipeline automation specialists.

MC: Why is it important to connect the genome and proteome worlds?Maria Martin (MM): The genome is the storehouse of the genetic material needed for an organism to function. Proteins are the primary effectors of the instructions encoded in our genomes and they and their products ultimately shape our cells, tissues, organs and bodies in response to our environment. Proteins provide an essential link between genome sequence and the eventual phenotype. The functional analysis of genomic and other large-scale biomedical datasets requires integrated information about many distinct types of biological entity, including individual genes, transcripts and proteins.

MC: Why has this been difficult previously?MM: Ensembl focuses on the annotation of transcripts in reference genomes using available cDNA, EST and RNA-seq data, while UniProt focuses on annotating protein sequences using experimental evidence from the literature, homologs in other species and proteomics experiments. The study of genomes and proteomes requires a very specialized scientific knowledge which needs to be combined to effectively map them.

MC: What do you hope the outcome of launching GIFTS will be?BF: The mappings that GIFTS pipelines produce will help the Ensembl and Uniprot teams update the data they present via their main sites. Using the GIFTS data will present a uniform view of mappings between the two domains and ensure that consistent information is presented. This provides an enormous benefit to those who use these mappings. Behind the public facing interface of GIFTS are tools used by the annotators and curators in the Ensembl and Uniprot groups. These tools enable them to review and improve mappings. As this process continues, it is hoped that over time canonical UniProt isoforms will be selected for all human genes and that these will match the MANE transcripts from Ensembl.

MC: Are there any intentions to launch a similar platform for other "omics" data?DZ: EMBL-EBI resources strive to be interoperable with each other, and this new bridge is merely strengthening a very tight network of data resources. For example, other EMBL-EBI resources, such as the Reactome pathway database or the Gene Expression Atlas already link directly and unambiguously to UniProt proteins or Ensembl genes. A sister project, Structure Integration with Function, Taxonomy and Sequence (SIFTS) now connects UniProt protein sequences to their 3D structures, stored in PDBe. All these interconnections are enabling researchers to make sense of all the resources at EMBL-EBI, as exemplified by our unified search utility.

Daniel Zerbino, Beth Flint and Maria Martin were speaking to Molly Campbell, Science Writer for Technology Networks.

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New Platform Connects the Genome and Proteome Worlds - Technology Networks

Abstract

The Scythians were a multitude of horse-warrior nomad cultures dwelling in the Eurasian steppe during the first millennium BCE. Because of the lack of first-hand written records, little is known about the origins and relations among the different cultures. To address these questions, we produced genome-wide data for 111 ancient individuals retrieved from 39 archaeological sites from the first millennia BCE and CE across the Central Asian Steppe. We uncovered major admixture events in the Late Bronze Age forming the genetic substratum for two main Iron Age gene-pools emerging around the Altai and the Urals respectively. Their demise was mirrored by new genetic turnovers, linked to the spread of the eastern nomad empires in the first centuries CE. Compared to the high genetic heterogeneity of the past, the homogenization of the present-day Kazakhs gene pool is notable, likely a result of 400 years of strict exogamous social rules.

The transition to the Iron Age (IA) marks one of the most important events in the history of Eurasia. At the turn of the first millennium BCE, changes in the archeological record attest to the rise of several nomad cultures across the steppe, from the Altai to the western fringe of the Pontic-Caspian region (1). These cultures are often collectively referred to as Scythians based on the common features found in their mortuary contexts (2). Compared to the preceding Bronze Age (BA) populations, the Scythians went through a transition from a sedentary to a nomadic cattle-breeding lifestyle, showed an increase in warfare and advancements in military technologies (e.g., new types of iron weapons and horseback riding techniques, such as introducing the use of a saddle), and the establishment of hierarchical elite-based societies (3).

Previous genomic studies have detected large-scale genetic turnovers (and therefore substantial human migrations) in the BA steppe, which eventually resulted in the formation of a homogeneous and widespread Middle and Late BA (LBA) gene pool that characterized the sedentary herders of the western and central steppe (steppe_MLBA) (47). The reasons that prompted the rapid decline of these MLBA cultures and the rise of the Scythians are still poorly understood. Scholars have pointed out, among the most relevant factors, the climatic humidification (8) and socioeconomic pressures from the neighboring farming civilizations, i.e., the ones linked to the Bactria Margiana Archaeological Complex (BMAC) (3). Three competing hypotheses have been debated regarding the origins of the Scythians: a Pontic-Caspian origin, supported by their assumed Iranian languages, a Kazakh Steppe origin supported by the archaeological findings, and a multiple independent origin from genetically distinct groups that adopted common cultural traits (2). The limited number of genomes so far retrieved from the IA steppe nomads provides a glimpse of their genetic diversity but is far from being sufficient to characterize complex patterns of admixture between various eastern and western Eurasian gene pools (912).

From an archaeological perspective, the earliest IA burials associated with nomad-warrior cultures were identified in the eastern fringes of the Kazakh Steppe, in Tuva and the Altai region (ninth century BCE) (13). Following this early evidence, the Tasmola culture in central and north Kazakhstan is among the earliest major IA nomad warrior cultures emerging (eighth to sixth century BCE) (13). These earlier groups were followed by the iconic Saka cultures located in southeastern Kazakhstan and the Tian Shan mountains (sixth to second century BCE), the Pazyryk culture centered in the Altai mountains (fifth to first century BCE-CE), and the Sarmatians that first appeared in the southern Ural region (sixth to second century BCE) and later are found westward as far as the northern Caucasus and eastern Europe (fourth BCE to fourth CE) (1, 1417). The nomad groups also influenced their sedentary neighbors, such as the ones associated with the Sargat cultural horizon (fifth to first century BCE) located in the northern forest-steppe zone between the Tobol and Irtysh rivers (3, 18).

After the IA, the Kazakh Steppe served as a center for the expansion of multiple empires, such as the Xiongnu and Xianbei chiefdoms from the east (19) and the Persian-related kingdoms from the south (e.g., Kangju) (20). These events brought the demise of the eastern Scythian cultures, but the demographic turnovers associated with this cultural transition remain poorly understood (20). Furthermore, forms of nomadic lifestyle persisted in the Kazakh Steppe throughout the centuries. A key event in the recent history of the nomad populations happened in the 15th to 16th century CE when all the tribes living in the territory of present-day Kazakhstan were organized and grouped into three main hordes (Zhuzs): Elder Zhuz, Middle Zhuz, and Junior Zhuz located in southeast, central/northeast, and west Kazakhstan, respectively (21, 22). This division was a political and religious compromise between different nomadic tribes, which were spread across Central Asia and had to protect themselves from external threats after the collapse of the Golden Horde. This set the basis for the foundation of the Kazakh Khanate (1465 to 1847 CE). Today, Kazakh groups in Kazakhstan still maintain their tribal affiliations and revere their nomadic history preserving some aspects of its culture (21). One of these traditions is the Zheti-ata, which consists of keeping track of the family tree up to seven generations by paternal line to avoid marriage between kins (23).

To understand the genetic structure of the different IA nomadic cultures as well as the demographic events associated with their origins and decline, we successfully generated genome-wide data from 111 ancient human individuals retrieved from 39 different archaeological sites across the Kazakh Steppe (Kazakhstan, Kyrgyzstan, and Russia) and one individual retrieved from a Hun elite burial located in present-day Hungary (text S1). Our dataset densely covers a time span ranging from the eighth century BCE to the fourth century CE and also includes three individuals from the medieval period (Fig. 1 and text S1). We also produced new genome-wide data from 96 modern-day Kazakh individuals belonging to several tribes affiliated to the three major Kazakh hordes (Zhuzh) covering the entire territory of present-day Kazakhstan to better understand how recent historical events have shaped the genetic structure of present-day nomads.

(A) Map showing the locations of the 39 archaeological sites where the 117 individuals were retrieved and (B) their respective dates in years BCE/CE. The dates reported are 14C-calibrated (2-sigma) ranges for the sites comprehending at least one individual directly radiocarbon-dated; if more individuals are dated, we report the lowest and the highest values across all of them. If for a site, no individuals are dated, we report the date ranges based on the archaeological context (data file S1). The sites are colored according to their cultural affiliation. This same culture-based color code (top right) is maintained for all the figures in the main text and the Supplementary Materials.

Genome-wide data for 117 ancient individuals were obtained using an in-solution DNA capture technique designed to enrich for 1,233,013 single-nucleotide polymorphisms (SNPs) commonly referred as 1240K capture (Materials and Methods). Genome-wide data for 96 present-day Kazakh individuals were generated with the Affymetrix Axiom Genome-wide HumanOrigins SNP-chip (HO) (Materials and Methods). After performing quality controls, we retained all the 96 modern Kazakh individuals and 111 ancient individuals with at least >20,000 SNPs covered, obtaining a median of 793,636 successfully recovered SNPs and 1.5 autosomal coverage on the 1240K panel across all individuals (Materials and Methods and data file S1).

We then merged the new data with a reference dataset of previously published modern and ancient individuals compiling a 1240KHO dataset consisting of 586,594 SNPs overlapping with the modern genotype data that we used for performing global population structure analyses [i.e., PCA (principal components analysis) and ADMIXTURE]. We also produced a 1240K-only dataset consisting of 1240K capture or whole-genome shotgun data pooled down to include 1240K sites only that we used for the rest of the analyses (Materials and Methods and tables S2 and S3). For population-based analyses, we grouped individuals according to their archaeological culture affiliation, spanning a defined time range after excluding genetic outliers shifted more than 2 SD from the median PCs of their respective group (Materials and Methods and table S1).

Overall, PCA and ADMIXTURE suggest that a substantial demographic shift occurred during the transition from the BA to the IA in the Kazakh Steppe (Fig. 2 and figs. S1 and S2). In contrast to the highly homogeneous steppe_MLBA cluster found across the Kazakh Steppe until the end of the second millennium BCE, the IA individuals are scattered across the PC space, most notably along PC1 and PC3. Their spread along these PCs suggests a varying degree of extra eastern Eurasian affinity compared to the MLBA population and extra affinity to southern populations ultimately related to the Neolithic Iranians and the Mesolithic Caucasus hunter-gatherers (from here on referred to as Iranian-related ancestry), respectively. Despite the high genetic variability, it is possible to appreciate homogeneous clusters of ancient individuals belonging to the same archaeological culture and/or geographic area (Fig. 2 and fig. S1). Following a chronological order, most of the individuals from the sites associated with the Early IA Tasmola culture (Tasmola_650BCE) and the published Saka_Kazakhstan_600BCE of central-north Kazakhstan cluster together in the middle of the PCA plot and show a uniform pattern of genetic components in ADMIXTURE analyses (Fig. 2, A and D, and figs. S1 and S2). The two previously published individuals from the Aldy Bel site in Tuva (Aldy_Bel_700BCE) also fall within this genetic cloud (Fig. 2A). This genetic profile persists in the later Middle and Late IA, shown by most individuals from the Pazyryk site of Berel (Pazyryk_Berel_50BCE) (Fig. 2B). This IA cluster is distinct from the previous steppe_MLBA groups inhabiting the same regions, most notably because of its substantial shift toward eastern Eurasians along PC1. In addition, we find outliers showing an even stronger shift to eastern Eurasians than the main cluster: two outliers from Pazyryk Berel time (Pazyryk_Berel_50BCE_o), three outliers from the Tasmola site of Birlik (Tasmola_Birlik_640BCE), and three of four individuals from the Korgantas phase of central-north Kazakhstan (24) (Fig. 2B and table S2). One female individual from Birlik (BIR013.A0101) with an eastern Eurasian genetic profile was unearthed with grave goods (a bronze mirror) that presented typical Eastern Steppe features (text S1).

(A to C) PC1 versus PC3 (outer plot) and PC1 versus PC2 (inner plot in the bottom right box) including all the IA, new and previously published individuals (filled symbols), relevant published temporally preceding groups (empty symbols), and present-day Kazakh individuals (small black points). The gray labels in this and the following panel indicate broad geographical groupings of the modern individuals used to calculate PCA that in the plots are shown as small gray points. The ancient samples are distributed in (A) to (C) sliced in three different time intervals as reported in the top right corner. (D) Histograms of ADMIXTURE analysis (K = 12; fig. S2) for the new IA and post-IA individuals and selected subset of temporally preceding groups maximizing key genetic components and a randomly selected subset of present-day Kazakh from the three main Zhuzs.

The classical IA Sakas from the Tian Shan region to the south (Saka_TianShan_600BCE, Saka_TianShan_400BCE, and previously published Pub_Saka_TianShan_200BCE) are distributed along a cline between the Tasmola/Pazyryk cluster and the Iranian-related gene pool, along PC3 (Fig. 2, A and B). A stronger affinity to the Neolithic Iranians is also found in ADMIXTURE analyses (Fig. 2D and fig. S2). The shift toward the Iranian-related gene pool is found as early as ~650 BCE in one Eleke_Sazy_650BCE individual (ESZ002) retrieved from an elite Saka burial, while three of four individuals from one of the earliest Tian Shan Saka site of Caspan_700BCE fall within the Tasmola/Pazyryk cloud.

The individuals associated with the sedentary Sargat culture in the forest-steppe zone north of the Kazakh Steppe (Sargat_300BCE) partially overlap with the Tasmola/Pazyryk cluster although forming a cloud in PCA that is shifted toward western Eurasians and toward the uppermost cline of northern Inner Eurasians (PC1 and PC2, respectively; Fig. 2B). In line with PCA, Sargat individuals carry a small proportion of a different type of northeast Asian ancestry not detected in the nomad groups further to the south (Fig. 2D).

With the exception of one outlier falling in the Tasmola/Pazyryk cloud, the individuals associated with the Sarmatian culture are highly homogeneous despite being spread over a wide geographic area and time period (i.e., early Sarmatians_450BCE, late Sarmatians_150BCE, and western Sarmatians_CaspianSteppe_350BCE; Fig. 2, A and B). Our new data from seven early Sarmatian sites in central and western Kazakhstan (Sarmatians_450BCE) document that this gene pool was already widespread in this region during the early phases of the Sarmatian culture. Furthermore, Sarmatians show a sharp discontinuity from the other IA groups by forming a cluster shifted toward west Eurasians (Fig. 2 and table S2).

Genetic ancestry modeling of the IA groups performed with qpWave and qpAdm confirmed that the steppe_MLBA groups adequately approximate the western Eurasian ancestry source in IA Scythians while the preceding steppe_EBA (e.g., Yamnaya and Afanasievo) do not (data file S4). As an eastern Eurasian proxy, we chose LBA herders from Khovsgol in northern Mongolia based on their geographic and temporal proximity. Other eastern proxies fail the model because of a lack or an excess of affinity toward the Ancient North Eurasian (ANE) lineage (25). However, this two-way admixture model of Khovsgol + steppe_MLBA does not fully explain the genetic compositions of the Scythian gene pools (data file S4). We find that the missing piece matches well with a small contribution from a source related to ancient populations living in the southern regions of the Caucasus/Iran or Turan [we use the term Turan for consistency with (7), only its geographical meaning, designating the southern part of Central Asia; Fig. 3A]. The proportions of this ancestry increase through time and space: a negligible amount in the most northeastern Aldy_Bel_700BCE group, ~6% in the early Tasmola_650BCE, ~12% in Pazyryk_Berel_50BCE, ~10% in Sargat_300BCE, ~13% in Saka_TianShan_600BCE, and ~20% in Saka_TianShan_400BCE (Fig. 3A), in line with f4-statistics (table S2). Sarmatians also require 15 to 20% Iranian ancestry while carrying substantially less Khovsgol and more steppe_MLBA-related ancestry than the eastern Scythian groups.

(A) Fitting models for the main IA groups using LBA sources, the major genetic shift with the new East Asian influx (DevilsCave_N-like) observed in the Middle IA outliers and Korgantas. (B) Fitting models for the post-IA groups using IA groups as sources. A transparency factor is added to the models presenting poor fits (P < 0.05; only Konyr_Tobe_300CE). On the top is shown the color legend for the sources tested. (C) Summary of the admixture dates obtained with DATES for the main groups studied. The y axis is the temporal scale from BCE (negative) to CE (positive) dates. The x axis represents the results for the different target groups reported in the legends in each box using the two-way sources reported at the bottom of the three panels formed along the x axis (e.g., source1 + source2). The colored bars represent the date ranges of the culture, while the filled symbols show the admixture dates SEs obtained from DATES and converted into dates considering 29 years per generation starting from the median point of the cultures age. The three set of sources reported correspond to the summary of the main admixture events described in the text from left to right: the LBA formation of the Scythian gene pools; the BMAC-related influx increasing through time in the Tian Shan Sakas; and the new eastern influx starting in the IA and continuing throughout the centuries. A number-based key (the white numbers from 1 to 6 inside the black circles) connects different tests and analyses shown in the figure with the corresponding arrow in Fig. 4.

For Sarmatians and later Tian Shan Sakas, only the groups from Turan (i.e., Turan_ChL, BMAC, and postBMAC) match as sources, while groups from Iran and Caucasus fail; we chose BMAC and postBMAC as the representative proxies (Fig. 3A and data file S4). The extra eastern Eurasian influx in the outliers (Tasmola_Birlik_640BCE, Korgantas_300BCE, and Pazyryk_Berel_50BCE_o) is not sourced from the same eastern proxies as the previous groups (i.e., Khovsgol); instead, it can only be modeled with an ancient northeast Asian (ANA) lineage, represented by the early Neolithic groups from the Devils Gate Cave site in the Russian Far East (DevilsCave_N) (Fig. 3A and data file S4).

We observe an intensification of the new eastern Eurasian influx described above among the individuals from the early 1st millennium CE (Xianbei_Hun_Berel_300CE) as well as the later 7th- to 11th-millennium CE individuals (Karakaba_830CE and Kayalyk_950CE). They are scattered along PC1 from the main IA Tasmola/Pazyryk cluster toward the ANA groups (Fig. 2C). The two individuals associated with Hun elite burials dated from the third century CE, one from the site of Kurayly in the Aktobe region in western Kazakhstan and the other from Budapest, Hungary (Hun_elite_350CE), cluster closely together along this cline (Fig. 2C and figs. S1 to S3).

The individuals from the ancient city of Otyrar Oasis in southern Kazakhstan show a quite distinct genetic profile. Three of five individuals (Konyr_Tobe_300CE) fall close to the published Kangju_250CE individuals from a similar time period and region (11), between Sarmatians and BMAC (Fig. 2C). KNT005 is shifted toward BMAC in PCA (Fig. 2C and fig. S1). Furthermore, KNT005 is the only one carrying a South Asian Y haplogroup, L1a2 (data file S1), and showing a South Asian genetic component in ADMIXTURE (Fig. 2D and fig. S2). KNT004 is shifted in PC1 toward East Asians (figs. S1 to S3). Admixture models including ~10% South Asian and ~50% eastern Eurasian influx adequately explain KNT005 and KNT004, respectively (data file S4). In contrast, the individuals from the site of Alai Nura (Alai_Nura_300CE) in the Tian Shan mountains (~200 km east from the Konyr Tobe site) still lay along the IA cline of the Tian Shan Saka, with four individuals falling closer to Konyr_Tobe_300CE and four closer to the Tasmola/Pazyryk cloud (Fig. 2C and figs. S1 to S3).

Admixture dating with the DATES program reveal an early formation of the main Scythian gene pools during 1000 to 1500 BCE (Fig. 3C and fig. S4). DATES is designed to model only the two-way admixture, so to account for the estimated three-way models obtained with qpWave and qpAdm, we independently tested the three pairwise comparisons (steppe_MLBA, BMAC, and Khovsgol). DATES was successful in fitting exponential decays for the two western + eastern Eurasian pairs, steppe_MLBA + Khovsgol, and BMAC + Khovsgol, while failing in the western + western Eurasian pair (steppe_MLBA + BMAC) (fig. S4 and table S3). For each target, steppe_MLBA + Khovsgol and BMAC + Khovsgol yielded nearly identical admixture date estimates (table S3). We believe that our estimates mostly reflect an average date between the genetically distinguishable eastern (Khovsgol) and western (steppe_MLBA + BMAC) ancestries, weighted by the relative contribution from the two western sources, rather than reflecting a true simultaneous three-way admixture. It is noteworthy that DATES found increasingly younger admixture dates in the Tian Shan Saka groups as the BMAC-related ancestry increases: from Saka_TianShan_600BCE to the Saka_TianShan_400BCE and especially in the later Alai_Nura_300CE as well as for Pazyryk_Berel_50BCE and Sargat_300BCE with respect to the date of Tasmola_650BCE (~1100 to 900 BCE with respect to ~1300 to 1400 BCE; Fig. 3C). A small-scale gene flow from a BMAC-related source continued over IA may explain both the increase in the BMAC-related ancestry proportion and increasingly younger admixture dates (Fig. 3A). Again, the inferred dates reflect an average over the IA admixture with a BMAC-related source and the LBA one with steppe_MLBA; therefore, they are likely shifted toward older time periods than the actual time of the IA gene flow.

Confirming the results from qpAdm, the admixed individuals from Tasmola_Birlik_640BCE and Korgantas_300BCE (admixed_Eastern_out_IA) show very recent admixture dates (Fig. 3C, fig. S4, and table S3). The later groups of Xianbei_Hun_Berel_300CE, Hun_elite_350CE, and Karakaba_830CE further corroborate this trend of recent dates of admixture, revealing that this new eastern influx likely started in the IA and continued at least during the first centuries of the first millennium CE (Fig. 3C, fig. S4, and table S3).

PCA, ADMIXTURE, and CHROMOPAINTER/fineSTRUCTURE fine-scale haplotype-based analyses performed on present-day Kazakhs reveal a tight clustering and absence of detectable substructure among Kazakhs regardless of the geographic location or Zhuz affiliation (Fig. 2 and fig. S5). We still grouped the Kazakh individuals according to their Zhuz affiliations (which roughly reflects their geographic origin) and ran Globetrotter analyses following the pipeline in (26) as independent replicates to identify the different ancestry sources contributing to the gene pool of Kazakhs and date admixture events. Globetrotter analyses confirmed that the three groups have the same source composition and admixture dates and are a result of a complex mixture of different western, southern, and eastern Eurasian ancestries (table S4). The dates of admixture identified by Globetrotter highlight a narrow and recent time range for the formation of the present-day Kazakh gene pool, between 1341 and 1544 CE (table S5).

Our analysis of more than 100 ancient individuals from Central Asia shows that IA nomad populations of the Kazakh Steppe formed through extensive admixture, resulting from complex interactions between preceding MLBA populations from the steppe and the neighboring regions (Figs. 2A, 3, A and C, and 4A). Our findings shed new light onto the debate about the origins of the Scythian cultures. We do not find support for a western Pontic-Caspian steppe origin, which is, in fact, highly questioned by more recent historical/archeological work (1, 2). The Kazakh Steppe origin hypothesis finds instead a better correspondence with our results, but rather than finding support for one of the two extreme hypotheses, i.e., single origin with population diffusion versus multiple independent origins with only cultural transmission, we found evidence for at least two independent origins as well as population diffusion and admixture (Fig. 4B). In particular, the eastern groups are consistent with descending from a gene pool that formed as a result of a mixture between preceding local steppe_MLBA sources (which could be associated with different cultures such as Sintashta, Srubnaya, and Andronovo that are genetically homogeneous) and a specific eastern Eurasian source that was already present during the LBA in the neighboring northern Mongolia region (27). The genetic structure of the Early IA Tasmola culture of central and northern Kazakhstan is mostly composed of an equal mixture of these two ancestries, although smaller amounts of gene flow from an Iranian-related source are also required (Figs. 3A and 4A and data file S4). We found that overall BMAC-related populations from Turan provide the best fit to our models while Iranian-related sources further to the west, such as the BA groups from the northern Caucasus, fail (data file S4). These results corroborate the historical/archaeological hypotheses of a cultural connection between the southern civilizations and the northern steppe people (3). This BMAC influx continues in the later fourth- to first-century BCE-CE Scythian groups from the northeastern Pazyryk site of Berel and becomes increasingly higher and nonuniformly distributed in the southeastern Saka individuals from the Tian Shan mountains (Figs. 2, B and D, 3, A and C, and 4B; fig. S4; table S3; and data file S4).

(A) Formation of a three-way LBA admixture cline from which (B) eastern Scythian and western Sarmatian gene pools arose and spread throughout the Steppe and (C) a new source of eastern Eurasian ancestry influx admixing with the Scythian gene pools started in the IA and becoming predominant and widespread at northern latitudes during the Xianbei-Hun period. On the very southern tips of the Steppe, a very different ancestry shift occurred, likely linked with the expansion of the Persian world. The arrows represent the demographic processes analyzed in the present study and are numbered from 1 to 6 to connect them to the main results shown in Fig. 3 from which these inferences have been drawn.

The two previously published individuals from the Aldy-Bel culture of the Arzhan 2 site in the Tuva region fall within the main eastern Scythian genetic cluster, confirming that it was present also in the same site where the earliest Scythian burials are found (Fig. 2A). These data, coupled with recent findings from the IA transition in Mongolia (28), seem to point to an origin in the Altai area of a main genetic substratum that formed all the eastern Scythians (Fig. 4B). The western Sarmatians from the southern Ural region also formed as a result of admixture between the same three ancestral sources as the eastern Scythians (Fig. 3A). Nevertheless, the eastern Eurasian ancestry is present only in a small amount in Sarmatians (Fig. 3A). In addition, their early admixture dates (Fig. 3C) and the absence of an admixture cline between the Sarmatians and the eastern groups (Fig. 2, A, B, and D) suggest that the Sarmatians descend from a related but different LBA gene pool compared with the one that contributed to the eastern Scythians (likely differently located along an LBA admixture cline). Given the geographic location of the earliest Sarmatian sites found so far, we hypothesize that this gene pool originated in the LBA southern Ural area (Fig. 4B). More data from the later and westernmost Scythian cultures of the Caucasus and eastern Europe will provide a better understanding of their genetic affinities with the earlier Scythians from the Kazakh Steppe analyzed in the current study. Furthermore, our results show that the northern sedentary Sargat-related cultures show a close genetic proximity with the Scythians especially with the eastern nomad groups (Fig. 2B). The Sargats show additional affinity not found in the Scythian groups ultimately related to a northern Siberian lineage (Figs. 2D and 3A). This is consistent with the historical hypothesis that the Sargat people formed as a result of admixture between incoming Scythian groups and an unsampled local or neighboring population that possibly carried this extra Siberian ancestry (3, 18).

From the second half of the first millennium BCE, we detect a major genetic shift in a number of outliers that are interestingly linked with the emergence of the Korgantas culture that replaced the Tasmola in central Kazakhstan. In particular, we observe an influx from an eastern Eurasian source that is different from the one that contributed to the shift in the LBA (Figs. 3A and 4C and table S2). At the turn of the first millennium CE, this mixed genetic profile became widespread among the northeastern individuals associated with the Xianbei-Hun cultures and the later medieval individuals (Figs. 2, C and D, 3B, and 4C, and table S2). The highly variable admixture proportions and dates obtained for those individuals suggest that this was an ongoing process that characterized the first centuries CE (first to fifth century at least; Fig. 3C, fig. S4, and table S3). Additional genetic data from the first millennium CE will allow a more comprehensive understanding of the nature and the extent of this heterogeneity. Instead, in the southern Kazakhstan region, the individuals from the Konyr Tobe site located in the ancient city of Otyrar Oasis show a different genetic turnover mostly characterized by an increase in Iranian-related genetic ancestry, most likely reflecting the influence of the Persian empires (Fig. 4C) (20, 29). Outliers, with high eastern Eurasian admixture or with gene flow from South Asia, suggest that the population of this city at that time was heterogeneous (Fig. 2C and data file S4). During this period, Otyrar was a main center of the Kangju kingdom and a crossroad along the Silk Road (29). In the neighboring region of the Tian Shan mountains, in the third century CE site of Alai Nura, a genetic profile typical of the much earlier IA Tian Shan Sakas can still be found (Fig. 3B and data file S4).

The heterogeneity and geographic structuring observed during the IA, the Xianbei-Hun, and the medieval periods in Kazakhstan come in strong contrast with the genetic homogeneity observed among present-day Kazakhs (fig. S5). Fine-scale haplotype-based analyses confirmed this homogeneity and showed, in line with previous findings (26), that the Kazakh gene pool is a mixture of different western and eastern Eurasian sources (table S4). Our results on the ancient populations revealed that this was a result of the very complex demographic history, with multiple layers of western and eastern Eurasian ancestries mixing through time. The admixture dates obtained for present-day Kazakhs overlap with the period when the Kazakh Khanate was established (~15th century CE; table S5). Furthermore, the gene pool of present-day Kazakhs cannot be fully modeled as a mixture of post-IA northern Xianbei-Hun and southern Kangju-related gene pools (data file S4). These findings suggest that recent events, likely enfolding during the second millennium CE, were associated with more demographic turnovers in this region that ultimately lead to the homogenization of the Kazakh gene pool as a consequence of the establishment of the Kazakh Khanate with its strict exogamic rules (21).

We selected 48 samples for radiocarbon dating. They were chosen to be representative of the different cultures/genetic clusters observed or key genetic outliers. Additional 14 samples were already 14C-dated in previous studies (text S1), summing up to a total of 62 individuals directly 14C-dated (data file S1). For the new dates, the analyses were done at the Curt-Engelhorn-Zentrum Archaeometry gGmbH, Mannheim, Germany. Collagen was extracted from the bones, purified by ultrafiltration (>30 kDa), and freeze-dried. Then, the samples were combusted to CO2 in an elemental analyzer, and CO2 was converted to graphite via catalysis. The 14C/12C ratio was obtained using a mini radiocarbon dating systemaccelerator mass spectrometry. The resulting 14C ages were normalized to 13C = 25 per mil (30). The 14C ages were then calibrated (we considered the Cal 2 for downstream analyses) using the dataset INTCAL13 (31) and the software SwissCal 1.0 (30).

DNA from the ancient individuals analyzed in this study was obtained following strict sampling and extraction protocols performed in an ancient DNA clean room at the facilities of the Max Planck Institute for the Science of Human History, Jena, Germany. In brief, 40 to 70 mg of bone or tooth powder was used for DNA extraction following a previously published protocol, optimized for the retrieval of short DNA fragments (32). For the initial lysis step, the powder was incubated for 12 to 16 hours (37C) in 1 ml of extraction buffer containing 0.45 M EDTA (pH 8.0) and proteinase K (0.25 mg/ml) and subsequently purified using a binding buffer containing guanidine hydrochloride, sodium acetate (pH 5.2), and isopropanol (32), in combination with the High Pure Viral Nucleic Acid Large Volume Kit (Roche). Last, DNA extracts were eluted in 100 l of TET [10 mM tris-HCl, 1 mM EDTA (pH 8.0), and 0.05% Tween 20]. Following DNA extraction, 25 l of extract from each sample were used to produce double-stranded DNA libraries using a published protocol (33) with an initial treatment using the enzymes uracil-DNA glycosylase (UDG) and endonuclease VIII following a previously described procedure (34). This step allows for the partial removal of uracils resulting from postmortem DNA damage (cytosine deamination), retaining enough damage at the terminal nucleotides of the fragments to permit ancient DNA authentication. The resulting NSG libraries were quantified on a quantitative polymerase chain reaction (qPCR) instrument (LightCycler 96 System, Roche) using the IS7/IS8 primer set and DyNAmo SYBR Green qPCR Kit (Thermo Fisher Scientific) (33). Subsequently, libraries were double-indexed using a combination of indexing primers containing unique 8base pair (bp) identifiers (35). Ten-cycle indexing PCR reactions were carried out using Pfu Turbo Cx Hotstart DNA Polymerase (Agilent). PCR products were purified using the MinElute DNA purification kit (QIAGEN) and were subsequently qPCR-quantified using the IS5/IS6 primer set (35). Indexed libraries were then amplified with the IS5/IS6 primer set using the Herculase II Fusion DNA Polymerase (Agilent) to achieve a maximum of 10 copies per reaction, and amplification products were purified using the MinElute DNA purification kit (QIAGEN). Moreover, the concentration (nanograms per microliter) of amplified libraries was measured on an Agilent 4200 TapeStation instrument (Agilent) using the D1000 ScreenTape system (Agilent). Last, an equimolar pool of 69 of 117 UDG-half libraries was prepared for shotgun sequencing within the Max Planck Institute for the Science of Human History facilities on an Illumina HiSeq 4000 platform using a single-end 76-cycle sequencing kit. All the sequenced libraries showed high human endogenous DNA proportions (between 1 and 85% with only one library showing 0.8%) and ancient DNA characteristic damage patterns at the end of the fragments (3 end at least ~0.05%; data file S1). Therefore, all the sample libraries were enriched using DNA probes spanning 1,237,207 genome-wide SNPs known to be variable in human populations. For this, all libraries we reamplified using the Herculase II Fusion DNA Polymerase (Agilent) to achieve 1 to 2 mg of total DNA in 5.2 l (200 to 400 ng/l), they were then purified using the MinElute DNA purification kit (QIAGEN), and their concentrations were measured on a NanoDrop spectrophotometer (Thermo Fisher Scientific). All amplified libraries were subsequently captured following an established in-solution DNA capture protocol (5, 36, 37).

Genomic DNA from the 96 Kazakh individuals was extracted using the QIAamp DNA Mini Kit (QIAGEN, Germany) according to the manufacturers protocol. The DNA was quantified spectrophotometrically (Eppendorf BioPhotometer Plus) and fluorometrically (Qubit 2.0). The DNA samples were then genotyped for ~600,000 genome-wide SNPs with the Affymetrix Axiom Genome-wide Human Origins 1 (HO) array platform performed at the ATLAS Biolabs GmbH in Berlin (Germany). Quality controls were performed with PLINK v.1.9 (38). All the 96 individuals had a genotype success rate higher than 95%, and all SNPs had a success rate higher than 95% and were therefore kept for downstream analyses. We then merged our 96 individuals with 18 previously published Kazakh individuals also genotyped on a HumanOrigins array (26). On this dataset (N = 114), we estimated recent relatedness values among each pair of individuals with the --genome function restricting the analysis only on 73,076 SNPs with low linkage disequilibrium (LD) (r2 < 0.1) that was estimated setting the --indep-paiwise 50 100 0.1 parameters. We found only two couples with PI-HAT values [i.e., coefficient of relatedness (38)] compatible with a third- to second-degree relation (0.25 > PI-HAT > 0.125) and involved one couple of previously published Kazakh individuals (KZH-1611 and KZH-1750, PI-HAT = 0.23) and one couple formed by a new and a previously published individual (KZH-1650 and E01; PI-HAT = 0.19).

Raw data. Demultiplexing of the sequenced reads was done allowing only one mismatch in the indexes. Adaptor removal, mapping to the reference genome, and duplicate removal were done through the EAGER 1.92.32 workflow (39). We used AdapterRemoval v2.2.0 to remove adaptors discarding reads shorter than 30 bp (40). We then mapped the reads to Human Reference Genome Hs37d5 using the bwa v0.7.12 aln/samse alignment algorithm (41) with an edit distance parameter (-n) of 0.01 and a seed length (-l) of 32 and keeping only high-quality reads (phred mapping quality of 30) using Samtools v1.3 (42). We then used DeDup v0.12.2 to remove PCR duplicates (39).

Authentication and contamination estimates. We used mapDamage v2.0 (43) to assess the amount of deamination at the ends of the fragments on a subset of 100,000 high-quality reads using default parameters. We assessed exogenous human DNA contamination levels using ANGSD v0.910 (44) for nuclear (based on X chromosome heterozygosity levels in males) and Schmutzi (45) for mitochondrial DNA contamination. Among the males with enough coverage (i.e., >200 SNPs on X chromosome), none of the individuals had a contamination level of >7%, and only one had >4%. Even if the results are less reliable (i.e., <<200 SNPs), we removed from further analyses two males that showed signs of moderate nuclear contamination (>10%) that were also PCA outliers. Furthermore, none of the individuals (males and females) showed levels of mitochondrial contamination of >3% (data file S1).

Genotyping. We used pileupCaller (https://github.com/stschiff/sequenceTools) with the --randomHaploid mode to call haploid genotypes for each position captured on the 1240K panel by randomly choosing one high-quality base (phred base quality score of 30). To call transitions, we first clipped 2 bp from each end of the high-quality reads using the trimBam module of bamUtil v.1.0.13 (46) to reduce the numbers of wrong calls due to high deamination at the last two bases, while we used the full high-quality reads to call transversions. At this stage, we excluded from the analyses four individuals with the lowest coverage presenting <20,000 SNPs typed on the 1240K panel.

We then merged the newly produced genotype data of 111 ancient individuals with the 96 modern Kazakh and a reference panel composed of 2280 modern individuals genotyped with the HumanOrigins array (26, 47, 48) and 959 ancient individuals haploid genotypes obtained from a mix of 1240K capture and shotgun sequencing data (4, 6, 7, 911, 2527, 36, 4852) (data files S2 and S3). This 1240KHO dataset consisting of 586,594 overall SNPs was used for explorative global structure population genetic analyses. For fine-scale ancestry deconvolution and admixture dating analyses, we compiled a higher-coverage 1240K dataset merging only data obtained with the 1240K capture technique or whole-genome shotgun data pooled down to comprehend 1240K sites only (1,233,013 overall SNPs; data files S2 and S3).

Sex determination. Genetic sex was determined calculating the ratio between the coverage on the X and Y chromosomes over the one on the autosomes. We found highly consistent ratios, allowing us to confidently infer the sex of all the individuals. One individual showed a Y/autosomes proportion of 0.96 (data file S1). Since the X-based contamination estimates are extremely low and the X/autosomes ratio within the normal range for males, the most likely explanation is that this individual carries a XYY karyotype. This condition is known as the XYY syndrome and is relatively rare (1 in 1000 births) and largely asymptomatic (53). It commonly affects stature (i.e., increased height) and can slightly influence cognitive or behavioral functions (53).

Genetic relatedness estimation. We assessed relatedness between individuals by calculating the rate of mismatching alleles between every pair of individuals (pairwise mismatch rate) among the overlapping positions as described in (27, 54). The pairwise mismatch rate provides good evidence of close relationships such as identical individual/twins and first and second degrees (55). We detected a couple of first-degree relatives. The two individuals, a male and a female (ESZ001 and ESZ003), came from the same site (Eleke_Sazy_650BCE) and the same burial (Mound 4). Another first-degree couple was found in Taldy_7cBCE site (TAL003 and TAL004). We then identified a couple of second-degree relatives from the Karashoky_7cBCE site (KSH001 and KSH003) and a couple of possible second- to third-degree relatives between two individuals retrieved from two different Tasmola sites of Akbeit_7cBCE and Nurken_8cBCE (AKB001 and NUR002). We removed one individual per pair of related couples for downstream population-based analyses (data file S1).

We used Schmutzi to obtain the consensus sequence of the mitochondrial DNA with a q10 quality cutoff, and we used HaploGrep2 (56) to assign haplogroups. We used yHaplo (57) to assign Y chromosome haplogroups of the male individuals. To obtain Y chromosome genotypes, we used pileupCaller in the --majorityCall mode to call the allele supported by most reads for each Y chromosome SNP included in the 1240K panel (data file S1).

We applied the smartpca v16000 function in EIGENSOFT v6.0.1 package (58) on the 1240KHO dataset to run PCA with the lsqproject option to project the data of the ancient individuals on top of PCA calculated on the set of modern populations to bypass the high number of missing genotypes in the ancient data that would artificially shift the eigenvectors toward the origin of the axes. We used a set of 150 present-day Eurasian populations on which we projected our newly produced 111 ancient unrelated individuals that passed the quality controls together with other relevant published ancient genomes. We also ran a PCA only on the genotypes of the present-day Kazakh individuals. We then applied ADMIXTURE v.1.3.0. (59) unsupervised cluster analyses testing K = 2 to K = 16 on a set of worldwide ancient and modern individuals. For each K value tested, we performed 10 independent ADMIXTURE runs with a different random seed to check the convergence of log-likelihoods across the different runs. For each K value, we selected for consideration the run with the highest log-likelihood. We also estimated the cross-validation error (CV-err) for each K value to identify the most parsimonious models (i.e., increasing the number of K values does not produce a visible decrease in CV-err) to avoid overfitting. For ADMIXTURE analyses, we removed the variants with a minor allele frequency of <0.01, and we pruned the dataset, removing all the SNPs in LD with an r2 > 0.4 setting a 200-SNP sliding window with a 25-SNP step using the dedicated commands in PLINK. The pruned dataset consists of 206,728 SNPs, and we further removed from the analysis all the ancient individuals with a missingness rate higher than 95%, which corresponds to including individuals with at least ~10,000 nonmissing variants on this thinned dataset.

For the new ancient individuals produced in the current study, we first considered a site-based labeling system consisting of site name plus the age expressed in centuries BCE/CE referring to the median of the archeological time range of the site (e.g., Site_Name_400BCE). In the few cases of same sites presenting burials from different and discontinuous time periods, multiple unique names for the same site exist (e.g., Berel_50BCE and Berel_300CE). Following the recommendations in (60) for grouping the individuals into populations, we used a mixed system consisting of the archaeological cultures name and the archaeological age of the sites included in the group in centuries BCE/CE (e.g., Tasmola_650BCE). To respect the high levels of admixture and genetic variability observed within most of the ancient cultures studied, we identified and excluded as outliers only the individuals that exceeded 2 SD from the median of at least one of the first three PCs within their respective culture group (table S1).

In the cases of cultures represented by one site only, or by few individuals with highly admixed genetic profiles, we retained the site-based labels or used different grouping combinations depending on specific hypotheses and analyses tested as detailed in Results. We extended this labeling system also to previously published ancient individuals belonging to closely related cultures. Nevertheless, to limit potential batch effects due to different laboratory techniques and sequencing methods (i.e., shotgun or 1240K capture), we avoided grouping together our newly generated individuals with previously published ones even if belonging to the same age or culture, opting for using them as independent control groups for validation (data file S3). For consistency with the literature, the rest of the reference ancient and modern population labels and groupings were kept the same as in the original publications unless stated otherwise (data file S3).

All the f-statisticbased analyses were run using the dedicated programs in the ADMIXTOOLS package (47) on the 1240K dataset. We run outgroup-f3 analyses with qp3Pop (v400). We tested the forms f3(Test, X; Mbuti) for the Kazakh ancient individuals as Test against every other X individual/population included in the dataset. For the newly reported individuals, outgroup-f3 was run on a site-based grouping considering separate the PCA outliers. To test specific hypotheses detailed in the results, we also computed f4-statistics with qpDstat (v711) setting the f4mode: YES option. For both f3- and f4-statistics, we considered only the tests that had a number of overlapping SNPs of >30,000, and we considered a Z > |3| as a threshold for significance.

We then run f4-statisticbased ancestry decomposition analyses on the 1240K dataset using the qpWave and qpAdm (v632) pipeline (5, 61). SEs for the computed f-statistics were estimated using a block jackknife with a 5-centimorgan block. We used the following set of eight outgroups (OG1) by including representatives of western and eastern Eurasian and relevant non-Eurasian ancient lineages using directly ancient individuals or present-day proxies: Mbuti, Natufian, Anatolia_N, Ganj_Dareh_N, Villabruna, Onge, Ami, and Mixe. As sources, we used, when available, ancient populations from the closest available preceding time periods. We started by selecting proximal source populations for the IA groups by choosing representatives of the three main genetic ancestries found in the MLBA in the Kazakh Steppe and the surrounding regions. Specifically, we used as western ancestry sources a chosen set of steppe_MLBA groups as well as the earlier steppe_EBA (i.e., Yamnaya and Afanasievo) for completeness of analysis. We selected two groups from the west and central clusters described in (7): Sintashta_MLBA and Srubnaya as representative of the western cultures from the southern Ural area (steppe_MLBA_west) and Dali:MLBA and Krasnoyarsk_MLBA from northeastern Kazakhstan and the Minusinsk Basin in Russia, respectively, as representative of the eastern cluster showing higher affinity to preceding local hunter-gatherer populations and ultimately to the ANE-related ancestry (steppe_MLBA_central). As sources of East Asian ancestries, we used previously published Eneolithic and Early BA individuals from the Baikal region (Baikal_EN and Baikal_EBA) and from the Minusinsk Basin (Okunevo) and LBA individuals from Khovsgol site in northern Mongolia (Khovsgol) as well as Neolithic individuals from the Amur River Basin representative of a deep north East Asian lineage (DevilsCave_N) presenting a high genetic continuity with modern individuals from the same region (52, 62). As third Iranian-related sources, we used the available Eneolithic groups from Iran (Iran_ChL and Hajji_Firuz_C), the MLBA groups from the Caucasus (Caucasus_MBA_North_Caucasus, Caucasus_Late_Maykop, and Caucasus_Kura_Araxes), Armenia_LBA, Eneolithic from Turan (Geoksiur_EN and Tepe_Hissar_C), and BA from Turan associated with the Bactria-Margiana complex or BMAC (Gonur1_BA) and later MLBA postBMAC (Sappali:Tepe_BA, Bustan_BA, and Dzharkutan1_BA). We first performed 1648 qpWave/qpAdm-independent tests for each target group, permuting all combinations of two-way (N = 16) and three-way (N = 96) sources (data file S4). For the IA outliers and the later CE groups, we used the preceding IA groups as first sources and tested different second and eventually third sources (when two-way tests failed) to narrow down closer proxies that could explain the nature of the observed genetic turnovers. For the modeling of present Kazakh Zhuz, we used the 1240KHO dataset using the same set of outgroups used for the ancient (albeit the modern populations are represented by more individuals in the 1240KHO with respect to the 1240K dataset; data file S2). We tested two-way models (data file S4) with all the later CE individuals from the northern latitude, showing the eastern Eurasian influx as the first source (Xiambei_Hun_Berel_300CE, Hun_elite_350CE, Karakaba_830CE, and Kayalyk_950CE) and the southern CE individuals with Iranian-related influx as the second source (Konyr_Tobe_300CE and Alai_Nura_300CE).

We used DATES (7) on the 1240K dataset to date the admixture events identified from previous analyses in the IA and post-IA Kazakh individuals. The method is conceptually similar to commonly used admixture-dating methods based on LD such as ALDER (63), although instead of calculating the weighted LD decay, which would require high coverage with virtually no missing data, DATES use the decay of ancestry covariance (AC) coefficients between pairs of overlapping SNPs over increasing genetic distance. As for the LD-based methods, an exponential function can be fitted to the decay of weighted AC as genetic distance increases to infer admixture parameters such as the number of generations since admixture (63). We then considered a standard 29 years per generation to convert the generation times into years since admixture (7). DATES assumes a two-way admixture; therefore, we used as sources pairwise combinations of the best proxies resulted from qpAdm modeling analyses. In choosing the source populations, we also considered that the method is sensitive to sample sizes and coverage, preferring proxies with a higher number of individuals or, when possible, pooling together genetically homogeneous populations to reduce statistical noise (table S3). In choosing the target individuals, for sites with more complex chronology (i.e., containing burials belonging to different time periods), we included only individuals directly 14C-dated to reduce the errors due to incorrect context dating.

We reconstructed the phase of haplotypes for the modern Kazakh individuals together with the set of worldwide modern populations present in the 1240KHO dataset using SHAPEIT2 v2.r790 (64) with default parameters and using HapMap phase 3 recombination maps. To explore the fine-scale population structure among present-day Kazakh individuals, we applied the haplotype-based CHROMOPAINTERv2/fineSTRUCTURE pipeline (65) on the Central Asian Southern Steppe populations present in the dataset plus all the Kazakh individuals (96 new and 18 previously published). We first estimated the mutation/emission and the switch rate parameters with 10 steps of the Expectation-Maximization algorithm on a subset of chromosomes {4, 10, 15, 22} using each individual as donor and recipient. Then, we averaged the values across chromosomes (normalized by the number of SNPs per chromosome) and individuals, and we used these mutation/emission and switch rate parameters to run CHROMOPAINTER again on all chromosomes, considering a parameter k = 50 to specify the number of expected chunks to define a region. The obtained matrix of haplotype-sharing chunk counts was summed up across all the 22 autosomes and submitted to the fineSTRUCTURE clustering algorithm version fs2.1 (65). We ran fineSTRUCTURE pipeline by setting 1,000,000 burn-in Markov chain Monte Carlo iterations, followed by additional 2,000,000 iterations and sampling the inferred clustering patterns every 10,000 runs. Last, we set 1,000,000 additional hill-climbing steps to improve posterior probability and merge clusters in a stepwise fashion. Individuals were hierarchically assembled into clusters until reaching the final configuration tree. We then applied the GLOBETROTTER algorithm (66) using the Kazakhs, grouped according to their Zhuz affiliation, as targets and a set of 85 non-Inner Eurasian populations as reference groups following the same pipeline detailed in (26) to date admixture and identify the main contributing sources. All GLOBETROTTER runs were conducted according to the guidelines reported in (66) and performing a first run standardizing over a null individual.

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