Biology:Haplogroup O-M95
| Haplogroup O-M95 | |
|---|---|
| Possible time of origin | 40+ kya |
| Coalescence age | 20–40 kya[1] |
| Possible place of origin | Guangxi, Southern China |
| Ancestor | O-P31 |
| Descendants | O-M88, O-M297, O2a1*-M95, O2a1a-F789, O2a1b*-F1252, O2a1b1*-M88, and O2a1b1a -F761 |
| Defining mutations | M95, F709, F987/M1300, F1931/M1362, F2176/M1376, F2254/M1383, F2917/M1436, F4233/M1404 |
Haplogroup O1b1a1a-M95 (also known as O-M95 or M95, previously denoted O2a/O2a1 under ISOGG 2006–2014) is a human Y-chromosome (chrY) DNA haplogroup, a descendant branch of haplogroup O-P31, and the dominant chrY haplogroup in most Austroasiatic-speaking populations of Southeast Asia. It is found at especially high frequencies in areas of South Central China bordering Vietnam, as well as in East India among the Munda people of Chota Nagpur Plateau in Jharkhand state.[2] In some populations of Island Southeast Asia (ISEA) it is fixed, likely due to population bottlenecks.
Origin
The genetic origin of O-M95 is uncertain, but TMRCA and haplogroup diversity estimates suggest an origin in Guangxi, China.[3] From there, it likely spread eastwards into modern East India, resulting in the concentration among indigenous Munda populations.
Distribution
Haplogroup O-M95 is distributed widely in Asia, from southern India to the Altai Mountains and Central Asia in the west, and from Indonesia to northern China and Japan in the east. It is found only at marginally low frequencies of approximately 1% at the periphery of its distribution in southern India, Central Asia, northern China, and Japan, but many populations within the vast intervening territory in South Asia, Southeast Asia, and southern China display a greatly elevated frequency of Haplogroup O-M95 Y-chromosomes. Patrilines within Haplogroup O-M95 predominate among the Austroasiatic-speaking populations of South and Southeast Asia, such as the Khmer of Cambodia and the Khasi of Meghalaya in northeastern India. Some researchers have reported that slightly over half of all men in a composite sample of Austroasiatic speakers belonged to Haplogroup O-M95. Haplogroup O-M122, which attains its peak frequency among the Sino-Tibetan and Hmong–Mien peoples of China and Southeast Asia, and Haplogroup O-M119, which predominates among Taiwanese aborigines and many populations of the Philippines, also generally occur among speakers of Austroasiatic languages in South China and the Indochinese Peninsula, but usually at much lower frequencies than Haplogroup O-M95. The hypothesis that Haplogroup O-M95 was the major Y-chromosome haplogroup of the proto-Austroasiatic population is strengthened by the fact that Haplogroup O-M95 is the only haplogroup found among many Austroasiatic-speaking tribes, such as the Mlabri people of Thailand, Mang people of southern China and northern Vietnam, Juang of mainland India, and the Nicobarese and Shompen of the Nicobar Islands (Sahoo 2006 and Trivedi 2006).
Outside of the region in which Austroasiatic languages are currently spoken or have a historically attested presence, Haplogroup O-M95 reaches its highest frequencies among the populations of the islands of Sumatra, Java, Bali, and Borneo in western and central Indonesia (Underhill 2001). Haplogroup O-M95 has been found to be by far the most common Y-chromosome haplogroup among the Balinese, occurring in approximately 58.6% (323/551) of a sample of Balinese men; Haplogroup O-M119 and Haplogroup O-M122, which are typical of Austronesian peoples outside of Malaysia and Indonesia, were observed in only 18.1% (100/551) and 6.9% (38/551) of Balinese men (Karafet 2005). Haplogroup O-M95 has also been found to be the most frequently occurring haplogroup among Malay men in Singapore (Yong 2006). The reason for its substantial presence in these populations, all of which are Austronesian-speaking, is yet to be elucidated.
Subclade distribution
- O-PK4 This lineage has been relocated upstream of M95 following a paper published on the subject in 2011.(Shi Yan et al. 2011) Found in three samples of Han Chinese: 3/65 = 4.6% South China, 1/129 = 0.8% North China, 1/167 = 0.6% East China.
- O-M88 This lineage is frequently found among Hani, She people, Vietnamese with a moderate distribution among Tai peoples, Cambodians, Qiang, Hlai, Miao, Yao, Taiwanese aborigines, populations of Borneo (Hurles 2005), Han Chinese of Sichuan, Guangxi, and Guangdong, and Pashtuns (Khaliq 2006)
- O-M297 More research is needed on this lineage. It is claimed to be downstream from M95 and parallel to M88.
Phylogenetics
Phylogenetic history
Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.
| YCC 2002/2008 (Shorthand) | (α) | (β) | (γ) | (δ) | (ε) | (ζ) | (η) | YCC 2002 (Longhand) | YCC 2005 (Longhand) | YCC 2008 (Longhand) | YCC 2010r (Longhand) | ISOGG 2006 | ISOGG 2007 | ISOGG 2008 | ISOGG 2009 | ISOGG 2010 | ISOGG 2011 | ISOGG 2012 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| O-M175 | 26 | VII | 1U | 28 | Eu16 | H9 | I | O* | O | O | O | O | O | O | O | O | O | O |
| O-M119 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1* | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a |
| O-M101 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1a | O1a1 | O1a1a | O1a1a | O1a1 | O1a1 | O1a1a | O1a1a | O1a1a | O1a1a | O1a1a |
| O-M50 | 26 | VII | 1U | 32 | Eu16 | H10 | H | O1b | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 |
| O-P31 | 26 | VII | 1U | 33 | Eu16 | H5 | I | O2* | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 |
| O-M95 | 26 | VII | 1U | 34 | Eu16 | H11 | G | O2a* | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a1 | O2a1 |
| O-M88 | 26 | VII | 1U | 34 | Eu16 | H12 | G | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1a | O2a1a |
| O-SRY465 | 20 | VII | 1U | 35 | Eu16 | H5 | I | O2b* | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b |
| O-47z | 5 | VII | 1U | 26 | Eu16 | H5 | I | O2b1 | O2b1a | O2b1 | O2b1 | O2b1a | O2b1a | O2b1 | O2b1 | O2b1 | O2b1 | O2b1 |
| O-M122 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3* | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 |
| O-M121 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3a | O3a | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1a | O3a1a |
| O-M164 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3b | O3b | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a1b | O3a1b |
| O-M159 | 13 | VII | 1U | 31 | Eu16 | H6 | L | O3c | O3c | O3a3a | O3a3a | O3a3 | O3a3 | O3a3a | O3a3a | O3a3a | O3a3a | O3a3a |
| O-M7 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d* | O3c | O3a3b | O3a3b | O3a4 | O3a4 | O3a3b | O3a3b | O3a3b | O3a2b | O3a2b |
| O-M113 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d1 | O3c1 | O3a3b1 | O3a3b1 | - | O3a4a | O3a3b1 | O3a3b1 | O3a3b1 | O3a2b1 | O3a2b1 |
| O-M134 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e* | O3d | O3a3c | O3a3c | O3a5 | O3a5 | O3a3c | O3a3c | O3a3c | O3a2c1 | O3a2c1 |
| O-M117 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1* | O3d1 | O3a3c1 | O3a3c1 | O3a5a | O3a5a | O3a3c1 | O3a3c1 | O3a3c1 | O3a2c1a | O3a2c1a |
| O-M162 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1a | O3d1a | O3a3c1a | O3a3c1a | O3a5a1 | O3a5a1 | O3a3c1a | O3a3c1a | O3a3c1a | O3a2c1a1 | O3a2c1a1 |
Research publications
The following research teams per their publications were represented in the creation of the YCC Tree.
Phylogenetic trees
This phylogenetic tree of haplogroup O subclades is based on the YCC 2008 tree (Karafet 2008) and subsequent published research.
- O-M95 (M95)
- O-M88 (M88, M111)
Table of frequencies of O-M95(xM88/M111)
| Population | Frequency | Count | Source | SNPs |
|---|---|---|---|---|
| Nicobarese | 1.00 | 11 | Kumar 2007 | M95(xM88) |
| Juang | 0.980 | 49 | Kumar 2007 | M95(xM88) |
| Lamet | 0.857 | 35 | Cai 2011 | M95(xM88) |
| Korku | 0.814 | 59 | Kumar 2007 | M95(xM88) |
| Inh | 0.794 | 34 | Cai 2011 | M95(xM88) |
| Katu | 0.689 | 45 | Cai 2011 | M95(xM88) |
| Mal | 0.660 | 50 | Cai 2011 | M95(xM88) |
| Ho | 0.658 | 79 | Kumar 2007 | M95(xM88) |
| Bo | 0.643 | 28 | Cai 2011 | M95(xM88) |
| Talieng | 0.629 | 35 | Cai 2011 | M95(xM88) |
| Brau | 0.625 | 32 | Cai 2011 | M95(xM88) |
| Khmu | 0.608 | 51 | Cai 2011 | M95(xM88) |
| Oy | 0.600 | 50 | Cai 2011 | M95(xM88) |
| Korwa | 0.595 | 42 | Kumar 2007 | M95(xM88) |
| Li (Hlai) | 0.588 | 34 | Xue 2006 | M95(xM88) |
| Balinese | 0.573 | 641 | Karafet 2010 | M95(xM111) |
| Alak | 0.567 | 30 | Cai 2011 | M95(xM88) |
| Suy | 0.564 | 39 | Cai 2011 | M95(xM88) |
| Bit | 0.536 | 28 | Cai 2011 | M95(xM88) |
| Aheu | 0.526 | 38 | Cai 2011 | M95(xM88) |
| Bugan | 0.500 | 32 | Cai 2011 | M95(xM88) |
| Java (mostly sampled in Dieng) | 0.492 | 61 | Karafet 2010 | M95(xM111) |
| Ngeq | 0.486 | 35 | Cai 2011 | M95(xM88) |
| Jeh | 0.469 | 32 | Cai 2011 | M95(xM88) |
| Santhal | 0.468 | 109 | Kumar 2007 | M95(xM88) |
| Munda | 0.453 | 53 | Kumar 2007 | M95(xM88) |
| Laven | 0.420 | 50 | Cai 2011 | M95(xM88) |
| So | 0.420 | 50 | Cai 2011 | M95(xM88) |
| Muong | 0.417 | 12 | Cai 2011 | M95(xM88) |
| Khasi | 0.413 | 92 | Kumar 2007 | M95(xM88) |
| Kharia | 0.389 | 36 | Kumar 2007 | M95(xM88) |
| Buyi | 0.371 | 35 | Xue 2006 | M95(xM88) |
| Lao (Luang Prabang, Laos) | 0.360 | 25 | He 2012 | M95(xM88) |
| Kinh | 0.333 | 15 | Cai 2011 | M95(xM88) |
| Oraon | 0.319 | 91 | Kumar 2007 | M95(xM88) |
| Banjarmasin, Indonesia | 0.318 | 22 | Hurles 2005 | M95(xM88) |
| Malaysia | 0.313 | 32 | Karafet 2010 | M95(xM111) |
| Mountain Kimmun | 0.313 | 32 | Cai 2011 | M95(xM88) |
| Blang | 0.308 | 52 | Cai 2011 | M95(xM88) |
| Miao (Yunnan) | 0.306 | 49 | Cai 2011 | M95(xM88) |
| Cham (Binh Thuan, Vietnam) | 0.305 | 59 | He 2012 | M95(xM88) |
| Lowland Kimmun | 0.244 | 41 | Cai 2011 | M95(xM88) |
| Zhuang | 0.235 | 166 | Chen 2006 | M95(xM111) |
| Palyu | 0.233 | 30 | Cai 2011 | M95(xM88) |
| Kota Kinabalu, Malaysia | 0.215 | 65 | Hurles 2005 | M95(xM88) |
| Northern Mien | 0.212 | 33 | Cai 2011 | M95(xM88) |
| Flower-head Mien | 0.211 | 19 | Cai 2011 | M95(xM88) |
| Borneo (Indonesia) | 0.209 | 86 | Karafet 2010 | M95(xM111) |
| Southern Mien | 0.194 | 31 | Cai 2011 | M95(xM88) |
| Garo | 0.182 | 33 | Kumar 2007 | M95(xM88) |
| Blue Kimmun | 0.179 | 28 | Cai 2011 | M95(xM88) |
| Thai (Northern Thailand) | 0.176 | 17 | He 2012 | M95(xM88) |
| Xinhmul | 0.172 | 29 | Cai 2011 | M95(xM88) |
| Malagasy | 0.171 | 35 | Hurles 2005 | M95(xM88) |
| Miao (Guizhou) | 0.163 | 49 | Cai 2011 | M95(xM88) |
| Lowland Yao | 0.161 | 31 | Cai 2011 | M95(xM88) |
| Batak Toba (Sumatra) | 0.158 | 38 | Karafet 2010 | M95(xM111) |
| Daur | 0.154 | 39 | Xue 2006 | M95(xM88) |
| Western Mien | 0.149 | 47 | Cai 2011 | M95(xM88) |
| Mandar (Sulawesi) | 0.130 | 54 | Karafet 2010 | M95(xM111) |
| Pahng | 0.129 | 31 | Cai 2011 | M95(xM88) |
| Kinh (Hanoi, Vietnam) | 0.118 | 76 | He 2012 | M95(xM88) |
| Kataang | 0.108 | 37 | Cai 2011 | M95(xM88) |
| Han (South China) | 0.092 | 65 | Yan 2011 | PK4(xM88) |
| Qiang | 0.091 | 33 | Xue 2006 | M95(xM88) |
| Top Board Mien | 0.091 | 11 | Cai 2011 | M95(xM88) |
| Thin Board Mien | 0.091 | 11 | Cai 2011 | M95(xM88) |
| Miao (Hunan) | 0.090 | 100 | Cai 2011 | M95(xM88) |
| She | 0.088 | 34 | Xue 2006 | M95(xM88) |
| Native Mien | 0.073 | 41 | Cai 2011 | M95(xM88) |
| Vietnamese | 0.071 | 70 | Karafet 2010 | M95(xM111) |
| Han Chinese (China) | 0.061 | 165 | Karafet 2010 | M95(xM111) |
| Hmong Daw (Laos) | 0.059 | 51 | Cai 2011 | M95(xM88) |
| Hani | 0.059 | 34 | Xue 2006 | M95(xM88) |
| Yao (Liannan, Guangdong) | 0.057 | 35 | Xue 2006 | M95(xM88) |
| Bunu | 0.056 | 36 | Cai 2011 | M95(xM88) |
| Kapingamarangi | 0.048 | 21 | Hurles 2005 | M95(xM88) |
| Flores | 0.046 | 394 | Karafet 2010 | M95(xM111) |
| Japanese | 0.043 | 47 | Xue 2006 | M95(xM88) |
| Western Samoa | 0.040 | 25 | Hurles 2005 | M95(xM88) |
| Ewenki (China) | 0.038 | 26 | Xue 2006 | M95(xM88) |
| Northern She (Zhejiang) | 0.036 | 56 | Cai 2011 | M95(xM88) |
| Miao (China) | 0.034 | 58 | Karafet 2010 | M95(xM111) |
| Han (Lanzhou, Gansu) | 0.033 | 30 | Xue 2006 | M95(xM88) |
| Han (Yili, Xinjiang) | 0.031 | 32 | Xue 2006 | M95(x88) |
| Han (North China) | 0.031 | 129 | Yan 2011 | PK4(xM88) |
| Han (Chengdu, Sichuan) | 0.029 | 34 | Xue 2006 | M95(xM88) |
| Han (East China) | 0.024 | 167 | Yan 2011 | PK4(xM88) |
| Japanese | 0.024 | 210 | Hammer 2006 | M95(xM111) |
| Philippines | 0.021 | 48 | Karafet 2010 | M95(xM111) |
| Yao (China) | 0.017 | 60 | Karafet 2010 | M95(xM111) |
| Sumba | 0.003 | 350 | Karafet 2010 | M95(xM111) |
Table of frequencies of O-M88/M111
| Population | Frequency | Count | Source | SNPs |
|---|---|---|---|---|
| Xinhmul | 0.690 | 29 | Cai 2011 | M88 |
| Hani | 0.441 | 34 | Xue 2006 | M88 |
| She | 0.353 | 51 | Karafet 2010 | M111 |
| Suy | 0.308 | 39 | Cai 2011 | M88 |
| Kinh (Hanoi, Vietnam) | 0.303 | 76 | He 2012 | M88 |
| Lowland Yao | 0.290 | 31 | Cai 2011 | M88 |
| Kataang | 0.270 | 37 | Cai 2011 | M88 |
| Zaomin | 0.216 | 37 | Cai 2011 | M88 |
| Vietnamese | 0.200 | 70 | Karafet 2010 | M111 |
| Buyi | 0.171 | 35 | Xue 2006 | M88 |
| Lao (Luang Prabang, Laos) | 0.120 | 25 | He 2012 | M88 |
| Han (Chengdu, Sichuan) | 0.118 | 34 | Xue 2006 | M88 |
| Cham (Binh Thuan, Vietnam) | 0.085 | 59 | He 2012 | M88 |
| Zhuang | 0.072 | 166 | Chen 2006 | M111 |
| Miao (China) | 0.069 | 58 | Karafet 2010 | M111 |
| Thai (Northern Thailand) | 0.059 | 17 | He 2012 | M88 |
| Han (China) | 0.055 | 165 | Karafet 2010 | M111 |
| Taiwanese aborigines | 0.051 | 39 | Hurles 2005 | M88 |
| Banjarmasin, Indonesia | 0.045 | 22 | Hurles 2005 | M88 |
| Pathans (Dir, Pakistan) | 0.042 | 96 | Firasat 2007 | M88, M111 |
| Malaysia | 0.031 | 32 | Karafet 2010 | M111 |
| Kota Kinabalu, Malaysia | 0.031 | 65 | Hurles 2005 | M88 |
| Qiang | 0.030 | 33 | Xue 2006 | M88 |
| Li (Hlai) | 0.029 | 34 | Xue 2006 | M88 |
| Yao (Liannan, Guangdong) | 0.029 | 35 | Xue 2006 | M88 |
| Philippines | 0.021 | 48 | Karafet 2010 | M111 |
| Taiwanese aborigines | 0.021 | 48 | Karafet 2010 | M111 |
| Yao (China) | 0.017 | 60 | Karafet 2010 | M111 |
See also
Genetics
- genetic genealogy
- Haplogroup
- Haplotype
- Human Y-chromosome DNA haplogroup
- molecular phylogeny
- Paragroup
- Subclade
- Y-chromosome haplogroups by populations
- Y-DNA haplogroups by ethnic groups
- Y-DNA haplogroups by populations of East and Southeast Asia
Y-DNA O subclades
References
Footnotes
Works cited
Books
- Underhill, Peter (2005). "Chapter 17: A synopsis of extant Y chromosome diversity in East Asia and Oceania". in Sagart, Laurent; Blench, Roger; Sanchez-Mazas, Alicia. The Peopling of East Asia: Putting Together Archaeology, Linguistics and Genetics. Psychology Press. pp. 297–314. ISBN 9780415322423.
Conference Posters
- Yong, R.Y.Y.; Gan, L.S.H.; Khripin, Y.; Yap, V.B.; Yap, E.P.H. (2006). "Workshop 6 Genomic Variation and Diversity: Association of Y chromosome variation with paternal ancestry origin of three ethnic populations in Singapore". HUGO's 11th Human Genome Meeting Helsinki Fair Centre, Helsinki, Finland, Wed 31 May to Sat 3 June 2006. Helsinki, Finland. http://hgm2006.hugo-international.org/Abstracts/Publish/WorkshopPosters/WorkshopPosters06/hgm128.html.
Journals
- Firasat, Sadaf; Khaliq, Shagufta; Mohyuddin, Aisha; Papaioannou, Myrto; Tyler-Smith, Chris; Underhill, Peter A; Ayub, Qasim (2006). "Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan". European Journal of Human Genetics 15 (1): 121–6. doi:10.1038/sj.ejhg.5201726. PMID 17047675. PMC 2588664. http://www.nature.com/ejhg/journal/v15/n1/full/5201726a.html.
- Fornarino, Simona; Pala, Maria; Battaglia, Vincenza; Maranta, Ramona; Achilli, Alessandro; Modiano, Guido; Torroni, Antonio; Semino, Ornella et al. (2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): A reservoir of genetic variation". BMC Evolutionary Biology 9 (1): 154. doi:10.1186/1471-2148-9-154. PMID 19573232. PMC 2720951. http://www.biomedcentral.com/1471-2148/9/154.
- Hurles, M; Sykes, B; Jobling, M; Forster, P (2005). "The Dual Origin of the Malagasy in Island Southeast Asia and East Africa: Evidence from Maternal and Paternal Lineages". The American Journal of Human Genetics 76 (5): 894–901. doi:10.1086/430051. PMID 15793703. PMC 1199379. http://linkinghub.elsevier.com/retrieve/pii/S0002-9297(07)60736-8.
- Karafet, Tatiana M.; Lansing, J. S.; Redd, Alan J.; Watkins, Joseph C.; Surata, S. P. K.; Arthawiguna, W. A.; Mayer, Laura; Bamshad, Michael et al. (2005). "Balinese Y-Chromosome Perspective on the Peopling of Indonesia: Genetic Contributions from Pre-Neolithic Hunter-Gatherers, Austronesian Farmers, and Indian Traders". Human Biology 77 (1): 93–114. doi:10.1353/hub.2005.0030. PMID 16114819.
- Sahoo, Sanghamitra; Kashyap, V.K. (2006). "Phylogeography of mitochondrial DNA and Y-Chromosome haplogroups reveal asymmetric gene flow in populations of Eastern India". American Journal of Physical Anthropology 131 (1): 84–97. doi:10.1002/ajpa.20399. PMID 16485297.
- Trivedi, Rajni; Sitalaximi, T.; Banerjee, Jheelam; Singh, Anamika; Sircar, P. K.; Kashyap, V. K. (2006). "Molecular insights into the origins of the Shompen, a declining population of the Nicobar archipelago". Journal of Human Genetics 51 (3): 217–26. doi:10.1007/s10038-005-0349-2. PMID 16453062.
- Shi Yan; Chuan-Chao Wang; Hui Li; Shi-Lin Li; Li Jin; The Genographic Consortium (2011). "An updated tree of Y-chromosome Haplogroup O and revised phylogenetic positions of mutations P164 and PK4". European Journal of Human Genetics 19 (9): 1013–1015. doi:10.1038/ejhg.2011.64. PMID 21505448.
Further reading
- Hammer, Michael F.; Karafet, Tatiana M.; Park, Hwayong; Omoto, Keiichi; Harihara, Shinji; Stoneking, Mark; Horai, Satoshi (2005). "Dual origins of the Japanese: Common ground for hunter-gatherer and farmer Y chromosomes" (PDF). Journal of Human Genetics 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082. http://www.eva.mpg.de/genetics/pdf/Japan.pdf.
- Shi, Hong; Dong, Yong-li; Wen, Bo; Xiao, Chun-Jie; Underhill, Peter A.; Shen, Pei-Dong; Chakraborty, Ranajit; Jin, Li et al. (2005). "Y-Chromosome Evidence of Southern Origin of the East Asian–Specific Haplogroup O3-M122". The American Journal of Human Genetics 77 (3): 408–19. doi:10.1086/444436. PMID 16080116. PMC 1226206. http://linkinghub.elsevier.com/retrieve/pii/S0002-9297(07)63021-3.
- Thanseem, Ismail; Thangaraj, Kumarasamy; Chaubey, Gyaneshwer; Singh, Vijay; Bhaskar, Lakkakula VKS; Reddy, B Mohan; Reddy, Alla G; Singh, Lalji (2006). "Genetic affinities among the lower castes and tribal groups of India: Inference from Y chromosome and mitochondrial DNA". BMC Genetics 7 (1): 42. doi:10.1186/1471-2156-7-42. PMID 16893451. PMC 1569435. http://www.biomedcentral.com/1471-2156/7/42.
- ↑ Zhang, Xiaoming; Liao, Shiyu; Qi, Xuebin; Liu, Jiewei; Kampuansai, Jatupol; Zhang, Hui; Yang, Zhaohui; Serey, Bun et al. (20 October 2015). "Y-chromosome diversity suggests southern origin and Paleolithic backwave migration of Austro-Asiatic speakers from eastern Asia to the Indian subcontinent" (in en). Scientific Reports (Nature Publishing Group) 5 (1): 15486. doi:10.1038/srep15486. ISSN 2045-2322. https://www.nature.com/articles/srep15486.
- ↑ Zhang, Xiaoming; Liao, Shiyu; Qi, Xuebin; Liu, Jiewei; Kampuansai, Jatupol; Zhang, Hui; Yang, Zhaohui; Serey, Bun et al. (2015-10-20). "Y-chromosome diversity suggests southern origin and Paleolithic backwave migration of Austro-Asiatic speakers from eastern Asia to the Indian subcontinent" (in en). Scientific Reports (Nature Publishing Group) 5 (1): 15486. doi:10.1038/srep15486. ISSN 2045-2322. https://www.nature.com/articles/srep15486.
- ↑ Zhang, Xiaoming; Kampuansai, Jatupol; Qi, Xuebin; Yan, Shi; Yang, Zhaohui; Serey, Bun; Sovannary, Tuot; Bunnath, Long et al. (2014-06-27). "An Updated Phylogeny of the Human Y-Chromosome Lineage O2a-M95 with Novel SNPs" (in en). PLOS ONE (Public Library of Science) 9 (6): e101020. doi:10.1371/journal.pone.0101020. ISSN 1932-6203. PMID 24972021. PMC 4074153. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0101020.
