Haplogroup O-M176

Haplogroup O-M176 (aka O-SRY465) or O1b2 is a human Y-chromosome DNA haplogroup. It is best known for its part in the settlement of Korea and Japan. It is a descendant of Haplogroup O-P31, and it has been estimated to share a most recent common ancestor with its nearest outgroup, Haplogroup O-K18, approximately 28,000 [95% CI 25,800 <-> 30,300] years before present.[1]

Haplogroup O-M176
O1b2-M176'
Possible time of origin28,000 [95% CI 25,800 <-> 30,300] years before present[1]
Coalescence age25,900 [95% CI 23,400 <-> 28,400] years before present (YFull[1][2])
Possible place of originManchuria or a nearby part of northern East Asia[3][4]
AncestorO-P31
Defining mutationsM176/SRY465, P49, 022454
Highest frequencies'Koreans, Japanese, Ryukyuans, Manchus

Distribution

Haplogroup O-M176 is found mainly in the northernmost parts of East Asia, from the Uriankhai and Zakhchin peoples of western Mongolia (Katoh 2004) to the Japanese of Japan, though it also has been detected sporadically in the Buryats (Jin 2003). It's been detected with moderate frequencies in Udegeys (Jin 2010) of southern Siberia, rarely among populations of Southeast Asia including Indonesia (Hammer 2006 and Jin 2003), the Philippines (Jin 2003), Thailand (Jin 2003), and Vietnam (Hammer 2006 and Jin 2003), and Micronesians (Hammer 2006). This haplogroup is found with its highest frequency and diversity values among modern populations of Japan and Korea and is rare in most populations in China. Among Han Chinese, it has been detected in some samples of Han Chinese from Beijing (1/51, Jin 2003 and Kim 2011),[5] Xi'an (1/34, Kim 2011),[5] one Han Chinese in Henan,[6] Han Chinese in Taiwan (2/352 = 0.57%, including one of 34 Hakka people and one of 258 miscellaneous Han volunteers),[7] Han Chinese from East China sampled from the infertility clinic at the Affiliated Hospitals of Nanjing Medical University at Jiangsu (6/1147 = 0.52%, Lu 2009), Wuhan (1/160),[8] and South China outside of Jiangsu, Anhui, Zhejiang, and Shanghai (1/65).[9] Among ethnic minorities in China, haplogroup O-M176 has been detected with high frequency in samples of Koreans in China (Xue 2006 and Katoh 2004) and with generally much lower frequency among Manchus (Xue 2006, Katoh 2004, and Karafet 2001), Hezhe people,[10] Daurs,[10] Evenks,[11] Sibes (Xue 2006), Kham Tibetans,[12] and Hui.[13]

Mitsuru Sakitani suggests that haplogroup O1b2, which is common in today Koreans, Japanese and some Manchu, are one of the carriers of Yangtze civilization. As the Yangtze civilization declined several tribes crossed westward and northerly, to the Shandong peninsula, the Korean Peninsula and the Japanese archipelago.[14] Another study calls the haplogroup O1b1 as the major Austroasiatic paternal lineage and the haplogroup O1b2 (of Koreans and Japanese) as the "para-Austroasiatic" paternal lineage.[15]

Subclade distribution

Paragroup O-M176*

Y-DNA that belongs to O-M176(xK10, F3356) has been found in an individual from Hiroshima,[2] an individual from Fukushima,[2] an individual from Beijing,[2] and 1% (7/706) of a sample of males collected in Seoul and Daejeon.[16]

O-M176(x47z) has been found in approximately 3.5%[17] to 9.9%[18] of Japanese males. However, most of those individuals probably belong to subclades of O-K10(x47z).

O-K10

The majority of extant members of O-M176 belong to the subclade O-K10 (or O-F3356). O-K10 subsumes the prolific subclades O-47z, which occurs with especially high frequency in Japan, and O-L682, which occurs with especially high frequency in Korea, in addition to a relatively rare subclade, O-K3, which has been found among Han Chinese in Hunan,[2] Jiangxi,[2] and Henan.[19] O-L682 and O-K3 are linked by 18 SNPs that define the O-K4 clade, and thus their members are more closely related to one another by paternal lineage than any of them is related to any member of O-47z.

An example of Y-DNA that belongs to O-K10 but neither O-47z nor O-K4 has been found in an individual in Tokyo, Japan. This individual's Y-DNA is estimated to share a most recent common ancestor with O-47z and O-K4 roughly around the same time as the most recent common ancestor of those latter two clades, about 7,200 [95% CI 6,200 <-> 8,200] ybp.[1]

O-F3356(x47z, L682) has been found in 2% (14/706) of a sample of Koreans collected in Seoul and Daejeon, South Korea.[16] However, the status of these individuals' Y-DNA in regard to K4, K3, and phylogenetically equivalent SNPs has not been published.

O-47z

Haplogroup O-47z
O1b2a1-47z
Possible time of origin7,870 [95% CI 5,720–12,630] years ago (Hammer 2006)

7,100 [95% CI 6,100 <-> 8,300] ybp[1]
Possible place of originJapanese Archipelago(Hammer 2006) or Korean Peninsula(see Jin 2003)
AncestorO-M176
Defining mutations47z
Highest frequencies'Japanese, Ryukyuans, Koreans, Manchus

O-47z or O-CTS11986 is a subclade of O-K10. It is found with high frequency among the Japanese and Ryukyuan populations of Japan, and with lower frequency among Koreans.

Haplogroup O-47z has been detected in approximately 24% of males who speak a Japonic language, while it has not been found at all among Ainu males whose Y-DNA has been tested in two genetic studies (Tajima 2004, n=16; Hammer 2006, n=4). Based on the STR haplotype diversity within Haplogroup O-47z, it has been estimated in a study published in 2006 that this haplogroup has expanded from a single founder who has lived approximately 3,810 (95% CI 1,640 <–> 7,960) years before present in a model according to which continuous, pure exponential population growth is assumed.[11] In a paper published in 2016, the time to most recent common ancestor of a set of fifteen members of the O-47z clade, all from the JPT (Japanese in Tokyo, Japan) sample of the 1000 Genomes Project, was estimated to be 4,500 years using a relatively slow mutation rate (μ = 0.76 x 10−9 per bp per year as according to Qiaomei Fu et al. 2014) or 3,900 years using a relatively fast mutation rate (μ = 0.888 x 10−9 per bp per year as according to A. Helgason et al. 2015).[17] Haplogroup O-47z also has been found among samples of modern Koreans, though with low frequency in comparison to both the frequency of O-47z in samples of Japanese and the frequency of O-M176(x47z) in samples of Koreans.

O-K4

O-K4 is a subclade of O-K10. It includes at least two subclades, O-L682 and O-K3, which have been estimated to share a most recent common ancestor approximately 6,100 [95% CI 5,000 <-> 7,200] years before present.[2]

O-K3
Haplogroup O-F940
O1b2a2b-F940
Possible time of origin3,500 [2,000-13,000]
Possible place of originManchuria or Korean Peninsula
AncestorO-F2868
Defining mutationsCTS12145, F1912, F2206, F2703, F940, K3
Highest frequencies'Manchurian, Manchu Mongolian, Manchu Han
  • Manchus 0-26% (katoh et al 2005)
  • Manchu Mongolian 0-4% (Guo et al 2015)
  • Manchu Han 0-4% (Liu et al 2014)

The O-K3 (or O-F940) lineage is a subclade of O-K4 that has been observed to date in three individuals from Hunan,[2] one individual from Jiangxi,[2] and one individual from Henan.[19]

O-L682
Haplogroup O-L682
O1b2a2a-L682
Possible time of origin6,300 [95% CI 4,700 <-> 8,000] ybp[1]
Possible place of originKorean Peninsula or Manchuria
AncestorO-M176, O-F3356
Defining mutationsL682
Highest frequencies'Koreans, Hezhen, Udege, Japanese, Ryukyuans, Manchus
O1b2a3-CTS10687

The O-L682 subclade of O-K4 is believed to be related to Native Korean population. One study has found O-L682 Y-DNA in 19% (134/706) of Koreans sampled in Seoul and Daejeon.[16] O-L682 also has been found in Japanese in Tokyo, Okayama, Kōchi, and the US, Chinese in Shanxi, Shandong, and Beijing,[2] and Nanai people in China. Its descendants appear to have begun rapidly increasing in number at approximately the same time as those of its distant cousin O-47z, perhaps 4,000 years ago.[2]

O1b2*-R220
O1b2*-R144
O1b2a-CTS3505

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-M17526VII1U28Eu16H9IO*OOOOOOOOOO
O-M11926VII1U32Eu16H9HO1*O1aO1aO1aO1aO1aO1aO1aO1aO1aO1a
O-M10126VII1U32Eu16H9HO1aO1a1O1a1aO1a1aO1a1O1a1O1a1aO1a1aO1a1aO1a1aO1a1a
O-M5026VII1U32Eu16H10HO1bO1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2O1a2
O-P3126VII1U33Eu16H5IO2*O2O2O2O2O2O2O2O2O2O2
O-M9526VII1U34Eu16H11GO2a*O2aO2aO2aO2aO2aO2aO2aO2aO2a1O2a1
O-M8826VII1U34Eu16H12GO2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1O2a1aO2a1a
O-SRY46520VII1U35Eu16H5IO2b*O2bO2bO2bO2bO2bO2bO2bO2bO2bO2b
O-47z5VII1U26Eu16H5IO2b1O2b1aO2b1O2b1O2b1aO2b1aO2b1O2b1O2b1O2b1O2b1
O-M12226VII1U29Eu16H6LO3*O3O3O3O3O3O3O3O3O3O3
O-M12126VII1U29Eu16H6LO3aO3aO3a1O3a1O3a1O3a1O3a1O3a1O3a1O3a1aO3a1a
O-M16426VII1U29Eu16H6LO3bO3bO3a2O3a2O3a2O3a2O3a2O3a2O3a2O3a1bO3a1b
O-M15913VII1U31Eu16H6LO3cO3cO3a3aO3a3aO3a3O3a3O3a3aO3a3aO3a3aO3a3aO3a3a
O-M726VII1U29Eu16H7LO3d*O3cO3a3bO3a3bO3a4O3a4O3a3bO3a3bO3a3bO3a2bO3a2b
O-M11326VII1U29Eu16H7LO3d1O3c1O3a3b1O3a3b1-O3a4aO3a3b1O3a3b1O3a3b1O3a2b1O3a2b1
O-M13426VII1U30Eu16H8LO3e*O3dO3a3cO3a3cO3a5O3a5O3a3cO3a3cO3a3cO3a2c1O3a2c1
O-M11726VII1U30Eu16H8LO3e1*O3d1O3a3c1O3a3c1O3a5aO3a5aO3a3c1O3a3c1O3a3c1O3a2c1aO3a2c1a
O-M16226VII1U30Eu16H8LO3e1aO3d1aO3a3c1aO3a3c1aO3a5a1O3a5a1O3a3c1aO3a3c1aO3a3c1aO3a2c1a1O3a2c1a1

Original research publications

The following research teams per their publications were represented in the creation of the YCC Tree.

  • α Jobling and Tyler-Smith 2000 and Kaladjieva 2001
  • β Underhill 2000
  • γ Hammer 2001
  • δ Karafet 2001
  • ε Semino 2000
  • ζ Su 1999
  • η Capelli 2001

Phylogenetic trees

This phylogenetic tree of haplogroup O subclades is based on the YCC 2008 tree (Karafet 2008) and subsequent published research.

  • O1b2 (IMS-JST022454, L272.2, M176/Page63/SRY465, M302, P49, F1942/Page92)
    • O1b2a (F1942/Page92)
      • O1b2a1 (CTS9259)
        • O1b2a1a (F3356)
          • O1b2a1a1 (47z, CTS713, CTS11986)
          • O1b2a1a2 (F2868, F3110, K4)
            • O1b2a1a2a (L682)
            • O1b2a1a2b (F940, F1912, F3390)
          • O1b2a1a3 (CTS10687, F1813, F1800)
        • O1b2a1b (CTS562)
      • O1b2a2 (Page90)

Table of frequencies of O-M176

Population Frequency Sample Size SNPs Source
Korean (Gangwon)0.39763M176(x47z)=20
47z=5
Kim 2011
Korean
(National Biobank of Korea)
0.377300M176(x47z)=88
47z=25
Park 2013
South Korea0.37375M176/P49(x47z)=25
47z=3
Hammer 2006
Japanese (Shizuoka)0.3446147z=13
M176/P49(x47z)=8
Hammer 2006
Korean (Daejeon)0.338133M176(x47z)=30
47z=15
Park 2012
Japanese0.33526347z=66
M176/JST022454(x47z)=22
Nonaka 2007
Korean (Jeju)0.32287M176(x47z)=20
47z=8
Kim 2011
Japanese (Kyushu)0.3215347z=15
M176/P49(x47z)=2
Hammer 2006
Korean (Seoul)0.316573M176(x47z)=125
47z=56
Park 2012
Korean (Jeolla)0.31190M176(x47z)=21
47z=7
Kim 2011
Japanese (Aomori)0.3082647z=7
M176/P49(x47z)=1
Hammer 2006
Korean (Chungcheong)0.30672M176(x47z)=15
47z=7
Kim 2011
Japanese (Tokushima)0.3007047z=17
M176/P49(x47z)=4
Hammer 2006
Korean (Gyeongsang)0.29884M176(x47z)=15
47z=10
Kim 2011
Japanese0.29315747z=38
M176(x47z)=8
Kim 2011
Korean (Seoul/Gyeonggi)0.282110M176(x47z)=23
47z=8
Kim 2011
Korean (PRC)0.28025M176(x47z)=5
47z=2
Xue 2006
Korean (Korea)0.27943M176(x47z)=6
47z=6
Xue 2006
Japanese0.2774747z=11
M176(x47z)=2
Xue 2006
Manchurians0.2714847z=9
M176(x47z)=4
Jin 2009
Korean (Seoul & Daejeon)0.269216M176(x47z)=37
47z=21
Kim 2007
Japanese0.26210747z=21
M176(x47z)=7
Jin 2009
Okinawa0.2224547z=5
M176/P49(x47z)=5
Hammer 2006
Korean0.201154M176(x47z)=22
47z=9
Jin 2009
Hezhe0.12140M176(L682)=2HGDP 2009
Udeges0.10140M176(L682)=2Jin 2010
Hezhe0.08140M176(L682)=2Xue 2006
Han (Beijing)0.02051M176(x47z)=1Kim 2011
Manchu0.05735M176(x47z)=2Xue 2006
Uriankhai (Mongolia)0.05060M176=3Katoh 2005
Mongol (NE Mongolia)0.05020M176=1DiCristofaro 2013
Hezhe (PRC)0.04445M176(x47z)=2Xue 2006
Manchu0.03852M176/P49(x47z)=2Hammer 2006
Zakhchin (Mongolia)0.03360M176=2Katoh 2005
Manchurian0.03330M176(x47z)=1Kim 2011
Buryat0.02836M176(x47z)=1Kim 2011
Nanai0.02737M176(L682)=2Bogunov et al 2015
Daur0.02639M176(x47z)=1Xue 2006
Evenk (PRC)0.02441M176/P49(x47z)=1Hammer 2006
Xibe0.02441M176(x47z)=1Xue 2006
Buryat0.02050M176(x47z)=1Jin 2009
Mongols (Mongolia)0.006160M176=1DiCristofaro 2013
Hakka (Taiwan)0.01934M176=1Trejaut 2014
Han (Taiwan)0.004258M176=1Trejaut 2014
Zhuang0.00020M176/P49=0Hammer 2006
Oroqen0.00022M176/P49=0Hammer 2006
Hanoi, Vietnam0.00024M176=0Trejaut 2014
Kalimantan0.00025M176=0Trejaut 2014
Evenk (PRC)0.00026M176=0Xue 2006
Sumatra0.00026M176=0Trejaut 2014
Akha (Thailand)0.00027M176=0Trejaut 2014
Alor0.00028M176=0Karafet 2010
Han (Lanzhou)0.00030M176=0Xue 2006
Even0.00031M176/P49=0Hammer 2006
Oroqen0.00031M176=0Xue 2006
Uyghur (Ürümqi)0.00031M176=0Xue 2006
Han (Yili)0.00032M176=0Xue 2006
Malay0.00032M176/P49=0Hammer 2006
Australian aborigines0.00033M176/P49=0Hammer 2006
Qiang0.00033M176=0Xue 2006
Han (Chengdu)0.00034M176=0Xue 2006
Hani (PRC)0.00034M176=0Xue 2006
Li0.00034M176=0Xue 2006
She0.00034M176=0Xue 2006
Buyi0.00035M176=0Xue 2006
Han (Harbin)0.00035M176=0Xue 2006
Han (Meixian)0.00035M176=0Xue 2006
Hui (PRC)0.00035M176=0Xue 2006
Tibetan0.00035M176=0Xue 2006
Yao (Bama)0.00035M176=0Xue 2006
Yao (Liannan)0.00035M176=0Xue 2006
Batak Toba (Sumatra)0.00038M176=0Karafet 2010
Uyghur (Yili)0.00039M176=0Xue 2006
East Indonesia0.00040M176=0Trejaut 2014
Han (Guangdong)0.00040M176/P49=0Hammer 2006
Yi (Butuo, Sichuan)0.00043M176/P49=0Hammer 2006
Northern Han0.00044M176/P49=0Hammer 2006
Khalkh0.00045M176=0Kim 2011
Mongol (Inner Mongolia)0.00045M176=0Xue 2006
Papua New Guinea0.00046M176/P49=0Hammer 2006
Khalkh0.00048M176=0Jin 2009
Philippines0.00048M176/P49=0Hammer 2006
Taiwanese aborigines0.00048M176/P49=0Hammer 2006
Tujia0.00049M176/P49=0Hammer 2006
She0.00051M176/P49=0Hammer 2006
Melanesia0.00053M176/P49=0Hammer 2006
Mandar (Sulawesi)0.00054M176=0Karafet 2010
Han (Fujian)0.00055M176=0Trejaut 2014
Indonesia (East)0.00055M176/P49=0Hammer 2006
Miao0.00058M176/P49=0Hammer 2006
Han (Yunnan)0.00060M176=0Kim 2011
Minnan (Taiwan)0.00060M176=0Trejaut 2014
Nias0.00060M176=0Karafet 2010
Polynesia0.00060M176/P49=0Hammer 2006
Yao0.00060M176/P49=0Hammer 2006
Java0.00061M176=0Karafet 2010
Filipino0.00064M176=0Kim 2011
Mongol (Outer Mongolia)0.00065M176=0Xue 2006
Uyghur0.00067M176/P49=0Hammer 2006
Mentawai0.00074M176=0Karafet 2010
Thailand0.00075M176=0Trejaut 2014
Buryat0.00081M176/P49=0Hammer 2006
Han (Taiwan)0.00084M176/P49=0Hammer 2006
Borneo0.00086M176=0Karafet 2010
Sri Lanka0.00091M176/P49=0Hammer 2006
Lembata0.00092M176=0Karafet 2010
Evenk (Russia)0.00095M176/P49=0Hammer 2006
Altai0.00098M176/P49=0Hammer 2006
Tibet0.000105M176/P49=0Hammer 2006
Java0.000141M176=0Trejaut 2014
Philippines0.000146M176=0Trejaut 2014
Mongolia0.000149M176/P49=0Hammer 2006
Sumba0.000350M176=0Karafet 2010
Taiwan mountain tribes0.000355M176=0Trejaut 2014
Taiwan plains tribes0.000370M176=0Trejaut 2014
Flores0.000394M176=0Karafet 2010
India0.000405M176/P49=0Hammer 2006
Bali0.000641M176=0Karafet 2010

See also

Genetics

Y-DNA O subclades

  • O-47z
  • O-M101
  • O-M113
  • O-M117
  • O-M119
  • O-M121
  • O-M122
  • O-M134
  • O-M159
  • O-M162
  • O-M164
  • O-M175
  • O-M176
  • O-M50
  • O-M7
  • O-M88
  • O-M95
  • O-MSY2.2
  • O-P31

Y-DNA backbone tree

Phylogenetic tree of human Y-chromosome DNA haplogroups [χ 1][χ 2]
"Y-chromosomal Adam"
A00 A0-T [χ 3]
A0 A1 [χ 4]
A1a A1b
A1b1 BT
B CT
DE CF
D E C F
F1  F2  F3  GHIJK
G HIJK
IJK H
IJ K
I   J     LT [χ 5]       K2 [χ 6]
L     T    K2a [χ 7]        K2b [χ 8]     K2c     K2d K2e [χ 9]  
K-M2313 [χ 10]     K2b1 [χ 11] P [χ 12]
NO   S [χ 13]  M [χ 14]    P1     P2
N O Q R

References

Footnotes

  1. 256/800=32.0% O-M176 in a pool of all Japanese samples of (Xue 2006), (Katoh 2004), (Jin 2009), (Nonaka 2007), (Poznik 2016), and all non-Ainu and non-Okinawan Japanese samples of (Hammer 2006).
  2. 202/677=29.8% O-M176 in a pool of all ethnic South Korean samples of (Hammer 2006), (Xue 2006), (Katoh 2004), (Kim 2007), and (Park 2013)
  3. 30/132=22.7% O-M176 in a pool of all Okinawan data from (Hammer 2006) and (Nonaka 2007)
  4. 30/123=24.3% O-M176 in a pool of all ethnic North Korea samples of Template:Hary
  5. 45/232=19.4% O-M176 in a pool of all Manchu samples of (Karafet 2001), (Jin 2003), (Katoh 2004), and (Xue 2006)
  6. 8/98=8.16% O-M176 in a pool of all Nanai samples of (Xue 2006), Template:HGDP
  7. 2/20=10% O-M176 in a pool of All Udege samples of Template:Hary
  8. 150/628=23.9% O-47z in a pool of all non-Ainu and non-Okinawan Japanese samples of (Jin 2003), (Hammer 2006), (Xue 2006), and (Nonaka 2007)
  9. 22/132=16.7% O-47z in a pool of all Okinawan samples of Hammer 2006 and Nonaka 2007
  10. 41/519=7.9% O-47z in a pool of all ethnic Korean samples of (Jin 2003), (Hammer 2006), (Xue 2006), and (Kim 2007)
  11. 9/135=6.7% O-47z in a pool of all "Manchu" or "Manchurian" samples of (Hammer 2006), (Xue 2006), and (Jin 2009)
  12. 41/519=7.9% O-L682 in a pool of all ethnic Korean samples of (Yoo 2014), (Katoh 2004), and (Kim 2011)
  13. 22/132=16.7% O-47z in a pool of all Okinawan samples of Hammer 2006 and Nonaka 2007
  14. 150/628=23.9% O-47z in a pool of all non-Ainu and non-Okinawan Japanese samples of (Jin 2003), (Hammer 2006), (Xue 2006), and (Nonaka 2007)
  15. 9/135=6.7% O-47z in a pool of all "Manchu" or "Manchurian" samples of (Hammer 2006), (Xue 2006), and (Jin 2009)

Works cited

  1. YFull Haplogroup YTree v6.01 at 04 January 2018
  2. YFull Haplogroup YTree v5.04 at 16 May 2017
  3. Kim, Soon-Hee; Kim, Ki-Cheol; Shin, Dong-Jik; et al. "High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea". Investigative Genetics. 2011 (2): 10.
  4. Balaresque, Patricia; Poulet, Nicolas; Cussat-Blanc, Sylvain; et al. (2015). "Y-chromosome descent clusters and male differential reproductive success: young lineage expansions dominate Asian pastoral nomadic populations". European Journal of Human Genetics. 23 (10): 1413–1422. doi:10.1038/ejhg.2014.285. PMC 4430317. PMID 25585703.
  5. Soon-Hee Kim 2011, High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea
  6. Yan, Shi; Wang, Chuan-Chao; Zheng, Hong-Xiang; Wang, Wei; Qin, Zhen-Dong; Wei, Lan-Hai; Wang, Yi; Pan, Xue-Dong; Fu, Wen-Qing; He, Yun-Gang; Xiong, Li-Jun; Jin, Wen-Fei; Li, Shi-Lin; An, Yu; Li, Hui; Jin, Li (2014). "Y Chromosomes of 40% Chinese Descend from Three Neolithic Super-Grandfathers". PLOS ONE. 9 (8): e105691. doi:10.1371/journal.pone.0105691. PMC 4149484. PMID 25170956.
  7. Trejaut, Jean A; Poloni, Estella S; Yen, Ju-Chen; et al. (2014). "Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia". BMC Genetics. 15: 77. doi:10.1186/1471-2156-15-77. PMC 4083334. PMID 24965575.
  8. Huang Dai-Xin, Yang Qing-En, Yin Hui et al., "Genetic Polymorphism of 23 Y Chromosome Biallelic Markers in Wuhan Han Population," HEREDITAS (Beijing) 28 (7) 791~798, 2006
  9. Yan, Shi; Chuan-Chao, Wang; Hui, Li; Li, Shi-Lin; Jin, Li; Schurr, Theodore G; Santos, Fabricio R; Quintana-Murci, Lluis; Bertranpetit, Jaume; Comas, David; Tyler-Smith, Chris; Zalloua, Pierre A; Balanovska, Elena; Balanovsky, Oleg; John Mitchell, R; Jin, Li; Soodyall, Himla; Pitchappan, Ramasamy; Cooper, Alan; Matisoo-Smith, Lisa; Royyuru, Ajay K; Platt, Daniel E; Parida, Laxmi; Blue-Smith, Jason; Soria Hernanz, David F; Spencer Wells, R (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. PMC 3179364. PMID 21505448.
  10. Yali Xue, Tatiana Zerjal, Weidong Bao, Suling Zhu, Qunfang Shu, Jiujin Xu, Ruofu Du, Songbin Fu, Pu Li, Matthew E. Hurles, Huanming Yang, and Chris Tyler-Smith, "Male Demography in East Asia: A North–South Contrast in Human Population Expansion Times." Genetics 172: 2431–2439 (April 2006).
  11. Hammer, Michael F.; Karafet, Tatiana M.; Park, Hwayong; Omoto, Keiichi; Harihara, Shinji; Stoneking, Mark; Horai, Satoshi (2006). "Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes". Journal of Human Genetics. 51: 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082.
  12. Wang, C-C; Wang, L-X; Shrestha, R; Zhang, M; Huang, X-Y; et al. (2014). "Genetic Structure of Qiangic Populations Residing in the Western Sichuan Corridor". PLoS ONE. 9 (8): e103772. doi:10.1371/journal.pone.0103772. PMC 4121179. PMID 25090432.
  13. Lu Yan (2011), "Genetic Mixture of Populations in Western China." Shanghai: Fudan University, 2011: 1-84. (Doctoral dissertation in Chinese: 陆艳, “中国西部人群的遗传混合”, 上海:复旦大学,2011: 1-84.)
  14. 崎谷満『DNA・考古・言語の学際研究が示す新・日本列島史』(勉誠出版 2009年
  15. Robbeets, Martine; Savelyev, Alexander (2017-12-21). Language Dispersal Beyond Farming. John Benjamins Publishing Company. ISBN 9789027264640.
  16. Yeun Kwon, So; Young Lee, Hwan; Young Lee, Eun; Ick Yang, Woo; Shin, Kyoung-Jin (2015). "Confirmation of Y haplogroup tree topologies with newly suggested Y-SNPs for the C2, O2b and O3a subhaplogroups". Forensic Science International: Genetics. 19: 42–46. doi:10.1016/j.fsigen.2015.06.003. PMID 26103100.
  17. Poznik, G. David; Xue, Yali; Mendez, Fernando L.; et al. (June 2016). "", "Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences". Nature Genetics. 48 (6): 593–599. doi:10.1038/ng.3559. PMC 4884158. PMID 27111036.
  18. Youichi Sato, Toshikatsu Shinka, Ashraf A. Ewis, Aiko Yamauchi, Teruaki Iwamoto, and Yutaka Nakahori, "Overview of genetic variation in the Y chromosome of modern Japanese males." Anthropological Science Vol. 122(3), 131–136, 2014.
  19. Yan, S; Wang, C-C; Zheng, H-X; Wang, W; Qin, Z-D; et al. (2014). "Y Chromosomes of 40% Chinese Descend from Three Neolithic Super-Grandfathers". PLoS ONE. 9 (8): e105691. doi:10.1371/journal.pone.0105691. PMC 4149484. PMID 25170956.

Further reading

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.