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18th dynast were haplogroup R1b/K?
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[QUOTE]Originally posted by the lioness,: [QB] [QUOTE]Originally posted by Djehuti: [qb] Again, is there a definitive study showing Tut's SNPs to be R1b in his Y chromosome and K in his mitochondria? I find that hard to believe considering his STRs along with that of his Amarna family members. From the JAMA report: As many have pointed out their STRs match those of Sub-Saharans not Eurasians so how does explain this discrepancy? [/qb][/QUOTE]what about page 1 of this thread and URL Link in second post? That is 2020 based on the 2010 Jama _________________________ Also in more detail in this other article: Also one exception to the R1b, Yuya's G2 https://www.researchgate.net/publication/353306320_Maternal_and_paternal_lineages_in_King_Tutankhamun%27s_family [b]Maternal and paternal lineages in King Tutankhamun’s family. February 2020[/b] In book: Guardian of Ancient Egypt: Essays in Honor of Zahi HawassPublisher: Czech Institute of Egyptology Project: Ancient Egyptian Genetics Project Authors: Yehia Z Gad,[ Somaia Ismail, Dina Fathalla, Rabab Khairat, Suzan Fares, Ahmed Zakaria Gad, Rama Saad, Amal Moustafa, Eslam ElShahat, Naglaa H. Abu Mandil, Mohamed Fateen, Hisham Elleithy, Sally Wasef, Albert R Zink, Zahi Hawass, Carsten M Pusch [IMG]https://images2.imgbox.com/40/9a/tc7x6cZi_o.png[/IMG] [QUOTE] The AmpFlSTR Y filer PCR amplification Kit (Applied Biosystems, Foster City, California) was used to analyze the Y-chromosome specific haplotype profles. The kit included sixteen human Y-chromosome DNA markers with sizes ranging between 99 bp and 324 bp, and a mean amplifcation size of 200 bp. All markers were tetranucleotide repetitive microsatellites with the exception of DYS392, DYS438 and DYS448, which displayed, respectively, trinucleotide, pentanucleotide and hexanucleotide repeat motifs. DNA templates were amplified according to the manufacturer’s protocol with some modications that involved decreasing the concentration of primers by 40% and increasing the AmpliTaq DNA polymerase concentration by 50%. Detection of the amplified PCR products was carried out using the ABI Genetic Analyzer 3130, Data collection Software v3.0 and GeneMapper ID v3.2 (Applied Biosystems).The majority rule was employed for STR allele designation, where a predominant peak was generated at least 10 times [i.e. each exceeding the threshold of 50 relative fluorescence units] per mummy, using various bone samples from different body areas and monitored for slippage (Hawass et al. 2010, 638–647). A final consensus profile of each investigated mummy was constructed using the reproducible data of the generated partial profiles (Cowen et al. 2011, 400–406) [/QUOTE] [/QB][/QUOTE]
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