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Thread: Geno 2.0 Results

  1. #31
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    Quote Originally Posted by noman View Post
    I have no hope on Living DNA. Their wait time is never-ending.
    I can't get my raw data directly from helix because that would cost me: (Exome+ Data) $499.00

    I copied the data from Geno 2.0 raw data and pasted them in Morley DNA and that's what I got. I thought to transfer geno to FTDNA, but FTDNA doesn't accept Helix transferred data files.

    wat.

    That's a lot of R1b SNPs xD

    https://www.yfull.com/tree/R-Z6

    I couldn't find L179 or L180 on YFull, so Z6 would be the most downstream mutation present on YFull. Z6 appears to be exclusive to NW Europe, with the TMRCA being about 2200 ybp.

    If LivingDNA is off the table, I would consider testing with YSEQ's R2-M479 panel ($93 inc. shipping). You could also test for individual SNPs.

    I would test for M479 first. If negative I would test for M269.
    Y-DNA (ISOGG 2019): R2a2b1b2a1a1-Y1383*

    YFull Line (From R-M207):

    M207+ ---> M479+ ---> M124+ ---> P267+ ---> Y12100+ ---> Y8763+ ---> Y8766+ ---> V3714+ ---> SK2142+ ---> Y1377+ ---> Y1379+ ---> Z29271+ ---> Y1383+ -X-> Y154917-

    Important Y-DNA negatives (within R2a-M124): L295-, Y5080-, L1069-, F1092-, L288-, L263-

    Extra mtDNA rCRS mutations: 207A, (315.1C), (523-), (524-), 2404C, 6150A, 8898T, 9755A, 15433T

    FTDNA Kit: IN41220

    GEDmatch Kit (MyHeritage): KC4074281

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  3. #32
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    U7a

    Pakistan United States of America Azad Kashmir Jammu and Kashmir
    Quote Originally Posted by aaronbee2010 View Post
    wat.

    That's a lot of R1b SNPs xD

    https://www.yfull.com/tree/R-Z6

    I couldn't find L179 or L180 on YFull, so Z6 would be the most downstream mutation present on YFull. Z6 appears to be exclusive to NW Europe, with the TMRCA being about 2200 ybp.

    If LivingDNA is off the table, I would consider testing with YSEQ's R2-M479 panel ($93 inc. shipping). You could also test for individual SNPs.

    I would test for M479 first. If negative I would test for M269.
    I am routing for YSEQ. Wish me luck!
    Kashmir

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  5. #33
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    Quote Originally Posted by noman View Post
    I am routing for YSEQ. Wish me luck!
    Won't be disappointed. They're a bit slow but worth it.
    Deg Teg Fateh - Victory to Charity and Arms

    Punjab, Punjabi, Fateh.

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  7. #34
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    Quote Originally Posted by MonkeyDLuffy View Post
    Won't be disappointed. They're a bit slow but worth it.
    I second this. I've only ordered individual SNPs but they've never let me down.
    Y-DNA (ISOGG 2019): R2a2b1b2a1a1-Y1383*

    YFull Line (From R-M207):

    M207+ ---> M479+ ---> M124+ ---> P267+ ---> Y12100+ ---> Y8763+ ---> Y8766+ ---> V3714+ ---> SK2142+ ---> Y1377+ ---> Y1379+ ---> Z29271+ ---> Y1383+ -X-> Y154917-

    Important Y-DNA negatives (within R2a-M124): L295-, Y5080-, L1069-, F1092-, L288-, L263-

    Extra mtDNA rCRS mutations: 207A, (315.1C), (523-), (524-), 2404C, 6150A, 8898T, 9755A, 15433T

    FTDNA Kit: IN41220

    GEDmatch Kit (MyHeritage): KC4074281

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     noman (01-09-2019)

  9. #35
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    U7a

    Pakistan United States of America Azad Kashmir Jammu and Kashmir
    Meanwhile, I would like to say THANK YOU to "ArmandoR1b", whom I sent my all three DNA data files (23&me, Ancestry DNA, and Geno). He went through my files, and figured out that my Y DNA is R2a2. Thank you ArmandoR1b once again!
    Thank you "laltota" for your recommendation.
    Last edited by noman; 01-13-2019 at 10:26 PM.
    Kashmir

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  11. #36
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    Quote Originally Posted by noman View Post
    Meanwhile, I would like to say THANK YOU to "ArmandoR1b", whom I sent my all three DNA data files (23&me, Ancestry DNA, and Geno". He went through my files, and figured out that my Y DNA is R2a2. Thank you ArmandoR1b once again!
    Thank you "laltota" for your recommendation.
    See, I told you that you belonged to the #R2Squad!

    Given that you know this now, I would strongly recommend the R2-M479 Superclade Panel from YSEQ, considering that LivingDNA is probably a lost cause at this point xD
    Y-DNA (ISOGG 2019): R2a2b1b2a1a1-Y1383*

    YFull Line (From R-M207):

    M207+ ---> M479+ ---> M124+ ---> P267+ ---> Y12100+ ---> Y8763+ ---> Y8766+ ---> V3714+ ---> SK2142+ ---> Y1377+ ---> Y1379+ ---> Z29271+ ---> Y1383+ -X-> Y154917-

    Important Y-DNA negatives (within R2a-M124): L295-, Y5080-, L1069-, F1092-, L288-, L263-

    Extra mtDNA rCRS mutations: 207A, (315.1C), (523-), (524-), 2404C, 6150A, 8898T, 9755A, 15433T

    FTDNA Kit: IN41220

    GEDmatch Kit (MyHeritage): KC4074281

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  13. #37
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    Quote Originally Posted by aaronbee2010 View Post
    See, I told you that you belonged to the #R2Squad!

    Given that you know this now, I would strongly recommend the R2-M479 Superclade Panel from YSEQ, considering that LivingDNA is probably a lost cause at this point xD
    Yea, R2 forever!

    I am ordering YSEQ now. Any recommendations for mt?
    Kashmir

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  15. #38
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    Quote Originally Posted by noman View Post
    Yea, R2 forever!

    I am ordering YSEQ now. Any recommendations for mt?
    Plug your 23andMe file into James Licks mtDNA predictor and see what your most detailed result is first. You might not want to look at other tests afterwards. On another note:

    L o n g
    L i v e
    R 2
    Y-DNA (ISOGG 2019): R2a2b1b2a1a1-Y1383*

    YFull Line (From R-M207):

    M207+ ---> M479+ ---> M124+ ---> P267+ ---> Y12100+ ---> Y8763+ ---> Y8766+ ---> V3714+ ---> SK2142+ ---> Y1377+ ---> Y1379+ ---> Z29271+ ---> Y1383+ -X-> Y154917-

    Important Y-DNA negatives (within R2a-M124): L295-, Y5080-, L1069-, F1092-, L288-, L263-

    Extra mtDNA rCRS mutations: 207A, (315.1C), (523-), (524-), 2404C, 6150A, 8898T, 9755A, 15433T

    FTDNA Kit: IN41220

    GEDmatch Kit (MyHeritage): KC4074281

  16. #39
    Registered Users
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    Sex
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    Chauhan
    Y-DNA
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    U7a

    Pakistan United States of America Azad Kashmir Jammu and Kashmir
    Quote Originally Posted by aaronbee2010 View Post
    Plug your 23andMe file into James Licks mtDNA predictor and see what your most detailed result is first. You might not want to look at other tests afterwards. On another note:

    L o n g
    L i v e
    R 2
    mthap version 0.19b (2015-05-11); haplogroup data version PhyloTree Build 17 (2016-02-18) +mods
    raw data source 23&me.txt (14MB )

    Found 5062 markers at 3267 positions covering 19.7% of mtDNA.

    Markers found (shown as differences to rCRS):

    HVR2: 73G 152C 263G
    CR: 750G 980C 1438G 1811G 2706G 5360T 7028T 8277I 8684T 8860G 11467G 13500C 14569A 14766T
    HVR1: (16519C)

    IMPORTANT NOTE: The above marker list is almost certainly incomplete due to limitations of genotyping technology and is not comparable to mtDNA sequencing results. It should not be used with services or tools that expect sequencing results, such as mitosearch.

    Best mtDNA Haplogroup Matches:
    1) U7
    Defining Markers for haplogroup U7:
    HVR2: 73G 152C 263G
    CR: 750G 980C 1438G 1811G 2706G 3741T 4769G 5360T 7028T 8137T 8684T 8860G 10142T 11467G 11719A 12308G 12372A 13500C 14569A 14766T 15326G
    HVR1: (16309G) 16318T

    Marker path from rCRS to haplogroup U7 (plus extra markers):
    H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 14766T ⇨ R0 ⇨ 73G 11719A ⇨ R ⇨ 11467G 12308G 12372A ⇨ U ⇨ 1811G ⇨ U2'3'4'7'8'9 ⇨ 152C 980C 3741T 5360T8137T 8684T 10142T 13500C 14569A (16309G) 16318T ⇨ U7 ⇨ 8277I (16519C)

    Imperfect Match. Your results contained differences with this haplogroup:
    Matches(16): 73G 152C 263G 750G 980C 1438G 1811G 2706G 5360T 7028T 8684T 8860G 11467G 13500C 14569A 14766T
    Mismatches(1): 4769A
    Extras(1): 8277I (16519C)
    No-Calls(6): 3741T 10142T 11719A 12308G 12372A 16318T
    Untested(2): 8137 15326 16309


    2) U7a
    Defining Markers for haplogroup U7a:
    HVR2: 73G 151T 152C 263G
    CR: 750G 980C 1438G 1811G 2706G 3741T 4769G 5360T 7028T 8137T 8684T 8860G 10142T 11467G 11719A 12308G 12372A 13500C 14569A 14766T 15326G
    HVR1: (16309G) 16318T

    Marker path from rCRS to haplogroup U7a (plus extra markers):
    H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 14766T ⇨ R0 ⇨ 73G 11719A ⇨ R ⇨ 11467G 12308G 12372A ⇨ U ⇨ 1811G ⇨ U2'3'4'7'8'9 ⇨ 152C 980C 3741T 5360T8137T 8684T 10142T 13500C 14569A (16309G) 16318T ⇨ U7 ⇨ 151T ⇨ U7a ⇨ 8277I (16519C)

    Imperfect Match. Your results contained differences with this haplogroup:
    Matches(16): 73G 152C 263G 750G 980C 1438G 1811G 2706G 5360T 7028T 8684T 8860G 11467G 13500C 14569A 14766T
    Mismatches(1): 4769A
    Extras(1): 8277I (16519C)
    No-Calls(7): 151T 3741T 10142T 11719A 12308G 12372A 16318T
    Untested(2): 8137 15326 16309


    3) U7a2
    Defining Markers for haplogroup U7a2:
    HVR2: 73G 151T 152C 263G
    CR: 750G 980C 1438G 1811G 2706G 3741T 4502C 4769G 5360T 7028T 8137T 8684T 8860G 10142T 11467G 11719A 12308G 12372A 13500C 14569A 14766T 15326G
    HVR1: (16309G) 16318T

    Marker path from rCRS to haplogroup U7a2 (plus extra markers):
    H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 14766T ⇨ R0 ⇨ 73G 11719A ⇨ R ⇨ 11467G 12308G 12372A ⇨ U ⇨ 1811G ⇨ U2'3'4'7'8'9 ⇨ 152C 980C 3741T 5360T8137T 8684T 10142T 13500C 14569A (16309G) 16318T ⇨ U7 ⇨ 151T ⇨ U7a ⇨ 4502C ⇨ U7a2 ⇨ 8277I (16519C)

    Imperfect Match. Your results contained differences with this haplogroup:
    Matches(16): 73G 152C 263G 750G 980C 1438G 1811G 2706G 5360T 7028T 8684T 8860G 11467G 13500C 14569A 14766T
    Mismatches(1): 4769A
    Extras(1): 8277I (16519C)
    No-Calls(7): 151T 3741T 10142T 11719A 12308G 12372A 16318T
    Untested(3): 4502 8137 15326 16309


    Is that a good option?

    https://www.yseq.net/product_info.ph...d5171b5cbd29fd
    Last edited by noman; 01-14-2019 at 02:22 AM.
    Kashmir

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  18. #40
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    Posts
    271
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    Location
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    Ethnicity
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    Nationality
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    U7a3a

    England United Kingdom India India Punjab
    Quote Originally Posted by noman View Post
    mthap version 0.19b (2015-05-11); haplogroup data version PhyloTree Build 17 (2016-02-18) +mods
    raw data source 23&me.txt (14MB )

    Found 5062 markers at 3267 positions covering 19.7% of mtDNA.

    Markers found (shown as differences to rCRS):

    HVR2: 73G 152C 263G
    CR: 750G 980C 1438G 1811G 2706G 5360T 7028T 8277I 8684T 8860G 11467G 13500C 14569A 14766T
    HVR1: (16519C)

    IMPORTANT NOTE: The above marker list is almost certainly incomplete due to limitations of genotyping technology and is not comparable to mtDNA sequencing results. It should not be used with services or tools that expect sequencing results, such as mitosearch.

    Best mtDNA Haplogroup Matches:
    1) U7
    Defining Markers for haplogroup U7:
    HVR2: 73G 152C 263G
    CR: 750G 980C 1438G 1811G 2706G 3741T 4769G 5360T 7028T 8137T 8684T 8860G 10142T 11467G 11719A 12308G 12372A 13500C 14569A 14766T 15326G
    HVR1: (16309G) 16318T

    Marker path from rCRS to haplogroup U7 (plus extra markers):
    H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 14766T ⇨ R0 ⇨ 73G 11719A ⇨ R ⇨ 11467G 12308G 12372A ⇨ U ⇨ 1811G ⇨ U2'3'4'7'8'9 ⇨ 152C 980C 3741T 5360T8137T 8684T 10142T 13500C 14569A (16309G) 16318T ⇨ U7 ⇨ 8277I (16519C)

    Imperfect Match. Your results contained differences with this haplogroup:
    Matches(16): 73G 152C 263G 750G 980C 1438G 1811G 2706G 5360T 7028T 8684T 8860G 11467G 13500C 14569A 14766T
    Mismatches(1): 4769A
    Extras(1): 8277I (16519C)
    No-Calls(6): 3741T 10142T 11719A 12308G 12372A 16318T
    Untested(2): 8137 15326 16309


    2) U7a
    Defining Markers for haplogroup U7a:
    HVR2: 73G 151T 152C 263G
    CR: 750G 980C 1438G 1811G 2706G 3741T 4769G 5360T 7028T 8137T 8684T 8860G 10142T 11467G 11719A 12308G 12372A 13500C 14569A 14766T 15326G
    HVR1: (16309G) 16318T

    Marker path from rCRS to haplogroup U7a (plus extra markers):
    H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 14766T ⇨ R0 ⇨ 73G 11719A ⇨ R ⇨ 11467G 12308G 12372A ⇨ U ⇨ 1811G ⇨ U2'3'4'7'8'9 ⇨ 152C 980C 3741T 5360T8137T 8684T 10142T 13500C 14569A (16309G) 16318T ⇨ U7 ⇨ 151T ⇨ U7a ⇨ 8277I (16519C)

    Imperfect Match. Your results contained differences with this haplogroup:
    Matches(16): 73G 152C 263G 750G 980C 1438G 1811G 2706G 5360T 7028T 8684T 8860G 11467G 13500C 14569A 14766T
    Mismatches(1): 4769A
    Extras(1): 8277I (16519C)
    No-Calls(7): 151T 3741T 10142T 11719A 12308G 12372A 16318T
    Untested(2): 8137 15326 16309


    3) U7a2
    Defining Markers for haplogroup U7a2:
    HVR2: 73G 151T 152C 263G
    CR: 750G 980C 1438G 1811G 2706G 3741T 4502C 4769G 5360T 7028T 8137T 8684T 8860G 10142T 11467G 11719A 12308G 12372A 13500C 14569A 14766T 15326G
    HVR1: (16309G) 16318T

    Marker path from rCRS to haplogroup U7a2 (plus extra markers):
    H2a2a1(rCRS) ⇨ 263G ⇨ H2a2a ⇨ 8860G 15326G ⇨ H2a2 ⇨ 750G ⇨ H2a ⇨ 4769G ⇨ H2 ⇨ 1438G ⇨ H ⇨ 2706G 7028T ⇨ HV ⇨ 14766T ⇨ R0 ⇨ 73G 11719A ⇨ R ⇨ 11467G 12308G 12372A ⇨ U ⇨ 1811G ⇨ U2'3'4'7'8'9 ⇨ 152C 980C 3741T 5360T8137T 8684T 10142T 13500C 14569A (16309G) 16318T ⇨ U7 ⇨ 151T ⇨ U7a ⇨ 4502C ⇨ U7a2 ⇨ 8277I (16519C)

    Imperfect Match. Your results contained differences with this haplogroup:
    Matches(16): 73G 152C 263G 750G 980C 1438G 1811G 2706G 5360T 7028T 8684T 8860G 11467G 13500C 14569A 14766T
    Mismatches(1): 4769A
    Extras(1): 8277I (16519C)
    No-Calls(7): 151T 3741T 10142T 11719A 12308G 12372A 16318T
    Untested(3): 4502 8137 15326 16309


    Is that a good option?

    https://www.yseq.net/product_info.ph...d5171b5cbd29fd
    RIP. You haven't even been confirmed for anything beyond U7. I got a mtDNA sequence from FTDNA when it was on offer. It's expensive but I don't regret purchasing it at all. Your mtDNA result will be as detailed as the PhyloTree will allow, which unfortunately is not very detailed for U7. For a full sequence, $165 is actually pretty good lol

    What you could do is compare your mtDNA results to the samples from the Sahakyan et al study (Supplementary Dataset 2) and using their nomenclature, you can get a mtDNA subclade far more detailed than PhyloTree.

    I would look at DNA files from other companies first, however if that doesn't go very well, then a full sequence is a very good test.
    Y-DNA (ISOGG 2019): R2a2b1b2a1a1-Y1383*

    YFull Line (From R-M207):

    M207+ ---> M479+ ---> M124+ ---> P267+ ---> Y12100+ ---> Y8763+ ---> Y8766+ ---> V3714+ ---> SK2142+ ---> Y1377+ ---> Y1379+ ---> Z29271+ ---> Y1383+ -X-> Y154917-

    Important Y-DNA negatives (within R2a-M124): L295-, Y5080-, L1069-, F1092-, L288-, L263-

    Extra mtDNA rCRS mutations: 207A, (315.1C), (523-), (524-), 2404C, 6150A, 8898T, 9755A, 15433T

    FTDNA Kit: IN41220

    GEDmatch Kit (MyHeritage): KC4074281

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