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From the standpoint of mtDNA testing: If you test Norman's mtDNA, then there is no need to test the others. Mutations in mtDNA are rare. In a given line, hundreds of years (or over a thousand years) can go by without a mutation. Even if there is a mutational difference in close relatives, it would not...Last edited by Everwaiting; 2 July 2016, 12:17 AM.
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Hi Rich,
If I understand the relationships correctly: Mary Elizabeth Irvine is your paternal grandmother; Norman is your father's brother; and Joan is the daughter of your father's sister. If so, then mtDNA testing is only needed from ONE of these relatives. This is because all three...
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Yes, you are correct. Testing your uncle will give you mtDNA information for his mother, his maternal grandmother, and so on. The mtFull-Sequence will enable you to determine the exact subclade status of that mtDNA line, now and in the future as new branches are found.
Some of the value...
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Benefit of mtFull-Sequence vs. Geno 2.0, etc., for mtDNA Information
I wholeheartedly agree with the comments above. Adding some additional details to the discussion: The mtFull-Sequence test fills in 81% of the mtDNA data that is not targeted with the Geno 2.0+ test. There is no way...
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Geno 2.0 recently updated its haplogroup labels to correspond with the latest version of the official mtDNA tree (dated 2014), known as the PhyloTree: Build 16. On the other hand, FTDNA last updated its mtDNA haplogroup labels in 2012, and they correspond with Build 14 of the PhyloTree. So new haplogroups/subclades...
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mtFull-Sequence Test: Record-Breaking Turnaround Time!
For the past several months, FTDNA has been turning out mtFull-Sequence results more and more quickly. But today, I am in disbelief. My project just received three sets of results that were ordered TWO weeks ago. That's right... a 2-week turn-around time for mt-results ordered during the recent sale....
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Post Moved to Different Category
Moving Post to Correct Topic CategoryLast edited by Everwaiting; 15 September 2015, 10:58 PM. Reason: Moving Post to Correct Topic Category
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I received that email (Admin. of I Haplogroup mtDNA Project)...
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Yes, as you know (clarifying for any who may not know), if you uploaded full-sequence results to James Lick's program, your data is 100% complete, so there would be no gaps at all. The "gaps" (untested markers) could only happen with 23andMe or Genographic Project testing, which, apparently,...
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P.S. I see that T2b has MANY subclades... up to T2b33. Many of these might also be divided into additional branches. It is likely that you belong to a subclade of T2b. James Lick's program seems to support this by saying there are "imperfect matches," which generally means your data shows...
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An "imperfect match" would mean that you are shown to have some (but not all) of the mutations defining a particular subclade. Usually, this is due to gaps in your 23andMe data at those mtDNA positions.
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With full-sequence testing, there are some fool-proof and very reliable ways to keep track of your most up-to-date subclade:
(1) Compare your results to the PhyloTree to see if you carry defining mutations below your current subclade designation.
(2) Use James Lick's tool, which is traditionally...
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Due to the continuing growth of the mtDNA tree, each time the PhyloTree is updated, a large batch of new subclade discoveries are added. Therefore, many people will belong to more refined subclades in the future that have not yet been identified.
Anyone with full-sequence testing is...
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