Why Y DNA testing?

Why DNA testing at a full platform genetic genealogy company?

Why Y STRs and how are they used?

Why Y SNPs and how are they used?

Why Big Y Next Generation Sequencing for discovering SNPs?

Should I upgrade Y STRs, even if I have limited or no matches?

What are SNP Packs and which should I consider?

What are terminal SNPs? novel SNPs private and public SNPs?

What myFTDNA Profile Settings are important?

The Y chromosome can only be passed from father to son and as such is passed almost completely unchanged. Changes or mutations occur every couple of generations but those mutations are also passed on giving each male lineage a unique signature that grows in uniqueness over the generations. The mutations can be thought of as a path of bread crumbs or footprints in the snow that never wash away. As we follow the path back through the woods we can find common ancestors with other people and potentially origins information.

Comparisons between potentially related people allows us to build a descendants tree back to a common ancestor. This can be used as a proof for genealogical records but can go way back into ancient times to understand where our people came from and how as we compare with historical and archaeological records. Your Y DNA has tremendous potential to track lineages from the head to the toe, from the ancient to the present.

The comparison method for tree building is simple, just compare validated mutations across potential relatives. If you have two brothers that have the same mutation unique to them then you can legitimately assume their most recent common ancestor, their father, had it. If you check a male cousin and he has the same mutation you can back up a step and know the grandfather had it. However, you need apples to apples comparisons of test results. It is of little value to do tests that few others are doing. Think of this as a team sport. You have to get others potentially related to take the same tests as you do or find them in the matching database. This is why the size of the matching database and recruiting efforts are so important.
https://www.familytreedna.com/why-ftdna.aspx

Y DNA tracking is both very granular, sensitive to the generations, and consistent, due to the father-son inheritance staying intact. However, it only tracks a paternal lineage, your father's father's father, etc. Still, this can be applied across your family tree. Every mother has a father. The key is to find male relatives, male cousins and uncles, and get them Y DNA tested while you can.

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FTDNA provides much more than bare bones DNA tests. They have a true laboratory and our not just a test remarketeer. They have no annual subscription charges, but provide a comprehensive platform for genetic genealogy including:

1. A robust project management web based platform for sharing and categorizing information that is critical to the newbies, future generations and non-technicians.

2. The largest accessible and compliant matching database for Y genetic genealogy. This is a database of real people who’ve shown some inclination for spending their own money on DNA testing.

3. Integrated and backward-compatible data management, which is the foundation of a large matching database. Old Deep Clade, Advanced Test SNPs, SNP Packs and Big Y results are all used for haplotree and haplogroup assignment and project display.

4. Convenience because of multiple test types (Big Y, STR panels, SNP Packs, mtDNA, Family Finder, etc.) available based on DNA samples that are safely stored.

4. Family tree and GEDCOM support integrated to DNA matching results.

5. Reasonable pricing which helps attract the most genetic genealogy testers.

6. Faster test processing time for SNP Pack and Big Y tests because they own their lab and test in-house.

7. They are an early feeder of your SNPs into a broader set of offerings including products from National Geographic Society organization sponsored tests that are used all over the world.

8. Excellent record and prospects as a proven on-going, self-funding concern.

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STRs are very useful in a multi-pronged approach, but should not be used out of context with SNPs. STRs support the formation of useful matching database because:

1) They have long legacy of usage and standardization, even beyond genealogy into forensic sciences.
2) They are consistently measured in standard STR based panels.
3) For the legacy STRs (111), everyone gets measured and issues like no calls are rare.

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Big Y is probably the most important Y DNA test that you can take because it goes beyond testing for public and known SNPs. Big Y discovers your own line of SNPs rather than just the known SNPs. Here's an analogy to help explain Big Y using the Lewis and Clark Expedition with an aviation twist.

Lewis and Clark's primary objectives included to explore and map the newly acquired territory, find a practical route across the western half of continent. They left St. Louis in 1804 and arrived at the Pacific Ocean late 1805. In this analogy, we think of the Pacific Coast as our genetic genealogy homeland, a place or status where our genealogically known family connects to the Y DNA tree of mankind. It is not the same for all of us, as each of our families has a distinctive location. Lewis and Clark founded what would be Fort Clastrop on he edge of Astoria, Oregon. From Astoria Column, a tower, you can see the Pacific Ocean, the Cascade Mountains and the Columbia River.

Single SNP testing is like flying a two seater from St. Louis and hoping to land in Astoria without knowing where Astoria is. The plane is low priced and reliable but has bad gas mileage. More importantly, Astoria may not even have coordinates on the map yet or a landing strip. This kind of approach is most applicable when someone who is highly probable to be on the edge of your genealogically known family has already done a Big Y test and has built a very tall tower or lighthouse to go with a new landing strip. That tower in Astoria could be thought as a super version of Astoria Column and it is built with 111 Y STRs.

Fixed SNP panel/pack testing is like flying the two seater from St. Louis hopscotching across the country, landing at a handful of small airports and getting out and taking a good set of photos at each location and then deciding the next location to fly to.  Fixed SNP packs/panels are a good, low entry price way to go, but suffer the same problem any fixed SNP test suffers. What if your Astoria hasn't been discovered? Perhaps, even your State of Oregon has not been discovered. You also might have troubles if your eyesight or navigation system isn't so good. For good navigation you'd want to have at least 67 Y STRs although 111 is a better long term investment.

Big Y Discovery testing is like having a super high speed, fuel efficient jet traversing back and forth on multiple paths high across the sky on mostly clear days taking special photos of the countryside between St. Louis and the Pacific Coast. It is scanning over 11 million locations. If your Astoria turns out to be San Diego, Long Beach or Tacoma, that's okay. Big Y is accomplishing what Lewis and Clark were doing, mapping the route for settlers to follow in the form of lower entry price tests. Unfortunately, your family of genealogical record might not even be on the maps for the mass migration of settlers to come, that is without Big Y discovery testing. It's just a fact of the Y chromosome just as it is of the geography. The settlers won't go to a place when they don't know where it is or even know it exists.

Only a member of your genealogical family can discover your Astoria and erect the Astoria Column of 111 STRs for the settlers. We need leaders from each family.

I'm asking you to start thinking about Big Y if you haven't already. Be a lead-explorer! There are now several thousand Big Y results completed. It works. Big Y results can come in as quickly as 4 weeks (FTDNA uses an 8-10 week estimate). Pooling of resources at the project/family/surname levels can help share the cost, but be look for holiday, DNA Day, Father's Day sales promotions.

https://www.familytreedna.com/learn/y-dna-testing/big-y/
https://en.wikipedia.org/wiki/Lewis_and_Clark_Expedition
https://en.wikipedia.org/wiki/Astoria_Column

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Yes, upgrading can still be of benefit. There is no magic in the STR panels and what one panel, such as 1-12, shows does not guarantee that another panel, such as 68-111, will not have new matches. The STR panels are essentially a random arrangement of STRs.

Here is my personal case (as of June 2015). Every case will be different. We probably don't care about the averages, we probably just care about our individual case and the related individuals. I remember going through this by incrementally upgrading over the years and realized I would have been smarter to have bitten the bullet from the git go. I try not to add up the money of nickel and diming myself to death.

This is generally what I saw along the way. Although there were more people in the mix from when I actually went through the incremental STR upgrades from 12 to 25, then from 25 to 37, then from 37 to 67, then to 96 (to fill out Ysearch) and then finally to 111 which included a rebuy of some in the 96.

A) 48 people at 12 STRs; 6 at GD=0, 41 at GD=1.
I remember at the time when I had only 12 STRs. I was frustrated as there were no patterns and there were people with Italian names, those from Latin America and Central Asia. There was no one with my last name and very few that looked at Irish (my lineage) at all. It just didn't make any sense. I do have a surname variant in the mix today, but he wasn't there when I went through this step and he has never replied to my emails.
After encouragement from others and the recommendation received to go to the gold standard (I was told back then) of 67 STRs, I instead took a small step and upgraded to 25 STRs. Here is what I now see on that screen.

B) 7 matches at 25 STRs, but only two of those were on the 12 STR matches report so there are five new individuals. (0 at GD=0, 0 at GD=1, 7 at GD=2).
It was apparent to me there was no magic in the first 12 STRs. They were not scientifically selected to support genetic genealogy. I think they were just happenstance of the early academic studies and what worked for them. At 25 STRs still I saw no patterns although I got rid some of the strangest geographies. I probably stewed for a year before going to 37 STRs.

C) 4 matches at 37 STRs, but only two of those were on the 25 STR matches report, so I have two new individuals at 37 STRs. (0 at GD=0, 0 at GD=1, 0 at GD=2, 2 at GD=3, 2 at GD=4).
I thought was getting somewhere at 37 STRs as I now was down to British Isles sounding names but nothing that seemed to have a relationship to my family's genealogy and history. A GD of 3 at 37 STRs is not that good so I knew I should have gone to 67 STRs prior. I am slower learner, but I went ahead to the next step. I resigned myself that I probably wasn't getting anywhere, but at worst case I would be a leader and establish where I fit in the matching database so others could find me in the future.

D) 19 matches at 67, but I dropped one of my 37 STR matches while gaining 16 new matches. (0 at GD=0, 0 at GD=1, 0 at GD=2, 0 at GD=3, 2 at GD=4, 2 at GD=5, 4 at GD=6, 11 at GD=7).
What's up with that? I have 19 people on 67 matches screen while only 4 on my 37 matches. The answer is there is no magic in the STRs included by panel at 1-12, 13-25, 26-37 and 38-67. It turns out I can see I have a couple red herring STRs in my 1-12 and 13-25 panel results which were throwing things off. These were very recent mutations that made me look more distantly related to people I was related to 300-500 and 500-1100 years ago.

At 67 STRs, a clear pattern emerged, FINALLY. The clear majority of matches were either residents of Wales or had Welsh surnames. There was one new person, with the a surname that just didn't fit at all. I pretty much ignored him, which was a mistake, and started contacting the Welsh related people. Since my surname is Walsh this all started to make sense. Another clear pattern emerged that the veteran hobbyists pointed out to me. I had a pair of slow moving STRs that was emerging as a distinctive pattern within the matches.

E) 3 matches at 111, one that appeared for the first time at 111 STRs, the other two were only on the 67 STRs matches screen. None of these three 111 matches were on my 12, 25 or 37 STR matches screen. (0 at GDs 0 thru 6, 1 at GD=6 2 at GD=10).
The GD=6 at 111 is pretty good, but it was the unexpected surname. I knew I had to contact him. It turns out he had not (at the time) updated his MDKA and he knew there was a surname change. The ancestor was of a surname variant of mine and from the same county in Ireland as my most distant known ancestor. We've now both taken Big Y and have identified an SNP that only we two share that is in the range of 200 to 500 years old. It's now included in SNP packs and panels so someone else may stumble up on us without having to go through the expense we did. These people in my 111 STR matches group are ones that I would be willing to contribute/pool money for discovery testing like Big Y. Ironically, there is some magic (rhyme or reason) in the panels. The 68-111 panel was organized last and was specifically organized for smoothly behaving STRs that are useful for genetic genealogy. The problem is you have to buy the other STRs to get to the 68-111 panel anyway. There are tens of thousands people in the FTDNA database at 111 STRs. It is has been the new gold standard for some time.

Will you see patterns like I saw as I upgraded? Maybe, maybe not. Your individual case might be entirely different. However, here is the key and it depends, it depends on your curiosity and interest in genetic genealogy. You don't know what you will find until you test, which is why we test. Essentially, we are on an exploration and discovery mission. We don't know what's on the other side. No guarantees, and for goodness sake, don't spend money you need for something else, but if you are interested I think advanced testing can be very valuable.

STRs are additive to SNPs at the end of the branches and twigs of the tree. In Big Y, there is an SNP about one of every four generations, actually father-son transmissions. If you go all the way to 111 STRs, the rate of a change to 1-111 STR panels is about one every three generations. When you multiply the probabilities we see that there is an opportunity for mutation one of every two father-son transmissions or 50% of the time on average. This is very granular. We are moving towards discerning grandfathers from grandsons. This is very helpful when your genealogical records trail hits a brickwall.

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SNP Packs are a set of SNPs known to be relevant to a particular subclade (branch). They represent FTDNA's known version of the haplotree for that particular subclade and may have additional SNPs where the exact branching position is unknown. Packs may also have phylogenetic equivalent SNPs which are extremely powerful for finding new branching and cross-checking results. Everyone who orders a pack gets tested for every SNP in the pack. This is a major difference between the old tree-traversing one a time SNP deep clade testing packages. FTDNA SNP Packs are not dependent on the tree as all SNPs in the pack are tested.

Big Y is a more advanced testing for SNPs as described in the Lewis and Clark Expedition analogy. SNP Packs can not discover your own lineage of SNPs, just check you against the tree of known SNPs. However, SNP Packs are very economical as they include from 100 to 160 SNPs per pack. Generally, the price is less than a dollar per SNP.

Below is a list of SNP Packs currently available. If you are unsure which pack you want, ask for help. The general and safe rule for people who have done limited or no SNP testing is do Big Y but if your budget doesn't allow that, do the main Backbone SNP Pack for your haplogroup, be it R1b-M343&M269, I-M253, I-P215, etc. It is the lowest price pack to date and will place you in a major haplogroup that will allow the administrators to move you to the right subgroup in the project.

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Terminal SNPs are the SNPs that mark an individual's placement on the haplotree on their most youthful known branch. An individual's terminal SNP is not permanent as updates to the hapotree may change the known branching. This is particularly apparent when new Big Y results show up as good matches for an existing Big Y result. Big Y testers invariably have their own list of novel SNPs.

Novel SNPs are just SNPs that are not known and/or documented. We find novel SNPs from Big Y discovery testing. The new SNPs are oftentimes unnamed, but even if named they are private to just that tester. These are also called singleton SNPs. The first Big Y tester with a set of new or novel SNPs may find they sit there, latent.

Novel SNPs often become public as additional people test. As new Big Y results come in and some of the novel SNPs are found in another individual, a new subclade or branch on the haplotree is discovered. When the branch is documented and submitted to those who maintain haplotrees, the novel SNPs are no longer novel. They are now public SNPs on the haplotree, shared by more than one person. This will cause a new haplogroup label to be generated for both the new Big Y tester and the original Big Y tester within whom the then novel SNPs were discovered. This is why Big Y testing is so important. It's how we build out the tree. See above, "Why Big Y Next Generation Sequencing for discovering SNPs?"

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