Showing posts with label Cece Moore. Show all posts
Showing posts with label Cece Moore. Show all posts

Sunday, August 14, 2016

A Month Abroad - Part Two - GRIP

This is the second in my series of blogs on my recent four weeks in the US. Part One is here.

Genealogical Research Institute of Pittsburgh
Two years ago, I participated in the inaugural course in Practical Genetic Genealogy at the Genealogical Research Institute of Pittsburgh (GRIP). The knowledge and the friendships from that week helped propel me along the path I have chosen in genetic genealogy.

This year, they offered Advanced Genetic Genealogy in their July session. This is the way GRIP describes the course:
If you believe that you are ready to graduate from the basics of genetic genealogy and take the next step in genetic genealogy education, then this is the course for you. Be prepared for a fast-paced learning experience intended for the genealogist who has experience applying DNA testing to family history research and has a strong foundational understanding of genetic genealogy concepts.We will demonstrate and discuss methods used by expert genetic genealogists to get the most out of DNA results, utilizing all four types of DNA, in conjunction with documentary evidence to advance knowledge of an individual’s family tree. Genetic genealogy’s application to unknown parentage search will also be examined and resources explored for when unexpected results are encountered.  We will end each day with a discussion session to enhance and reinforce the day’s coursework.Upon completion of this course, students will have gained insight into how to take their own genetic genealogy research to the next level and what it takes to assist others in this pursuit.
Nearly all the instruction was from CeCe Moore and Blaine Bettinger, who also taught two years ago. This is the curriculum.
One hundred forty pages of syllabus for this rich program
As I did two years ago, I stayed with Aunt Betty and Uncle Ken in Squirrel Hill rather than in the LaRoche College dormitory and rented a car for the twenty minute morning drive and the thirty minute afternoon return trip. Each day after morning services, I picked up a donut and a bagel at the kosher Dunkin Donuts to get me through the day.

The audio visual equipment in the room we were assigned was excellent, with everything shown on two large screens in the front of the room and a screen in the back to enable the  instructor to see it while facing the class. We were in four rows of stadium seating, with plugs for our computers on the table and adequate WiFi. The ratio of women to men was less overwhelming than last time. There were several people I knew, from the earlier course and from other places. The class list had forty-nine names, but it didn't feel like an overly large group. Only one or two aside from me expressed any special interest in Jewish DNA.

As before, I helped myself to a front row seat.

The course itself was outstanding and after more than one session, I (and others) said "this session was worth the entire price of admission." Of course this was helped by the fact that I am better equipped to handle the more advanced material than I was two years ago.

Among the stand-out sessions were Blaine on "Advanced Applications foir Third Party Tools" and CeCe on Ethnicity and Admixture, Unknown Parentage and Triangulation. The former included a really nice presentation of Kathy Johnston's Visual Phasing which identifies grandparents' segments based on three sibling-grandchildren. I had never seen this before. It is really very clever.

Both the unknown parentage session and those on admixture led to Jewish issues and CeCe showed herself to be much more knowledgeable and much more comfortable with the Jewish DNA than she had been two years ago. I told her that I was proud of her for her progress. She thanked me publicly for not giving her a hard time and for staying awake. (The latter was a problem last time.)

There was alot of emphasis on things specific to Ancestry and 23 & Me, and since I work with neither (though I tested with 23 & Me) I was quite unfamiliar with the material. I made a decision then that when in Seattle I would go to the Ancestry booth, give them some spit.- then put up the bare bones of a tree. I am pleased to report that I followed through on that. Even if I do not need it for my own research, I really need to know how this works as part of being a professional.

I still have to do something about 23 & Me which I have been ignoring because I find it user-unfriendly to say the least.

Although I am still skeptical about the whole notion of the companies' ethnicity analyses, I saw how CeCe uses them to help identify unknown parents. I was intrigued by the 23 & Me ethnicity results which are by chromosome, rather than just an aggregate blob. I would like to see FTDNA do something like that. I seem to have picked up on what CeCe was doing, as I was quite on the ball in the session on case studies. Of course, I do not use this much in real life, so I am not sure how to keep sharp on that analysis.

The attitude of Ancestry's "we'll do the work for you so you don't need to see the data" policy was analyzed under the harshest of lights. Good things were said about triangulation in that and other contexts.

There was a lot of discussion during Blaine's session on "Ethical and Legal Considerations." Judy Russell was a participant in the course so she had what to say on the subject. (Judy and I crossed swords more than a few times, but it was all in a friendly way. I think.)

Debbie Parker Wayne did one session - on "Reporting and Citing DNA results." It started off very dry with alot of reading from the slides, but it picked up and  ended up being quite useful.

Two students who are geneticists - Brianne Kirkpatrick and Beth Balkite - gave a session on "The Intersection of Genetic Genealogy and Genetic Counseling"  which gave us a different perspective on the whole topic.

Many of the participants in the course already work at a high level so student participation in the discussions was both interesting and useful. I think I held my own in that department.

If I had to boil it down to one sentence, I'd say that the course was way beyond my expectations, which were high to begin with.

I also enjoyed the general GRIP experience even though I was not a visitor to the cafeteria and did not stay for the evening programs. I wish I could say I look forward to doing this again as Elissa Scalise Powell and Debbie Deal put together a fine week of programming, but the non-DNA topics are pretty irrelevant for me and I don't see another DNA course in the near future.

There was one evening program in which I participated - the one on Wednesday when I gave a presentation "Lessons in Jewish DNA - One Man's Successes and What He Learned on the Journey." It was well attended and well received. A few people bought my book and a few others who had bought it online gave it to me to sign.

Triangulation: Jim Bartlett
While we are are on the subject of triangulation, which I mentioned a few paragraphs ago, let me mention that during the week after GRIP I spent a wonderful day with Jim Bartlett the segmentologist.

What got the ball rolling on that was a bloggers party at the home of Pat Richley-Erickson (aka Dear Myrtle) after RootsTech. Lara Diamond introduced me to Carol Petranek, the Co-Director of the Washington DC Family History Center. Carol said that it would be nice if I could speak at one of their Saturday programs, which of course I cannot. But since I knew then that I'd be in Baltimore on the twenty-fourth of July, I offered her the twenty-fifth. One thing led to another and I ended up with an invitation to speak that evening at the Fairfax (Virginia) Genealogical Society, with Jim Bartlett as my host.

I already knew that he liked my book and I have had a tremendous respect for his engineer's approach to DNA analysis, particularly triangulation. We went on for many hours and he showed me exactly how he does his analysis. It is still difficult for me to dive into this at that level both because of the Jewish issues and because I am doing a single-surname project, not just my own personal genealogy. This means I'd have to build an Excel analysis with additional dimensions.

I felt as though I had known Jim well, perhaps in a previous life. He and his wife Olivia were gracious hosts - as were all the people I stayed with during my trip. Actually, Jim and I met at the home of one of my wife's cousins and the three of us had a pleasant time together.

Jim is also known by the email address "gedmatch3" so I decided to run the Lazarus-Endogamy talk I had prepared for Seattle by him to see what he thought. He was the only person to see it before the actual presentation.

Jim and I on TV
Tuesday, after my Fairfax presentation, Jim and I were back in Fairfax for two interviews on Sidney Sacks' local TV show, Tracing Your Family Roots. In one Jim and Sidney's wife Arline interviewed me about my book and the other was more of a three way discussion, though officially Arline was interviewing both of us. I was not at my smoothest.

After they are shown locally, they will be available on line. I'll post links when I have them.

Part Three is here. Part Four is here. And finally, Part Five is here.

Wednesday, June 8, 2016

London and Toronto

I'm afraid that blogging from actual events is more than I can handle and both events have been covered by blogs, Facebook posts and tweets, but having spent nearly a week abroad, I figure I should say something here, if only for my own record.

As I write this, I am in my home office expecting to get a call any minute from the fellow delivering my suitcase. Each of the three legs of my trip included a stopover in Brussels and two of the three times my suitcase was not loaded onto the connecting flight. In London, they delivered it to my hotel at 1:20 AM, in time for my four o'clock taxi. Here they are not in such a rush, but since it's mostly laundry, neither am I.

London
The Wednesday evening program was sponsored by the Jewish Genealogical Society of Great Britain and the Guild of One-Name Studies (of which I am a member). The program was organized by Jeanette Rosenberg of the JGS and most of the attendees are members of that organization. The audience also included my wife's brother and one of her cousins with his wife.

Jeanette's husband Mark Nicholls picked me up at the airport after what seemed an interminable wait at Border Control, plus filling out papers for the missing suitcase. They took me from the hotel to the program site and back.

Paul Howse of the Guild did the introductions.

With Debbie Kennett, in my traveling clothes
Debbie Kennett spoke first. She gave a nice, professional, comprehensive introduction to the whole notion of DNA and its use in genealogy research. (She also addressed - aggressively - some of the nonsense that is being published in the field.)

I followed with the latest iteration of my basic DNA talk that has accompanied the publication of ENDOGAMY: One Family, One People. I have renamed it Lessons
With Paul Howse (right)
in Jewish DNA - One Man's Successes and What He Learned on the Journey
. It was well received. We took questions together afterwards and in most cases we both had what to say.

Debbie and I exchanged signatures on our books. Hers was on the reading list for the course I took at GRIP two years ago.

My thanks to Mark Nicholls for the photos.

Toronto
My friend and colleague Lara Diamond and I were invited to the first-ever Jewish stream of the Ontario Genealogical Society Conference, where we heard some of the top speakers in the field. Much of the conference was centered on matters Canadian, which didn't much interest either of us. But there were also some top-notch speakers including CeCe Moore and Judy Russell, whom I already knew, and Maurice Gleason whom I knew only by reputation.

There were some of the usual vendors, but mostly Canadian groups with limited appeal for those of us with no Canadian interests. (Actually, my grandfather arrived in the US via Montreal and St. Albans Vermont, at age seven with his mother and an older brother and sister. That was 1904. The rest of the family had preceded them in stages.
Actually, Uncle Dave was nine and Aunt Bessie was a bit older



































Friday, I listened to Maurice on the basics of Y-DNA research. Mostly basic stuff with a lot on the FTDNA surname projects. Even knowing much of the material, I can usually learn something from a new speaker and such was the case here.

I spoke Friday afternoon at a special "by invitation only" seminar for the Genetic Genealogy Special Interest Group of the Toronto branch of the Society, on Observations on the DNA of Populations Who "Marry Within the Tribe." This was a first-time event for this talk and it was well-received.

Lara and I both went to the Jewish neighborhood for Shabbat and I met several very nice couples, all of whom had done genealogies of their families. It made me think about how much genealogy is being done outside what we consider the genealogy community. It is important to harness all these private projects so that others can see their work in a searchable format, learn from it and perhaps connect to them. (Programs like Geni.com where people can change each others' data are not the solution.) I don't think this is being addressed. I don't even think that we are aware of the scope of such works. 

I imagine that the non-Jewish world has the same phenomenon.


Lara at 8:30, from her blog
Bright and early at 8:30 Sunday morning Lara spoke about ancestral movement in Europe in a talk called Movement Between Towns in Eastern Europe (aka Ancestral Towns May Not Have Been So Ancestral). It was a good crowd and it went well. (We aren't competing or anything, but she had more people than I.)

Shamelessly lifted from Lara's blog
I followed with my basic DNA talk, Lessons, in a different room, then we went back to Lara's room for her second talk Jewish Genealogy Research in Ukraine. It was largely the same people she had at 8:30, so they must have liked it.

Later, I did a Pop-up presentation in the hallway - fifteen minutes showing two case studies, while Lara did some "Ask the Expert" consulting.

We moved on to a panel discussion on the future of genetic genealogy, including the panel's thoughts on the long-term viability of the testing companies who control all our spit-and-swab data and many of the analytical tools. The final program was a keynote address by CeCe Moore to a packed auditorium where she impressed everyone with her stories of people who had searched successfully for their birth families. The folks doing that kind of work are having a real affect on peoples' lives.

Sunday evening, I gave a non-DNA talk to the JGS of Toronto. Perhaps they'll have me back to do DNA.

You can see Lara's more detailed descriptions of the conference here and here.

After I arrived in Toronto Thursday, I met with a fellow who had a few weak matches with my family and wanted to talk about trying to nail down the possible Jewish background of his grandfather. That is not the kind of thing that holds much interest for me as it is all so remote and tenuous, but he found it useful and attended my other talks. I thought something similar awaited me Monday morning, when I had a meeting scheduled with a man whose family matched mine on our Y-DNA line.

I was wrong. This one was real. A few days earlier, the latest Avotaynu had an article by Rachel Unkefer, J. B. Royal and Wim Penninx called Y-DNA Evidence for an Ashkenzai Lineage's Iberian Origin. This study is being done on a haplogroup called FGC20747 and it includes my line. It appears to include the Goldlust line as well, and one of the Goldlusts was my Monday meeting. As a result of our meeting, they have now joined that project and we look forward to learning more about our joint heritage, which appears headed for the days of the Inquisition - not generation after generation, but in a more macro view.

As my own work has concentrated on the past 220 years, I really do not fully understand this type of Y-DNA research but between the GRIP course next month and some personal mentoring from Rachel afterwards, I hope to enhance my understanding.

It was a good conference and a great experience. Many thanks to JGS Toronto president  Marla Waltman - whose mother matches over forty Pikholz descendants from Skalat and who was responsible for creating the Jewish stream and inviting Lara and me to speak. Les Kelman, too, facilitated our participation.

Housekeeping Notes
Suitcase arrived.

The call for papers for RootsTech2017 has gone out. I may submit some proposals for that February event. I have also submitted proposals for the Federation of Genealogical Societies conference in Pittsburgh at the end of August of next year.

I have another second cousin lined up for a DNA test as soon as we find out about the Fathers' Day sale prices. Perhaps some others of you will also sign up.

Only a month before my summer trip and things are falling into place nicely. I'll write more later but in the meantime, you can see some of it here.

Wednesday, January 28, 2015

Small Segments (and Endogamy)

The issue of small segments
When we compare autosomal matches on the basis of individual chromosomes, there is a natural tendency to concentrate on the larger segments. If you match someone on 30 or 40 centiMorgans (cM), it is clearly a good match. Small matches of one or two cM get overlooked - often deliberately.

When I first began looking at segment matches, I wondered about that because all my DNA came from my parents, grandparents and great-grandparents, even the smallest segments and if I match someone who got those same segments from his ancestors, perhaps both of us got them from a common ancestor.

After I raised this question several times at the GRIP course last summer, CeCe Moore convinced me otherwise by agreeing with me. That is, she agreed that these small segments - I prefer the term slivers - had to have come from somewhere in my past but since they are small, they probably came from so far back that searching for a common ancestor on that basis would not be a productive use of my time.

FamilyTreeDNA's chromosome browser starts showing matching segments with a minimum of five cM, but you can raise it to ten cM or lower it to three or even one cM. GEDmatch suggests seven cM, but you can change that to whatever you wish. But when you download raw data or total matches, you can pretty much do as you like.

There are researchers who begin any examination of matches by deleting all segments that are less than whatever minimum threshhold they set for themselves, never looking at those small segments again. Some go so far as to say that it is wrong to look at small segments.

When I met with Kitty Cooper and Gaye Tannenbaum in Salt Lake City last summer, we discussed the logic of starting with nine or ten cM but once you have a segment of that size, other smaller matches - perhaps even four cM - become relevant.

Not everyone takes this approach. One of the most consistent and convincing champions of using small segments is Roberta Estes of DNA Explained. Roberta has defended advocated the use of very small segments for triangulation and is rightly proud of her successes in having done so. Last week, Roberta posted a long blog after several weeks of laying the foundation. As you can see from what she writes, Roberta is a friend of this blog and I want to make a number of comments on what she wrote.

Moshe Hersch (And you thought we were finished with him!)
But first I want to show you something I found during the last few days in my own work which demonstrates the importance of very small segments.

Some weeks back, I concluded a discussion of two men named Moshe Hersch Pikholz, whom I thought might be the same man. Great-great-grandchildren of one (Charles and Leonora, second cousins to one another) and great-great-grandchildren of the other (Jane and Nan, also second cousins to one another) did Family Finder tests.

The maternal grandmothers of Charles and Leonora (sisters) are the daughters of two Pikholz parents whose relationship to one another is unknown. Aside from that, Leonora's maternal grandfather also has two Pikholz parents, in this case first cousins. So on one hand, Charles and Leonora have extra doses of Pikholz DNA, but on the other hand it makes it very difficult to say for certain which ancestor contributed what, moreso than with normal European-Jewish endogamy.

Nonetheless, I concluded that the genetic match between the two pairs of second cousins was good enough to demonstrate that the two Moshe Hersch Pikholz are indeed the same person.

This week, I took a closer look at chromosome 20 of the four cousins, using GEDmatch at a threshhold of 5 cM..
The bar graph is illustrative but it is not at all proportional.
In the first segment of chromosome 20 (the left side of the bar graph and the top row in the two charts above) Charles and Jane have a large match of 34.1 cM. Both match Leonora on the first part of that segment and both match Nan on the second part. Leonora and Nan do not match each other, but that is not a problem. I don't need all four to match.

The second segment (the right side of the bar graph and the second row in the two charts) is not so simple. Here we have a match of 60 cM between Jane and Nan, part of which matches Charles and part of which matches Leonora. Charles and Leonora are not a match. However nearly a quarter of Charles' match with Nan and Jane overlaps with Leonora's match with Nan and Jane. If this description is complete and correct, something must be wrong, because it is inconsistent.

I asked Roberta what she thought and she suggested that I lower the threshhold as far as possible. Perhaps, she suggested, there are some small segments that explain the inconsistency.

So I lowered the threshhold to one cM.

The long blue bar at the top right is the 60 cM match between Jane and Nan. The medium-sized blue bar at the right of the third line is the 24.5 cM match between Jane and Leonora. The bottom right where there is supposedly no match between Charles and Leonora, we see a series of about a dozen small matches in the same segment where Jane and Nan match. It is as though the long matching segment, to use Roberta's phrase, "has been chopped up." Or if you prefer, disintegrated.

If we ignore the red breaks, Charles' match with Leonora extends nearly all the way to the right end of Jane's match with Nan. Not only that, but Leonora's match with Charles extends Leonora nearly all the way to the left. If we count the small segments, all four line up very well together. To me it is clear that the 60 cM segment that Nan and Jane share came from Moshe Hersch (or his wife, assuming he had only one) and that it began to break down somewhere along the ancestors of Charles and Leonora, perhaps as early as their great-grandmother.

This may not always work so neatly and so conclusively, but to repeat a mantra of Roberta's, if you throw out the small segments even before you begin your analysis, you will never see this obvious result.

But that does not mean that I have totally signed on to Roberta's attachment to small segments. When you are talking about matches that are only small segments, the kind that do not overlap large ones, CeCe is probably right. It's generally not a productive use of my time to examine them.

That is even more valid when talking about endogamous populations where we know in advance that there are distant common ancestors simply by virtue of our being Jewish. For us, the strategy I discussed with Kitty Cooper, looking at smaller segments once you have a large match as an umbrella, is still the way to go. How large is large and how small is small is still a matter of personal preference - and mine is to be conservative. To quote myself in another context "If it might be wrong, it doesn't belong."

For the non-endogamous, such as Roberta, you can probably afford to be more liberal.

A Study Using Small Segment Matching, by Roberta Estes
I  am going to step through Roberta's blog and comment as I go along.

Sherlock Holmes is quoted as saying "When you have eliminated the impossible, whatever remains, however improbable, must be the truth." That does not mean that if we have nothing to go on aside from DNA, then DNA must have contain a usable truth. Maybe yes and maybe no.

Roberta writes " So we need to establish guidelines and ways to know if those small segments are reliable or not." I say, very carefully. Different circumstances require different tools and also create different opportunities. I want to read what all the experienced experts have to say but then I want to make my own decisions for my own families. Usually I will write about those decisions and will entertain debate. Ridicule, not so much. Genetic genealogy is way too new to have hard and fast rules, especially ones that begin :You can't..."

Roberta is obviously correct when she says "assuming the position that something can’t be done simply assures that it won’t be." That is true for an individual project which discards small segments according to some rule, as well as studies on small segment research as a genre. Roberta says correctly "The only way we, as a community, are ever going to figure out how to work with small segments successfully and reliably is to, well, work with them." To that I add if you have a few cases that are proven based on small segments, there are almost certainly many others which are not proven because those small segments were never examined.

I am well-aware that my work is different from that of most others because I an not looking for "new" relatives, rather looking to figure out how the ones I know fit together.  One-name studies is a legitimate field with its own requirements and opportunities.

Finding three people who match on the same segment may be "the commonly accepted gold standard of autosomal DNA triangulation within the industry" but among the endogamous, we strive for the platinum standard. There are too many ways to be wrong if you have only three people using segments that are not large enough and not numerous enough.

Sometimes I want to get more than one trangulation within a potential family group. I suppose that has to do with endogamy. I think of these multiple triangulation scenarios like this.

Roberta's Sarah Hickerson article "was meant to be an article encouraging people to utilize genetic genealogy for not only finding their ancestor and proving known connections, but breaking down brick walls." Absolutely. Many of us read to find not only ideas but encouragement. And some of us write not to show how smart we are but to bring others to the point where they say "I can do this too."

Roberta, please note - for some of us 5-6 generations does not qualify as "low hanging fruit."  And still our small segments can be useful.

I can understand that FTDNA and the other companies must draw a line dividing matches from non-matches. But it would me very very helpful if we could get at our non-matches on FTDNA's chromosome browser. Not everyone is on GEDmatch.

I think that will do.

Thursday, July 31, 2014

Breaking With Tradition

I was planning to blog my usual Sunday morning about the two programs I have attended these past two weeks, but it is too much, so I am putting this up now and will do the second half probably Monday.

DNA at GRIP
The week before last was the course in Practical Genetic Genealogy at GRIP in Pittsburgh. It was a wonderful course with excellent instructors. I really wish I could bring up the lectures again in podcast form, but that is not an option.

If I had any illusions about there being some simple solution to the endogamy problem - endogamy being the tendency of certain groups to marry within a relatively small tribe - those illusions would be banished. To be sure, our three wonderful lecturers, Debbie Parker Wayne, Blaine Bettinger and CeCe Moore referred to Ashkenazi Jewish endogamy frequently, but it was generally as an example of where the usual rules do not work.

(I sat in the center of the front row and was rather undisciplined when it came to comments and questions, and all three of them were very graceful about it. As were the other students. And everyone was very concerned for me and my family because of the war going on in Israel.)

The course was well-structured and included homework, which we'd go over at the end of the following day.

If I had to name one lesson I took away from the course it is that although the smaller matching segments may indeed be real, they are probably more generations in the past and it is not an efficient use of my time to be looking at them. I should really be concentrating on only the larger matches.

Of course, that and getting more family members to test.

During the course, I received test results for my third cousin once removed, Ralph, and it showed some really nice matches that brought smiles to the lecturers as well. I'll probably discuss those matches in about two weeks.

Wednesday evening, I gave a talk to people from the entire program (the DNA course and the five others) on "Special Challenges of Jewish Genealogy." For the most part, they hadn't a clue about what we have to deal with as researchers, aside from our unusual alphabet. There were probably forty people in attendance and it was well-received.

I suppose I shouldn't have been surprised that many of the people in the class take clients and want to upgrade their DNA skills in order to better serve their clients or widen their client base. That may work for the general population, but I wonder whether Jewish clients would be patient with all the difficulties and ambiguities. ("This is all I get for my money?") For now, I am sticking to the Pikholz Project and my other families, plus lending a hand elsewhere when I can.

I did not tweet or blog the course, but I did put a few things I learned at GRIPitt.org on Facebook:
Things I have learned at GRIPitt.org - everyone but me pronounces it "autozomal" as though it were written with a "z."

Things I learned at GRIPitt.org. CeCe Moore says that the day is coming when we will be able to get DNA from more obscure sources. So Save and label your gf's false teeth, your gm's hair, your father's baseball cap etc etc. But NOT in plastic, which promortes bacteria.
And tell people (us!) you have it so we can create the demand.


Things I learned at GRIPitt.org: Genealogists will stand in line for ten minutes to get M&Ms and bottled water.

Things I learned at GRIPitt.org: The world of genealogy is full of old friends whom I haven't met yet.
The week as a whole was wonderful and I came away with a lot of old friends. I had had some contact with some of the students before the course, as well as exchanges with some of the instructors (from my course and others). Now I consider them my friends. A few have asked me a week later how things are going in Israel.

There should be a class picture here, but they have not been distributed yet.

I had a feeling of swimming with the big fish. I spoke briefly with Judy Russell, Cyndi sat next to me the first evening, Kikmberly Powell of the APG Quarterly was in our course, and more.

My new old friend Pittsburgher Elissa Scalise Powell put together a really nice program.

A bonus for the week was spending time with Aunt Betty and Uncle Ken, as I stayed there during the course and for three days beforehand.


Housekeeping Notes
Although I don't use it myself, I am sad to see the demise of The Master Genealogist. It's another step on the road that leads to only online trees, where we will no longer be able to maintain definitive databases distinct from illustrative websites.