The next IAJGS International Conference on Jewish Genealogy will be taking place July 6-10, 2015 in Jerusalem, Israel. It is the 35th conference, the first having been held in 1981 in New York City, and it is the 4th conference to be held in Jerusalem.
The conference will be taking place in the Ramada Jerusalem Hotel, not far from the entrance to the city (the same location as the 2004 conference). Before the conference, there will be a program on Shabbat (starting Friday July 3 and Saturday July 4) for those interested, and a travel day on Sunday (July 5) before the conference starts (on Monday).
The conference website is now up, and they are accepting registrations for those outside of Israel (registration for residents of Israel is coming soon). There is an early-bird discount for those who register up until April 14, 2015.
For those interested in speaking, they are now accepting proposals. You can propose a lecture (45 minutes), workshop (105 minutes in the computer lab), or panel discussion (105 minutes with up to 5 people on a single topic). Proposals must be submitted via the web site. Note that in my experience the system for submitting papers does not work in Safari on a Mac – use Chrome or Firefox instead. You can submit your proposal by going to the Speaker Service Center page on the web site, and filling out the form. Lectures can be in English, Hebrew or French.
The information you need to provide when filling out the form includes:
Full name, mailing address, email address, and telephone number of presenter(s)(If a panel proposal, details for each panelist are required)
Brief biographical sketch – (up to 50 words)
Summary of recent presentation experience (up to 150 words)
Title of presentation (up to 15 words)
Presentation type (lecture, workshop, or panel)
Brief description of the presentation (up to 150 words)
Audience skill level (beginner, intermediate, advanced or all)
Preferred language of delivery (English, Hebrew, French)
For some reason, it seems you must finish your proposal within about 20 minutes of starting it, or it will log you out, and your submission will be lost. As such I suggest figuring out what you’re going to write for each of the above entries in advance, and just paste each entry in when you open up the form.
Each speaker can submit up to five proposals, and a maximum of three proposals will be accepted per speaker. For more details on speaking, see the Call for Papers on the conference web site.
While researching my previous post about MyHeritage’s new integration with 23andMe, I came across a new study being done by 23andMe on Irritable Bowel Syndrome (IBD) and its related diseases – Ulcerative Colitis and Crohn’s Disease (two very common diseases, particularly among Ashkenazi Jews). The study is being sponsored by drug company Pfizer, and it seeking 10,000 participants.
To join the study you must have been diagnosed with either UC or Crohn’s by a doctor, live in the US, have access to the Internet, and be at least six years old (from 6 to 17 you must have parental consent). If you qualify, they send you a saliva collection kit with a return envelope, and you must send back a saliva sample and fill out some online surveys related to your condition.
There’s actually one more qualification for the study, or rather a disqualification – if you are already a customer of 23andMe, you cannot participate in this study. If you are already a customer you can fill out some surveys, but it’s not clear if your DNA data will be included in the study.
Interestingly, both Ulcerative Colitis and Crohn’s Disease are significantly more common among Ashkenazi Jews than the general population. This probably means that Jewish participants in this study will outnumber their percentage of the general population. It also might mean that if you have the genetic markers that predispose you to these diseases, joining this study might connect you to a large number of potential relatives, since the group is self-selecting, and if the genetic markers are familial, then you’re more likely to find genetic relatives than on average when there are 10,000 other people with the same condition as you.
So what do you get for joining the study, besides knowledge that you are helping further scientific research that might one day benefit you personally?
Well, for one you get lifetime access to 23andMe’s Personal Genome Service. For the moment that only deals with genetic genealogy, not the health information that 23andMe previously offered (and still offers to customers who signed up before the ban), but that might return in the future. However, if you’re reading this post, chances are you are interested in genealogy, and if you have one of the very common diseases they are researching, and have not yet signed up for 23andMe, this will save you a $99 sign up fee for their service.
The only thing different about the account on 23andMe you receive compared to a regular 23andMe customer who would sign up at the same time, is that it seems you cannot participate in the customer forums. The other difference is of course that you know your DNA is being contributed to a specific study on a disease you have.
So if you have Ulcerative Colitis or Crohn’s Disease, and have not yet signed up for 23andMe, this is a good opportunity to further science and to get access to 23andMe for free. Go check out the 23andMe IBD Study page for further information.
In one of the more interesting announcements in the genealogy world of late, MyHeritage has announced a partnership with genetic testing company 23andMe.
Unlike the partnership between MyHeritage and Family Tree DNA which dates back to 2008 and was extended in 2012, this new partnership is not just an affiliate sales relationship.
MyHeritage has announced that they will be integrating their service directly with 23andMe, allowing one to confirm relationships in your tree on MyHeritage using the DNA data on 23andMe. Certainly a very interesting development, and it will be interesting to see how far they go with this integration.
It will also be interesting to see how the other players in this field respond to this development. MyHeritage, in addition to their namesake site also runs the large Geni.com family tree site. Will Family Tree DNA stay partnered with MyHeritage? Will they seek similar integration with MyHeritage? Will that even be allowed by 23andMe?
If not, will they seek to partner with another large family tree web site? Ancestry.com has their own family trees, but also their own DNA tests, so it would seem that’s not possible. From there, the size of family tree sites drops dramatically. TribalPages? OneGreatFamily? WikiTree? If the integration is done right, this creates a real strategic advantage for MyHeritage and 23andMe, that it would seem only Ancestry.com can really compete with at this stage.
See MyHeritage CEO Gilad Japheth speak about the new partnership on Bloomberg TV here:
and read more on MyHeritage’s blog post announcing the new partnership.