When it comes time to write the stories of your ancestors’ lives, whether you want to write a blog post or a book, you are going to want more than names, places and dates. These lists of facts make for boring reading. This lecture will reveal Janice’s secret method to uncovering hidden episodes of our ancestors’ lives that bring their stories to life.

Often the hardest part of writing an ancestor’s story is getting started. Learn how to use MyHeritage tools and features to outline, write and share family stories with ease.

Learn how to conquer family history writer’s block with 50 fun and practical tips for getting words on the page.

You may be missing 30% of genealogy discoveries if you’re not digging into issues of old periodicals for biographical profiles, stories about ancestral churches or schools, how-to tips for researching a locale, indexes and transcripts of local records. Learn to find and access this content using PERSI, the Periodical Source Index, NOW AVAILABLE FOR FREE on the Allen County Public Library website, and hear success stories that can inspire your own searches.

Illegitimacy. Poverty. Footloose fathers. Record destruction. Name changes. Conflicting data. Forged Bibles. Careless research by predecessors. All these problems can be overcome even when all are combined into one perplexing person. This session presents eight basic principles on which sound research is grounded. For each, it demonstrates how to apply that principle, drawing upon the presenter’s famed case that proved James Ball of Virginia, Tennessee, Mississippi, Arkansas, Oklahoma, and Texas, to be the father of a child born to an unmarried mother in 1824 Louisiana. *** This class requires an active webinar membership to attend. ***

MyHeritage has been breaking new ground with genetic genealogy research technology since the MyHeritage DNA test was first introduced in 2016. Join MyHeritage Product Manager Gal Zrihen for an overview of all the new and exciting developments in MyHeritage’s DNA features and capabilities.

By now you’ve all heard about 3-2-1 computer backup. Having three copies of your data makes sense, but this relies on knowing where your data is in the first place. Is everything on your computer? What about the external drive in the closet? Or the SD cards in the drawer? Is some of your data in a cloud application, and what happens to that data if you forget to pay the subscription? I call this problem “Data Scatter” and it is the enemy of the 3-2-1 backup model. It’s hard to back up all your data if the primary copies are scattered everywhere. Let’s walk through the problem and we’ll propose a few things you can do to reign in your data and give the 3-2-1 backup model a fighting chance.

Following the founding of the colony of Australia, individuals born in the British Empire were considered British subjects, irrespective of the nationality of their parents. Residents of Australia whose native place was outside of the British Empire were not afforded the same rights and privileges as British subjects. These rights, in particular the right to buy land and vote, could be conferred to an individual by a process known as naturalisation. This bureaucratic process generated multiple sets of records that contain a wealth of genealogical information. This talk will outline the complex history of naturalisation in Australia, the changing terminology used, how, when and why naturalisation records were created, and discuss the likely availability of records and for whom they may have been created.

Autosomal DNA tests are utilized in genetic genealogy to solve historic research questions by exploring the genetic traces left by deceased ancestors in the genomes of their living descendants. Any given descendant only inherits a portion of their ancestor’s DNA, and different descendants inherit different portions of that DNA. Based on the relationships between tested descendants of a research subject, it is possible to estimate how much of an ancestor’s DNA is represented in any given database. This information can help in prioritization of testing candidates and can also aid in interpretation of shared DNA between multiple groups of individuals.