From a young age, Paul Woodbury fell in love with genealogy research. To pursue his passion for this field, he studied genetics and family history at Brigham Young University. To aid in his desire to share his knowledge with others, he has also re
I checked out your webinar re: downloading data from 23andMe. How do I turn a raw data file into one that will work with your match list for creating citations?
Raw data is differet from match list downloads, and they are now not in use for security reasons., You can still download to Gedmatch with rawdata, there tier 1 needs to pay. And you can learn Dna painter chromosome painter with copying, but this video is not of use today.
LL
Lana Litke
7 months ago
I cannot believe it is so easy to populate the columns once you have the 1st one. That is a huge time saver I can take elsewhere. Thank you for making citations simple. In the 1st row I used a different font colour for the 3 things we need to input: Tester’s name, Month, and Year. You can’t get much easier than that!
Genealogy Standards spells out eight documentation standards, which give genealogists guidance for documenting genealogical writing. They also provide guidance for citation content, while allowing flexibility in the sequencing and structuring of citations supporting genealogical statements. This presentation will review the standards and provide examples of applying their principles.
Genealogy Standards spells out eight documentation standards, which give genealogists guidance for documenting genealogical writing. They also provide guidance for citation content, while allowing flexibility in the sequencing and structuring of citations supporting genealogical statements. This presentation will review the standards and provide examples of applying their principles.
Record As You Go, Cite As You Go, & File As You Go
Genealogists tend to get very excited about new records and sources they come across in their research. So much so that they grab a quick copy, download it to default folders, and move on to the next item without thoroughly exploring the source first. All too often they don't take…
Genealogists tend to get very excited about new records and sources they come across in their research. So much so that they grab a quick copy, download it to default folders, and move on to the next item without thoroughly exploring the source first. All too often they don't take…
Learning to write genealogical citations is part art, part science and potentially terrifying. Learn what important components to note while researching, and how to put them together while writing to subdue the panic, and produce quality work.
Learning to write genealogical citations is part art, part science and potentially terrifying. Learn what important components to note while researching, and how to put them together while writing to subdue the panic, and produce quality work.
Sources and Citations Made Simple, Standard, and Powerful
If genealogy without documentation is mythology, recording our citations is essential to sound genealogical research. In this webinar, Geoff Rasmussen will 1) explain what makes a good citation, 2) demonstrate how to properly and consistently record the citation, and 3) provide insider tips and tricks for using Legacy's SourceWriter.
If genealogy without documentation is mythology, recording our citations is essential to sound genealogical research. In this webinar, Geoff Rasmussen will 1) explain what makes a good citation, 2) demonstrate how to properly and consistently record the citation, and 3) provide insider tips and tricks for using Legacy's SourceWriter.
Anchors are the Way: Leveraging Multiple forms of DNA Evidence in your Research
Autosomal DNA, Y-DNA, X-DNA, and mtDNA testing and results all have their pros and cons for helping to solve a genealogy mystery. When used in tandem, the synergy of these various forms of DNA evidence aids in pinpointing (or ruling out) relationship scenarios and the source of shared DNA.
Autosomal DNA, Y-DNA, X-DNA, and mtDNA testing and results all have their pros and cons for helping to solve a genealogy mystery. When used in tandem, the synergy of these various forms of DNA evidence aids in pinpointing (or ruling out) relationship scenarios and the source of shared DNA.
Fishing in Your Match List with MyHeritage DNA Tools
MyHeritage's AutoClusters are a great way to start exploring the clusters of your genetic cousins and narrow in on potentially pertinent genetic cousins, but sometimes AutoClusters can only take you so far. Learn to leverage MyHeritage's Theories of Family Relativity, shared matching and DNA match labeling to isolate pertinent genetic cousins for a research question and solve your family history mysteries.
MyHeritage's AutoClusters are a great way to start exploring the clusters of your genetic cousins and narrow in on potentially pertinent genetic cousins, but sometimes AutoClusters can only take you so far. Learn to leverage MyHeritage's Theories of Family Relativity, shared matching and DNA match labeling to isolate pertinent genetic cousins for a research question and solve your family history mysteries.
Covering Your Bases: An Introduction to Autosomal DNA Coverage
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.
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.
Right Place, Right Time, Right Person: Intersections of DNA and Document Evidence
While genetic evidence can aid in the resolution of research obstacles, at the end of the day, genetic genealogy is just genealogy and must be considered within the context of documentary evidence. Even so, the aims of documentary research to make sense of anomalies in genetic evidence often center around finding the right person in the right place at the right time to be an ancestor of a research subject. Learn how to creatively use documentary evidence to recognize and detect intersections of DNA and document evidence.
While genetic evidence can aid in the resolution of research obstacles, at the end of the day, genetic genealogy is just genealogy and must be considered within the context of documentary evidence. Even so, the aims of documentary research to make sense of anomalies in genetic evidence often center around finding the right person in the right place at the right time to be an ancestor of a research subject. Learn how to creatively use documentary evidence to recognize and detect intersections of DNA and document evidence.
Seeking the Best Evidence: Targeted Testing for Genetic Genealogy Proof
According to the genealogical proof standard, part of pursuing thoroughly exhaustive research is seeking the best available evidence to address a research question. In genetic genealogy research problems, the evidence we use is the test results of living descendants of a research subject, and pursuing the best evidence requires targeted testing of those whose DNA is most likely to help address the research question. In this session, learn to identify, prioritize and invite the best testing candidates to address a research question.
According to the genealogical proof standard, part of pursuing thoroughly exhaustive research is seeking the best available evidence to address a research question. In genetic genealogy research problems, the evidence we use is the test results of living descendants of a research subject, and pursuing the best evidence requires targeted testing of those whose DNA is most likely to help address the research question. In this session, learn to identify, prioritize and invite the best testing candidates to address a research question.
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Blown away by this, what a fantastic explanation. I feel I can give this is a try.
Very helpful!
I checked out your webinar re: downloading data from 23andMe. How do I turn a raw data file into one that will work with your match list for creating citations?
Raw data is differet from match list downloads, and they are now not in use for security reasons., You can still download to Gedmatch with rawdata, there tier 1 needs to pay. And you can learn Dna painter chromosome painter with copying, but this video is not of use today.
I cannot believe it is so easy to populate the columns once you have the 1st one. That is a huge time saver I can take elsewhere. Thank you for making citations simple. In the 1st row I used a different font colour for the 3 things we need to input: Tester’s name, Month, and Year. You can’t get much easier than that!
Thanks! Very easy and straightforward. Will be useful.