Editorial
In This Issue of JoGG
T.
This is the first issue of the
Journal of Genetic Genealogy (JoGG), a new on-line journal. JoGG will appear quarterly and will feature
original articles, columns, letters, news items, and editorials.
Three original articles form the
heart of this inaugural issue. Gareth
Henson discusses the three-copy STR marker, DYF399S1, which he shows to be
associated with the four-copy marker, DYS464.
Henson makes a convincing case that this new marker would make a very
good addition to the toolkits of genetic genealogists. Hopefully, one of the commercial labs will
take note.
My own article on the haplogroup
predictor algorithm is not completely new since some of the information has
been posted on my web site, but JoGG seemed the natural place for a complete
presentation of the approach. Also, the
results of testing the program with 100 R1b and 50 I1a haplotypes are
presented.
Ellen Coffman-Levy has written a
wonderful review of genetic research that sheds light on the origins of the
Jewish people, particularly the Ashkenazi Jews.
She has skillfully interwoven the results of historical and genetic
research to produce the first coherent synthesis of the available information.
Ann Turner will contribute a regular
column for JoGG entitled “’Satiable Curiosity,” designed to connect the needs
and resources of the genealogy community with those of the professional
genetics community. The hundreds of
surname and other family or haplogroup projects constitute a tremendous
reservoir of valuable information, of which most geneticists are unaware. Turner seeks to connect project
administrators with professional geneticists and she proposes new genetics
projects that would be potentially helpful to both the genealogy and genetics
communities. Those of us interested in
genealogy are always talking about the study that we wish would be done, and
many geneticists, especially students, are looking for interesting projects to
do. Getting these needs together would
be a win-win proposition. Ann’s first
column suggests that “redundant” SNPs need further investigation and that those
SNPs leading to Haplogroup Q could be studied using participants from surname
projects who have been proven to be members of Q.
Book reviews letters to the editor, and a news section are not included in this first
issue, but we hope they will be in subsequent issues. If you would be interested in contributing in
these areas, please contact me.
JoGG was organized with
I have agreed to become the editor
for at least the first year of publication.
I welcome your ideas and your feedback.