[33]

Illustrations for the STRs: https://www.google.com/search >


search “Short Tandem Repeats” > choose "images for Short Tandem Repeats"

[34]

STR names ‘DYSddd’: all STRs have a unique identification number (e.g. 393, 442),


with DYS, DYZ, or DYF prefixes: ‘D’ stands for DNA, ‘Y’ stands for Y chromosome,


and S, Z, or F shows the complexity of the repeat segment: ‘S’ is a unique segment,


‘Z’ has repetitive segments at one site, ‘F’ has multiple copies on the Y chromosome.


https://www.familytreedna.com/


learn/y-dna-testing/y-str/dys-dyz-dyf-prefixes-y-dna-str-names-mean

[35]

Y-STR markers (mutation rates): https://en.wikipedia.org/wiki/List_of_Y-STR_markers

[36]

Genetic Distance (GD) (hybrid mutation counts, or infinite allele model)


a. Hybrid Mutation Model: stepwise mutation model, assumes each mutation changes


    the allele value by exactly one, so a difference of two means that two mutations


    occurred, and a difference of three means that three mutations occurred.


b. Infinite Allele Mutation Model: assumes that the entire difference between allele


    values, no matter how large, is the result of one mutation.


    http://www.mymcgee.com/tools/yutility.html?mode=ftdna_mode

[37]

The Western Atlantic Modal Haplotype (WAMH) (standard set of 12 STR markers):


http://isogg.org/wiki/Western_Atlantic_Modal_Haplotype

[38]

The Irish Modal Haplotype (IMH) and the (North West) NW Irish project


http://www.isogg.org/wiki/NW_Irish

[39]

The Y Chromosome Consortium: http://isogg.org/wiki/Y_Chromosome_Consortium

[40]

“Let's All Start Using Terminal SNP Labels Instead of Y Haplogroup Subclade Names,


Okay?", by CeCe Moore, September 20, 2012, on her blog, Your Genetic Genealogist:


http://www.yourgeneticgenealogist.com/2012/09/lets-all-start-using-terminal-snp.html

[41]

(North West) NW Irish Y-DNA haplogroup project: http://isogg.org/wiki/NW_Irish


and Haplogroup R1b (> R1b-M222): https://en.wikipedia.org/wiki/Haplogroup_R1b

[42]

SNP names include a ‘discovery’ prefix and sequential number; some of the codes are


*A* and *L* by Thomas Krahn, MSc (Dipl.-Ing.), YSEQ.net, Berlin, Germany [30]


*DF* by anonymous researcher(s) using publicly available full-genome-sequence data


*FGC* by Full Genomes Corporation, Rockville, Maryland [28]


 M  by Peter Underhill, Ph.D. of Stanford University, Palo Alto, California


  P  by Michael Hammer, Ph.D. of University of Arizona, Tuscon, Arizona


*S* by James F. Wilson, D.Phil. at Edinburgh University, Scotland


*Y* by the Y Full Team using data from next-generation sequencing samples [29]

[43]

SNP data: The Big Tree: Mutations: http://www.ytree.net/SNPIndex.php


e.g. Names / POSITION-ANC-DER / Region / STR Blocks


      FGC19846      18114115-T-G                         FGC19846


. . . FGC19849       22437424-C-T     DYZ19       FGC19846

[44]

SNP data: SNPedia Wiki for Personal Genomics: http://snpedia.com/index.php/SNPedia


_______________________________________________________________________________________________________

McAninch Y-DNA Status Report 2016: Source Notes and References: Notes [33] to [44]

McAninch Family History NL v.XXIV n.1 / April 2016 / Copyright Frank McAninch / pg.2016-17


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