Autosomal Kit Analysis
Analysis of raw autosomal kit files has been undertaken for a group of Y-DNA related Johnston relatives, other Johns(t)on(e) participants, and a small group of non-related control subjects. These raw autosomal kit files have been provided by participants from Ancestry, FTDNA, and 23andme autosomal tests.
The purpose is to determine whether it is possible to determine genealogical relationships between these individuals for distant relationships (5th/6th cousins).
Testing Methodology
Build 36 tests use the HapMap 2008-03_rel22_B36 recombination rates for calculating centimorgans
Build 37 tests use the HapMap 2011-01_phaseII_B37 recombination rates for calculating centimorgans
Build 36 tests use the Human Genome hg18-GRC36 autosomal gene position files to determine which gene the SNP resides in
Build 37 tests use the Human Genome hg19-GRC37 autosomal gene position files to determine which gene the SNP resides in
No call results (– in FTDNA and 00 in Ancestry) are ignored; treated as if the SNP was not tested in either kit
Only SNPs that were tested in both test participants are compared
Where a participant has tests from Ancestry and FTDNA the results are combined before performing matching (version 3)
Segment lengths are for Half Identical Region (HIR) matching
No allowances are made for mutations
Kits from different companies (Ancestry vs FTDNA) are difficult to compare and can lead to incorrect matching results
Weighting is used to filter out false positives; weighting is calculated as the multiplication of SNP count times cMs for each segment
Thresholds are used for each segment before it is considered genealogically relevant
Thresholds for each segment are set at: 5.0 cMs, 500 SNPs, and 3000 SNP-cMs weighting
Thresholds for the total of all segments passing their threshold levels is set at 3000 SNP-cMs weighting
Testing Results
Summary of findings