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Ancient sample BR2 matches living people

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After converting the raw sequence reads of Ancient Hungarian Bronze Age genome (BR2) into a genotyped file, I uploaded to GEDMatch as kit# F999933 to see if there are any matches. Interestingly, he has matches with living people!

1-to-Many

GEDMatch matches

1-to-1

I went ahead to see how solid are these matching segments by pulling a few top matches. I restricted at 800 SNPs / 8 cM to get the longest possible segments no errors.

9.7 cM matching segment

9.9 cM matching segment

Triangulation

I was even able to triangulate matches.
Triangulation of segments.

Related Blogs:




Let me know what you make of this.

Ust'-Ishim's Y-DNA and mt-DNA Analysis

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Ust'-Ishim is a high-quality genome sequence of modern human from Siberia. The authors date it to be 45,000-year-old. Raw data is available here. I downloaded it and started to convert into formats familiar to genetic genealogists (or genotyping it).

I finished processing Y-DNA and mt-DNA and uploaded here which contains Y-SNPs and mtDNA mutations.

Y-Haplogroup

The Y-Haplogroup is K-M526 (or K2)
ISOGG K2 Y-Tree

Y-STR Markers

DYS39312
DYS6409
DYS49012
DYS45511
DYS57616
DYS45816
DYS4508
DYS449.214
DYS45411
DYS48122
DYS56811
DYS48713
DYS39111
DYS4349
DYS43912
DYS43810
DYS43612
DYS6419
DYS4728
DYS49210
DYS64311
DYS63811
DYS53311
GATA-A1015
DYS44414
DYS42513
DYS395S1a/b15
DYS385a/b12
DYS46112
DYS54912
DYS59410
DYS48516
DYS5789
DYS55715
DYS406S111
DYS448.28
DYS459a/b9
DYS464a/b/c/d15

YSearch.org kit# is 9T6BJ

mtDNA Haplogroup

The mt-Haplogroup is R. It is also positive for atleast 4 subclades below R. Hence, it is safe to consider it to be R.

mt-DNA Haplogroup R


Ignoring the mutations that aren't considered for the mt-Tree, below is the closest match I can find.



The authors mentioned the mitochondrial mutation rate of 1.8 × 10−8 to 3.2 × 10−8 per site per year based on the age of the bone and the human chimp-split common ancestor (which I don't believe as there is no proof) but trust the direct pedigree method in mutation rate calculations.

1.8 × 10−8 to 3.2 × 10−8 per site per year is nothing but 1 mutation every 1886 to 3353 years. So, the common ancestor between Ust'-Ishim and JQ703641.1 is 45000 years + time for 2 mutations gives a range of 48772-51706 years. Now, from this common ancestor, JQ703641.1 has 11 mutations. Which means, time for 11 mutations gives a range of 20746 to 36883 years. If we subtract these years from the common ancestor, we should get the time as 0 or close to it because JQ703641.1 is still living. Instead we get the age of  JQ703641.1 as 14823 - 28026 years as the age of JQ703641.1 which is clearly wrong. I can only infer from this either mutation rate used is wrong or 14C dating is wrong or both.

However, I want to estimate the age through direct pedigree method which I consider accurate. In this method, mutations are calculated based on what is found in known pedigree/family tree. This is far more superior than unknown assumptions like human chimp split which cannot be verified. You can see all academic references for Direct pedigree method in True Age of mt-Eve based on Direct Pedigree Method.  Direct pedigree method gives an estimate of 0.02353 mutations per generation or 1 mutation every 42 generations. If we consider 1 generation is 20 years, than 42 mutations is 840 years. Hence, 11 mutations of JQ703641.1 will take 9240 years back in time for the common ancestor. Then, 2 mutations from 9240 years gives only 7560 years ago. To get the range, I will use the lower limit found in direct pedigree method which is 1 mutations every 15 transmission events (which is through excluding the no-mutation experiment). If we use this, we get the age as 5400 years back which is 2160 years less as the lower limit. Hence, the upper limit can be confidently put as 9720 years ago. Hence, the actual age of Ust'-Ishim can only be within 5400 to 9720 years back using direct pedigree method.

Let me know what you think.

Gökhem2 Ancient DNA Analysis

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The authors had generated between 0.01 to 2.2-fold genome wide coverage for 6 neolithic hunter-gathers from pitted ware culture, 4 neolithic farmers from funnel beaker culture and 1 late Mesolithic hunter-gatherer. I converted the raw data of Gökhem2 excavated in Sweden into formats familiar to genetic genealogists and made available here. I also filtered with SNPs tested by DNA testing companies like FTDNA, 23andMe and Ancestry and upload to GEDMatch as kit# F999934.

Admixture

Dodecad V3 Admixture Calculator

Eurogenes Admixture Calculator

MDLP Admixture Calculator

Eye Color


Runs of Homozygosity

RoH reveals parents of Gökhem2 are not related in their genealogical timeframe.

Mt-DNA

After merging mtDNA output from all runs, I get 149 mutations! That's really strange. However, processed files each run can always be referred inside the folder having the accession number. The best mt-Haplogroups are identified as  H1c, H1k1, H1ax, H1b1g with 107 mismatches on the tree.

Ancient Hungarian BR2 DNA in FTDNA

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I was able to upload the ancient BR2 sample which has matches with living people into FTDNA using the free autosomal transfer available for 23andme V3/Ancestry files. There are 43 additional matches apart from the top 20.

FTDNA Screenshot
The only problem is, it's locked. To unlock, I need  4 additional transfers using the reference link from the BR2 kit. Below is the link.

If you have a 23andme V3 or Ancestry autosomal files and already match above 7 cM in GEDMatch and suspect you could match this ancient sample in FTDNA database as well, then I encourage you to use the above link to transfer into FTDNA database. 



If you do match this ancient sample BR2 in FTDNA, you are welcome to join the Ancient DNA project.

How long back in time will a large compound segment match?

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There has been a few Ancient DNA matching living people. So, I thought of calculating how far can a segment length of 1000 SNPs / 10 cM can go back in a highly endogamous society.

Direct estimates from genome sequencing of relatives suggest that mutation rate is about 1.1 × 10-8 which implies that an average of 70 new mutations arise in the human diploid genome per generation1. There are 2,881,033,286 base-pairs in all 22 chromosomes. This means, the probability of a mutation occurring in a particular allele is 70 / (2,881,033,286 x 2) ~ 1.1 × 10-8 per allele per generation.  However, in terms of a matching segment, only the SNPs differ and the base-pairs in between do match except a few novel variants.

So, let's consider a segment of 10 cM with 1000 SNPs. The probability of a mutation occurring on a segment of 1000 SNPs is = 1.1 × 10-8 x 1000. We don't multiply by 2 because, we are calculating for a single strand match. This gives a rate of 0.000011 mutations per generation for 1000 SNP segment. This is nothing but, 1 mutation every 91000 generations. Hence, if we take a 10 cM / 1000 SNP compound segment, it is very much possible for anyone truly related to match ancient DNA as a 3rd to 4th cousin.

I feel happy for people who match Ancient DNA. I wish I could match one.

1 Keightley, Peter D. "Rates and fitness consequences of new mutations in humans."Genetics 190, no. 2 (2012): 295-304.

Founder Population and Fallen Angels: A Christian Perspective

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Irrespective of whether you are a Christian or not, there are some manuscripts and the Torah provides a glimpse of antediluvian world, which must not be ignored. It was filled with amazing things like people living nearly a thousand years and another group called 'sons of God' taking daughters of men as wives and producing a giant race.

Based on medical research and the description given in the Bible, Goliath of Gath who was defeated by David, might have had hereditary gigantism1. This gives us a clue that a union between a group referred as 'sons of God' and the daughters born to human families resulted in another group called nephilim who had some different phenotypes and gigantism is one of them. Many interpret sons of God as direct creations of God. This union between sons of God and daughters of men giving birth to another group called nephilim and the admixture resulted in present day humans.

After doing some Math on how long back in time will a large compound segment match, I learnt that if Adam & Eve were living just 6000 years back, then it is indeed possible to get a rough count on the number of fallen angels based on mutations among populations. To begin with, we will consider 6000 years as roughly 300 generations, assuming 1 generation is 20 years. We also know that there will be 70 new mutations per generation2 . Hence, for 300 generations, there must be only 21000 mutations for any person from Adam. Hence, the genetic distance between any two humans living today must be 42000 mutations. This is true if Adam was the only common ancestor. However, we don't have just 42000 mutations but much more than that. Any two unrelated humans are ~99.7% identical. This means, there are 0.3% differences, which translates to 2,881,033,286 * 0.3% = 8.64 million mutations. If any two individuals differ by only 42000 mutations if they ever had only 1 ancestor, how many different ancestors would make 8.46 million mutations between any two individuals? The answer is 8.64 million / 42000 = ~206.

Hence, including Adam & Eve, there should have been around 206 total common ancestors before 300 generations. These ~206 other common ancestors could be the fallen angels.

Interestingly, the book of Enoch chapter 4 verse 7-8 specifies the number of fallen angels which counts to 200.
And these are the names of their leaders: Sêmîazâz, their leader, Arâkîba, Râmêêl, Kôkabîêl, Tâmîêl, Râmîêl, Dânêl, Êzêqêêl, Barâqîjâl, Asâêl, Armârôs, Batârêl, Anânêl, Zaqîêl, Samsâpêêl, Satarêl, Tûrêl, Jômjâêl, Sariêl. These are their chiefs of tens.
Even though the book of Enoch is apocryphal which mentions the number of fallen angels as 200, genetically, the number of founder population distinct to each other including Adam & Eve is ~206.

1 Donnelly, Deirdre E., and Patrick J. Morrison. "Hereditary Gigantism-the biblical giant Goliath and his brothers."The Ulster medical journal 83, no. 2 (2014): 86.
2 Keightley, Peter D. "Rates and fitness consequences of new mutations in humans."Genetics 190, no. 2 (2012): 295-304.

Ust'-Ishim Ancient DNA Analysis

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The authors provided a high-quality genome sequence of a 45,000-year-old modern human from Siberia. I converted this raw data of Ust'-Ishim into formats familiar to genetic genealogists and uploaded here. I also filtered with SNPs tested by DNA testing companies like FTDNA, 23andMe and Ancestry and upload to GEDMatch as kit# F999935.

Admixture


Dodecad V3 Admixture

Eurogenes K15 Admixture

MDLP Admixture
Did you notice that Ust'-Ishim had significant South Indian/South Asian?

Eye Color


Eye Color in GEDmatch

Runs of Homozygosity

RoH reveals parents of Ust'-Ishim are not related in their genealogical timeframe.

Y-DNA and Mt-DNA

The Y-Haplogroup is K-M526 (or K2). The mt-Haplogroup is R. For more information, please refer to the other blog Ust'-Ishim's Y-DNA and mt-DNA Analysis.

HIrisPlex Eye and Hair Colour Report

PBlueEye0.717687808
PIntermediateEye0.0705954
PBrownEye0.211716792
Full_AUC_BlueEye0.940398377
Full_AUC_IntermediateEye0.743643077
Full_AUC_BrownEye0.945280146
Numb_missingSNPs_Eye0
Name_missingSNPs_Eye
AUC_Loss_BlueEye0
AUC_Loss_IntermediateEye0
AUC_Loss_BrownEye0
PBlondHair0.181988131
PBrownHair0.414160283
PRedHair0.001216703
PBlackHair0.402634883
Full_AUC_BlondHair0.810615722
Full_AUC_BrownHair0.75106119
Full_AUC_RedHair0.922711998
Full_AUC_BlackHair0.848113996
Numb_missingSNPs_Hair2
Name_missingSNPs_Hairrs86insA_A / Y152OCH_A
AUC_Loss_BlondHair0.004212153
AUC_Loss_BrownHair0.000578154
AUC_Loss_RedHair0.010694627
AUC_Loss_BlackHair0.000144711
PLightHair0.351583723
PDarkHair0.648416277
Full_AUC_HairShade0.905443611
Numb_missingSNPs_HairShade0
Name_missingSNPs_HairShade
AUC_Loss_HairShade0
Ref: http://www.erasmusmc.nl/47743/3604975/HIris?lang=en

Below is the closest hair color match I can get.



Kit in FTDNA

I also uploaded the Ust'-Ishim kit into FTDNA using their free autosomal transfer program. FTDNA database has 1 match!

FTDNA Database
Segment Matches for that 1 match

The kit is locked. If you have a 23andme V3 file or Ancestry autosomal file, please use the below link to transfer into FTDNA database. If 4 such people use the below reference link, the Ust'-Ishim kit in FTDNA database gets unlocked.


Clovis Anzick ethnic makeup in FTDNA myOrigins

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I just received an email that Clovis Anzick kit is unlocked. So, immediately, I went to see the ethnic makeup.

FTDNA myOrigin for Clovis Anzick kit
Below are the ethnic makeup of close matches for comparison.

Ethnic Makeup of close matches to Clovis Anzick


New force, global anisotropy and the changes in β-decay rate of radioactive elements

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Last month, I posted, Accuracy of the ages of ancient DNA samples discussing the recent findings in nuclear physics based on Jenkins Fischbach Effect which affects radiometric decay rates and thus influence the ages of ancient bio-samples.

Now, a new paper is published in American Journal of Astronomy and Astrophysics suggesting a "new force" that influences β-decay rate of radioactive elements.

Abstract

The review of experimental studies results of a global anisotropy of physical space and new interaction in nature based on analyzing fluctuations in the intensity of the β-decay of radioactive elements are presented. The explanation of the results, based on a hypothesis as to the global anisotropy of physical space caused by the existence of cosmological vector potential AG in limits of theory of byuon, is given. It is shown that vector AG has the following coordinates in the second equatorial coordinate system: right ascension α = 293° ± 15°; declination δ = 36° ± 10°.

The abstract is more technical jargon but introduction is a bit more clear.
(Introduction - New force, global anisotropy and the
changes in β-decay rate of radioactive elements)

Let's see the experiment conclusions.

(Conclusion - New force, global anisotropy and the
changes in β-decay rate of radioactive elements)

So, how does this affect genetic genealogists who look beyond genealogical time-frame and anthropologists? Decay of 146147N is β− decay. I believe it will take years or even decades to recognize the fault in most age related radiometric calculations by assuming a constant nuclear decay rate having no external influence. Having proved the external influence of nuclear decay rates mentioned in this paper as "New force" and "Jenkins Fischbach Effect" using Sun's neutrinos, it will take years to accept the fault in the existing radiometric dating techniques and formulate a more correct method for age calculation of ancient bio-samples.

PDF Link: doi: 10.11648/j.ajaa.s.20140202.12 

Kostenki14 Ancient DNA Analysis

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The origin of contemporary Europeans remains contentious. The authors obtained a genome sequence from Kostenki 14 in European Russia dating to 38,700 to 36,200 years ago, one of the oldest fossils of Anatomically Modern Humans from Europe. I converted this raw data of Kostenki 14 into formats familiar to genetic genealogists and uploaded here. I also filtered with SNPs tested by DNA testing companies like FTDNA, 23andMe and Ancestry and upload to GEDMatch as kit# F999936.

Admixture

Dodecad v3

Eurogenes

MDLP


Eye Color



Runs of Homozygosity

RoH reveals parents of Kostenki14 are not related in their genealogical timeframe.

Y-DNA and mt-DNA

Y-Haplogroup is C-V199 and mt-Haplogroup is U2b

Archaic DNA matches

K14 seems to be closer to Ust'-Ishim/LBK/Loschbour than other ancients when viewed at 1 cM/ 100 SNPs in GEDmatch.

Comparison to other Ancient samples.

Triangulated Ancient DNA Segments

The segment Chr8: 51067154 - 52075739 has 197 SNPs / 1 Mb which occurs in all Loschbour, BR2, Kostenki14, NE1 ancient DNA samples. Based on other autosomal segment matches, below is how all 4 ancients are related through autosomal DNA. "Loschbour/BR2/Kostenki14/NE1" means, the common ancestor for all 4 ancient DNA samples.


GEDmatch 1-to-many

K14 does have matches with living people around less than 10.
Matches in GEDmatch


Ust'-Ishim Ancient DNA has matches with living people!

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The authors provided a high-quality genome sequence of a 45,000-year-old modern human from Siberia. I converted this raw data of Ust'-Ishim into formats familiar to genetic genealogists. I also filtered with SNPs tested by DNA testing companies like FTDNA, 23andMe and Ancestry and upload to GEDMatch as kit# F999935. I also transferred the kit to FTDNA. Interestingly, the 45000 year old sample as mentioned by authors is having matches with living people as recent cousins.

GEDmatch Matches

There are several matches in GEDmatch.
Matches at 500 SNPs / 5 cM

FTDNA Matches

FamilyTreeDNA has 1 match.
Matches in FTDNA


Do you have any matching segments?

Related  BlogUst'-Ishim Ancient DNA Analysis

NE1 Ancient DNA Analysis

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The Great Hungarian Plain was a crossroads of cultural transformations that have shaped European prehistory. The authors had analysed a 5,000-year transect of human genomes, sampled from petrous bones giving consistently excellent endogenous DNA yields, from 13 Hungarian Neolithic, Copper, Bronze and Iron Age burials including two to high (~22 × ) and seven to ~1 × coverage, to investigate the impact of these on Europe’s genetic landscape. I converted the raw data of NE1 from Polgár-Ferenci-hát site in Hungary into formats familiar to genetic genealogists and uploaded here. I also filtered with SNPs tested by DNA testing companies like FTDNA, 23andMe and Ancestry and uploaded to GEDmatch as kit# F999937.

Admixture

Dodecad v3

Eurogenes

MDLP


Eye Color

Eye Color


Runs of Homozygosity

RoH reveals parents of Kostenki14 are not related in their genealogical timeframe.

Mt-DNA

NE1 is a female and she belongs to mt-Haplogroup U5b2c

Archaic DNA matches

GEDmatch Archaic DNA Matches.
(Note: Browser seems to cache the image for GEDmatch's Archaic DNA matches. So, if you get same result when you change the thresholds, make sure you refresh the browser).

NE1 is so closely related to LBK. Below is at 700 SNPs / 7 cM. It has 2 matching segments at 500 SNPs / 5 cM.

NE1 and LBK.

 BR2 is also related to NE1. BR2 could possibly be a descendant of NE1.

NE1 and BR2

Ust'-Ishim could be an ancestor to NE1.

NE1 and Ust'-Ishim

Loschbour could also be an ancestor to NE1.

NE1 and Loschbour

HIrisPlex Eye and Hair Colour DNA Phenotyping

PBlueEye0.798765
PIntermediateEye0.078415
PBrownEye0.12282
Full_AUC_BlueEye0.940398
Full_AUC_IntermediateEye0.743643
Full_AUC_BrownEye0.94528
Numb_missingSNPs_Eye0
Name_missingSNPs_Eye
AUC_Loss_BlueEye0
AUC_Loss_IntermediateEye0
AUC_Loss_BrownEye0
PBlondHair0.052597
PBrownHair0.401653
PRedHair0.000564
PBlackHair0.545185
Full_AUC_BlondHair0.810616
Full_AUC_BrownHair0.751061
Full_AUC_RedHair0.922712
Full_AUC_BlackHair0.848114
Numb_missingSNPs_Hair3
Name_missingSNPs_Hairrs86insA_A / Y152OCH_A / rs2228479_A
AUC_Loss_BlondHair0.004374
AUC_Loss_BrownHair0.002165
AUC_Loss_RedHair0.010717
AUC_Loss_BlackHair0.002165
PLightHair0.154469
PDarkHair0.845531
Full_AUC_HairShade0.905444
Numb_missingSNPs_HairShade1
Name_missingSNPs_HairShaders2228479_A
AUC_Loss_HairShade0.000133

S. Walsh, L. Chaitanya, L. Clarisse, L. Wirken, J. Draus-Barini, L. Kovatsi, H. Maeda, T. Ishikawa, T. Sijen, P. de Knijff, W. Branicki, F. Liu, M. Kayser, Developmental validation of the HIrisPlex system: DNA-based eye and hair colour prediction for forensic and anthropological usage. Forensic Science International: Genetics. Submitted. 

According to HIrisPlex, NE1 had Blue hair and Brownish/Black hair.


Kit in FTDNA Database


NE1 has matches in FTDNA. I want to thank Roberta and FTDNA for helping to unlock ancient DNA kits.

Matches in FTDNA

GEDmatch Archaic DNA matches

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I would like to thank John Olson from GEDmatch for preparing an excellent tool to compare all ancient DNA uploaded to GEDmatch in one page. The tool allows to reduce the cM as low as 0.5. However, based on my experience and experiments, always try to use 1.5 to 2 cM and above.

Please note, if you see the page giving the exact same results even after changing the thresholds, make sure you refresh the page using F5 key (this seems to be a bug?).

While it is useful to compare your autosomal DNA with ancient DNA kits, it is also helpful to see how other ancient DNA matches with each other. For the below comparisions, I had used 2 cM.















Google+ Awesome trick for the previous post images ...

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Google+ automatically created an awesome trick motion image based on the previous post images which were uploaded. Just thought of sharing this ...

Previous Post: GEDmatch Archaic DNA matches

Autosomal Pedigree Creator Tutorial

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This is a tool to automatically create pedigree trees based on segment matches from a set of autosomal files. This tool will also let you know how a segment match of an unrelated genetic match is related and through whom.

Project Page:Autosomal Pedigree Creator

Getting Started

Folder StructureDownload the Autosomal Pedigree Creator.zip file from the website which is usually less than 1 Mb and extracting it gives you the following files and folders.
  • bin – contains bare minimum Graphviz binaries required to convert a .gv dot to PNG image file.
  • data – intermediate folder
  • ibd – intermediate folder
  • tmp – intermediate folder
  • Autosomal Pedigree Creator.exe – Executable
  • README.txt – Readme file giving a quick overview of the software just in case you haven’t looked at the website.

Kit Preparation

In order to use this tool, some basic preparation must be done. It is just renaming the files with humanly readable filenames. Please don’t change the file extensions. Please use only alphabets.
E.g.,
  • 264652-autosomal-o37-results.csv.gz can be renamed to Felix.gz
  • 264652-autosomal-o37-results.csv can be renamed to Felix
  • genome_v3_Full_20131006120000.zip can be renamed to Felix.zip
Once renamed, place all the renamed kits into a folder. This folder will be selected from the interface.

User Interface




Usage of this tool is self-explanatory and below are the brief steps.
  1. Click Browse and select folder where you had placed all the prepared kits.
  2. Dump All –This option is only required when you have kits totally unrelated to each other and you want to dump every possible segment connection.
  3. Click start and the process begins. The process can go on for a few minutes to several hours depending on the number of autosomal DNA files.

Execution

The process executes sometimes for several hours. The progress seems to get stuck at 15% and then at 75%. This is not really stuck but it tries to extract as much information as possible in order to construct the tree and it does not know how far it has to go. Also, each comparison is done in parallel equal to the number of processors in your computer to accelerate the process.

Pedigree Output

When the process finishes, a PNG file called pedigree.png will automatically open which contains the tree. For some reason if the PNG file didn’t open, then you can always find the file in the root folder of Autosomal Pedigree Creator.


 The tool uses Graphviz to generate the PNG file output from a .gv dot file. The .gv file can be found inside the tmp folder as tree.gv.

Tracing the Connection

For some reason, if you want to check a connection between two common ancestors or two autosomal files, you can do so by following the below procedure.

In the pedigree output, each line is a match, the terminals are autosomal files and the 4 letter ovals are common ancestors. The mapping between these 4 letters and what it means can be found inside tmp folder in the file common_ancestors.csv which can be opened in excel.

As mentioned each arrow is a connection or a matching segment or a group of segments from a common ancestor.



XML Representation

The complete list of common ancestors and how each are related is present in the XML file atree.xml.



This file contains the common ancestor CA tag and the list of segments that match. Please note that all the sub nodes match all the segments at the parent level. Even though the root element is ADAM-EVE, its sub nodes are not automatically connected to the root. The root element is just for the sake of having a root element in XML and is not reproduced in the pedigree tree.

The XML is generated from a text file ‘atree.txt’. The XML file is simply a hierarchical representation of the text file.



Matching Segments

All matching segments can be found inside the ‘ibd’ folder. Please note ‘ibd’ is just a folder name and does not automatically mean they haven’t had recombination or Identity By Descent. However, all matching segments inside ‘ibd’ folder are compound segments.



Opening a file say, Arulraj-Chandrakumar-Esther-SathiaGnanaraj means, the segment is common across Arulraj, Chandrakumar, Esther and SathiaGnanaraj autosomal files and it represents the common ancestor for the kits involved.



Output Interpretation



You might wonder why there are some common ancestors represented as 4 chars in ovals but has only one descendant common ancestor also represented as 4 chars in ovals. The reason is because, these intermediate common ancestors do have population data or segments matching the individuals but does not match the parents. If you want to include all such matching segments from population data, you can enable ‘Dump All’ option. However, be warned that ‘Dump All’ can create a clumsy pedigree because every individual may match every common ancestor depending on how close they are related.

The above output which is closely correct, but still requires some manual intervention and adjustments to get accurate pedigree.

For the above pedigree, below are the true relations.
  • Felix (self)
  • Chandrakumar (Father)
  • Selvarani (Mother)
  • Sathia Gnanaraj (Paternal grandfather)
  • Esther (Wife)
  • Arulraj (Father in law)
There is no common ancestors between Felix and Chandrakumar (because Chandrakumar is my father). So, VLXQ name represented as a common ancestor between myself and my father is none other than my father himself. Similarly for all parent/child relations. It is not possible to automate this using computer algorithms because, a computer can only say if a relation is parent/child but it cannot find who the parent is unless it has all the required data surrounding it which is not possible or feasible all the time. Changing the parent/child relations will lead to the below modified pedigree.



As you can see, I can infer the following from the autosomal pedigree tree.
  • My wife’s tree is separate line.
  • There are three individual common ancestors giving three lines.
  • My parents are distant cousins.
The above tutorial can also be downloaded here: Autosomal Pedigree Creator.pdf 

Let me know if you find this tool useful and know what you found.

Ancient Hungarian Neolithic (NE1) DNA matches living people!

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The Great Hungarian Plain was a crossroads of cultural transformations that have shaped European prehistory. The authors had analysed a 5,000-year transect of human genomes, sampled from petrous bones giving consistently excellent endogenous DNA yields, from 13 Hungarian Neolithic, Copper, Bronze and Iron Age burials including two to high (~22 × ) and seven to ~1 × coverage, to investigate the impact of these on Europe’s genetic landscape. I converted the raw data of NE1 from Polgár-Ferenci-hát site in Hungary into formats familiar to genetic genealogists and uploaded here. I also filtered with SNPs tested by DNA testing companies like FTDNA, 23andMe and Ancestry and uploaded to GEDmatch as kit# F999937. After batch processing, NE1 has significant matches with living people.

Matches on GEDmatch


Top NE1 matches in GEDmatch

Matches in FTDNA


Top FTDNA matches for NE1.

Related Blog:

Ust'-Ishim has Warrior Gene 3 Repeats

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After building the Warrior Gene Test, I thought of checking the ancients for warrior gene 3 repeats. It is interesting to note that Ust'-Ishim has warrior gene (MAO-A) 3 Repeats. No other ancients male have warrior gene 3 repeats. NE1 being a female also has warrior gene (3 repeats) on one copy of X-Chromosome.

I also ran through the OpenSNP dump (downloaded a month back) to see who else have Warrior Gene 3R and below are the list.

UserFile
Jasmine496
Svan3
Svan903
Jonathan689
George Smith738
sagan4
Alexandre Bolze749
Txguy750
Robert Wilmott907
biotechdj73
Kazumichi SATO1689
Nathan1013
Brandon80
Bastian Greshake9
Tornpie1204
vpl88
david raska1273
Bryan E109
William Childress1361
R.M. Holston8
George G. Stradtman, Jr.1486
Rosie Redfield94
Ian Logan1505
Eugenio Battaglia1585
Max1594
K. Thomas Pickard125
frenchboy146
Razib Khan12
Mom to AG173
Mikko Ojanen208
mtDNA T2b7a2 (The clan of Tara)854
Daniel Hartnell240
Gestalt242
Mo23
f0rky268
Grant Brunner270
Matt Jordan273
Beau Gunderson27
jtw287
Petar Ivanov293
John Kemeny31
Matt Di Pasquale299
ab owain471
Roberta ohler336
zane5546339
Rebecca O'Meara342
tomarak39
Donald Meek388
James Smith389
Joerg Rings41
Joerg Rings864
Jerry Kezar866
moeffju395
David Cooper427
Jeff Hammerbacher431
John Wilkins865
Muriel Hykes449
Glenn Hammonds451
Steven Berry478
dayna494

FamilytreeDNA's 2nd Mystery Rewards

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On top of reduced prices for holiday sale, FamilyTreeDNA is providing Mystery Rewards for existing customers every week. Since I manage 11 kits of whom all of them are my close relatives and I already used what I want last week itself, I thought of sharing it here and will be sharing for consecutive weeks until the end of this year when the offer ends.

Y-DNA
$25 off Y37, Y67, or Y111 R5HLXNJ4
$10 off Y37, Y67, or Y111 R5M7KY1H
$10 off Y37, Y67, or Y111 R5RUIH63
Autosomal
$10 off Family Finder R5R53WX7
$5 off Family Finder R53PQAD9
$5 off Family Finder R5ZA9I51
Mt-DNA
$10 off mtFull Sequence R5RB4ZMO
$10 off mtFull Sequence R5ACYW1W
Any purchase
$10 off any purchase R5680KTU
$5 off any purchase R5AKKFLV

Please note that once a code is used, it can't be used again. So, it's first come first serve.

NE1 Ancient DNA is BRCA1 Positive

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I am grateful for a volunteer who shared the autosomal raw data positive for BRCA1. I used the raw data to build a tool called BRCA1 Test that can quickly and effectively test for BRCA1 positive for a particular type of mutation.

Based on the tool, I analysed the ancients to see if I can find anyone is with BRCA1 positive and found that only NE1 ancient DNA is indeed positive for this mutation.

If you have a factoid result or any of the gene results BRCA1 or warrior or CCR5 etc and also had done Autosomal DNA testing for genetic genealogy, and willing to share your DNA with me, please send them to me and I can build a tool to test them for the benefit of others.

How the ancients are related to each other

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I used the Autosomal Pedigree Creator to create the below pedigree using matching compound segments.


It seems BR2, Loschbour, NE1, LBK and NE6 has more compound segments from population that the rest of the ancients.

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