• Conn Cétchathach

    (Conn of the Hundred Battles) 

     

    Conn Cétchathach mac Tuathail, 110th Ard rí na h'Éireann, is the son of Fedlimid Rechtmar and Ughna, Princess of Denmark.  

The Quinn Genetic Genealogy Project

Welcome to the Quinn Genetic Genealogy Project Portal.  This website is privately maintained by T. Allen Quinn the current curator, administrator, researcher and resident historian for the lines associated with Laughlin Quin, Born between 1703-1712 in Dublin, Ireland having passed in the Newport District of Carteret County on the 4th of February, 1774.  

Laughlin's Last Will and Testament and death was proved by Governor J. Martin in New Bern on the 5th of February when William Coale presented the will to Governor Martin and the Letter's Testimentary were to be provided to the governor.  The will was placed in the Governor's personal papers instead of being filed at the Carteret County Court House in Beaufort which would have been the correct place to file the will.  The question for me has always been to determine why the will was taken to the Royal Governor in New Bern versus the far closer County Courthouse in Beaufort Town unless William Coale had other business in Newport on the 5th of February.  The will was discovered and identified as Secretary of State Papers in the Colonial & State Records of North Carolina.

After physically investigating this box of artifacts along with the will itself, it became fairly clear that the contents of this box were not organized by any particular subject.  Rather, the loose contents contained a wide range of the governor's private articles for a handful of local men, some priminant and some not.  The contents were retrieved from Tryon Palace on the governor's office on 25 April 1775 when Whigs attacked Tryon Palace and Governor Martin and his family fled New Bern.  The governor sent his family to Elizabeth's in Whitehouse, New York and himeself took refuge on board the sloop-of-war Cruiser, transferring his headquarters to Fort Johnston on the Cape Fear River.  

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DNA and Quinn Genealogy

The purpose of the project is to help you identify your QUINN lineage genetically as you research traditional historic records and find new places to look.  That said, you are always encouraged to ask for help.  What you will find in some cases is that what you thought you knew about your specific surname may be incorrect, or not completely accurate.

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Understanding DNA

Base Page Data @ https://www.familytreedna.com/understanding-dna.aspx to view with graphics.

DNA is the carrier of our genetic information, and is passed down from generation to generation. All of the cells in our bodies, except red blood cells, contain a copy of our DNA.

At conception, a person receives DNA from both the father and mother. We each have 23 pairs of chromosomes. Of each pair, one was received from the father and one was received from the mother. These 23 pairs of chromosomes are known as nuclear DNA because, with the exception of red blood cells, they reside in the nucleus of every cell in our body.

The 23rd chromosome is known as the sex chromosome. As with the other chromosomes, one is inherited from the father, and one from the mother. The 23rd chromosome from the mother is always an X. From the father, a person either inherits an X chromosome or a Y chromosome. The chromosome inherited from the father determines their gender. An X from the father would result in an XX combination, which is a female. A Y from the father would result in an XY combination, which is a male.

We also inherit our mitochondrial DNA, mtDNA, from our mother, and none from our father. Mitochondrial DNA is located outside the nucleus of the cell.
 

DNA is made up of four bases: adenine (A), cytosine (C), thymine (T), and guanine (G). The order of these bases is called the DNA sequence.

Whenever a particular base is present on one side, its complementary base is found on the other side. In the example above, see how the bases always occur in complementary pairs. Guanine (green) always pairs with cytosine (red) and thymine (yellow) always pairs with adenine (blue). So we can write the DNA sequence by listing the bases along either one of the two sides. In the example shown, one side reads:

T G T T C G T C etc.

For Genetic Genealogy, which is the application of DNA testing to genealogy research, two types of DNA can provide information useful in conjunction with genealogy research. These two types are the Y chromosome and mitochondrial DNA.

Y-Chromosome DNA

The Y chromosome is transmitted from father to son. Testing the Y chromosome provides information about the direct male line, meaning the father to his father and so on. The locations tested on the Y chromosome are called markers. Occasionally a mutation occurs at one of the markers in the Y chromosome. Mutations are simply small changes in the DNA sequence. They are natural occurrences and take place at random intervals. Overall, they are estimated to occur once every 500 generations per marker. Mutations can sometimes be valuable in identifying branches of a family tree.

Each marker has a name assigned to it by the scientific community, such as DYS#391, DYS#439 or GATA H4. The scientists classify these markers as Short Tandem Repeats

STRs

The markers used in our standard Y-DNA Tests are classified by scientists as Short Tandem Repeats, STR. They are called because at each of these marker locations a short DNA code repeats itself. The result for a marker is the number of times the code repeats at that location and is called the allele value. Each marker has a name assigned to it by the scientific community, such as DYS391, DYS439 or GATA H4.

The result received for a Y-DNA test is a string of allele values called a haplotype. Here is an example of a haplotype for someone who took the Y-DNA 37 marker test:

https://www.familytreedna.com/v3/img/bg_navBar.png) repeat-x rgb(26, 47, 75);">PANEL 1
LOCUS
1
2
3
4
5
6
7
8
9
10
11
12
DYS#
393
390
19*
391
385a
385b
426
388
439
389-1
392
389-2
ALLELES
12
24
14
10
11
15
12
12
12
13
13
29
https://www.familytreedna.com/v3/img/bg_navBar.png) repeat-x rgb(26, 47, 75);">PANEL 2
LOCUS
13
14
15
16
17
18
19
20
21
22
23
24
25
DYS#
458
459a
459b
455
454
447
437
448
449
464a**
464b**
464c**
464d**
ALLELES
17
9
10
11
12
24
15
19
28
15
16
17
17

*Also known as DYS 394
**On 5/19/2003, these values were adjusted down by 1 point due to a change in Lab nomenclature.

You can read about using Short Tandem Repeats on the y-Chromosome to compare results.

Surname Project

A Surname Project is a project which is established to test and compare those with a common surname and variants. A Surname Project has a leader known as the Group Administrator. This person assists the members with understanding their results, typically interprets the results for the group, and may publish this information in a newsletter or web site.

There are a wide variety of applications for Y-DNA testing. Y-DNA testing can be used to confirm the paper genealogical research for your family tree. It can determine which family trees with the same or variant surnames are related, and can provide clues to help you with your genealogy research. These are just a few of the applications for Y-DNA testing.

Since the Y chromosome is only found in men, those who take the Y-DNA test must be males. For females who are interested in the Y-DNA result for their surname or family tree, a close male relative with that surname would need to provide the sample.

Y-DNA Haplogroups

Using the results of a Y-DNA marker test, Family Tree DNA estimates the tester’s haplogroup. The haplogroup identifies the person's major population group and provides information about the ancient origin of the male line. Family Tree DNA also offers a haplogroup test which participants can use to confirm their haplogroup assignment. The “Backbone” haplogroup test confirms the base haplogroup assignment, and the “Deep Clade” haplogroup test identifies the branch of the haplogroup the person belongs to.

SNPs

Using the results of any of our Y-DNA tests, Family Tree DNA also predicts the haplogroup. The haplogroup identifies the person's major population group and provides information about the ancient origin of the male line. Family Tree DNA also offers a haplogroup test which participants can use to confirm their haplogroup assignment. The "Backbone" haplogroup test confirms the base haplogroup assignment, and the "Deep Clade" haplogroup test identifies the branch of the haplogroup the person belongs to. You may read more about y-chromosome and SNP testing...click here

Mitochondrial DNA

Mitochondrial is passed from mother to child. Since only females pass on their mtDNA, testing the mtDNA tells about the mother, to her mother, and so on along the direct maternal line. Both males and females receive mtDNA from their mothers, so both men and women can test their mtDNA.

While mutations occur in mitochondrial DNA, the rate of mutation is relatively slow. Over thousands of years these mutations build up so that one female line will have a sequence distinguishable from another. As people spread throughout the world, mutations occasionally occurred in different populations over time. This allows us to test the mtDNA to identify the world origin of a person's lineage.

mtDNA is tested and the result is compared to a reference sequence called the Cambridge Reference Sequence (CRS). By comparing an mtDNA sequence to the CRS, we can identify the ancient lineage to which you belong, called the haplogroup. Many haplogroups are continent-specific and some of their branches are region-specific.

Mitochondrial Haplogroups

Haplogroups are labeled alphabetically. Today, anthropologists have identified certain haplogroups that originated in Africa, Europe, Asia, the islands of the Pacific, the Americas, and sometimes particular ethnic groups. Of course, haplogroups that are specific to one region are sometimes found in another, but this is due to more recent migration.