As I pointed out at the end of my last article, I made a mistake in my notes. Instead of simply deleting my mistake when I realized it, I did a strike-through and left it up so that others would see that I am accountable for my mistakes. I will never claim to be perfect and if I do make a mistake I expect to be called out on them. She has since edited the paper and removed Sarah Bollinger from the co-author list.
- It begins with her signing up on Zoobank on Oct. 25, 2012.
- The name of her paper and the species name is registered on Zoobank on Nov. 18, 2012.
- The Journal of Advanced Multidisciplinary Exploration in Zoology is registered on Zoobank on Jan. 9, 2013.
- A Scholastica page for this journal is created on Jan. 11, 2013.
- Denova Scientific Journal is registered on godaddy.com on Feb. 4, 2013.
- Denova Scientific Journal publishes Novel North American Hominins after she obtains journal and renames it.
Dr. Ketchum has repeatedly claimed that there was obscene scientific bias against her paper. That was the entire reason for having to purchase the journal.
As I laid out in my last article, Dr. Ketchum claims there’s no more data, while the paper says otherwise. She supplied 2.7Mbp, 2.1Mbp, and 0.53??Mbp for her 3 genomes. A single genome should be approximately 3Gbp or even 135Mbp for just the chromosome 11 section. That’s a substantial chunk of missing data.
Dear Mr. Weeast, Thank you for your email concerning the sequencing that we provided to Dr. Ketchum and co-workers. This work was performed as a fee for service. We have not been involved in the analysis of the results. Further, we are not at liberty and have no intention of discussing the laboratory results that we obtained with anyone but Dr. Ketchum or her colleagues. I would suggest that you direct your questions to her. Our core has only provided sequencing service for this study and we are not involved beyond that.All the best,Ward WakelandEdward K. Wakeland, Ph.D Edwin L. Cox Distinguished Chair in Immunology and Genetics Director, Walter M. and Helen D. Bader Center for Research on Arthritis and Autoimmune Diseases Director, IIMT Genomics Core Professor and Chairman, Department of Immunology
Notice he says there was no analysis done at their labs. None. Her paper claims otherwise:
In depth analysis of all three genomic sequences (samples 26, 31 and 140) was performed at the University of Texas, Southwestern and alignment confirmed by the University of North Texas Health Science Center. Using CLC Bio Genomic Workbench version 5.1, a subsample of extracted reads were assembled to create a consensus sequence using the human chromosome 11 ….So if they didn’t do the analysis, who did?
The following was a unsolicited commentary by A. John Marsh on a genealogy DNA page which scientists use to discuss mtDNA origin. This is not the complete discussion . However, it sums up the analysis.
T2 BIGFOOTS FOUND IN 5 DIFFERENT STATES:
Along with the fact that all Bigfoots seem to have several different mtDNA mutations from each other, they also are found in 5 different states. It suggests that if a single T2b human female mated with a Bigfoot male 13,000 years ago, that the descendants of the T2b ancestor have spread widely in USA since then.
AGE OF T2b:
Web site
http://www.nature.com/srep/2012/121018/srep00745/full/srep00745.html
If T2b is 12-10kya, and T1/ T2 coalesced about 19kya, T2b might very roughly originate about 10,000 to 15,000 years ago.
THINGS I NOTED ABOUT MUTATIONS DIFFERENT IN BIGFOOT AND HUMANS:
One thing I noted was that all the 52 number diverse T2b haplogroup listed humans in the T2 project had a mutation 146T, but none of the Bigfoot had that mutation. It seems in fact that all T haplogroup have 146T. I am guessing that the earliest common ancestor of all Bigfoots had a back mutation on that marker to the CRS value.
Another thing I noticed was that all Bigfoots which appear to have been tested on the lower number markers, have mutation 73G. Yet not one of the
52 human mtDNA T2b persons had the mutation 73G. Why not? Was 73G a very early mutation in the Bigfoot line?
All the fully tested 4 Bigfoots had the 263G mutation, but not one single one of the 52 humans had 263G. Why not?
It seems all human T2bs have have 16187C and 16189T, but no bigfoots have either. In fact, all human haplgroup T are postive for both these mutations, so presumably in the common ancestor of all Bigfoots there was a mutation reverting to CRS.
According to the Ketchum knockers, all the mtDNA Haplotypes in her project are modern contamination. All of these Bigfoot haplotypes are different.
Isn't it a bit puzzling that all of these humans mistaken as Bigfoot have different T2 mtDNA haplotypes, all have 73G and 263G mutations not found in humans, and all seem to have had back mutations on 146T, 16187C and 16189T, where these back mutations are apparently not found in any human T2b s?
John.
That sounds interesting. Dr. Ketchum was very excited. An hour earlier she posted:
"We just received permission to post. There will most likely be a new paper come from this so we will not post the new findings but you will see enough of the proof to validate the paper. I am SO excited!!!!!"
I apologize for tempering your excitement, but the thread is from Ancestry.com, not a genealogy DNA page. And A. John Marsh isn’t a scientist. He is an architect. A landscape architect to be precise, so according to Dr. Ketchum’s analysis of doctors, would that make him a lawn-chair scientist? But he built the excitement to write another paper... Did she see what he said about Q30 scores?
Does the Q30 quality scores of above 88 mean 30 times average coverage, and 88 percent of the genome reconstructed? Just my guess, I don't know what it means. But on the face of it, does the scores obtained hint at a reliable coverage?
The Foundations.
All of her foundations have one thing in common. They are businesses. All of the payment methods point to her paypal address at DNA Diagnostics. Claiming to run a non-profit while actually operating as a for-profit business is a serious matter. Even the newest foundation the Melba Ketchum Global Sasquatch Foundation announces itself as a non-profit, but is only registered in Texas as a business. It is not listed as a non-profit, nor is it listed in the pending applications for non-profit license.
You can do the texas look up here: https://ourcpa.cpa.state.tx.us/coa/Index.html and enter Global Sasquatch Foundation as the name
You can search the IRS non-profit list here: http://apps.irs.gov/app/eos/ and enter the same name with Garland, Texas as City and State. You can search both existing and those that have applied from that page.
This entire project may have started with a noble goal, but it’s obviously steered in an unknown direction. Perhaps the missing data also holds a key to the direction it’s going.
As before, I call on Dr. Ketchum to answer the questions. There are plenty of qualified scientists that can validate your data if it really says what you claim it does. What you released doesn't. I'm sure Mr. Marsh is a great guy and it looks like he's done a decent job with his family's history, but for Sasquatch it's going to take someone a little more experienced.
John, You are right on. Marsh's results are wrong, because he used the RSRS reference and Ketchum used the rCRS reference. I checked it out. Ketchum's T2b samples are the same as other T2b's in Genbank and the Family Tree DNA T2 project and the Cro-Magnon mtDNA sequence in GenBank. I checked them out with BLAST. "Rookie mistake."
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