tiistai 25. elokuuta 2020

RT PCR Test Fraud - Homo sapiens chromosome 8 defined in the WHO PCR test specs

  • The sequence “CTCCCTTTGTTGTGTTGT” is an 18-character primer sequence found in the WHO coronavirus PCR testing protocol document.
  • The primer sequences are what get amplified by the PCR process in order to be detected and designated a “positive” test result.
  • It just so happens this exact same 18-character sequence, verbatim, is also found on Homo sapiens chromosome 8!
  • As far as I can tell, this means that the WHO test kits should find a positive result in all humans

Bombshell Evidence: COVID RNA Base Pairs are Identical to Chromosome 8 Human DNA


One of the WHO primer sequences in the PCR test for SARS-CoV-2 is found in all human DNA

By Fauxlex – Apr 06.20

World Health Organization Coronavirus PCR Test Primer Sequence is Found in all Human DNA


The sequence “CTCCCTTTGTTGTGTTGT” is an 18-character primer sequence found in the WHO coronavirus PCR testing protocol document.

The primer sequences are what get amplified by the PCR process in order to be detected and designated a “positive” test result.

It just so happens this exact same 18-character sequence, verbatim, is also found on Homo sapiens chromosome 8!

As far as I can tell, this means that the WHO test kits should find a positive result in all humans. Can anyone explain this otherwise?

WHO Primer 2

Homo sapiens chromosome 8, GRCh38.p12 Primary Assembly
Sequence ID: NC_000008.11 Length: 145138636
Range 1: 63648346 to 63648363 is “CTCCCTTTGTTGTGTTGT”

Proof that human chromosome 8 has this exact same 18-character sequence. The sequence is shown at the bottom of the page. https://www.ncbi.nlm.nih.gov/nucleotide/NC_000008.11?report=genbank&log$=nuclalign&from=63648346&to=63648363

Fauxlex wrote in the comment section:
This is the WHO protocol. I also came across several private companies (Sigma-Aldrich, Thermo Fisher) whose PCR primer sequences were longer and had no such match. So I am not saying that ALL test kits belong to WHO, but if we were to find shenanigans we would expect to find it with the WHO. This really has me shaken, and I am really starting to believe that the WHO designed a test where they would be able to find a positive anywhere they wanted to find one. Also, the PCR test process is inherently very error-prone and even the WHO test may occasionally have false negatives. I’m stunned.

Read more at https://pieceofmindful.com/2020/04/06/bombshell-who-coronavirus-pcr-test-primer-sequence-is-found-in-all-human-dna/?fbclid=IwAR3MLXyv9d9VXwhKOJDKgwB6hIJqS0QLfFkMv8xqsLtRn8h9qFAjcR_V2rE

Very educational video that also exposes Gardasil.


3. CORONAVIRUS – WHERE’S THE SCIENCE?

Scroll down to: THE SCIENCE OF TESTING: https://thedoctorwithin.com/blog/2020/03/10/newsletter-march-2020/

Now for the bad news. What is the test they claim to use to identify this new bug in a patient? The test is called PCR. This is the classic polymerase chain reaction test, invented in the 80s by Dr Kary Mullis. In 40 years, doctors have never come up with any test more accurate than this very flawed, theoretical estimate of microbial activity.

The test produces loads of false positives, often failing to measure anything at all. No one is more critical of the test’s reliability than the inventor himself.

Dr. Kary Mullis, who won the Nobel prize for inventing PCR to detect HIV, [9] explains its limitations—why the PCR is not especially diagnostic, for HIV or for anything else:

“Quantitative PCR is an oxymoron. PCR is intended to identify substances qualitatively, but by its very nature is unsuited for estimating numbers. Although there is a common misimpression that the viral-load tests actually count the number of viruses in the blood, these tests cannot detect free, infectious viruses at all; they can only detect proteins that are believed, in some cases wrongly, to be unique to HIV.
.
“The tests can detect genetic sequences of viruses, but not viruses themselves.” [1]

Can’t identify viruses? Then how do we know all these people have the same disease, let alone the same novel disease?

This means that with all these people who have supposedly been PCR tested for COVID, there is still no conclusive diagnostic evidence that they have any coronaviruses at all. Let alone the same virus. According to the inventor of the primary diagnostic test. Red more at https://thedoctorwithin.com/blog/2020/03/10/newsletter-march-2020/


COVID19 is a catalyst for

1] World domination by the forces of darkness or
2] Man to open his/her mind and heart, speak the truth, use mask exemptions, protect the children, take back personal power and freedom from politicians Kontrolled by a new world dystopian order.

Evidence strongly suggests that a vote for ‘any’ politician is a vote for #1. You know the rest.

Please share this information. Thank you.

Without Prejudice and Without Recourse
Doreen A Agostino
http://freetobewealthy.net
Sent via hardwired computer
All wireless turned off to safeguard life

https://ourgreaterdestiny.org/2020/08/bombshell-evidence-covid-rna-base-pairs-are-identical-to-chromosome-8-human-dna/


 

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Chromosome 8

From Wikipedia, the free encyclopedia
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Chromosome 8
Human male karyotpe high resolution - Chromosome 8 cropped.png
Human chromosome 8 pair after G-banding.
One is from mother, one is from father.
Human male karyotpe high resolution - Chromosome 8.png
Chromosome 8 pair
in human male karyogram.
Features
Length (bp)145,138,636 bp
(GRCh38)[1]
No. of genes646 (CCDS)[2]
TypeAutosome
Centromere positionSubmetacentric[3]
(45.2 Mbp[4])
Complete gene lists
CCDSGene list
HGNCGene list
UniProtGene list
NCBIGene list
External map viewers
EnsemblChromosome 8
EntrezChromosome 8
NCBIChromosome 8
UCSCChromosome 8
Full DNA sequences
RefSeqNC_000008 (FASTA)
GenBankCM000670 (FASTA)

Chromosome 8 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 8 spans about 145 million base pairs (the building material of DNA) and represents between 4.5 and 5.0% of the total DNA in cells.[5]

About 8% of its genes are involved in brain development and function, and about 16% are involved in cancer. A unique feature of 8p is a region of about 15 megabases that appears to have a high mutation rate. This region shows a significant divergence between human and chimpanzee, suggesting that its high mutation rates have contributed to the evolution of the human brain.[5]

Genes[edit]

Number of genes[edit]

The following are some of the gene count estimates of human chromosome 8. Because researchers use different approaches to genome annotation their predictions of the number of genes on each chromosome varies (for technical details, see gene prediction). Among various projects, the collaborative consensus coding sequence project (CCDS) takes an extremely conservative strategy. So CCDS's gene number prediction represents a lower bound on the total number of human protein-coding genes.[6]

Estimated byProtein-coding genesNon-coding RNA genesPseudogenesSourceRelease date
CCDS646[2]2016-09-08
HGNC656242539[7]2017-05-12
Ensembl6701,052613[8]2017-03-29
UniProt703[9]2018-02-28
NCBI719848682[10][11][12]2017-05-19

Gene list[edit]

The following is a partial list of genes on human chromosome 8. For complete list, see the link in the infobox on the right.

  • ADHFE1 encoding protein Alcohol dehydrogenase, iron containing 1
  • AEG1 : Astrocyte Elevated Gene (linked to hepatocellular carcinoma and neuroblastoma)
  • ANK1: ankyrin 1, erythrocytic
  • Arc/Arg3.1
  • ASAH1: N-acylsphingosine amidohydrolase (acid ceramidase) 1
  • ASPH: encoding enzyme Aspartyl/asparaginyl beta-hydroxylase
  • AZIN1: encoding protein Antizyme inhibitor 1
  • BRF2: transcription factor IIIB 50 kDa subunit
  • C8orf32/WDYHV1: encoding enzyme Protein N-terminal glutamine amidohydrolase
  • C8orf33: chromosome 8, open reading frame 33
  • C8orf4: encoding protein Uncharacterized protein C8orf4
  • C8orf46: encoding protein chromosome 8 open reading frame 46 (C8orf46)
  • C8orf48 encoding protein C8orf48
  • C8orf58: chromosome 8 open reading frame 58
  • CCAT1: colon cancer associated transcript 1
  • CCDC25: coiled-coil domain containing protein 25
  • CHD7: chromodomain helicase DNA binding protein 7
  • CHMP4C: Charged multivesicular body protein 4c
  • CHRAC1 encoding protein Chromatin accessibility complex 1
  • CHRNA2: cholinergic receptor, nicotinic, alpha 2 (neuronal)
  • CLN8: ceroid-lipofuscinosis, neuronal 8
  • CNGB3: cyclic nucleotide gated channel beta 3
  • COH1: vacuolar protein sorting 13B
  • CRISPLD1 encoding protein Cysteine rich secretory protein LCCL domain containing 1
  • CSGALNACT1: Chondroitin sulfate N-acetylgalactosaminyltransferase 1
  • CTHRC1 encoding protein Collagen triple helix repeat containing 1
  • CYP11B1: cytochrome P450, family 11, subfamily B, polypeptide 1
  • CYP11B2: cytochrome P450, family 11, subfamily B, polypeptide 2
  • DCSTAMP: dendrocyte expressed seven transmembrane protein
  • DPYS: dihydropyrimidinase
  • EBAG9: Estrogen receptor binding site associated antigen 9
  • EPPK1: epiplakin
  • ERICH5 encoding protein Glutamate rich 5
  • ESCO2: establishment of sister chromatid cohesion N-acetyltransferase 2
  • EXT1: exostosin glycosyltransferase 1
  • EXTL3: exostosin-like glycosyltransferase 3
  • EYA1: EYA transcriptional coactivator and phosphatase 1
  • FABP9: fatty acid binding protein 9, testis
  • FAM167A: family with sequence similarity 167, member A
  • FAM203B: family with sequence similarity 203, member B
  • FAM83A: family with sequence similarity 83, member A
  • FAM83H: family with sequence similarity 83, member H
  • FBXO16 encoding protein F-box protein 16
  • FDFT1 encoding protein Farnesyl-diphosphate farnesyltransferase 1
  • FGFR1: fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)
  • FGL1: Fibrinogen-like protein 1
  • GDAP1: ganglioside-induced differentiation-associated protein 1
  • GDF6: growth differentiation factor 6
  • GPIHBP1: GPI-anchored high density lipoprotein binding protein 1
  • GRINA: encoding protein Glutamate receptor, ionotropic, N-methyl D-aspartate-associated protein 1 (glutamate binding)
  • GSDMC encoding protein Gasdermin C
  • GULOP pseudogene: responsible for human inability to produce Vitamin C
  • HGSNAT: heparan-alpha-glucosaminide N-acetyltransferase
  • HMBOX1: encoding protein Homeobox containing 1, also known as homeobox telomere-binding protein 1 (HOT1)
  • HRSP12 encoding enzyme Ribonuclease UK114
  • INTS8: integrator complex subunit 8
  • INTS9: integrator complex subunit 9
  • KCNQ3: potassium channel, voltage gated KQT-like subfamily Q, member 3.
  • KIAA0196: KIAA0196
  • KIF13B encoding protein Kinesin family member 13B
  • LACTB2: lactamase, beta 2
  • LAPTM4B: lysosomal-associated transmembrane protein 4B
  • LOC642658: encoding protein Basic helix-loop-helix transcription factor scleraxis
  • LPL: lipoprotein lipase
  • LSM1: U6 snRNA-associated Sm-like protein LSm1
  • MAK16: MAK16 homolog
  • MCPH1: microcephaly, primary autosomal recessive 1
  • MIR6850 encoding protein MicroRNA 6850
  • MRPL13 encoding protein Mitochondrial ribosomal protein L13
  • MYBL1 encoding protein MYB proto-oncogene like 1
  • NBN: nibrin
  • NDRG1: N-myc downstream regulated gene 1
  • NEF3: neurofilament 3 (150kDa medium)
  • NEFL: neurofilament, light polypeptide 68kDa
  • ODF1: outer dense fiber protein 1
  • OTUD6B: OTU domain containing 6B
  • PDP1: pyruvate dehydrogenase phosphatase catalytic subunit 1
  • PKIA: cAMP-dependent protein kinase inhibitor alpha
  • PLEC: plectin
  • PNMA2: paraneoplastic antigen Ma2
  • PREX2: phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2
  • PROSC: proline synthetase co-transcribe bacterial homolog protein
  • GLI4: encoding protein Gli family zinc finger 4
  • PURG encoding protein Purine-rich element binding protein G
  • PVT1: Pvt1 oncogene
  • RECQL4: RecQ protein-like 4
  • RNF5P1: ring finger protein 5 pseudogene 1
  • RRS1: ribosome biogenesis regulator homolog
  • RUNX1T1: runt-related transcription factor 1; translocated to, 1 (cyclin D-related)
  • SFTPC: surfactant protein C
  • SLC20A2: Sodium-dependent phosphate transporter 2
  • SLURP1: secreted LY6/PLAUR domain containing 1
  • SNAI2: snail homolog 2 (Drosophila)
  • SPAG11B: sperm-associated antigen 11B
  • STAU2: staufen double-stranded RNA binding protein 2
  • SYBU: Syntabulin
  • TG: thyroglobulin
  • THAP1: THAP domain containing, apoptosis associated protein 1
  • TMEM67: encoding protein Meckelin
  • TNFRSF11B: tumor necrosis factor receptor superfamily, member 11b
  • TONSL: encoding protein Tonsoku-like, DNA repair protein
  • TPA: tissue plasminogen activator
  • TRMT12: tRNA methyltransferase 12 homolog
  • TRPS1: trichorhinophalangeal syndrome I
  • TTI2 encoding protein TELO2 interacting protein 2
  • VCPIP1: valosin containing protein/p47 complex interacting protein 1
  • VMAT1: vesicular monoamine transporter protein
  • VPS13B: vacuolar protein sorting 13 homolog B (yeast)
  • VPS37A: vacuolar protein sorting 37 homolog A
  • WRN: Werner syndrome
  • YTHDF3: YTH N6-methyladenosine RNA binding protein 3
  • ZFP41: encoding protein ZFP41 zinc finger protein
  • ZHX2: zinc fingers and homeoboxes protein 2
  • ZMAT4: zinc finger matrin-type 4
  • ZNF16: zinc finger protein 16
  • ZNF395: encoding protein Zinc finger protein 395
  • ZNF517 encoding protein Zinc finger protein 517
  • ZNF696 encoding protein Zinc finger protein 696
  • ZNF703: zinc finger protein 703
  • ZNF706: zinc finger protein 706
  • ZNF707: encoding protein Zinc finger protein 707

Diseases and disorders[edit]

The following diseases and disorders are some of those related to genes on chromosome 8:

Cytogenetic band[edit]

G-banding ideograms of human chromosome 8
G-banding ideogram of human chromosome 8 in resolution 850 bphs. Band length in this diagram is proportional to base-pair length. This type of ideogram is generally used in genome browsers (e.g. Ensembl, UCSC Genome Browser).
G-banding patterns of human chromosome 8 in three different resolutions (400,[16] 550[17] and 850[4]). Band length in this diagram is based on the ideograms from ISCN (2013).[18] This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process.[19]
G-bands of human chromosome 8 in resolution 850 bphs[4]
Chr.Arm[20]Band[21]ISCN
start[22]
ISCN
stop[22]
Basepair
start
Basepair
stop
Stain[23]Density
8p23.3011512,300,000gneg
8p23.21153312,300,0016,300,000gpos75
8p23.13316906,300,00112,800,000gneg
8p2269099212,800,00119,200,000gpos100
8p21.3992117919,200,00123,500,000gneg
8p21.21179138023,500,00127,500,000gpos50
8p21.11380163927,500,00129,000,000gneg
8p12163918972,900,000136,700,000gpos75
8p11.231897204136,700,00138,500,000gneg
8p11.222041215638,500,00139,900,000gpos25
8p11.212156234339,900,00143,200,000gneg
8p11.12343247243,200,00145,200,000acen
8q11.12472264545,200,00147,200,000acen
8q11.212645281747,200,00151,300,000gneg
8q11.222817303351,300,00151,700,000gpos75
8q11.233033327751,700,00154,600,000gneg
8q12.13277349354,600,00160,600,000gpos50
8q12.23493362260,600,00161,300,000gneg
8q12.33622380961,300,00165,100,000gpos50
8q13.13809393865,100,00167,100,000gneg
8q13.23938409667,100,00169,600,000gpos50
8q13.34096431269,600,00172,000,000gneg
8q21.11431245457,200,000174,600,000gpos100
8q21.124545462874,600,00174,700,000gneg
8q21.134628485874,700,00183,500,000gpos75
8q21.24858495983,500,00185,900,000gneg
8q21.34959528985,900,00192,300,000gpos100
8q22.15289557792,300,00197,900,000gneg
8q22.25577569297,900,001100,500,000gpos25
8q22.356925922100,500,001105,100,000gneg
8q23.159226152105,100,001109,500,000gpos75
8q23.261526267109,500,001111,100,000gneg
8q23.362676611111,100,001116,700,000gpos100
8q24.1166116726116,700,001118,300,000gneg
8q24.1267266942118,300,001121,500,000gpos50
8q24.1369427244121,500,001126,300,000gneg
8q24.2172447431126,300,001130,400,000gpos50
8q24.2274317661130,400,001135,400,000gneg
8q24.2376617804135,400,001138,900,000gpos75
8q24.378048250138,900,001145,138,636gneg

References[edit]

  1. ^ "Human Genome Assembly GRCh38 - Genome Reference Consortium". National Center for Biotechnology Information. 2013-12-24. Retrieved 2017-03-04.
  2. ^ Jump up to:a b "Search results - 8[CHR] AND "Homo sapiens"[Organism] AND ("has ccds"[Properties] AND alive[prop]) - Gene". NCBI. CCDS Release 20 for Homo sapiens. 2016-09-08. Retrieved 2017-05-28.
  3. ^ Tom Strachan; Andrew Read (2 April 2010). Human Molecular Genetics. Garland Science. p. 45. ISBN 978-1-136-84407-2.
  4. ^ Jump up to:a b c Genome Decoration Page, NCBI. Ideogram data for Homo sapience (850 bphs, Assembly GRCh38.p3). Last update 2014-06-03. Retrieved 2017-04-26.
  5. ^ Jump up to:a b Tabarés-Seisdedos R, Rubenstein JL; Rubenstein (2009). "Chromosome 8p as a potential hub for developmental neuropsychiatric disorders: implications for schizophrenia, autism and cancer". Mol Psychiatry. 14 (6): 563–89. doi:10.1038/mp.2009.2. PMID 19204725.
  6. ^ Pertea M, Salzberg SL (2010). "Between a chicken and a grape: estimating the number of human genes". Genome Biol. 11 (5): 206. doi:10.1186/gb-2010-11-5-206. PMC 2898077. PMID 20441615.
  7. ^ "Statistics & Downloads for chromosome 8". HUGO Gene Nomenclature Committee. 2017-05-12. Retrieved 2017-05-19.
  8. ^ "Chromosome 8: Chromosome summary - Homo sapiens". Ensembl Release 88. 2017-03-29. Archived from the original on 2019-12-03. Retrieved 2017-05-19.
  9. ^ "Human chromosome 8: entries, gene names and cross-references to MIM". UniProt. 2018-02-28. Retrieved 2018-03-16.
  10. ^ "Search results - 8[CHR] AND "Homo sapiens"[Organism] AND ("genetype protein coding"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  11. ^ "Search results - 8[CHR] AND "Homo sapiens"[Organism] AND ( ("genetype miscrna"[Properties] OR "genetype ncrna"[Properties] OR "genetype rrna"[Properties] OR "genetype trna"[Properties] OR "genetype scrna"[Properties] OR "genetype snrna"[Properties] OR "genetype snorna"[Properties]) NOT "genetype protein coding"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  12. ^ "Search results - 8[CHR] AND "Homo sapiens"[Organism] AND ("genetype pseudo"[Properties] AND alive[prop]) - Gene". NCBI. 2017-05-19. Retrieved 2017-05-20.
  13. ^ Blouin JL, Dombroski BA, Nath SK, et al. (September 1998). "Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21". Nat. Genet. 20 (1): 70–3. doi:10.1038/1734. PMID 9731535.
  14. ^ Gurling HM, Kalsi G, Brynjolfson J, et al. (March 2001). "Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23". Am. J. Hum. Genet. 68 (3): 661–73. doi:10.1086/318788. PMC 1274479. PMID 11179014.
  15. ^ Suarez BK, Duan J, Sanders AR, et al. (February 2006). "Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample". Am. J. Hum. Genet. 78 (2): 315–33. doi:10.1086/500272. PMC 1380238. PMID 16400611.
  16. ^ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (400 bphs, Assembly GRCh38.p3). Last update 2014-03-04. Retrieved 2017-04-26.
  17. ^ Genome Decoration Page, NCBI. Ideogram data for Homo sapience (550 bphs, Assembly GRCh38.p3). Last update 2015-08-11. Retrieved 2017-04-26.
  18. ^ International Standing Committee on Human Cytogenetic Nomenclature (2013). ISCN 2013: An International System for Human Cytogenetic Nomenclature (2013). Karger Medical and Scientific Publishers. ISBN 978-3-318-02253-7.
  19. ^ Sethakulvichai, W.; Manitpornsut, S.; Wiboonrat, M.; Lilakiatsakun, W.; Assawamakin, A.; Tongsima, S. (2012). "Estimation of band level resolutions of human chromosome images". In Computer Science and Software Engineering (JCSSE), 2012 International Joint Conference on: 276–282. doi:10.1109/JCSSE.2012.6261965. ISBN 978-1-4673-1921-8.
  20. ^ "p": Short arm; "q": Long arm.
  21. ^ For cytogenetic banding nomenclature, see article locus.
  22. ^ Jump up to:a b These values (ISCN start/stop) are based on the length of bands/ideograms from the ISCN book, An International System for Human Cytogenetic Nomenclature (2013). Arbitrary unit.
  23. ^ gpos: Region which is positively stained by G banding, generally AT-rich and gene poor; gneg: Region which is negatively stained by G banding, generally CG-rich and gene rich; acen Centromere. var: Variable region; stalk: Stalk.

External links[edit]

  • National Institutes of Health. "Chromosome 8". Genetics Home Reference. Retrieved 2017-05-06.
  • "Chromosome 8". Human Genome Project Information Archive 1990–2003. Retrieved 2017-05-06.

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