On the subject of 
				
				the PCR test, the Family 
				Court of
				
				Weimar writes: 
				
					
					"The expert 
					witness Prof. Dr. med. Kappstein has already pointed out in 
					her testimony that the PCR test can only detect genetic 
					material, but not whether the RNA originates from viruses 
					that are capable of infection and thus capable of 
					replication (i.e. capable of reproduction)."
					
					
					
					Source
				
				
				The expert witness 
				Prof. Dr. rer. biol. hum. 
				
				Ulrike
				Kämmerer confirmed, in her testimony 
				on molecular biology, that a PCR test - even if it is carried 
				out correctly - cannot provide any information on whether a 
				person is infected with an active pathogen or not.
				
				This is because the test cannot distinguish between "dead" 
				matter, e.g. a completely harmless genome fragment as a remnant 
				of the body's own immune system's fight against a cold or flu 
				(such genome fragments can still be found many months after the 
				immune system has "dealt with" the problem) and "living" matter, 
				i.e. a "fresh" virus capable of reproducing.
				
				For example, PCR is also used in forensics to amplify residual 
				DNA from hair remains or other trace materials by means of PCR 
				in such a way that the genetic origin of a [putative] 
				perpetrator(s) can be identified ("genetic fingerprint").
				
				Even if everything is done "correctly" when carrying out the PCR, 
				including all preparatory steps (PCR design and establishment, 
				sample collection, preparation and PCR performance), and the 
				test is positive, i.e.,
				
					
					detects a genome sequence which may also 
				exist in one or even the specific "corona" virus sequence 
				(SARS-CoV-2), this does not mean, under any circumstances, that 
				the person who was tested positive is infected with a 
				replicating SARS-CoV-2 and is therefore infectious = dangerous 
				for other persons.
				
				
				Rather, in order to determine an active infection with 
				SARS-CoV-2, further - indeed specific - diagnostic methods, such 
				as the isolation of replicable viruses, must be used.
				
				Independent of the fact that, in principle, it is impossible to 
				detect an infection with the SARS-CoV-2 virus using the PCR 
				test, the results of a PCR test, according to the expert witness 
				Prof. Dr. Kämmerer, depend on a number of parameters which, 
				
				
					
						- 
						
						firstly, cause considerable uncertainties 
						 
- 
						
						secondly, can 
						be manipulated in such a way that many or few 
						(apparently) positive results are obtained 
				
				Of these sources of error, two striking ones may be singled out.
				 
				
					
					-
				One of these is the number of target genes to be tested. The WHO 
				guidelines reduced these from originally a sequence of three to 
				just one. 
					 
					
					The expert witness calculated that the use of only one 
				target gene to be tested in a mixed population of 100,000 tests, 
				with not a single person actually infected, would result in a 
				count of 2,690 false positives:
					
						
						this is based on a mean error 
				rate determined in an interlaboratory comparison. 
					
					
					Using three 
				target genes would result in only ten false positives.
If the 100,000 tests carried out were representative of 100,000 
				citizens of a city or district over a period of seven days, this 
				reduction in the number of target genes used would alone result 
				in a difference of 10 false positives compared to 2,690 false 
				positives in terms of the "daily incidence" and, depending on 
				this, the severity of the restrictions on the freedom of the 
				citizens.
If the correct "target number" of three or even better (as e.g. 
				in Thailand) up to six genes had been consistently used for the 
				PCR analysis, the rate of positive tests and thus the "7-day 
				incidence" would have been reduced almost completely to zero.
 
					
					
-
				Furthermore, the so-called 
					
					Ct-value, i.e. the number of 
				amplification/doubling steps up to which the test is still 
				considered "positive", is an additional source of error.
					
The expert witness points out that, according to unanimous 
				scientific opinion, all "positive" results that are only 
				detected from a Ct-value of 35 upwards have no scientific (i.e. 
				no evidence-based) foundation. 
					 
					
					In the Ct range 26-35, the test 
				can only be considered positive if it is matched with virus 
				cultivation. 
					 
					
					Yet the RT-qPCR test for the detection of 
				SARS-CoV-2, which was propagated worldwide with the help of 
					
					the 
				WHO, was (and following it, all other tests based on it as a 
				blueprint) set at 45 cycles without defining a Ct-value for 
				"positive".
In addition, when using the RT-q-PCR test, the WHO 
					Information 
				Notice for IVD Users 2020/05 must be observed (No. 12 of the 
				court's legal notes). 
					 
					
					Accordingly, if the 
				test result does not correspond to the clinical findings about 
				an examined person, a new sample must be taken and a further 
				examination performed, as well as a differential diagnostic; 
				only then, according to these guidelines, can a test be counted 
				as positive. 
					 
					
					According to the 
				expert report, the rapid antigen tests used for mass testing 
				cannot provide any information on infectivity, as they can only 
				detect protein components without any connection to an intact, 
				reproducible virus.
In order to allow an estimation of the infectivity of the tested 
				persons, the positive test carried out in each case (similar to 
				the RT-qPCR) would have to be individually compared with the 
				cultivability of viruses from the test sample, which is 
				impossible under the extremely variable and unverifiable test 
				conditions.
				
				
				Finally, the expert witness points out that the low specificity 
				of the tests causes a high rate of false positive results, which 
				lead to unnecessary personnel (quarantine) and social (e.g. 
				schools closed, "outbreak reports") consequences until they turn 
				out to be false alarms. 
				
				 
				
				The error, i.e. a high number of false 
				positives, is particularly high in tests on people who have no 
				symptoms.
				
				It remains to be noted that, in principle, neither the PCR test 
				nor the antigen rapid test can detect an infection with the 
				SARS-CoV-2 virus, as has been demonstrated by the expert 
				witness. 
				
				 
				
				Moreover, besides those described above, there are 
				other sources of error, which are listed in the expert opinion 
				as having serious effects, such that an adequate detection of 
				the infection with SARS-CoV-2 in [the Federal Constitutive 
				State, or Land, of] Thuringia (and nationwide) is not remotely 
				possible.
				
				In any case, the term "incidence" is misused by the Land 
				executive. 
				
				 
				
				"Incidence" actually means the occurrence of new 
				cases in a defined group of persons (repeatedly tested and, if 
				necessary, medically examined) in a defined period of time, cf. 
				No. 11 of the Legal Notes of the Court. 
				
				 
				
				In fact, however, 
				undefined groups of people are tested in undefined periods of 
				time, so that what is passed off as "incidence" is merely 
				reporting data, pure & simple.
				
				In any case, according to a meta-analysis study by medical 
				scientist and statistician John Ioannidis, one of the most cited 
				scientists worldwide, which was published in a WHO bulletin in 
				October 2020, the infection fatality rate is 0.23%, 
				
					
					which is no 
				higher than that of moderately severe influenza epidemics...
				
				
				Ioannidis also concluded, in a study published in January 2021, 
				that 
				lockdowns have no significant benefit.