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The extent of metabolomic alteration which occurs in haemolysed samples is unknown.
Although the storage history of the samples is unknown, the following conclusions can be drawn: Chinese papers are largely neutral with pH mostly between 6 and 8, with only a small proportion of samples with pH < 6 (10%).
However, we can not exclude that such differences pre-existed to the burial of the samples as both the pre-burial and burial history of the samples is unknown.
However, BRCA1 splicing pattern in breast tissue samples is unknown.
The cell linage of the lung cancer patient samples is unknown.
Most often the exact storage history of 'naturally' aged seed samples is unknown.
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The excipients of FK2 samples are unknown.
If the fault samples are unknown, they will be added in historical dataset and the SWKC-GS is used to partition the mixed dataset and update the clustering results for diagnosing new fault.
Similarly, the sensitivities of filovirus serological assays on bat samples are unknown.
As the source organisms of proteins from environmental samples are unknown, a detailed analysis of the taxonomic distribution is currently impossible.
Most studies (e.g. [18]) rely on the repetition of results to verify apparent homozygotes, since the true genotypes of the samples are unknown.
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