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All known mutations in two different genes in the patients' DNA samples were identified correctly.
Problem DNA samples were identified as rows for which the value on the diagonal (the self similarity) was small.
Twenty-one tumour DNA samples were identified by CGH to show gain of 2p material and these were selected for RT PCR analysis.
The genotypes of the DNA samples were identified without knowledge of the case or control status; 5% were randomly selected as a sample set of cases and controls that were genotyped by different investigators, and the reproducibility was 100%.
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Each DNA sample was identified by a number followed by the Lutzomyia species it was extracted from.
On the basis of DNA sequencing, 3 brain samples were identified as containing A. cantonensis DNA (GenBank accession nos. KP231729, KP231728, and KP231727).
The PCR positive samples were identified by DNA sequencing of the internal transcribed spacer (ITS) region of the rRNA gene.
The species of the fungus in the PCR positive samples were identified by DNA sequencing of the internal transcribed spacer (ITS) region of the rRNA gene.
However, a significant number of gender-specific DNA methylation differences between male and female samples were identified, which might play a role in gender-specific life span extension, for example, different gene expression regulation.
Therefore, only 34 Rhodiola samples were identified according to their DNA sequences.
Also in 2002 and 2003, 109 L2b-positive samples of 403 C. trachomatis DNA positive rectal samples were identified, of which 45 were strain L2b, and these have been described in a previous publication (5 ).
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