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The DH samples are distinguished by DH uGaN film (thickness, 120 nm) grown on the InGaN layer.
On the other hand, the cell culture samples are distinguished by a higher expression of genes associated with transcriptional regulation, e.g. Foxa2, Foxm1, Gata6, Hoxb2, Jmjd2c, Ppargc1a, and Tle1, and developmental processes, e.g. Bmp4 which is involved in the differentiation of mesenchymal cells.
Samples are distinguished by their locations in the multidimensional sample pool, each pool barcoded with a unique short DNA sequence.
Mutated samples are distinguished from normal samples by a 20-bp longer uncleaved exon 12 fragment on agarose gels (Salahshor S, et al, manuscript submitted).
Two methods were used to determine how well dysbiotic samples are distinguished from non-dysbiotic samples for multiple possible data types: multidimensional scaling (MDS) plots and BC dissimilarity indices.
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The morphology, crystallinity, elemental composition and light absorption capability of samples were distinguished based on various characterizations.
Some of these samples were distinguished by the fact that nitrogen was used in the manufacturing process.
In one experiment (identified as experiment 2 in Table S1), ten different samples were distinguished by adding unique "barcode -labeled amplification primers (provided as part of the SOLiD SREK kit).
Anopheles arabiensis samples were distinguished from other An.
Ten bands in pea and 12 bands in bean samples were distinguished in this region.
These samples were distinguished by higher potentials for gene transfer, pathogenicity, and the presence of ARGs.
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