10 research outputs found

    Verification of assay on amplified libraries with shotgun sequencing data.

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    1<p>As discussed in the methods section, the assay percentages are meant as a guide to compare samples and are not expected to match the absolute values yielded via shotgun sequencing.</p>2<p>The scaled shotgun sequencing results do not include reads without BLAST matches or reads which matched higher taxonomic levels (e.g., eukaryotes or metazoa).</p>3<p><i>N/A</i> indicates the primer set did not fluoresce before the negative control for the sample.</p

    Directions to interpret qPCR assay data.

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    <p>Follow the questions in the flowchart to compare the endogenous DNA content of different ancient plant samples. The least contaminated samples are best suited for shotgun sequencing.</p

    Taxonomic distribution of non-maize HiSeq 2000 reads from cDNA and DNA sets:

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    <p>(<b>a</b>) represents cDNA sample 935130, (<b>b</b>) represents cDNA sample 935230, and (<b>c</b>) represents a DNA shotgun sample from <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0050961#pone.0050961-Bannister1" target="_blank">[25]</a> 100,00 randomly sampled unmapped reads were used to perform BLAST searches and MEGAN was for taxonomic characterization of non-maize reference genome (non-B73) reads.</p

    Kernel and sample information and names.

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    <p>A total of 6 kernels were utilized for either RNA or DNA extraction only, or co-extracted for DNA and RNA. After nucleic acids were co-extracted, samples were divided into 2 aliquots, and RNA samples were DNase treated and DNA samples were RNase treated (see Methods and Supplementary Methods S1), and labeled with unique sample names.</p
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