34 research outputs found
Haplotype diversity, nucleotide diversity of different ploidy populations of <i>S</i>. <i>spontaneum</i> according to rDNA-ITS haplotype data.
Haplotype diversity, nucleotide diversity of different ploidy populations of S. spontaneum according to rDNA-ITS haplotype data.</p
Molecular variance (AMOVA) analysis among different ploidy populations according to rDNA-ITS haplotype data.
<p>Molecular variance (AMOVA) analysis among different ploidy populations according to rDNA-ITS haplotype data.</p
The GC content analysis of composition of ITS sequence of different ploidy populations of <i>S</i>. <i>spontaneum</i>.
<p>The GC content analysis of composition of ITS sequence of different ploidy populations of <i>S</i>. <i>spontaneum</i>.</p
Molecular variance (AMOVA) analysis among different ploidy populations according to rDNA-ITS haplotype data.
Molecular variance (AMOVA) analysis among different ploidy populations according to rDNA-ITS haplotype data.</p
The list of clones of <i>S</i>. <i>spontaneum</i> used in this study.
<p>The list of clones of <i>S</i>. <i>spontaneum</i> used in this study.</p
The analysis of variable sites of ITS sequence of different ploidy populations of <i>S</i>. <i>spontaneum</i>.
<p>The analysis of variable sites of ITS sequence of different ploidy populations of <i>S</i>. <i>spontaneum</i>.</p
Pairwise Gst (above the diagonal) and Nm (below the diagonal) among different ploidy populations according to rDNA-ITS data.
<p>Pairwise Gst (above the diagonal) and Nm (below the diagonal) among different ploidy populations according to rDNA-ITS data.</p
The ML and NJ phylogenetic tree based on rDNA-ITS haplotype data of different polyploid clones of <i>S</i>. <i>spontaneum</i>.
<p>The ML and NJ phylogenetic tree based on rDNA-ITS haplotype data of different polyploid clones of <i>S</i>. <i>spontaneum</i>.</p
Additional file 3: of An improved suppression subtractive hybridization technique to develop species-specific repetitive sequences from Erianthus arundinaceus (Saccharum complex)
Figure S3. Electrophoresis of secondary PCR products after SSH. M: 100 bp marker; Lanes 1–4: products of subtracted second PCR by 62 °C, 64 °C, 66 °C, 68 °C. 20 μM primers and 0.5 U LA Taq polymerase (a), 20 μM primers and 1 U LA Taq polymerase (b), 30 μM primers and 0.5 U LA Taq polymerase (c). (TIF 11035 kb
