The best scoring ML tree was selected from 30 GARLI analyses under a GTR model.

<p>Numbers above branches are ML bootstrap support values, and the numbers below branches are bootstrap support values.</p

Estimates of nucleotide diversity and test statistics for selection at DMC1 in polyploidy and diploid H genome.

<p>The N is the number of sequences analyzed, h is the number of haplotypes, n is the number of the sites (excluding sites with gaps/missing data), s is the number of segregating sites, π is the average pairwise diversity, θ_w is the diversity based on the number of segregating sites.</p>*<p>: Significant at α = 0.05.</p

Genetic diversity and diversity ratio in domesticated and non-domesticated gene regions of barley chromosomes.

<p>*: diversity ratio = (diversity of wild type—diversity of cultivated type)/diversity of wild type×100%</p><p>Genetic diversity and diversity ratio in domesticated and non-domesticated gene regions of barley chromosomes.</p

Legislative Documents

Also, variously referred to as: Senate bills; Senate documents; Senate legislative documents; legislative documents; and General Court documents

The SSR markers in domesticated regions and non-domesticated regions divided based on the genetic distance (cM).

<p>The location of SSR marker in each linkage group is mainly based on Varshney et al. (2007) [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0121106#pone.0121106.ref043" target="_blank">43</a>]. The dot on the chromosome represented the position of domesticated genes: <i>Ppd-H2</i> gene on chromosome 1H, <i>Ppd-H1</i> gene (top) and <i>Vrs1</i> gene (bottom) on chromosome 2H, <i>btr1</i> and <i>btr2</i> genes (linked tightly) on 3H, <i>Sgh1</i> gene on the 4H, main QTLs (<i>SD1</i>, top and <i>SD2</i>, bottom) on chromosome 5H, and <i>nud</i> gene on the chromosome 7H, No domesticated gene on 6H chromosome.</p

Additional file 12: of Transcriptome analysis reveals new microRNAs-mediated pathway involved in anther development in male sterile wheat

Table S8. Details of differentially expressed known and novel miRNAs in NN2 and SL2 plants. (XLSX 12 kb

Additional file 2: of Transcriptome analysis reveals new microRNAs-mediated pathway involved in anther development in male sterile wheat

Figure S1. Morphological features of wheat lines HZ09, 337S and Huamai 2566 at sowing time for short day-length/low temperature condition. (JPG 216 kb

Additional file 1: of Transcriptome analysis reveals new microRNAs-mediated pathway involved in anther development in male sterile wheat

Table S1. The primers used for qRT-PCR in this study. (XLSX 12 kb

Additional file 17: of Transcriptome analysis reveals new microRNAs-mediated pathway involved in anther development in male sterile wheat

Table S12. List of identified targets of differentially expressed miRNAs which were obtained from comparative analysis of SL1 and NN1, SL1 and NN1 together. (XLSX 53 kb

Additional file 10: of Transcriptome analysis reveals new microRNAs-mediated pathway involved in anther development in male sterile wheat

Figure S4. Venn charts of differentially expressed miRNAs between SL1 vs NN1 and SL2 vs NN2. (JPG 34 kb