<p>The genotypes show high variation with the reference when compared to pairwise combination of genotypes, indicating missing SNPs (a characteristic of RADseq) that could be imputed. Overall the numbers of SNPs between genotypes were found to be in the range of 442 to 1151.</p
<p><sup>a</sup> one sample failed to genotype.</p><p><sup>b</sup> two samples failed to genotype.</p...
Inexpensive short-read sequencing technologies applied to reduced representation genomes is revoluti...
SNP heritability, the proportion of phenotypic variance explained by SNPs, has been reported for man...
Genotype calls from RAD-seq data for 78 individuals against the Skylark reference genome. Only genot...
Effective population size (Ne) is a key parameter of population genetics. However, Ne remains challe...
<p>(A) Phylogenetic reconstruction based on the SNP of the 6,220 informative RAD markers (RAxML). Ge...
RAD genotypes at seven sex-associated loci in 286 individuals from the Wood River basin. Some loci ...
<p>Frequency of genotypes with missing data (left), and frequency of DArTseq SNPs (loci) with missin...
International audienceInexpensive short-read sequencing technologies applied to reduced representati...
RAD Sequencing (RAD-Seq) is an economical and efficient method for SNP discovery and genotyping. As ...
<p>We characterized 1611 informative RAD sites in 19 inbred lines by minor allele count (“MAC”) (max...
We present the allelic frequencies of all SNPs and natural populations. We provide information on t...
<p>Among 19 inbred lines, RAD SNPs with identical genotype patterns (LD of 1) were grouped into hapl...
genotypes for 20334 position are distributed over 16173 RAD loci; please refer to Table S1 in the ma...
<p>Summary of SNPs, Alleles, Haplotypes, and gene diversity inferred from RARseq data.</p
<p><sup>a</sup> one sample failed to genotype.</p><p><sup>b</sup> two samples failed to genotype.</p...
Inexpensive short-read sequencing technologies applied to reduced representation genomes is revoluti...
SNP heritability, the proportion of phenotypic variance explained by SNPs, has been reported for man...
Genotype calls from RAD-seq data for 78 individuals against the Skylark reference genome. Only genot...
Effective population size (Ne) is a key parameter of population genetics. However, Ne remains challe...
<p>(A) Phylogenetic reconstruction based on the SNP of the 6,220 informative RAD markers (RAxML). Ge...
RAD genotypes at seven sex-associated loci in 286 individuals from the Wood River basin. Some loci ...
<p>Frequency of genotypes with missing data (left), and frequency of DArTseq SNPs (loci) with missin...
International audienceInexpensive short-read sequencing technologies applied to reduced representati...
RAD Sequencing (RAD-Seq) is an economical and efficient method for SNP discovery and genotyping. As ...
<p>We characterized 1611 informative RAD sites in 19 inbred lines by minor allele count (“MAC”) (max...
We present the allelic frequencies of all SNPs and natural populations. We provide information on t...
<p>Among 19 inbred lines, RAD SNPs with identical genotype patterns (LD of 1) were grouped into hapl...
genotypes for 20334 position are distributed over 16173 RAD loci; please refer to Table S1 in the ma...
<p>Summary of SNPs, Alleles, Haplotypes, and gene diversity inferred from RARseq data.</p
<p><sup>a</sup> one sample failed to genotype.</p><p><sup>b</sup> two samples failed to genotype.</p...
Inexpensive short-read sequencing technologies applied to reduced representation genomes is revoluti...
SNP heritability, the proportion of phenotypic variance explained by SNPs, has been reported for man...