10 research outputs found
Genotypes
Genotypes: Individual genotypes for each sample at each of the 19,703 loci. Sample ID is population abbreviation (see Table 1) followed by "xXXX", where XXX is a three digit numerical identifier
Allele Frequencies
Allele Frequencies - The frequency of the major allele (P) is indicated for each of 19,703 SNP loci for each population (indicated by abbreviation as described in Table 1), including the global average MAF, and the global average genotype success rate (GSR)
LOSITAN-Rangewide
Input file for Lositan for all populations, 19,703 SNP
Ots_RADcatalog_21504SNPs
Pre-filtered RAD catalog of 21,504 SNP
Mantel-Hecht-Moran FST full matrices
Input files for Mantel test between Hecht Fst values and Moran et al. (2013) Fst values. Each set of Fst values are included in full matrix format in separate tabs of the Excel file. See Table S2 for corresponding triangular matrices and results of Mantel tests
RDA_AlleleFreq
Input file of allele frequencies for 19,703 SNPs for RD
GENEPOP-Rangewide_NeutralSNPs
Input file for GENEPO
PCA-adegenet_neutralSNPs
Input file for PCA in adgenet for all populations; 5,007 putatively adaptive SNP
RDA_BIOCLIMDATA
Input file of environmental factors included for RD
Hardy Weinberg equilibrium
Hardy Weinberg equilibrium: Locus summary by population including estimates of the genotyping success rate (GSR), the P-value from a chi-square test of the deviation from Hardy-Weinberg Equilibrium (HWE, * reported is the raw uncorrected p-value, the Bonferroni threshold p-value for 19,703 comparisons at α=0.05 level is 0.05/19703 = 0.00000254), the observed heterozygosity (Ho), the expected heterozygosity based on HWE (He), and the minor allele (Q) frequency (MAF). Populations are numbered according to Table 1, and the colored font corresponds to the lineage of the population (blue, North Coastal Lineage; red, South Coastal Lineage; green, Interior Columbia River Stream-Type Lineage)