vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more information
Genotype likelihoods in vcf file format for the full data set including all 621 individuals
VCF file containing genotype data at all 6136 SNP markers retained after quality filters and for all...
Single nucleotide polymorphism data for all individuals. Used for DAPC analyses and calculating f-st...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
This text file contains the filtered genetic data (SNP set) in variant call format (vcf). This inclu...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
Annotated VCF file containing allele frequency and read depths of the 14 samples described in Bergla...
VCF file with information of all 4559 SNPs used for analyses in the publication. It can be converted...
This is a .vcf file produced by calling variant genetic sites using samtools and bcftools. For each ...
This file is the set of single nucleotide polymorphisms and insertion/deletions in a population of D...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
A VCF file containing a random subset (1%) of all SNPs discovered in this study. This file was used ...
The VCF file containing alll SNPs identified by STACKS. This file was filtered and further used to a...
VCF file containing data for 1286 individuals and 12666 loci. Minor allele frequency cut-off of 0.05...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
Genotype likelihoods in vcf file format for the full data set including all 621 individuals
VCF file containing genotype data at all 6136 SNP markers retained after quality filters and for all...
Single nucleotide polymorphism data for all individuals. Used for DAPC analyses and calculating f-st...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
This text file contains the filtered genetic data (SNP set) in variant call format (vcf). This inclu...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
Annotated VCF file containing allele frequency and read depths of the 14 samples described in Bergla...
VCF file with information of all 4559 SNPs used for analyses in the publication. It can be converted...
This is a .vcf file produced by calling variant genetic sites using samtools and bcftools. For each ...
This file is the set of single nucleotide polymorphisms and insertion/deletions in a population of D...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
A VCF file containing a random subset (1%) of all SNPs discovered in this study. This file was used ...
The VCF file containing alll SNPs identified by STACKS. This file was filtered and further used to a...
VCF file containing data for 1286 individuals and 12666 loci. Minor allele frequency cut-off of 0.05...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
Genotype likelihoods in vcf file format for the full data set including all 621 individuals
VCF file containing genotype data at all 6136 SNP markers retained after quality filters and for all...
Single nucleotide polymorphism data for all individuals. Used for DAPC analyses and calculating f-st...
DOI
Add to ORKG