Publication date
April 2018
DOIAbstract
This is a vcf file containing the individuals genotyped using sdRADseq, analyzed separately. Only the pruned set of loci used in the analysis are contained in this file
This is a vcf file containing the individuals genotyped using sdRADseq, analyzed separately. Only the pruned set of loci used in the analysis are contained in this file
R script for converting 'vcf' data from SNP pipeline to a single datafile of genotype and read count...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
A vcf file containing all individuals, both sdRADseq and ddRADseq, when analyzed together using stac...
VCF file with ddRad-seq dataset. This dataset comprises 8788 polymorphic loci in a sample of 300 ind...
<p>.zip file containing a .vcf file with all individuals and all loci used in analyses</p
A VCF file containing a random subset (1%) of all SNPs discovered in this study. This file was used ...
Variant call file listing genotypes for the filtered set of SNPs in the initial scan used in downstr...
vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more info...
This is a .vcf file produced by calling variant genetic sites using samtools and bcftools. For each ...
This text file contains the filtered genetic data (SNP set) in variant call format (vcf). This inclu...
Single nucleotide polymorphism data set with only in-group individuals, used in DAPC and for calcula...
Data file containing the final (filtered) variants for all individuals that were used to build the s...
This is a .vcf file containing genotypes for Chloephaga picta at RAD loci. It was generated using th...
Single nucleotide polymorphism data for all individuals. Used for DAPC analyses and calculating f-st...
R script for converting 'vcf' data from SNP pipeline to a single datafile of genotype and read count...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
A vcf file containing all individuals, both sdRADseq and ddRADseq, when analyzed together using stac...
VCF file with ddRad-seq dataset. This dataset comprises 8788 polymorphic loci in a sample of 300 ind...
<p>.zip file containing a .vcf file with all individuals and all loci used in analyses</p
A VCF file containing a random subset (1%) of all SNPs discovered in this study. This file was used ...
Variant call file listing genotypes for the filtered set of SNPs in the initial scan used in downstr...
vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more info...
This is a .vcf file produced by calling variant genetic sites using samtools and bcftools. For each ...
This text file contains the filtered genetic data (SNP set) in variant call format (vcf). This inclu...
Single nucleotide polymorphism data set with only in-group individuals, used in DAPC and for calcula...
Data file containing the final (filtered) variants for all individuals that were used to build the s...
This is a .vcf file containing genotypes for Chloephaga picta at RAD loci. It was generated using th...
Single nucleotide polymorphism data for all individuals. Used for DAPC analyses and calculating f-st...
R script for converting 'vcf' data from SNP pipeline to a single datafile of genotype and read count...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
Add to ORKG