This file is the formatted input file for entropy, the hierarchical Bayesian model used in this study. The file contains data for a subset of SNPs, in a simplified genotype likelihood format. SNPs in this file have a minor allele frequency >0.05, and a maximum of 1 alternate allele. This file also contains only one locus per contig
A Single Nucleotide Polymorphism (SNP) is a position in the genome at which two or more of the possi...
<div>All structural variant, SNP and indel calls used for GWAS.<br></div><div>All filtered to have m...
The file contains the genotypes of all 948 individuals studied. Each row represents one individual.T...
This file is the formatted input file for entropy, the hierarchical Bayesian model used in this stud...
Input file for analysis with the "entropy" model. This file is a filtered version of the VCF file, i...
Input file for entropy including 1286 individuals and 12666 loci. Data are in genotype likelihood fo...
Genotype likelihoods (simplified from VCF) at 11,221 SNPs for 2785 individual Catostomus fish. This ...
Contains three genotype files (VCF) using either all twelve outcrossing populations, all eight selfi...
This text file contains the filtered genetic data (SNP set) in variant call format (vcf). This inclu...
The filtered SNP dataset used in Barth et al. as PLINK/MERLIN/Haploview text genotype table (.ped), ...
Text file (genepop input format) containing the genotypes used for population genomics analysis. The...
Abstract Rare variants are believed to play an important role in disease etiology. Recent advances i...
File with the individuals names and genotypes for the 1,047 SNPs used for the analyses
The distribution of genetic variation among populations is conveniently measured by Wright’s FST , w...
The directory contains data described by Le Scouarnec et al. (2015) for the rare variant association...
A Single Nucleotide Polymorphism (SNP) is a position in the genome at which two or more of the possi...
<div>All structural variant, SNP and indel calls used for GWAS.<br></div><div>All filtered to have m...
The file contains the genotypes of all 948 individuals studied. Each row represents one individual.T...
This file is the formatted input file for entropy, the hierarchical Bayesian model used in this stud...
Input file for analysis with the "entropy" model. This file is a filtered version of the VCF file, i...
Input file for entropy including 1286 individuals and 12666 loci. Data are in genotype likelihood fo...
Genotype likelihoods (simplified from VCF) at 11,221 SNPs for 2785 individual Catostomus fish. This ...
Contains three genotype files (VCF) using either all twelve outcrossing populations, all eight selfi...
This text file contains the filtered genetic data (SNP set) in variant call format (vcf). This inclu...
The filtered SNP dataset used in Barth et al. as PLINK/MERLIN/Haploview text genotype table (.ped), ...
Text file (genepop input format) containing the genotypes used for population genomics analysis. The...
Abstract Rare variants are believed to play an important role in disease etiology. Recent advances i...
File with the individuals names and genotypes for the 1,047 SNPs used for the analyses
The distribution of genetic variation among populations is conveniently measured by Wright’s FST , w...
The directory contains data described by Le Scouarnec et al. (2015) for the rare variant association...
A Single Nucleotide Polymorphism (SNP) is a position in the genome at which two or more of the possi...
<div>All structural variant, SNP and indel calls used for GWAS.<br></div><div>All filtered to have m...
The file contains the genotypes of all 948 individuals studied. Each row represents one individual.T...