This archive contains the vcf files listing all the high quality positions kept to draw the reference allele frequency distribution for samples Pvl07 to Pvl09. Please see the Materials and methods section for a detailed description
Variant Call Format file (GZipped) for individuals used for genotype-phenotype associations. Sample ...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
This is the raw VCF file containing all 32,978 variant genetic sites initially identified from assem...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more info...
Annotated VCF file containing allele frequency and read depths of the 14 samples described in Bergla...
The data archive contains VCF files derived from the sequenced X-QTL samples, allele frequency measu...
Fully filtered vcf file containing the genotypes for the 239 individuals genotyped at 5,907 single n...
Compressed (tgz) Vcf file containing a subset of high quality biallelic variant filtered out from th...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
VCF file containing data for 1286 individuals and 12666 loci. Minor allele frequency cut-off of 0.05...
This is the VCF of variants from the 117 M. tuberculosis samples that were used to construct the ref...
(A) Reference allele frequencies. Expected frequencies for hemizygote (F8) and heterozygote (VWF) po...
Variant Call Format file (GZipped) for individuals used for genotype-phenotype associations. Sample ...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
This is the raw VCF file containing all 32,978 variant genetic sites initially identified from assem...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
This archive contains the vcf files listing all the high quality positions kept to draw the referenc...
vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more info...
Annotated VCF file containing allele frequency and read depths of the 14 samples described in Bergla...
The data archive contains VCF files derived from the sequenced X-QTL samples, allele frequency measu...
Fully filtered vcf file containing the genotypes for the 239 individuals genotyped at 5,907 single n...
Compressed (tgz) Vcf file containing a subset of high quality biallelic variant filtered out from th...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
VCF file containing data for 1286 individuals and 12666 loci. Minor allele frequency cut-off of 0.05...
This is the VCF of variants from the 117 M. tuberculosis samples that were used to construct the ref...
(A) Reference allele frequencies. Expected frequencies for hemizygote (F8) and heterozygote (VWF) po...
Variant Call Format file (GZipped) for individuals used for genotype-phenotype associations. Sample ...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
This is the raw VCF file containing all 32,978 variant genetic sites initially identified from assem...