The data archive contains VCF files derived from the sequenced X-QTL samples, allele frequency measurements based on the VCF files and the R scripts used to process the allele frequency measurements to map and plot QTL
<p>Data, logs and code for genomic vcf genotypes file for the Morrow lab, D.melanogaster LHM sequenc...
This file contains 1) metadata that describes each sample used, 2) quality scores from sequencing on...
Variant Call Format file (GZipped) for individuals used for genotype-phenotype associations. Sample ...
vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more info...
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...
RAD, transcriptomic, and microsatellite data used in the manuscript, as well as inputs/outputs of an...
Annotated VCF file containing allele frequency and read depths of the 14 samples described in Bergla...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
VCF file containing data for 1286 individuals and 12666 loci. Minor allele frequency cut-off of 0.05...
This text file contains the filtered genetic data (SNP set) in variant call format (vcf). This inclu...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
This is a .vcf file produced by calling variant genetic sites using samtools and bcftools. For each ...
<p>Data, logs and code for genomic vcf genotypes file for the Morrow lab, D.melanogaster LHM sequenc...
This file contains 1) metadata that describes each sample used, 2) quality scores from sequencing on...
Variant Call Format file (GZipped) for individuals used for genotype-phenotype associations. Sample ...
vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more info...
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...
RAD, transcriptomic, and microsatellite data used in the manuscript, as well as inputs/outputs of an...
Annotated VCF file containing allele frequency and read depths of the 14 samples described in Bergla...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
VCF file containing data for 1286 individuals and 12666 loci. Minor allele frequency cut-off of 0.05...
This text file contains the filtered genetic data (SNP set) in variant call format (vcf). This inclu...
VCF file contains 255,290 bi-allelic SNPs identified from RADseq data from 182 samples using stacks ...
This is a .vcf file produced by calling variant genetic sites using samtools and bcftools. For each ...
<p>Data, logs and code for genomic vcf genotypes file for the Morrow lab, D.melanogaster LHM sequenc...
This file contains 1) metadata that describes each sample used, 2) quality scores from sequencing on...
Variant Call Format file (GZipped) for individuals used for genotype-phenotype associations. Sample ...
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