This is the raw VCF file containing all 32,978 variant genetic sites initially identified from assembled reads
This is a vcf file containing the individuals genotyped using sdRADseq, analyzed separately. Only th...
Variant calling files (VCF) for L. montandoni individuals. Archive consists of 2886 VCF files - one ...
The VCF file containing alll SNPs identified by STACKS. This file was filtered and further used to a...
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...
<p>VCF files describing the mutations contained in the sixty-seven groups of BRCA1 reads. These were...
Compressed vcf (variant call format) file containing the genetic data for the 206,047 single nucleot...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more info...
This VCF file includes genotype calls for all 37 individuals included in the study at both variant a...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
This file is the set of single nucleotide polymorphisms and insertion/deletions in a population of D...
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...
All variant sites initially identified for analysis of hybridization. This VCF was produced using sa...
This is a vcf file containing the individuals genotyped using sdRADseq, analyzed separately. Only th...
Variant calling files (VCF) for L. montandoni individuals. Archive consists of 2886 VCF files - one ...
The VCF file containing alll SNPs identified by STACKS. This file was filtered and further used to a...
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...
<p>VCF files describing the mutations contained in the sixty-seven groups of BRCA1 reads. These were...
Compressed vcf (variant call format) file containing the genetic data for the 206,047 single nucleot...
The VCF file sontains information on the genetic variants (SNPs) identified by exome resequencing ge...
vcf including SNPs on all chromosomes, and allele frequency estimates. See README file for more info...
This VCF file includes genotype calls for all 37 individuals included in the study at both variant a...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
This file is the set of single nucleotide polymorphisms and insertion/deletions in a population of D...
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...
All variant sites initially identified for analysis of hybridization. This VCF was produced using sa...
This is a vcf file containing the individuals genotyped using sdRADseq, analyzed separately. Only th...
Variant calling files (VCF) for L. montandoni individuals. Archive consists of 2886 VCF files - one ...
The VCF file containing alll SNPs identified by STACKS. This file was filtered and further used to a...
DOI
Add to ORKG