Variant call file listing genotypes for filtered SNPs after amplicon sequencing used in downstream analyses
SNPs identifiers in PED format relative to the PED file containing genotypes based on RAD sequencing
Amplicon sequencing (AmpSeq) is a practical, intuitive strategy with a semi-automated computational ...
Abstract Background Next-generation amplicon sequencing enables high-throughput genetic diagnostics,...
Variant call file listing genotypes for filtered SNPs after amplicon sequencing used in downstream a...
Variant call file listing genotypes for the filtered set of SNPs in the initial scan used in downstr...
Variant call file listing genotypes for the all SNPs in the initial scan in the vicinity of SNPs tar...
Variant Call Format files for chromosome encoded SNPs/InDels identified for each isolate from this s...
These are scripts we used for SNP variant calling. The locuslist provides a list of specific SNPs wh...
This file outlines the exact steps to filter variant calls into a final SNP data set. Lines are com...
The file contains the results of genotyping of analysed individuals with use of AmpliSAS pipeline. T...
In this file are the SNP data for all loci and all individuals, output by Stacks' populations module...
Filtered SNPs that have undergone VariantFiltration and also selection for presence in 75% of indivi...
File contains variant counts (snp calling) for each individual. This file was used to estimate genot...
Amplicon sequence variants (ASV) with significant differential abundance between d0 and all other da...
Raw SNP genotypes in PLINK format (i.e., .ped & .map file) before quality-control filtering
SNPs identifiers in PED format relative to the PED file containing genotypes based on RAD sequencing
Amplicon sequencing (AmpSeq) is a practical, intuitive strategy with a semi-automated computational ...
Abstract Background Next-generation amplicon sequencing enables high-throughput genetic diagnostics,...
Variant call file listing genotypes for filtered SNPs after amplicon sequencing used in downstream a...
Variant call file listing genotypes for the filtered set of SNPs in the initial scan used in downstr...
Variant call file listing genotypes for the all SNPs in the initial scan in the vicinity of SNPs tar...
Variant Call Format files for chromosome encoded SNPs/InDels identified for each isolate from this s...
These are scripts we used for SNP variant calling. The locuslist provides a list of specific SNPs wh...
This file outlines the exact steps to filter variant calls into a final SNP data set. Lines are com...
The file contains the results of genotyping of analysed individuals with use of AmpliSAS pipeline. T...
In this file are the SNP data for all loci and all individuals, output by Stacks' populations module...
Filtered SNPs that have undergone VariantFiltration and also selection for presence in 75% of indivi...
File contains variant counts (snp calling) for each individual. This file was used to estimate genot...
Amplicon sequence variants (ASV) with significant differential abundance between d0 and all other da...
Raw SNP genotypes in PLINK format (i.e., .ped & .map file) before quality-control filtering
SNPs identifiers in PED format relative to the PED file containing genotypes based on RAD sequencing
Amplicon sequencing (AmpSeq) is a practical, intuitive strategy with a semi-automated computational ...
Abstract Background Next-generation amplicon sequencing enables high-throughput genetic diagnostics,...
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