This text file contains scripts and notes for the steps used in converting raw Illumina GBS sequencing reads to individual genotypes (at both variant and invariant sites) across the genome. The resulting genotype files (in "012NA" format) were then used as input into R, for the rest of the analysis and production of figures
Configuration files and bash scripts used in the following study: "The genotype-phenotype map of an ...
This is a custom R script used to count the number of Haplotypic Alleles in a SNP table (in this cas...
Scripts accompanying Benonisdottir and Kong (2023), 'Studying the genetics of participation using fo...
This text file contains scripts and notes for the steps used in converting raw Illumina GBS sequenci...
This repository holds a short script that allows loading a genetic dataset (genotype calls) derived ...
This compressed directory contains the allele frequency data ('p*') and associated scripts for the a...
This folder contains genotypic information for variant sites only (no invariant sites) across the wh...
Scripts for aligning reads, calling SNPs and converting files for downstream population genomic anal...
This repository holds two short scripts: A) The first one with name "script_from_long_to_wide.r" is...
Making figures and tables for publication. Each zip archive contains input data, shell script to ini...
Genotyping-by-sequencing (GBS) and related methods are increasingly used for studies of non-model or...
Data and R scripts to generate Figures - Perspective paper on Gene Editing - Visscher et al. (2023) ...
Bam files and script used to conduct analyses for the article " Population genomic SNPs from epigene...
R and shell scripts to perform genome scan analyses. See README for details on how to use script
A major goal for biologists is to understand the connection between genes and phenotypic traits, and...
Configuration files and bash scripts used in the following study: "The genotype-phenotype map of an ...
This is a custom R script used to count the number of Haplotypic Alleles in a SNP table (in this cas...
Scripts accompanying Benonisdottir and Kong (2023), 'Studying the genetics of participation using fo...
This text file contains scripts and notes for the steps used in converting raw Illumina GBS sequenci...
This repository holds a short script that allows loading a genetic dataset (genotype calls) derived ...
This compressed directory contains the allele frequency data ('p*') and associated scripts for the a...
This folder contains genotypic information for variant sites only (no invariant sites) across the wh...
Scripts for aligning reads, calling SNPs and converting files for downstream population genomic anal...
This repository holds two short scripts: A) The first one with name "script_from_long_to_wide.r" is...
Making figures and tables for publication. Each zip archive contains input data, shell script to ini...
Genotyping-by-sequencing (GBS) and related methods are increasingly used for studies of non-model or...
Data and R scripts to generate Figures - Perspective paper on Gene Editing - Visscher et al. (2023) ...
Bam files and script used to conduct analyses for the article " Population genomic SNPs from epigene...
R and shell scripts to perform genome scan analyses. See README for details on how to use script
A major goal for biologists is to understand the connection between genes and phenotypic traits, and...
Configuration files and bash scripts used in the following study: "The genotype-phenotype map of an ...
This is a custom R script used to count the number of Haplotypic Alleles in a SNP table (in this cas...
Scripts accompanying Benonisdottir and Kong (2023), 'Studying the genetics of participation using fo...
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