This repository holds a short script that allows loading a genetic dataset (genotype calls) derived from OpenArray technology and transforming it into a handly-format file, which can be further imported to PLINK software. Basically, this script carries out a dataset manipulation and transformation from long to wide format. In order to run the script, you will need: An input file derived from OpenArray technology in the long format containing information for three columns (NCBI_SNP_Reference, Sample_ID and Genotype_Call). Change the arguments "aa" and "cc" according to your experimental design and characteristics
We created a suite of packages to enable analysis of extremely large genomic data sets (potentially ...
Script simulates selfing, and creation of full-sibling, half-sibling, and first cousins in proportio...
This compressed directory contains the allele frequency data ('p*') and associated scripts for the a...
This repository holds a short script that allows loading a genetic dataset (genotype calls) derived ...
This repository holds two short scripts: A) The first one with name "script_from_long_to_wide.r" is...
This text file contains scripts and notes for the steps used in converting raw Illumina GBS sequenci...
Genotyping microarrays are an important and widely-used tool in genetics. I present argyle, an R pac...
R markdown script used to generate the accession means that were used in the genome-wide association...
Supporting files for manuscript "Evolutionary histories of breast cancer and related clones". Conte...
This is a custom R script used to count the number of Haplotypic Alleles in a SNP table (in this cas...
Input file for estimation of the SNP error rate. The R script to analyse this file is provided by Ma...
This package contains the R-script used for simulating genetic data of two (or more) populations of ...
Input file for estimation of the SNP error rate. The R script to analyse this file is provided by Ma...
Input file for estimation of the SNP error rate. The R script to analyse this file is provided by Ma...
Input file for estimation of the SNP error rate. The R script to analyse this file is provided by Ma...
We created a suite of packages to enable analysis of extremely large genomic data sets (potentially ...
Script simulates selfing, and creation of full-sibling, half-sibling, and first cousins in proportio...
This compressed directory contains the allele frequency data ('p*') and associated scripts for the a...
This repository holds a short script that allows loading a genetic dataset (genotype calls) derived ...
This repository holds two short scripts: A) The first one with name "script_from_long_to_wide.r" is...
This text file contains scripts and notes for the steps used in converting raw Illumina GBS sequenci...
Genotyping microarrays are an important and widely-used tool in genetics. I present argyle, an R pac...
R markdown script used to generate the accession means that were used in the genome-wide association...
Supporting files for manuscript "Evolutionary histories of breast cancer and related clones". Conte...
This is a custom R script used to count the number of Haplotypic Alleles in a SNP table (in this cas...
Input file for estimation of the SNP error rate. The R script to analyse this file is provided by Ma...
This package contains the R-script used for simulating genetic data of two (or more) populations of ...
Input file for estimation of the SNP error rate. The R script to analyse this file is provided by Ma...
Input file for estimation of the SNP error rate. The R script to analyse this file is provided by Ma...
Input file for estimation of the SNP error rate. The R script to analyse this file is provided by Ma...
We created a suite of packages to enable analysis of extremely large genomic data sets (potentially ...
Script simulates selfing, and creation of full-sibling, half-sibling, and first cousins in proportio...
This compressed directory contains the allele frequency data ('p*') and associated scripts for the a...