This new release enable map-independent imputations of a VCF file created by STACKS. Two options are available for imputations: using Random Forest or the most frequent category. Before imputations, the VCF file can be filtered with: a whitelist of loci (to keep only specific loci...) a blacklist of individuals (to remove individuals or entire populations...) Also, a list of genotypes with bad coverage and/or genotype likelihood can be supplied to erase the genotypes before imputations (for more details look at the function: blacklist_erase_genotype)
<p>Given a pedigree tree of 3,671 Hutterites (1), 1,415 individuals in the three most recent generat...
These functions can be used to filter a vcf file. They can remove loci that have a given amount miss...
The advent of genome-wide association studies (GWAS) revolutionized the field of complex disease gen...
vcf2plink: to easily convert a VCF file created in STACKS to a PLINK input file (tped/tfam format)....
This new release introduce haplo2fstat function. Similar to the other 'haplo2...' functions, you can...
New release with imputations using Random Forest or the most frequent allele. The imputations comput...
This is the final cleaned and filtered VCF file used for downstream population genetic and landscape...
v.0.2.2 vcf2genepop: to easily convert a VCF file created in STACKS to a genepop input file. This ...
v.0.3.6 fixed a bug in vcf_imputation, the function now calls genomic_converter with all the bell...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
This utility sorts and (optionally) filters the rows/variants of a VCF file (containing data for 2 o...
Sample list and characteristics, imputed and non imputed vcf files. "h2dom.tar.gz" contains 3 files:...
v.0.3.0 Update that makes my coding life easier. Several internal functions to convert from a tidy...
This is the final cleaned and filtered VCF file output from the program ipyrad for our data (https:/...
National audienceThe software DiscoSnp++ is designed to detect genomic variants such as Single Nucle...
<p>Given a pedigree tree of 3,671 Hutterites (1), 1,415 individuals in the three most recent generat...
These functions can be used to filter a vcf file. They can remove loci that have a given amount miss...
The advent of genome-wide association studies (GWAS) revolutionized the field of complex disease gen...
vcf2plink: to easily convert a VCF file created in STACKS to a PLINK input file (tped/tfam format)....
This new release introduce haplo2fstat function. Similar to the other 'haplo2...' functions, you can...
New release with imputations using Random Forest or the most frequent allele. The imputations comput...
This is the final cleaned and filtered VCF file used for downstream population genetic and landscape...
v.0.2.2 vcf2genepop: to easily convert a VCF file created in STACKS to a genepop input file. This ...
v.0.3.6 fixed a bug in vcf_imputation, the function now calls genomic_converter with all the bell...
VCF file containing imputed genotype data belonging to 67 newly sequenced and publicly available anc...
This utility sorts and (optionally) filters the rows/variants of a VCF file (containing data for 2 o...
Sample list and characteristics, imputed and non imputed vcf files. "h2dom.tar.gz" contains 3 files:...
v.0.3.0 Update that makes my coding life easier. Several internal functions to convert from a tidy...
This is the final cleaned and filtered VCF file output from the program ipyrad for our data (https:/...
National audienceThe software DiscoSnp++ is designed to detect genomic variants such as Single Nucle...
<p>Given a pedigree tree of 3,671 Hutterites (1), 1,415 individuals in the three most recent generat...
These functions can be used to filter a vcf file. They can remove loci that have a given amount miss...
The advent of genome-wide association studies (GWAS) revolutionized the field of complex disease gen...