Publication date
October 2013
DOIAbstract
Python scripts used for VCF files filtering, Fst simulations and allele specific gene expression assesment
Python scripts used for VCF files filtering, Fst simulations and allele specific gene expression assesment
Scripts for aligning reads, calling SNPs and converting files for downstream population genomic anal...
R scripts for extraction of SNP types from .VCF files, and for PGLS analyses Phenotype data used in...
This zip file contains multiple Python scripts called by the scripts in the GenBank Main Scripts fil...
Python scripts used in study to generate results and posterior predictive simulations. Information a...
Sliding window analyses python3 script used to perform sliding window analyses over a vcf file in Ba...
The set of scripts used for SNPs calling, expression analyses, Fst calculation and pedigree-based si...
Python script that downsamples the population sizes and calculates the joint folded Site Frequency S...
Python scripts for processing of reactivity profiles for MS2 RNA which has undergone X-ray footprint...
Script to calculate allele frequencies from a filtered VCF (.geno) file. Open in a text editor to se...
Nucleotide alignments of individual chloroplast genes. Python scripts for removal of masked sites. D...
This file contains the python scripts used in this study. These scripts can be used to analysis next...
Python script that downsamples the population sizes and calculates the joint folded Site Frequency S...
A Python script to construct FASTA files containing reconstructed genome sequences of evolved clones...
All relevant scripts used to format files, analyse data and obtain results from sequence capture exp...
R script for converting 'vcf' data from SNP pipeline to a single datafile of genotype and read count...
Scripts for aligning reads, calling SNPs and converting files for downstream population genomic anal...
R scripts for extraction of SNP types from .VCF files, and for PGLS analyses Phenotype data used in...
This zip file contains multiple Python scripts called by the scripts in the GenBank Main Scripts fil...
Python scripts used in study to generate results and posterior predictive simulations. Information a...
Sliding window analyses python3 script used to perform sliding window analyses over a vcf file in Ba...
The set of scripts used for SNPs calling, expression analyses, Fst calculation and pedigree-based si...
Python script that downsamples the population sizes and calculates the joint folded Site Frequency S...
Python scripts for processing of reactivity profiles for MS2 RNA which has undergone X-ray footprint...
Script to calculate allele frequencies from a filtered VCF (.geno) file. Open in a text editor to se...
Nucleotide alignments of individual chloroplast genes. Python scripts for removal of masked sites. D...
This file contains the python scripts used in this study. These scripts can be used to analysis next...
Python script that downsamples the population sizes and calculates the joint folded Site Frequency S...
A Python script to construct FASTA files containing reconstructed genome sequences of evolved clones...
All relevant scripts used to format files, analyse data and obtain results from sequence capture exp...
R script for converting 'vcf' data from SNP pipeline to a single datafile of genotype and read count...
Scripts for aligning reads, calling SNPs and converting files for downstream population genomic anal...
R scripts for extraction of SNP types from .VCF files, and for PGLS analyses Phenotype data used in...
This zip file contains multiple Python scripts called by the scripts in the GenBank Main Scripts fil...
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