Script associated with the bioinformatics pipeline. The first script strings the programs together (used in Linux environment). The second script determines the SNPs and allelic variants. The third script creates the consensus sequences
Bolded boxes represent publicly-available software used in analyses. Consensus sequences, generated ...
These are the three final scripts used for generating the 5159 SNP matrix that was used as a basis f...
The rapidly advancing high-throughput and next generation sequencing technologies facilitate deeper ...
Script associated with the bioinformatics pipeline. The first script strings the programs together (...
Bioinformatics code for assembling transcriptomes, mapping reads, clustering gene families, performi...
Full scripts for bioinformatic pipeline as applied for sequence data analysis for Geisen et al. 2015...
The scripts used for the analysis of our manuscript "Optimized high-throughput screening of non-codi...
This repository compiles scripts that have been developed to analyse genomic data in manuscript BIOR...
Scripts for aligning reads, calling SNPs and converting files for downstream population genomic anal...
The file contains all the commandds used in this study to generate the final data. The bioinformatic...
Bash shell and python scripts used to prepare alignments for gene tree inference, phase alleles, and...
Consensus sequences of all loci used in analyses. Loci identifier numbers match those of other uploa...
A computer tool is described for comparison, analysis and search of genetic signals. The method is b...
The field of Genomics is aimed at complex analysis of genomes based on our knowledge of the nucleo...
Nucleotide alignments of individual chloroplast genes. Python scripts for removal of masked sites. D...
Bolded boxes represent publicly-available software used in analyses. Consensus sequences, generated ...
These are the three final scripts used for generating the 5159 SNP matrix that was used as a basis f...
The rapidly advancing high-throughput and next generation sequencing technologies facilitate deeper ...
Script associated with the bioinformatics pipeline. The first script strings the programs together (...
Bioinformatics code for assembling transcriptomes, mapping reads, clustering gene families, performi...
Full scripts for bioinformatic pipeline as applied for sequence data analysis for Geisen et al. 2015...
The scripts used for the analysis of our manuscript "Optimized high-throughput screening of non-codi...
This repository compiles scripts that have been developed to analyse genomic data in manuscript BIOR...
Scripts for aligning reads, calling SNPs and converting files for downstream population genomic anal...
The file contains all the commandds used in this study to generate the final data. The bioinformatic...
Bash shell and python scripts used to prepare alignments for gene tree inference, phase alleles, and...
Consensus sequences of all loci used in analyses. Loci identifier numbers match those of other uploa...
A computer tool is described for comparison, analysis and search of genetic signals. The method is b...
The field of Genomics is aimed at complex analysis of genomes based on our knowledge of the nucleo...
Nucleotide alignments of individual chloroplast genes. Python scripts for removal of masked sites. D...
Bolded boxes represent publicly-available software used in analyses. Consensus sequences, generated ...
These are the three final scripts used for generating the 5159 SNP matrix that was used as a basis f...
The rapidly advancing high-throughput and next generation sequencing technologies facilitate deeper ...