<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Dall'Olio GM</dc:creator>
  <dc:creator>Vahdati AR</dc:creator>
  <dc:creator>Bertranpetit J</dc:creator>
  <dc:creator>Wagner A</dc:creator>
  <dc:creator>Laayouni H</dc:creator>
  <dc:date>2015</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">SUMMARY
A wealth of large-scale genome sequencing projects opens the doors to new approaches to study the relationship between genotype and phenotype. One such opportunity is the possibility to apply genotype networks analysis to population genetics data. Genotype networks are a representation of the set of genotypes associated with a single phenotype, and they allow one to estimate properties such as the robustness of the phenotype to mutations, and the ability of its associated genotypes to evolve new adaptations. So far, though, genotype networks analysis has rarely been applied to population genetics data. To help fill this gap, here we present VCF2Networks, a tool to determine and study genotype network structure from single-nucleotide variant data.


AVAILABILITY AND IMPLEMENTATION
VCF2Networks is available at https://bitbucket.org/dalloliogm/vcf2networks.


CONTACT
giovanni.dallolio@kcl.ac.uk


SUPPLEMENTARY INFORMATION
Supplementary data are available at Bioinformatics online.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/236571</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1093/bioinformatics/btu650</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/25282646</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Bioinformatics (Oxford, England). - 2015</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Biological Evolution</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Gene Regulatory Networks</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Genetics, Population</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Genome, Human</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Genotype</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Phenotype</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Polymorphism, Single Nucleotide</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Software</dc:subject>
  <dc:title xmlns:ns10="xml" ns10:lang="en">VCF2Networks: applying genotype networks to single-nucleotide variants data.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
