<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>Anisimova M</dc:creator>
  <dc:creator>Pečerska J</dc:creator>
  <dc:creator>Schaper E</dc:creator>
  <dc:date>2015</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Tandem repeats (TRs) are frequently observed in genomes across all domains of life. Evidence suggests that some TRs are crucial for proteins with fundamental biological functions and can be associated with virulence, resistance, and infectious/neurodegenerative diseases. Genome-scale systematic studies of TRs have the potential to unveil core mechanisms governing TR evolution and TR roles in shaping genomes. However, TR-related studies are often non-trivial due to heterogeneous and sometimes fast evolving TR regions. In this review, we discuss these intricacies and their consequences. We present our recent contributions to computational and statistical approaches for TR significance testing, sequence profile-based TR annotation, TR-aware sequence alignment, phylogenetic analyses of TR unit number and order, and TR benchmarks. Importantly, all these methods explicitly rely on the evolutionary definition of a tandem repeat as a sequence of adjacent repeat units stemming from a common ancestor. The discussed work has a focus on protein TRs, yet is generally applicable to nucleic acid TRs, sharing similar features.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/55335</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3389/fbioe.2015.00031</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/25853125</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Frontiers in bioengineering and biotechnology. - 2015</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">molecular evolution</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">protein domain</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">sequence profile model</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">tandem repeat annotation</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">tandem repeats</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">Statistical approaches to detecting and analyzing tandem repeats in genomic sequences.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
