4.8 Article

An enhanced MITOMAP with a global mtDNA mutational phylogeny

Journal

NUCLEIC ACIDS RESEARCH
Volume 35, Issue -, Pages D823-D828

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkl927

Keywords

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Funding

  1. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL064017] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE ON AGING [R01AG013154] Funding Source: NIH RePORTER
  3. NATIONAL LIBRARY OF MEDICINE [T15LM007443] Funding Source: NIH RePORTER
  4. NHLBI NIH HHS [HL64017] Funding Source: Medline
  5. NIA NIH HHS [R01 AG024373, R01 AG013154, AG13154] Funding Source: Medline
  6. NINDS NIH HHS [NS213L8] Funding Source: Medline
  7. NLM NIH HHS [T15 LM007443] Funding Source: Medline

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The MITOMAP (http://www.mitomap.org) data system for the human mitochondrial genome has been greatly enhanced by the addition of a navigable mutational mitochondrial DNA (mtDNA) phylogenetic tree of similar to 3000 mtDNA coding region sequences plus expanded pathogenic mutation tables and a nuclear-mtDNA pseudogene (NUMT) data base. The phylogeny reconstructs the entire mutational history of the human mtDNA, thus defining the mtDNA haplogroups and differentiating ancient from recent mtDNA mutations. Pathogenic mutations are classified by both genotype and phenotype, and the NUMT sequences permits detection of spurious inclusion of pseudogene variants during mutation analysis. These additions position MITOMAP for the implementation of our automated mtDNA sequence analysis system, Mitomaster.

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