Maximum-likelihood estimation of site-specific mutation rates in human mitochondrial DNA from partial phylogenetic classification

Genetics

Volumn 180, Issue 3, 2008, Pages 1511-1524

  Rosset, Saharon ^a,b,c   Wells, R Spencer ^c   Soria Hernanz, David F ^c   Tyler Smith, Chris ^d,j   Royyuru, Ajay K ^b,c   Behar, Doron M ^e,k   Schurr, Theodore G ^f   Santos, Fabricio R ^g   Quintana Murci, Lluis ^h   Bertranpetit, Jaume ⁱ   Comas, David ⁱ   Balanovska, Elena ^j   Balanovsky, Oleg ^j   Mitchell, R John ^k   Jin, Li ^l   Soodyall, Himla ^m   Pitchappan, Ramasamy ⁿ   Cooper, Alan ^o   Blue Smith, Jason ^c   Hernanz, David Soria ^p  

^a TEL AVIV UNIVERSITY   (Israel)

^b IBM T J WATSON RESEARCH CENTER   (United States)

^c NATIONAL GEOGRAPHIC SOCIETY   (United States)

^d WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^e Molecular Medicine Laboratory   (Israel)

^f UNIVERSITY OF PENNSYLVANIA   (United States)

^g FEDERAL UNIVERSITY OF MINAS GERAIS   (Brazil)

^h INSTITUT PASTEUR   (France)

ⁱ UNIVERSITAT POMPEU FABRA   (Spain)

^j RESEARCH CENTRE FOR MEDICAL GENETICS   (Russian Federation)

^k LA TROBE UNIVERSITY   (Australia)

^l FUDAN UNIVERSITY   (China)

^m NATIONAL HEALTH LABORATORY SERVICE   (South Africa)

ⁿ MADURAI KAMARAJ UNIVERSITY   (India)

^o UNIVERSITY OF ADELAIDE   (Australia)

^p NONE

more..

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; DNA SEQUENCE; GENE DELETION; GENE INSERTION; GENE LOCUS; GENE SEQUENCE; HUMAN; HUMAN GENOME; MOLECULAR CLOCK; MUTATION RATE; NUCLEOTIDE BINDING SITE; PHYLOGENETIC TREE; PRIORITY JOURNAL; SEQUENCE ALIGNMENT; SHORT TANDEM REPEAT; SINGLE NUCLEOTIDE POLYMORPHISM; BIOLOGICAL MODEL; COMPUTER SIMULATION; GENETIC VARIABILITY; GENETICS; HAPLOTYPE; PHYLOGENY; POINT MUTATION; STATISTICAL MODEL;

COMPUTER SIMULATION; DNA, MITOCHONDRIAL; GENETIC VARIATION; HAPLOTYPES; HUMANS; LIKELIHOOD FUNCTIONS; MODELS, GENETIC; PHYLOGENY; POINT MUTATION;

EID: 59449085284     PISSN: 00166731     EISSN: 00166731     Source Type: Journal    
DOI: 10.1534/genetics.108.091116     Document Type: Article

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