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  • techniques. Advanced models of nucleotide substitution (gamma-distributed mutation rates, molecular clock models, codon models and analysis of selective press
    2 KB (212 words) - 00:09, 9 August 2006
  • This command plots the relative mutation rates at the first, second, and third codon positions. How does this fit wi
    28 KB (4,371 words) - 03:28, 14 April 2008
  • ...ration, unlike nuclear DNA which changes by 50% each generation. Since the mutation rate is easily measured, mtDNA is a powerful tool for tracking [[matrilinea
    5 KB (740 words) - 23:25, 29 December 2005
  • In genetics, a '''Transition''' is a mutation changing a [[purine]] to another [[purine]] nucleotide (A <-> G) or a [[pyr
    382 bytes (48 words) - 23:39, 29 December 2005
  • .... It can only be reverted by a spontaneous reversion. Because this type of mutation changes the chemical structure dramatically, the consequences of this chang
    541 bytes (73 words) - 23:41, 29 December 2005
  • ...use maximum parsimony uses unrooted trees, independent innovation and back-mutation are actually mathematically equivalent.
    6 KB (941 words) - 04:51, 13 September 2006
  • ...evolves rapidly. There are only four possible [[nucleotides]] and when [[mutation|DNA substitution]] rates are high, the probability that two lineages will i
    3 KB (371 words) - 04:51, 13 September 2006
  • ...a fundamental characteristic of healthy tissue. Failure of cell death (by mutation, infection, or otherwise) can, ironically, lead to the death of the organis
    11 KB (1,611 words) - 01:12, 9 July 2012
  • * [[wikipedia:Point accepted mutation]]
    4 KB (746 words) - 01:49, 17 October 2006
  • ==Nucleic acid sequence mutation== ;silent : Silent mutation restriction enzyme scan
    21 KB (2,762 words) - 01:04, 10 July 2012
  • '''[[wikipedia:Point Accepted Mutation|PAM]]''' ('''P'''oint '''A'''ccepted '''M'''utation)
    6 KB (932 words) - 01:07, 16 May 2008
  • # [http://shmpd.bii.a-star.edu.sg SHMPD: The Singapore Human Mutation and Polymorphism Database] # [http://www.hgmd.cf.ac.uk/ HGMD disease-causing mutations] (HGMD Human Gene Mutation Database)
    9 KB (1,252 words) - 22:15, 4 June 2008
  • ;Mendelian disorders : Phenotypes caused by a mutation (or mutations) in a single gene and inherited in a dominant, recessive or X ...>Edwards JR, Ruparel H, Ju J (2005). "Mass-spectrometry DNA sequencing". ''Mutation Research'', '''573'''(1–2): 3–12. PMID 15829234. {{doi|10.1016/j.mrfmmm
    14 KB (1,969 words) - 21:46, 17 July 2012