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Det sätt begreppsrelationer visas:
Sekvensinpassning
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Bredare villkor: | |
Anmärkning: | The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms.
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Annotation: | sequence refers to molec seq (amino acid or base); note category; DF: SEQ ALIGNMENT
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historyNote*: | 91
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publicMeSHNote*: | 91
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activeMeSHYear*: | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007X |
dateCreated*: | 1990-06-01X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 1992-05-18X |
recordAuthorizer*: | PLSX |
recordMaintainer*: | TAPX |
recordOriginator*: | PLSX |
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Termer och motsvarande begrepp: | Geenisekvenssien vertailu (fi) XGeenijaksojen vertailu (fi, ersatt) Sekvenslinjering (sv, ersatt) Sequence Alignment (en) Sequence Homology Determination (en, ersatt) |
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