ONKI3 | Medical Subject Headings

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suomeksi på svenska in English

The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Sequence Alignment

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Tutkimusmenetelmät ∟ Geenitekniikat ∟ Sequence Alignment 27 coordinate concepts ∟ Contig-kartoitus \| ∟ DNA-jalanjälkimenetelmä \| ∟ DNA-sormenjälkitutkimus \| ∟ Geeniekspression profiili \| ∟ Geenikartoitus \| ∟ Geenimanipulaatio \| ∟ Geeninsiirtomenetelmät \| ∟ Gene Targeting \| ∟ Geneettiset risteytykset \| ∟ Heterotsygoottien tunnistaminen \| ∟ In Situ Nick-End Labeling \| ∟ Kromatiini-immunopresipitaatio \| ∟ Molekylaarinen kloonaus \| ∟ Molekyylidiagnostiikka \| ∟ Molekyyliepidemiologia \| ∟ Molekyylikoetinmenetelmät \| ∟ Mutageenisuustestit \| ∟ Nuclease protection -menetelmät \| ∟ Nukleiinihappohybridisaatio \| ∟ Nukleiinihappojen denaturaatio \| ∟ Nukleiinihappomonistusmenetelmät \| ∟ Organismin kloonaus \| ∟ Restriktiokartoitus \| ∟ Sekvenssianalyysi \| ∟ Solutuman siirtomenetelmät \| ∟ Sukupuu \| ∟ Sytogeneettinen analyysi X
Broader terms:	Medical Subject Headings (MeSH) ∟ Tutkimusmenetelmät ∟ Geenitekniikat ∟ Sequence Alignment Geenitekniikat > Tutkimusmenetelmät > Medical Subject Headings (MeSH) X
Annotation:	sequence refers to molec seq (amino acid or base); note category; DF: SEQ ALIGNMENT X
historyNote*:	91 X
publicMeSHNote*:	91 X
Scope note:	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. X
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
Type:	Käsite X
Coordinate terms:	Contig-kartoitus \| DNA-jalanjälkimenetelmä \| DNA-sormenjälkitutkimus \| Geeniekspression profiili \| Geenikartoitus \| Geenimanipulaatio \| Geeninsiirtomenetelmät \| Gene Targeting \| Geneettiset risteytykset \| Heterotsygoottien tunnistaminen \| In Situ Nick-End Labeling \| Kromatiini-immunopresipitaatio \| Molekylaarinen kloonaus \| Molekyylidiagnostiikka \| Molekyyliepidemiologia \| Molekyylikoetinmenetelmät \| Mutageenisuustestit \| Nuclease protection -menetelmät \| Nukleiinihappohybridisaatio \| Nukleiinihappojen denaturaatio \| Nukleiinihappomonistusmenetelmät \| Organismin kloonaus \| Restriktiokartoitus \| Sekvenssianalyysi \| Solutuman siirtomenetelmät \| Sukupuu \| Sytogeneettinen analyysi X
URI:	X
Labels and equivalent concepts:	Geenisekvenssien vertailu (fi) Geenijaksojen vertailu (fi, replaced) Sekvensinpassning (sv) Sekvenslinjering (sv, replaced) Sequence Homology Determination (en, replaced) X
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