Flanking Gene Method: Difference between revisions

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[[Image:Flanking gene method.png|thumb|600px|right|[[GEvo]] analysis showing the flanking gene method.]]
[[Image:Flanking gene method2.png|thumb|600px|right|[[GEvo]] analysis showing the flanking gene method. The top panel represents a transposition event in one species as compared to uninterrupted genes in the orthologous region of another species in the panel below]]


The flanking gene method is a procedure which compares two neighboring [[syntenic]] gene pairs in order to identify transposed or deleted genes.  An example visualization of this method is shown to the right. Here, there are two pairs of syntenic genes (numbered 1 and 2).  
The flanking gene method is a procedure in which possible transposed genes are identified by comparing two neighboring [[syntenic]] gene pairs.  An example visualization of this method is shown to the right. In this visualization, a pair of genes (numbered 1 and 2) in Species A is being compared to an orthologous pair of genes (similarly numbered 1 and 2) in Species B.


Kieran, go wild.
In the procedure, sequential, adjoining genes (genes 1 and 2) are compared between two species (A and B). If said genes are from [[orthologous]] regions, one would assume the genes remain sequential. However, in a transposition event another gene (eg, gene X in red) inserts itself between two otherwise sequential genes. In this case, gene X is a possible transposed gene, identified by its presence in Species B between genes 1 and 2 which would be otherwise adjoining each other. This method of identification is previously described in Freeling et al 2008.


 
Further analysis uses an additional species as an outgroup to determine whether or not gene X is, in fact, an [[insertion]] between genes 1 an 2 rather than merely a gene in sequence that's been [[deleted]].
the location of two sequential genes in a region orthologous between two species such that, given a pair of genes 1 and 2, if gene X is present between the two genes in one species but not the other (such that  Species A=1 X 2, Species B=1 2), gene X is denoted as a possible transposed gene (as previously described in Freeling et al 2008).  An outgroup (Species C) is used  to distinguish between gene transposition in Species A and gene deletion in Species B.

Latest revision as of 20:49, 17 May 2010

GEvo analysis showing the flanking gene method. The top panel represents a transposition event in one species as compared to uninterrupted genes in the orthologous region of another species in the panel below

The flanking gene method is a procedure in which possible transposed genes are identified by comparing two neighboring syntenic gene pairs. An example visualization of this method is shown to the right. In this visualization, a pair of genes (numbered 1 and 2) in Species A is being compared to an orthologous pair of genes (similarly numbered 1 and 2) in Species B.

In the procedure, sequential, adjoining genes (genes 1 and 2) are compared between two species (A and B). If said genes are from orthologous regions, one would assume the genes remain sequential. However, in a transposition event another gene (eg, gene X in red) inserts itself between two otherwise sequential genes. In this case, gene X is a possible transposed gene, identified by its presence in Species B between genes 1 and 2 which would be otherwise adjoining each other. This method of identification is previously described in Freeling et al 2008.

Further analysis uses an additional species as an outgroup to determine whether or not gene X is, in fact, an insertion between genes 1 an 2 rather than merely a gene in sequence that's been deleted.