Skip to content

Commit

Permalink
Fix more relative links
Browse files Browse the repository at this point in the history
  • Loading branch information
trvrb committed Jan 11, 2017
1 parent 25d1faf commit caac31f
Show file tree
Hide file tree
Showing 2 changed files with 2 additions and 2 deletions.
2 changes: 1 addition & 1 deletion recombination/r_squared/README.md
Original file line number Diff line number Diff line change
@@ -1,3 +1,3 @@
![](https://github.com/blab/siv-cst/blob/master/figures/png/FigS1.png)
![](../../figures/png/FigS1.png)
##Extensive divergence makes sitewise measures of genetic linkage ineffective
For pairs of biallelic sites (ignoring rare variants), R^2 was used to estimate how strongly the allele in one site predicts the allele in the second site, with values of 0 indicating no linkage and 1 indicating perfect linkage. The mean value of R^2 was 0.044, indicating very low levels of linkage overall.
2 changes: 1 addition & 1 deletion recombination/rspr/README.md
Original file line number Diff line number Diff line change
@@ -1,4 +1,4 @@
![](https://github.com/blab/siv-cst/blob/master/figures/png/FigS2.png)
![](../../figures/png/FigS2.png)

## Figure S2: No evidence of linkage between nonadjacent segments of the SIV genome.
The alignment used for GARD analyses (LANL compendium with HIV overrepresentation reduced) was split along the breakpoints identified by GARD to yield the 12 genomic segments, and a maximum likelihood tree was constructed for each. The number of steps required to turn one tree topology into another was assessed for each pair of trees with the Rooted Subtree-Prune-and-Regraft (rSPR) package. Segment pairs with similar topologies have lower scores than segments with less similar topologies.

0 comments on commit caac31f

Please sign in to comment.