I'm trying to join two datasets where a variable (or position along a genome) in one dataset fits within a range in the second (gene start/stop position). However, positions are not unique, but nested within an additional column (chromosome). The same goes for the gene start/stop positions. My goal is to link each position with the corresponding annotation and effect.
For example:
library(sqldf)
set.seed(100)
a <- data.frame(
annotation = sample(c("this", "that", "other"), 3, replace=TRUE),
start = seq(1, 30, 10),
chr = sample(1:3, 3, replace=TRUE)
)
a$stop <- a$start + 10
b <- data.frame(
chr = sample(1:3, 3, replace=TRUE),
position = sample(1:15, 3, replace=TRUE),
effect = sample(c("high", "low"), 3, replace=TRUE)
)
An SQL inner join gets me part of the way there:
df<-sqldf("SELECT a.start, a.stop, a.annotation, b.effect, b.position
FROM a, b
inner JOIN a b on(b.position >= a.start and b.position <= a.stop);")
But this doesn't account for the repetition of position per chromosome. I'm having conceptual trouble wrapping this into a loop or apply function.
I'm not wedded to SQL, it's just how I tackled a simpler problem previously. I'm also not sure that making an additional index column is appropriate since I have thousands of chromosome values.
My desired output would look like the following:
df$chr<-c("NA","2","2")
start stop annotation effect position chr
1 1 11 this high 3 NA
2 1 11 this high 10 NA
3 11 21 this low 14 2
Where each position
has been placed between the start
and stop
points on the correct chr
, or given NA
where no points on a chr
match.