Hi guys,
The genotype imputation need human genetic map file, whose format is like(in chr1):
position COMBINED_rate(cM/Mb) Genetic_Map(cM)
55550 0 0
568322 0 0
568527 0 0
721290 2.685807669 0.410292036939447
723819 2.8222713027 0.417429561063975
723891 2.9813105581 0.417644215424158
728242 2.9806151254 0.430612871834774
729948 3.0780969498 0.435864105231133
740857 3.075133293 0.46941073432447
There are 3 columns, the first column is physical position united in bp, which is easy to understand. The second and third column is recombination rate(cM/Mb) and genetic position(cM, centiMorgan). I'm confused about the values in column 2 and 3.
Let's take the 4th row as an example. I know 721290 means the 721290th position on chr1. So what's the 2.68 and 0.41 represent for? I looked up some webpages and learned that "A centiMorgan is a unit of genetic distance that represents a 1% probability of recombination during meiosis." But I still cannot figure out the what's the meaning of 0.41/2.68 at position 721290.
Can anyone explain it to me? Thanks!
Tao
For the first SNP on the rest of the chromosomes there is a rate(cM/Mb) > 0 when cM is 0. First chromosome is not good example. How is this calculated or it is inferred somehow. For instance this is first 5 on chromosome 2:
How do you get
0.5043954585
?