The read counts are based on a whole-exome sequencing (WES) data
from Simons Foundation Autism Research Initiative with the accession number
SRR1301329. One million reads are randomly sampled from the raw data to
generate the read counts.
Arguments
Details
A two-column matrix.
The first column is the frequency \(j = 1,2,\dots\); and the second column
is \(N_j\), the number of reads observed exactly \(j\) times in the
data.