SRR1301329_1M_read {preseqR} | R Documentation |
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.
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.
Simons Foundation Autism Research Initiative (https://www.sfari.org/).
##load library
library(preseqR)
##load data
data(SRR1301329_1M_read)