SRR1301329_1M_read | 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,…; 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)
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