SRR611492 | R Documentation |
The coverage histogram is based on a single-cell whole-genome sequencing data (scWGS) through MALBAK protocol. The accession number of the raw data is SRR1301329. Only forward reads are used to generate the coverage histogram.
A two-column matrix. The first column is the frequency j = 1,2,…; and the second column is N_j, the number of nucleotides in the genome covered exactly j times.
Zong, C., Lu, S., Chapman, A. R., & Xie, X. S. (2012). Genome-wide detection of single-nucleotide and copy-number variations of a single human cell. Science, 338(6114), 1622-1626.
##load library library(preseqR) ##load data data(SRR611492)
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