SRR1301329_1M_read: Read counts of a WES data
In preseqR: Predicting Species Accumulation Curves
Description
Details
References
Examples
Description
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.
Details
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.
References
Simons Foundation Autism Research Initiative (https://www.sfari.org/).
Examples
1
2
3
4
5
##load library
library(preseqR)
##load data
data(SRR1301329_1M_read)
preseqR documentation built on May 2, 2019, 6:39 a.m.
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Description Details References Examples
Description
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.
Details
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.
References
Simons Foundation Autism Research Initiative (https://www.sfari.org/).
Examples
1 2 3 4 5 | ##load library
library(preseqR)
##load data
data(SRR1301329_1M_read)
|
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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