Releases: dcgerard/seqgendiff
Releases · dcgerard/seqgendiff
v0.4.1
seqgendiff 0.4.1
- I added
select_counts()
, a function that will subsample the rows (genes)
and columns (samples) of a RNA-seq count matrix. It is generally
recommended that you do this subsampling each iteration of a simulation
study so that your results do not depend on the specific structure of
your data. The samples are just selected randomly. There are four different
criteria for selecting the genes. - I also added citation information. This will be updated after I submit
the manuscript to bioRxiv.
v0.4.0
This is a major release. poisthin()
is now defunct. The main functions are now thin_diff()
, thin_2group()
, thin_lib()
, thin_gene()
, and thin_all()
. thin_diff()
allows for general designs beyond the two-group model, and the rest of the functions are special cases of thin_diff()
.