Closed liuwd15 closed 3 years ago
Hi @liuwd15
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The DESCRIPTION file for this package is:
Package: tomoda
Title: Tomo-seq data analysis
Version: 0.99.0
Authors@R:
person(given = "Wendao",
family = "Liu",
role = c("aut", "cre"),
email = "liuwd15@tsinghua.org.cn",
comment = c(ORCID = "0000-0002-5124-9338"))
Description: This package provides many easy-to-use methods to analyze and
visualize tomo-seq data. The main purpose of the package is to find zones
with similar transcriptional profiles and spatially expressed genes in a
tomo-seq sample. Several visulization functions are available to create
high quality and easy-to-modify plots.
Depends: R (>= 4.0.0)
Imports:
methods,
stats,
grDevices,
reshape2,
Rtsne,
umap,
colorRamps,
ggplot2,
ggrepel,
SummarizedExperiment
License: MIT + file LICENSE
Encoding: UTF-8
Roxygen: list(markdown = TRUE)
RoxygenNote: 7.1.1
Suggests:
knitr,
rmarkdown,
BiocStyle,
testthat
URL: https://github.com/liuwd15/tomoda
BugReports: https://github.com/liuwd15/tomoda/issues
biocViews:
GeneExpression,
Sequencing,
RNASeq,
Transcriptomics,
Clustering,
Visualization
VignetteBuilder: knitr
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Hi Wendao Liu, @liuwd15
Thank you for your submission to Bioconductor. Please see the review below. Feel free to post any questions or comments below.
Best regards, Marcel
SummarizedExperiment()
). Otherwise,
use lower case for 'plain' functions.base::scale
vs Scale
and stats::kmeans
vs KMeans
).
Please add a more descriptive name to your functions or consider renaming them.r BiocStyle::Biocpkg('tomoda')
when accepted.SummarizedExperiment
to represent the example dataset
(zh.data
)Normalize
and Scale
operations be part of your CreateTomo
function?.gitignore
file in the vignettes folder (.R
and .html
files
do not belong in the directory).CreateTomo
should support both matrix
and SummarizedExperiment
inputs.CreateTomo
function.CreateTomo
to something like checkTomo
as 'Tomo' is not
really a class or subclass of SummarizedExperiment
.CreateTomo
function.SummarizedExperiment
is the main data representation. The
GetMatrix
function is repeated code for assay(se, i = "counts")
and should
be removed. The documentation should inform users to use the assay
function
to extract a matrix.cat
and use message
instead to notify the user.HClust
and KMeans
seem to be thin wrappers for hclust
and kmeans
and
consider including the convenience functions inside the main CreateTomo
,
if at all.FindPeakGene
(assays(object)$scaled
).
Allow the user to input the scaled assay name (scaled
) using an argument.
This applies to other functions that use assays(object)$scaled
etc.assay
rather than assays
when extracting oneFindPeakGene
for
loop when
nperm > 0
.BiocManger::install
code chunkReceived a valid push on git.bioconductor.org; starting a build for commit id: b44e45d4a8ccab5c0cadddf761c954d0be2a2be0
Hi Marcel @LiNk-NY, Thanks for your comments. I have updated the package and here are my responses to your comments. I followed most of your comments but left a few unchanged. The reasons are explained below.
The vignette is now 80 column-wide.
Now r BiocStyle::Biocpkg('tomoda')
is used.
In my opinion, most users will start with a read count matrix
rather than a SummarizedExperiment object
. The example matrix is useful as I show how to create the SummarizedExperiment object from a read count matrix. If the dataset is saved as a SummarizedExperiment object, users may not understand how to prepare their data. Therefore I believe saving the example dataset as matrix is reasonable.
Normalization and scaling are now added into createTomo
.
Color-blind friendly default colors from RColorBrewer
are used for heatmaps now.
.gitignore
in this directory is removed.
createTomo
now supports matrix and SummarizedExperiment inputs by using S4 generics and methods.
Normalization and scaling are now added into createTomo
.
Although there is no class named Tomo, I believe that createTomo
shows the meanings of "creating an object representing tomo-seq data" better than checkTomo
, so I leave this name unchanged.
More details in documentation are added.
GetMatrix
is replaced with assay
. Accessing matrices using assay
is demonstrated in the vignette.
cat
and print
is replaced with message
.
hierarchClust
(old name HClust
) returns a hclust
object so it cannot be added into createTomo
. Besides, I plan to add more clustering algorithms in future versions, so I do not think adding clustering functions in createTomo
is a good idea.
Functions using data of certain assays now have the augument matrix
, which tells the functions which assay to work on. Default values are provided so that users do not always need to specify it.
assays
are replaced with assay
.
Allocate and fill strategy is used in FindPeakGene
.
There is BiocManager::install("tomoda")
in Installation.
Dear Package contributor,
This is the automated single package builder at bioconductor.org.
Your package has been built on Linux, Mac, and Windows.
On one or more platforms, the build results were: "WARNINGS". This may mean there is a problem with the package that you need to fix. Or it may mean that there is a problem with the build system itself.
Please see the build report for more details. This link will be active for 21 days.
Remember: if you submitted your package after July 7th, 2020,
when making changes to your repository push to
git@git.bioconductor.org:packages/tomoda
to trigger a new build.
A quick tutorial for setting up remotes and pushing to upstream can be found here.
Received a valid push on git.bioconductor.org; starting a build for commit id: 1233335b2ebcd93acccefeda53f3304184fad8ce
Dear Package contributor,
This is the automated single package builder at bioconductor.org.
Your package has been built on Linux, Mac, and Windows.
Congratulations! The package built without errors or warnings on all platforms.
Please see the build report for more details. This link will be active for 21 days.
Remember: if you submitted your package after July 7th, 2020,
when making changes to your repository push to
git@git.bioconductor.org:packages/tomoda
to trigger a new build.
A quick tutorial for setting up remotes and pushing to upstream can be found here.
Hi Wendao Liu, @liuwd15
Thank you for making those changes. They look great!
I would consider renaming the createTomo.matrix
function into something that resembles an S3 method less. Perhaps tomoMatrix
?
I will accept your package. Thank you for your contribution.
Best regards, Marcel
Your package has been accepted. It will be added to the Bioconductor nightly builds.
Thank you for contributing to Bioconductor!
Hi Marcel @LiNk-NY,
Thanks for reviewing and accepting this package.
createTomo.matrix
and createTomo.SummarizedExperiment
are renamed into tomoMatrix
and tomoSummarizedExperiment
now.
Best, Wendao
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