Back to Multiple platform build/check report for BioC 3.19:   simplified   long
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This page was generated on 2024-06-18 17:59 -0400 (Tue, 18 Jun 2024).

HostnameOSArch (*)R versionInstalled pkgs
nebbiolo1Linux (Ubuntu 22.04.3 LTS)x86_644.4.0 (2024-04-24) -- "Puppy Cup" 4758
palomino3Windows Server 2022 Datacenterx644.4.0 (2024-04-24 ucrt) -- "Puppy Cup" 4492
merida1macOS 12.7.4 Montereyx86_644.4.0 (2024-04-24) -- "Puppy Cup" 4464
kjohnson1macOS 13.6.6 Venturaarm644.4.0 (2024-04-24) -- "Puppy Cup" 4464
Click on any hostname to see more info about the system (e.g. compilers)      (*) as reported by 'uname -p', except on Windows and Mac OS X

Package 1900/2300HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
scMerge 1.20.0  (landing page)
Yingxin Lin
Snapshot Date: 2024-06-16 14:00 -0400 (Sun, 16 Jun 2024)
git_url: https://git.bioconductor.org/packages/scMerge
git_branch: RELEASE_3_19
git_last_commit: 0b5d058
git_last_commit_date: 2024-04-30 11:14:29 -0400 (Tue, 30 Apr 2024)
nebbiolo1Linux (Ubuntu 22.04.3 LTS) / x86_64  OK    OK    OK  UNNEEDED, same version is already published
palomino3Windows Server 2022 Datacenter / x64  OK    OK    OK    OK  UNNEEDED, same version is already published
merida1macOS 12.7.4 Monterey / x86_64  OK    OK    OK    OK  UNNEEDED, same version is already published
kjohnson1macOS 13.6.6 Ventura / arm64  OK    OK    OK    OK  UNNEEDED, same version is already published


CHECK results for scMerge on palomino3

To the developers/maintainers of the scMerge package:
- Allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/scMerge.git to reflect on this report. See Troubleshooting Build Report for more information.
- Use the following Renviron settings to reproduce errors and warnings.
- If 'R CMD check' started to fail recently on the Linux builder(s) over a missing dependency, add the missing dependency to 'Suggests:' in your DESCRIPTION file. See Renviron.bioc for more information.

raw results


Summary

Package: scMerge
Version: 1.20.0
Command: F:\biocbuild\bbs-3.19-bioc\R\bin\R.exe CMD check --no-multiarch --install=check:scMerge.install-out.txt --library=F:\biocbuild\bbs-3.19-bioc\R\library --no-vignettes --timings scMerge_1.20.0.tar.gz
StartedAt: 2024-06-17 11:13:23 -0400 (Mon, 17 Jun 2024)
EndedAt: 2024-06-17 11:29:00 -0400 (Mon, 17 Jun 2024)
EllapsedTime: 937.5 seconds
RetCode: 0
Status:   OK  
CheckDir: scMerge.Rcheck
Warnings: 0

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   F:\biocbuild\bbs-3.19-bioc\R\bin\R.exe CMD check --no-multiarch --install=check:scMerge.install-out.txt --library=F:\biocbuild\bbs-3.19-bioc\R\library --no-vignettes --timings scMerge_1.20.0.tar.gz
###
##############################################################################
##############################################################################


* using log directory 'F:/biocbuild/bbs-3.19-bioc/meat/scMerge.Rcheck'
* using R version 4.4.0 (2024-04-24 ucrt)
* using platform: x86_64-w64-mingw32
* R was compiled by
    gcc.exe (GCC) 13.2.0
    GNU Fortran (GCC) 13.2.0
* running under: Windows Server 2022 x64 (build 20348)
* using session charset: UTF-8
* using option '--no-vignettes'
* checking for file 'scMerge/DESCRIPTION' ... OK
* checking extension type ... Package
* this is package 'scMerge' version '1.20.0'
* package encoding: UTF-8
* checking package namespace information ... OK
* checking package dependencies ... OK
* checking if this is a source package ... OK
* checking if there is a namespace ... OK
* checking for hidden files and directories ... OK
* checking for portable file names ... OK
* checking whether package 'scMerge' can be installed ... OK
* checking installed package size ... OK
* checking package directory ... OK
* checking 'build' directory ... OK
* checking DESCRIPTION meta-information ... OK
* checking top-level files ... OK
* checking for left-over files ... OK
* checking index information ... OK
* checking package subdirectories ... OK
* checking code files for non-ASCII characters ... OK
* checking R files for syntax errors ... OK
* checking whether the package can be loaded ... OK
* checking whether the package can be loaded with stated dependencies ... OK
* checking whether the package can be unloaded cleanly ... OK
* checking whether the namespace can be loaded with stated dependencies ... OK
* checking whether the namespace can be unloaded cleanly ... OK
* checking dependencies in R code ... OK
* checking S3 generic/method consistency ... OK
* checking replacement functions ... OK
* checking foreign function calls ... OK
* checking R code for possible problems ... OK
* checking Rd files ... NOTE
checkRd: (-1) scMerge.Rd:85: Lost braces in \itemize; \value handles \item{}{} directly
checkRd: (-1) scMerge.Rd:86: Lost braces in \itemize; \value handles \item{}{} directly
checkRd: (-1) scMerge2.Rd:82: Lost braces in \itemize; \value handles \item{}{} directly
checkRd: (-1) scMerge2.Rd:83: Lost braces in \itemize; \value handles \item{}{} directly
checkRd: (-1) scMerge2.Rd:84: Lost braces in \itemize; \value handles \item{}{} directly
* checking Rd metadata ... OK
* checking Rd cross-references ... OK
* checking for missing documentation entries ... OK
* checking for code/documentation mismatches ... OK
* checking Rd \usage sections ... OK
* checking Rd contents ... OK
* checking for unstated dependencies in examples ... OK
* checking contents of 'data' directory ... OK
* checking data for non-ASCII characters ... OK
* checking data for ASCII and uncompressed saves ... OK
* checking files in 'vignettes' ... OK
* checking examples ... OK
Examples with CPU (user + system) or elapsed time > 5s
                user system elapsed
scMerge2h      14.89   2.89   18.18
getAdjustedMat  4.90   2.91    8.05
scMerge2        4.61   2.64    7.42
* checking for unstated dependencies in 'tests' ... OK
* checking tests ...
  Running 'testthat.R'
 OK
* checking for unstated dependencies in vignettes ... OK
* checking package vignettes ... OK
* checking running R code from vignettes ... SKIPPED
* checking re-building of vignette outputs ... SKIPPED
* checking PDF version of manual ... OK
* DONE

Status: 1 NOTE
See
  'F:/biocbuild/bbs-3.19-bioc/meat/scMerge.Rcheck/00check.log'
for details.


Installation output

scMerge.Rcheck/00install.out

##############################################################################
##############################################################################
###
### Running command:
###
###   F:\biocbuild\bbs-3.19-bioc\R\bin\R.exe CMD INSTALL scMerge
###
##############################################################################
##############################################################################


* installing to library 'F:/biocbuild/bbs-3.19-bioc/R/library'
* installing *source* package 'scMerge' ...
** using staged installation
** R
** data
** inst
** byte-compile and prepare package for lazy loading
** help
*** installing help indices
** building package indices
** installing vignettes
** testing if installed package can be loaded from temporary location
** testing if installed package can be loaded from final location
** testing if installed package keeps a record of temporary installation path
* DONE (scMerge)

Tests output

scMerge.Rcheck/tests/testthat.Rout


R version 4.4.0 (2024-04-24 ucrt) -- "Puppy Cup"
Copyright (C) 2024 The R Foundation for Statistical Computing
Platform: x86_64-w64-mingw32/x64

R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.

R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.

Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.

> library(testthat)
> library(scMerge)
> 
> test_check("scMerge")
Dimension of the replicates mapping matrix: 
[1] 100   3
Dimension of the replicates mapping matrix: 
[1] 100   3
Dimension of the replicates mapping matrix: 
[1] 100   3
Dimension of the replicates mapping matrix: 
[1] 200   3
Dimension of the replicates mapping matrix: 
[1] 200   3
Dimension of the replicates mapping matrix: 
[1] 200   3
Dimension of the replicates mapping matrix: 
[1] 200   3
Dimension of the replicates mapping matrix: 
[1] 200   4
Dimension of the replicates mapping matrix: 
[1] 200   3
Selecting optimal RUVk 
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    75 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     3     1       1
2     2     1       2
3     1     1       3
4     1     2       1
5     2     2       2
6     3     2       3
Dimension of the replicates mapping matrix: 
[1] 200   3
Could not find a  batch  column in colData(sce_combine)[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   89
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   86
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047  100
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 1, data1"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   89
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 1, data2"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   86
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 2, data1"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047  100
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   89
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047  117
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 1, data1"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   89
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 2, data1"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047  117
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   50
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   50
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   50
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   50
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   86
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047  101
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 1, data1"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   50
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 1, data2"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   50
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 1, data3"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   50
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 1, data4"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   50
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 2, data1"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047   86
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
[1] "Hierarchical merging level 3, data1"
[1] "Cluster within batch"
[1] "Normalising data"
[1] "Constructing pseudo-bulk"
Dimension of pseudo-bulk expression: [1] 1047  101
[1] "Identifying MNC using pseudo-bulk:"
[1] "Running RUV"
Selecting optimal RUVk 
No cell type info, replicate matrix will be used as cell type info 
Performing supervised scMerge with: 
 1. Cell type information 
 2. No cell type indices 
 3. No mutual nearest neighbour clustering 
Performing semi-supervised scMerge with: 
 1. Cell type information 
 2. No cell type indices 
 3. Mutual nearest neighbour clustering 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    75 HVG were found 
 5. Calculating supervised clustering list 
 6. Create Mutual Nearest Clusters. Preview cells-to-cell_type matching graph and matrix:
  group batch cluster
1     3     1       1
2     2     1       2
3     1     1       3
4     3     2       1
5     2     2       2
6     1     2       3
Performing semi-supervised scMerge with: 
 1. Cell type information 
 2. No cell type indices 
 3. Mutual nearest neighbour clustering 
 4. No supplied marker but supplied marker_list for MNN clustering 
    Taking the union of marker_list as the markers 
 5. Calculating supervised clustering list 
 6. Create Mutual Nearest Clusters. Preview cells-to-cell_type matching graph and matrix:
  group batch cluster
1     2     1       1
2     3     1       2
3     1     1       3
4     4     2       1
5     5     2       2
6     1     2       3
Performing semi-supervised scMerge with: 
 1. Cell type information 
 2. No cell type indices 
 3. Mutual nearest neighbour clustering 
 5. Calculating supervised clustering list 
 6. Create Mutual Nearest Clusters. Preview cells-to-cell_type matching graph and matrix:
  group batch cluster
1     2     1       1
2     3     1       2
3     1     1       3
4     4     2       1
5     5     2       2
6     1     2       3
Performing semi-supervised scMerge with: 
 1. Cell type information 
 2. No cell type indices 
 3. Mutual nearest neighbour clustering 
 5. Calculating supervised clustering list 
 6. Create Mutual Nearest Clusters. Preview cells-to-cell_type matching graph and matrix:
  group batch cluster
1     2     1       1
2     3     1       2
3     1     1       3
4     4     2       1
5     5     2       2
6     1     2       3
Performing semi-supervised scMerge with: 
 1. Cell type information 
 2. Cell type indices 
 3. No mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    75 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     3     1       1
2     2     1       2
3     1     1       3
4     1     2       1
5     2     2       2
6     3     2       3
 7. Finishing semi-supervised scMerge with subsets of known cell type 
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    75 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     3     1       1
2     2     1       2
3     1     1       3
4     3     2       1
5     2     2       2
6     1     2       3
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker but supplied marker_list for MNN clustering 
    Taking the union of marker_list as the markers 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     1     1       1
2     2     1       2
3     3     1       3
4     1     2       1
5     4     2       2
6     5     2       3
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     1     1       1
2     2     1       2
3     3     1       3
4     4     2       1
5     5     2       2
6     1     2       3
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    75 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     3     1       1
2     2     1       2
3     1     1       3
4     1     2       1
5     3     2       2
6     2     2       3
 7. Performing semi-supervised scMerge with wanted variation 
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    75 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     3     1       1
2     2     1       2
3     1     1       3
4     3     2       1
5     2     2       2
6     1     2       3
 7. Performing semi-supervised scMerge with wanted variation 
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    36 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     2     1       1
2     1     1       2
3     3     1       3
4     1     2       1
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    36 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     2     1       1
2     3     1       2
3     1     1       3
4     1     2       1
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    63 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     3     1       1
2     2     1       2
3     1     1       3
4     2     2       1
5     1     2       2
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    63 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     3     1       1
2     2     1       2
3     1     1       3
4     2     2       1
5     1     2       2
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    24 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     1     1       1
2     2     2       1
3     1     3       1
Performing unsupervised scMerge with: 
 1. No cell type information 
 2. Cell type indices not relevant here 
 3. Mutual nearest neighbour matching 
 4. No supplied marker and no supplied marker_list for MNN clustering 
    Finding Highly Variable Genes for clustering 
    24 HVG were found 
 5. PCA and Kmeans clustering will be performed on each batch 
 6. Create Mutual Nearest Clusters. Preview cells-cell_type matching output matrix: 
  group batch cluster
1     1     1       1
2     2     2       1
3     1     3       1

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[ FAIL 0 | WARN 85 | SKIP 0 | PASS 42 ]

[ FAIL 0 | WARN 85 | SKIP 0 | PASS 42 ]
> 
> proc.time()
   user  system elapsed 
 166.07   50.50  217.67 

Example timings

scMerge.Rcheck/scMerge-Ex.timings

nameusersystemelapsed
fastRUVIII1.720.041.76
getAdjustedMat4.902.918.05
ruvSimulate1.950.172.13
scMerge2.330.132.45
scMerge24.612.647.42
scMerge2h14.89 2.8918.18
scRUVIII2.050.172.22
scRUVg0.030.000.03
scReplicate0.370.000.37
scSEGIndex4.100.014.11
sce_cbind0.790.150.94