Guandong Shang
| Snapshot Date: 2023-03-28 14:00:22 -0400 (Tue, 28 Mar 2023) |
| git_url: https://git.bioconductor.org/packages/FindIT2 |
| git_branch: devel |
| git_last_commit: db4c20d |
| git_last_commit_date: 2022-11-01 11:25:15 -0400 (Tue, 01 Nov 2022) |
| Back to Multiple platform build/check report for BioC 3.17: simplified long |
|
This page was generated on 2023-03-29 11:06:13 -0400 (Wed, 29 Mar 2023).
| Hostname | OS | Arch (*) | R version | Installed pkgs |
|---|---|---|---|---|
| nebbiolo1 | Linux (Ubuntu 22.04.1 LTS) | x86_64 | R Under development (unstable) (2023-03-16 r83996) -- "Unsuffered Consequences" | 4547 |
| palomino3 | Windows Server 2022 Datacenter | x64 | R Under development (unstable) (2023-03-15 r83984 ucrt) -- "Unsuffered Consequences" | 4308 |
| merida1 | macOS 10.14.6 Mojave | x86_64 | R Under development (unstable) (2023-03-16 r83985) -- "Unsuffered Consequences" | 4301 |
| 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 | ||||
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To the developers/maintainers of the FindIT2 package: - Please allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/FindIT2.git to reflect on this report. See How and When does the builder pull? When will my changes propagate? for more information. - Make sure to use the following settings in order to reproduce any error or warning you see on this page. |
| Package 686/2195 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
| FindIT2 1.5.0 (landing page) Guandong Shang
| nebbiolo1 | Linux (Ubuntu 22.04.1 LTS) / x86_64 | OK | OK | OK | | ||||||||
| palomino3 | Windows Server 2022 Datacenter / x64 | OK | OK | OK | OK | | ||||||||
| merida1 | macOS 10.14.6 Mojave / x86_64 | OK | OK | OK | OK | | ||||||||
| Package: FindIT2 |
| Version: 1.5.0 |
| Command: /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings FindIT2_1.5.0.tar.gz |
| StartedAt: 2023-03-29 00:26:19 -0400 (Wed, 29 Mar 2023) |
| EndedAt: 2023-03-29 00:40:58 -0400 (Wed, 29 Mar 2023) |
| EllapsedTime: 878.8 seconds |
| RetCode: 0 |
| Status: OK |
| CheckDir: FindIT2.Rcheck |
| Warnings: 0 |
##############################################################################
##############################################################################
###
### Running command:
###
### /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings FindIT2_1.5.0.tar.gz
###
##############################################################################
##############################################################################
* using log directory ‘/Users/biocbuild/bbs-3.17-bioc/meat/FindIT2.Rcheck’
* using R Under development (unstable) (2023-03-16 r83985)
* using platform: x86_64-apple-darwin17.0 (64-bit)
* R was compiled by
Apple clang version 12.0.0 (clang-1200.0.32.29)
GNU Fortran (GCC) 8.2.0
* running under: macOS Mojave 10.14.6
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘FindIT2/DESCRIPTION’ ... OK
* this is package ‘FindIT2’ version ‘1.5.0’
* 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 for sufficient/correct file permissions ... OK
* checking whether package ‘FindIT2’ 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 R 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 ... OK
* 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
findIT_regionRP 11.938 0.130 16.047
calcRP_region 10.176 0.212 14.537
calcRP_coverage 6.547 0.504 10.086
plot_peakGeneCor 6.667 0.063 9.245
calcRP_TFHit 6.427 0.175 9.521
enhancerPromoterCor 6.250 0.069 8.402
peakGeneCor 5.310 0.042 7.150
integrate_ChIP_RNA 4.159 0.034 5.511
* checking for unstated dependencies in ‘tests’ ... OK
* checking tests ...
Running ‘testthat.R’
OK
* checking for unstated dependencies in vignettes ... OK
* checking package vignettes in ‘inst/doc’ ... OK
* checking running R code from vignettes ... SKIPPED
* checking re-building of vignette outputs ... SKIPPED
* checking PDF version of manual ... OK
* DONE
Status: OK
FindIT2.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### /Library/Frameworks/R.framework/Resources/bin/R CMD INSTALL FindIT2 ### ############################################################################## ############################################################################## * installing to library ‘/Library/Frameworks/R.framework/Versions/4.3/Resources/library’ * installing *source* package ‘FindIT2’ ... ** 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 (FindIT2)
FindIT2.Rcheck/tests/testthat.Rout
R Under development (unstable) (2023-03-16 r83985) -- "Unsuffered Consequences"
Copyright (C) 2023 The R Foundation for Statistical Computing
Platform: x86_64-apple-darwin17.0 (64-bit)
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(FindIT2)
Loading required package: GenomicRanges
Loading required package: stats4
Loading required package: BiocGenerics
Attaching package: 'BiocGenerics'
The following objects are masked from 'package:stats':
IQR, mad, sd, var, xtabs
The following objects are masked from 'package:base':
Filter, Find, Map, Position, Reduce, anyDuplicated, aperm, append,
as.data.frame, basename, cbind, colnames, dirname, do.call,
duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table,
tapply, union, unique, unsplit, which.max, which.min
Loading required package: S4Vectors
Attaching package: 'S4Vectors'
The following objects are masked from 'package:base':
I, expand.grid, unname
Loading required package: IRanges
Loading required package: GenomeInfoDb
> if (!requireNamespace("TxDb.Athaliana.BioMart.plantsmart28")) {
+ stop("unable to load TxDb.Athaliana.BioMart.plantsmart28")
+ }
Loading required namespace: TxDb.Athaliana.BioMart.plantsmart28
>
> test_check("FindIT2")
>> preparing gene features information... 2023-03-29 00:38:16
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:38:20
>> preparing weight info... 2023-03-29 00:38:20
>> loading E50h_sampleChr5.bw info... 2023-03-29 00:38:21
------------
>> extracting and calcluating Chr5 signal... 2023-03-29 00:38:21
>> dealing with Chr5 left gene signal... 2023-03-29 00:38:28
>> norming Chr5RP accoring to the whole Chr RP... 2023-03-29 00:38:29
>> merging all Chr RP together... 2023-03-29 00:38:29
>> done 2023-03-29 00:38:29
>> checking seqlevels match... 2023-03-29 00:38:29
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region... 2023-03-29 00:38:29
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:38:31
>> finding overlap peak in gene scan region... 2023-03-29 00:38:31
>> dealing with left peak not your gene scan region... 2023-03-29 00:38:31
>> merging two set peaks... 2023-03-29 00:38:32
>> calculating distance and dealing with gene strand... 2023-03-29 00:38:32
>> merging all info together ... 2023-03-29 00:38:32
>> done 2023-03-29 00:38:32
>> calculating peakCenter to TSS using peak-gene pair... 2023-03-29 00:38:32
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2023-03-29 00:38:35
>> calculating RP using centerToTSS and peak score2023-03-29 00:38:35
>> merging all info together 2023-03-29 00:38:41
>> done 2023-03-29 00:38:43
>> calculating peakCenter to TSS using peak-gene pair... 2023-03-29 00:38:43
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2023-03-29 00:38:46
>> calculating RP using centerToTSS and peak score2023-03-29 00:38:46
>> merging all info together 2023-03-29 00:38:54
>> done 2023-03-29 00:38:55
>> checking seqlevels match... 2023-03-29 00:38:55
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region... 2023-03-29 00:38:56
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:38:58
>> finding overlap peak in gene scan region... 2023-03-29 00:38:58
>> dealing with left peak not your gene scan region... 2023-03-29 00:38:58
>> merging two set peaks... 2023-03-29 00:38:58
>> calculating distance and dealing with gene strand... 2023-03-29 00:38:58
>> merging all info together ... 2023-03-29 00:38:59
>> done 2023-03-29 00:38:59
>> calculating peakCenter to TSS using peak-gene pair... 2023-03-29 00:38:59
>> calculating RP using centerToTSS and TF hit 2023-03-29 00:39:01
>> merging all info together 2023-03-29 00:39:01
>> done 2023-03-29 00:39:01
>> calculating peakCenter to TSS using peak-gene pair... 2023-03-29 00:39:01
>> calculating RP using centerToTSS and TF hit 2023-03-29 00:39:03
>> merging all info together 2023-03-29 00:39:03
>> done 2023-03-29 00:39:03
>> checking seqlevels match... 2023-03-29 00:39:05
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region... 2023-03-29 00:39:05
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:39:08
>> finding overlap peak in gene scan region... 2023-03-29 00:39:08
>> dealing with left peak not your gene scan region... 2023-03-29 00:39:08
>> merging two set peaks... 2023-03-29 00:39:08
>> calculating distance and dealing with gene strand... 2023-03-29 00:39:08
>> merging all info together ... 2023-03-29 00:39:09
>> done 2023-03-29 00:39:09
>> calculating peakCenter to TSS using peak-gene pair... 2023-03-29 00:39:09
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2023-03-29 00:39:12
>> calculating RP using centerToTSS and peak score2023-03-29 00:39:12
>> merging all info together 2023-03-29 00:39:17
>> done 2023-03-29 00:39:18
>> extracting RP info from regionRP... 2023-03-29 00:39:20
>> dealing with TF_GR_databse... 2023-03-29 00:39:20
>> calculating percent and p-value... 2023-03-29 00:39:20
>> dealing withE5_0h_R1... 2023-03-29 00:39:20
>> dealing withE5_0h_R2... 2023-03-29 00:39:20
>> dealing withE5_4h_R1... 2023-03-29 00:39:21
>> dealing withE5_4h_R2... 2023-03-29 00:39:21
>> dealing withE5_8h_R1... 2023-03-29 00:39:21
>> dealing withE5_8h_R2... 2023-03-29 00:39:21
>> dealing withE5_16h_R1... 2023-03-29 00:39:21
>> dealing withE5_16h_R2... 2023-03-29 00:39:21
>> dealing withE5_24h_R1... 2023-03-29 00:39:21
>> dealing withE5_24h_R2... 2023-03-29 00:39:22
>> dealing withE5_48h_R1... 2023-03-29 00:39:22
>> dealing withE5_48h_R2... 2023-03-29 00:39:22
>> dealing withE5_48h_R3... 2023-03-29 00:39:22
>> dealing withE5_72h_R1... 2023-03-29 00:39:22
>> dealing withE5_72h_R2... 2023-03-29 00:39:22
>> dealing withE5_72h_R3... 2023-03-29 00:39:22
>> merging all info together... 2023-03-29 00:39:22
>> done 2023-03-29 00:39:23
>> preparing gene features information... 2023-03-29 00:39:23
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:39:25
>> calculating p-value for each TF, which may be time consuming... 2023-03-29 00:39:25
>> merging all info together... 2023-03-29 00:39:25
>> done 2023-03-29 00:39:25
>> dealing with TF_GR_database... 2023-03-29 00:39:26
>> calculating coef and converting into z-score using INT... 2023-03-29 00:39:26
>> dealing with E5_0h_R1... 2023-03-29 00:39:26
>> dealing with E5_0h_R2... 2023-03-29 00:39:27
>> dealing with E5_4h_R1... 2023-03-29 00:39:27
>> dealing with E5_4h_R2... 2023-03-29 00:39:27
>> dealing with E5_8h_R1... 2023-03-29 00:39:27
>> dealing with E5_8h_R2... 2023-03-29 00:39:28
>> dealing with E5_16h_R1... 2023-03-29 00:39:28
>> dealing with E5_16h_R2... 2023-03-29 00:39:28
>> dealing with E5_24h_R1... 2023-03-29 00:39:28
>> dealing with E5_24h_R2... 2023-03-29 00:39:28
>> dealing with E5_48h_R1... 2023-03-29 00:39:29
>> dealing with E5_48h_R2... 2023-03-29 00:39:29
>> dealing with E5_48h_R3... 2023-03-29 00:39:29
>> dealing with E5_72h_R1... 2023-03-29 00:39:29
>> dealing with E5_72h_R2... 2023-03-29 00:39:29
>> dealing with E5_72h_R3... 2023-03-29 00:39:30
>> merging all info together... 2023-03-29 00:39:30
>> done 2023-03-29 00:39:30
>> checking seqlevels match... 2023-03-29 00:39:31
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region... 2023-03-29 00:39:31
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:39:33
>> finding overlap peak in gene scan region... 2023-03-29 00:39:33
>> dealing with left peak not your gene scan region... 2023-03-29 00:39:33
>> merging two set peaks... 2023-03-29 00:39:33
>> calculating distance and dealing with gene strand... 2023-03-29 00:39:33
>> merging all info together ... 2023-03-29 00:39:34
>> done 2023-03-29 00:39:34
>> calculating peakCenter to TSS using peak-gene pair... 2023-03-29 00:39:34
>> calculating RP using centerToTSS and TF hit 2023-03-29 00:39:35
>> merging all info together 2023-03-29 00:39:36
>> done 2023-03-29 00:39:36
>> checking seqlevels match... 2023-03-29 00:39:37
>> your peak_GR seqlevel:5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match... 2023-03-29 00:39:37
>> your peak_GR seqlevel:Chr5 Chr6...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match... 2023-03-29 00:39:45
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match... 2023-03-29 00:39:45
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2023-03-29 00:39:45
>> finding nearest gene and calculating distance... 2023-03-29 00:39:47
>> dealing with gene strand ... 2023-03-29 00:39:47
>> merging all info together ... 2023-03-29 00:39:47
>> done 2023-03-29 00:39:48
>> checking seqlevels match... 2023-03-29 00:39:48
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match... 2023-03-29 00:39:48
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2023-03-29 00:39:48
>> finding nearest gene and calculating distance... 2023-03-29 00:39:50
>> dealing with gene strand ... 2023-03-29 00:39:50
>> merging all info together ... 2023-03-29 00:39:50
>> done 2023-03-29 00:39:50
>> checking seqlevels match... 2023-03-29 00:39:53
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match... 2023-03-29 00:39:54
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2023-03-29 00:39:54
>> finding nearest gene and calculating distance... 2023-03-29 00:39:55
>> dealing with gene strand ... 2023-03-29 00:39:56
>> merging all info together ... 2023-03-29 00:39:56
>> done 2023-03-29 00:39:56
>> checking seqlevels match... 2023-03-29 00:39:58
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match... 2023-03-29 00:39:58
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2023-03-29 00:39:58
>> finding nearest gene and calculating distance... 2023-03-29 00:40:00
>> dealing with gene strand ... 2023-03-29 00:40:01
>> merging all info together ... 2023-03-29 00:40:01
>> done 2023-03-29 00:40:01
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match... 2023-03-29 00:40:03
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match... 2023-03-29 00:40:03
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2023-03-29 00:40:03
>> finding nearest gene and calculating distance... 2023-03-29 00:40:05
>> dealing with gene strand ... 2023-03-29 00:40:05
>> merging all info together ... 2023-03-29 00:40:05
>> done 2023-03-29 00:40:05
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match... 2023-03-29 00:40:08
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match... 2023-03-29 00:40:10
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:40:12
>> checking seqlevels match... 2023-03-29 00:40:14
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:40:16
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2023-03-29 00:40:20
>> merging all info together... 2023-03-29 00:40:20
>> done 2023-03-29 00:40:20
>> checking seqlevels match... 2023-03-29 00:40:20
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> using scanPromoter parameter to scan promoter for each gene... 2023-03-29 00:40:21
>> checking seqlevels match... 2023-03-29 00:40:21
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:40:23
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene... 2023-03-29 00:40:24
>> checking seqlevels match... 2023-03-29 00:40:24
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:40:26
>> calculating cor and pvalue, which may be time consuming... 2023-03-29 00:40:26
>> merging all info together... 2023-03-29 00:40:27
>> done 2023-03-29 00:40:27
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2023-03-29 00:40:27
>> merging all info together... 2023-03-29 00:40:27
>> done 2023-03-29 00:40:27
>> checking seqlevels match... 2023-03-29 00:40:28
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region... 2023-03-29 00:40:28
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:40:30
>> finding overlap peak in gene scan region... 2023-03-29 00:40:30
>> dealing with left peak not your gene scan region... 2023-03-29 00:40:30
>> merging two set peaks... 2023-03-29 00:40:30
>> calculating distance and dealing with gene strand... 2023-03-29 00:40:31
>> merging all info together ... 2023-03-29 00:40:31
>> done 2023-03-29 00:40:31
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2023-03-29 00:40:35
>> merging all info together... 2023-03-29 00:40:35
>> done 2023-03-29 00:40:36
>> checking seqlevels match... 2023-03-29 00:40:36
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> using scanPromoter parameter to scan promoter for each gene... 2023-03-29 00:40:36
>> checking seqlevels match... 2023-03-29 00:40:36
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:40:38
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene... 2023-03-29 00:40:39
>> checking seqlevels match... 2023-03-29 00:40:39
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming... 2023-03-29 00:40:41
>> calculating cor and pvalue, which may be time consuming... 2023-03-29 00:40:41
>> merging all info together... 2023-03-29 00:40:42
>> done 2023-03-29 00:40:42
Joining with `by = join_by(feature_id)`
Joining with `by = join_by(feature_id)`
`geom_smooth()` using formula = 'y ~ x'
Joining with `by = join_by(feature_id)`
Joining with `by = join_by(feature_id)`
`geom_smooth()` using formula = 'y ~ x'
[ FAIL 0 | WARN 0 | SKIP 0 | PASS 65 ]
>
> proc.time()
user system elapsed
130.711 2.509 179.574
FindIT2.Rcheck/FindIT2-Ex.timings
| name | user | system | elapsed | |
| TF_target_database | 0.001 | 0.000 | 0.001 | |
| calcRP_TFHit | 6.427 | 0.175 | 9.521 | |
| calcRP_coverage | 6.547 | 0.504 | 10.086 | |
| calcRP_region | 10.176 | 0.212 | 14.537 | |
| enhancerPromoterCor | 6.250 | 0.069 | 8.402 | |
| findIT_MARA | 0.933 | 0.053 | 1.270 | |
| findIT_TFHit | 1.873 | 0.046 | 2.595 | |
| findIT_TTPair | 0.155 | 0.007 | 0.225 | |
| findIT_enrichFisher | 0.329 | 0.005 | 0.440 | |
| findIT_enrichWilcox | 0.365 | 0.006 | 0.497 | |
| findIT_regionRP | 11.938 | 0.130 | 16.047 | |
| getAssocPairNumber | 2.332 | 0.026 | 3.152 | |
| integrate_ChIP_RNA | 4.159 | 0.034 | 5.511 | |
| integrate_replicates | 0.003 | 0.000 | 0.004 | |
| jaccard_findIT_TTpair | 0.214 | 0.006 | 0.285 | |
| jaccard_findIT_enrichFisher | 0.435 | 0.004 | 0.581 | |
| loadPeakFile | 0.124 | 0.001 | 0.166 | |
| mm_geneBound | 2.455 | 0.030 | 3.211 | |
| mm_geneScan | 2.407 | 0.029 | 3.105 | |
| mm_nearestGene | 2.179 | 0.026 | 2.904 | |
| peakGeneCor | 5.310 | 0.042 | 7.150 | |
| plot_annoDistance | 2.963 | 0.033 | 3.933 | |
| plot_peakGeneAlias_summary | 2.683 | 0.024 | 3.604 | |
| plot_peakGeneCor | 6.667 | 0.063 | 9.245 | |
| test_geneSet | 0.001 | 0.000 | 0.001 | |