Guandong Shang
| Snapshot Date: 2022-01-26 13:55:18 -0500 (Wed, 26 Jan 2022) |
| git_url: https://git.bioconductor.org/packages/FindIT2 |
| git_branch: master |
| git_last_commit: 4c4fab3 |
| git_last_commit_date: 2021-12-28 22:18:58 -0500 (Tue, 28 Dec 2021) |
| Back to Multiple platform build/check report for BioC 3.15 |
|
This page was generated on 2022-01-27 11:10:36 -0500 (Thu, 27 Jan 2022).
| Hostname | OS | Arch (*) | R version | Installed pkgs |
|---|---|---|---|---|
| nebbiolo1 | Linux (Ubuntu 20.04.4 LTS) | x86_64 | R Under development (unstable) (2022-01-05 r81451) -- "Unsuffered Consequences" | 4167 |
| riesling1 | Windows Server 2019 Standard | x64 | R Under development (unstable) (2021-11-21 r81221) -- "Unsuffered Consequences" | 4062 |
| palomino3 | Windows Server 2022 Datacenter | x64 | R Under development (unstable) (2021-12-21 r81400 ucrt) -- "Unsuffered Consequences" | 4004 |
| merida1 | macOS 10.14.6 Mojave | x86_64 | R Under development (unstable) (2022-01-05 r81451) -- "Unsuffered Consequences" | 4121 |
| 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 | ||||
|
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? here for more information. - Make sure to use the following settings in order to reproduce any error or warning you see on this page. |
| Package 641/2077 | Hostname | OS / Arch | INSTALL | BUILD | CHECK | BUILD BIN | ||||||||
| FindIT2 1.1.3 (landing page) Guandong Shang
| nebbiolo1 | Linux (Ubuntu 20.04.4 LTS) / x86_64 | OK | OK | OK | | ||||||||
| riesling1 | Windows Server 2019 Standard / x64 | OK | OK | OK | NA | |||||||||
| 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: 1.1.3 |
| 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_1.1.3.tar.gz |
| StartedAt: 2022-01-27 00:59:38 -0500 (Thu, 27 Jan 2022) |
| EndedAt: 2022-01-27 01:08:56 -0500 (Thu, 27 Jan 2022) |
| EllapsedTime: 557.8 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_1.1.3.tar.gz
###
##############################################################################
##############################################################################
* using log directory ‘/Users/biocbuild/bbs-3.15-bioc/meat/FindIT2.Rcheck’
* using R Under development (unstable) (2022-01-05 r81451)
* using platform: x86_64-apple-darwin17.0 (64-bit)
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘FindIT2/DESCRIPTION’ ... OK
* this is package ‘FindIT2’ version ‘1.1.3’
* 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 ... NOTE
Found the following hidden files and directories:
.git_fetch_output.txt
.git_merge_output.txt
These were most likely included in error. See section ‘Package
structure’ in the ‘Writing R Extensions’ manual.
* 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 11.095 0.140 11.261
calcRP_region 9.012 0.176 9.205
calcRP_coverage 6.970 0.725 7.712
calcRP_TFHit 6.239 0.223 6.580
plot_peakGeneCor 5.488 0.059 5.556
enhancerPromoterCor 4.947 0.051 5.014
* 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: 1 NOTE
See
‘/Users/biocbuild/bbs-3.15-bioc/meat/FindIT2.Rcheck/00check.log’
for details.
FindIT2.Rcheck/00install.out
############################################################################## ############################################################################## ### ### Running command: ### ### /Library/Frameworks/R.framework/Resources/bin/R CMD INSTALL FindIT2 ### ############################################################################## ############################################################################## * installing to library ‘/Library/Frameworks/R.framework/Versions/4.2/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) (2022-01-05 r81451) -- "Unsuffered Consequences"
Copyright (C) 2022 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, 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... 2022-01-27 01:07:08
>> some scan range may cross Chr bound, trimming... 2022-01-27 01:07:10
>> preparing weight info... 2022-01-27 01:07:10
>> loading E50h_sampleChr5.bw info... 2022-01-27 01:07:10
------------
>> extracting and calcluating Chr5 signal... 2022-01-27 01:07:11
>> dealing with Chr5 left gene signal... 2022-01-27 01:07:15
>> norming Chr5RP accoring to the whole Chr RP... 2022-01-27 01:07:15
>> merging all Chr RP together... 2022-01-27 01:07:15
>> done 2022-01-27 01:07:15
>> checking seqlevels match... 2022-01-27 01:07:16
>> 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... 2022-01-27 01:07:16
>> some scan range may cross Chr bound, trimming... 2022-01-27 01:07:17
>> finding overlap peak in gene scan region... 2022-01-27 01:07:17
>> dealing with left peak not your gene scan region... 2022-01-27 01:07:17
>> merging two set peaks... 2022-01-27 01:07:18
>> calculating distance and dealing with gene strand... 2022-01-27 01:07:18
>> merging all info together ... 2022-01-27 01:07:18
>> done 2022-01-27 01:07:18
>> calculating peakCenter to TSS using peak-gene pair... 2022-01-27 01:07:18
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2022-01-27 01:07:19
>> calculating RP using centerToTSS and peak score2022-01-27 01:07:19
>> merging all info together 2022-01-27 01:07:24
>> done 2022-01-27 01:07:26
>> calculating peakCenter to TSS using peak-gene pair... 2022-01-27 01:07:26
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2022-01-27 01:07:27
>> calculating RP using centerToTSS and peak score2022-01-27 01:07:27
>> merging all info together 2022-01-27 01:07:32
>> done 2022-01-27 01:07:33
>> checking seqlevels match... 2022-01-27 01:07:33
>> 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... 2022-01-27 01:07:34
>> some scan range may cross Chr bound, trimming... 2022-01-27 01:07:35
>> finding overlap peak in gene scan region... 2022-01-27 01:07:35
>> dealing with left peak not your gene scan region... 2022-01-27 01:07:35
>> merging two set peaks... 2022-01-27 01:07:35
>> calculating distance and dealing with gene strand... 2022-01-27 01:07:35
>> merging all info together ... 2022-01-27 01:07:35
>> done 2022-01-27 01:07:35
>> calculating peakCenter to TSS using peak-gene pair... 2022-01-27 01:07:35
>> calculating RP using centerToTSS and TF hit 2022-01-27 01:07:37
>> merging all info together 2022-01-27 01:07:37
>> done 2022-01-27 01:07:37
>> calculating peakCenter to TSS using peak-gene pair... 2022-01-27 01:07:37
>> calculating RP using centerToTSS and TF hit 2022-01-27 01:07:38
>> merging all info together 2022-01-27 01:07:38
>> done 2022-01-27 01:07:39
>> checking seqlevels match... 2022-01-27 01:07:40
>> 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... 2022-01-27 01:07:40
>> some scan range may cross Chr bound, trimming... 2022-01-27 01:07:41
>> finding overlap peak in gene scan region... 2022-01-27 01:07:41
>> dealing with left peak not your gene scan region... 2022-01-27 01:07:41
>> merging two set peaks... 2022-01-27 01:07:42
>> calculating distance and dealing with gene strand... 2022-01-27 01:07:42
>> merging all info together ... 2022-01-27 01:07:42
>> done 2022-01-27 01:07:42
>> calculating peakCenter to TSS using peak-gene pair... 2022-01-27 01:07:42
>> pre-filling 1356 noAssoc peak gene's RP with 0... 2022-01-27 01:07:43
>> calculating RP using centerToTSS and peak score2022-01-27 01:07:43
>> merging all info together 2022-01-27 01:07:48
>> done 2022-01-27 01:07:48
>> extracting RP info from regionRP... 2022-01-27 01:07:50
>> dealing with TF_GR_databse... 2022-01-27 01:07:50
>> calculating percent and p-value... 2022-01-27 01:07:50
>> dealing withE5_0h_R1... 2022-01-27 01:07:50
>> dealing withE5_0h_R2... 2022-01-27 01:07:50
>> dealing withE5_4h_R1... 2022-01-27 01:07:50
>> dealing withE5_4h_R2... 2022-01-27 01:07:50
>> dealing withE5_8h_R1... 2022-01-27 01:07:50
>> dealing withE5_8h_R2... 2022-01-27 01:07:50
>> dealing withE5_16h_R1... 2022-01-27 01:07:50
>> dealing withE5_16h_R2... 2022-01-27 01:07:50
>> dealing withE5_24h_R1... 2022-01-27 01:07:50
>> dealing withE5_24h_R2... 2022-01-27 01:07:50
>> dealing withE5_48h_R1... 2022-01-27 01:07:50
>> dealing withE5_48h_R2... 2022-01-27 01:07:50
>> dealing withE5_48h_R3... 2022-01-27 01:07:51
>> dealing withE5_72h_R1... 2022-01-27 01:07:51
>> dealing withE5_72h_R2... 2022-01-27 01:07:51
>> dealing withE5_72h_R3... 2022-01-27 01:07:51
>> merging all info together... 2022-01-27 01:07:51
>> done 2022-01-27 01:07:51
>> preparing gene features information... 2022-01-27 01:07:52
>> some scan range may cross Chr bound, trimming... 2022-01-27 01:07:53
>> calculating p-value for each TF, which may be time consuming... 2022-01-27 01:07:53
>> merging all info together... 2022-01-27 01:07:53
>> done 2022-01-27 01:07:53
>> dealing with TF_GR_database... 2022-01-27 01:07:53
>> calculating coef and converting into z-score using INT... 2022-01-27 01:07:54
>> dealing withE5_0h_R1... 2022-01-27 01:07:54
>> dealing withE5_0h_R2... 2022-01-27 01:07:54
>> dealing withE5_4h_R1... 2022-01-27 01:07:54
>> dealing withE5_4h_R2... 2022-01-27 01:07:55
>> dealing withE5_8h_R1... 2022-01-27 01:07:55
>> dealing withE5_8h_R2... 2022-01-27 01:07:55
>> dealing withE5_16h_R1... 2022-01-27 01:07:55
>> dealing withE5_16h_R2... 2022-01-27 01:07:55
>> dealing withE5_24h_R1... 2022-01-27 01:07:55
>> dealing withE5_24h_R2... 2022-01-27 01:07:56
>> dealing withE5_48h_R1... 2022-01-27 01:07:56
>> dealing withE5_48h_R2... 2022-01-27 01:07:56
>> dealing withE5_48h_R3... 2022-01-27 01:07:56
>> dealing withE5_72h_R1... 2022-01-27 01:07:56
>> dealing withE5_72h_R2... 2022-01-27 01:07:56
>> dealing withE5_72h_R3... 2022-01-27 01:07:57
>> merging all info together... 2022-01-27 01:07:57
>> done 2022-01-27 01:07:57
>> checking seqlevels match... 2022-01-27 01:07:57
>> 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... 2022-01-27 01:07:57
>> some scan range may cross Chr bound, trimming... 2022-01-27 01:07:59
>> finding overlap peak in gene scan region... 2022-01-27 01:07:59
>> dealing with left peak not your gene scan region... 2022-01-27 01:07:59
>> merging two set peaks... 2022-01-27 01:07:59
>> calculating distance and dealing with gene strand... 2022-01-27 01:07:59
>> merging all info together ... 2022-01-27 01:07:59
>> done 2022-01-27 01:07:59
>> calculating peakCenter to TSS using peak-gene pair... 2022-01-27 01:07:59
>> calculating RP using centerToTSS and TF hit 2022-01-27 01:08:00
>> merging all info together 2022-01-27 01:08:00
>> done 2022-01-27 01:08:01
>> checking seqlevels match... 2022-01-27 01:08:01
>> your peak_GR seqlevel:5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match... 2022-01-27 01:08:02
>> your peak_GR seqlevel:Chr5 Chr6...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match... 2022-01-27 01:08:08
>> 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... 2022-01-27 01:08:08
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2022-01-27 01:08:08
>> finding nearest gene and calculating distance... 2022-01-27 01:08:09
>> dealing with gene strand ... 2022-01-27 01:08:09
>> merging all info together ... 2022-01-27 01:08:09
>> done 2022-01-27 01:08:09
>> checking seqlevels match... 2022-01-27 01:08:10
>> 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
>> checking seqlevels match... 2022-01-27 01:08:10
>> 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
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information... 2022-01-27 01:08:10
>> finding nearest gene and calculating distance... 2022-01-27 01:08:11
>> dealing with gene strand ... 2022-01-27 01:08:11
>> merging all info together ... 2022-01-27 01:08:11
>> done 2022-01-27 01:08:11
>> checking seqlevels match... 2022-01-27 01:08:13
>> 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... 2022-01-27 01:08:13
>> 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... 2022-01-27 01:08:13
>> finding nearest gene and calculating distance... 2022-01-27 01:08:14
>> dealing with gene strand ... 2022-01-27 01:08:14
>> merging all info together ... 2022-01-27 01:08:14
>> done 2022-01-27 01:08:14
>> checking seqlevels match... 2022-01-27 01:08:16
>> 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... 2022-01-27 01:08:16
>> 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... 2022-01-27 01:08:16
>> finding nearest gene and calculating distance... 2022-01-27 01:08:17
>> dealing with gene strand ... 2022-01-27 01:08:18
>> merging all info together ... 2022-01-27 01:08:18
>> done 2022-01-27 01:08:18
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match... 2022-01-27 01:08:19
>> 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... 2022-01-27 01:08:19
>> 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... 2022-01-27 01:08:19
>> finding nearest gene and calculating distance... 2022-01-27 01:08:20
>> dealing with gene strand ... 2022-01-27 01:08:21
>> merging all info together ... 2022-01-27 01:08:21
>> done 2022-01-27 01:08:21
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match... 2022-01-27 01:08:22
>> 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... 2022-01-27 01:08:24
>> 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... 2022-01-27 01:08:25
>> checking seqlevels match... 2022-01-27 01:08:27
>> 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... 2022-01-27 01:08:28
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2022-01-27 01:08:31
>> merging all info together... 2022-01-27 01:08:31
>> done 2022-01-27 01:08:31
>> checking seqlevels match... 2022-01-27 01:08:31
>> 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
>> using scanPromoter parameter to scan promoter for each gene... 2022-01-27 01:08:31
>> checking seqlevels match... 2022-01-27 01:08:31
>> 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
>> some scan range may cross Chr bound, trimming... 2022-01-27 01:08:32
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene... 2022-01-27 01:08:33
>> checking seqlevels match... 2022-01-27 01:08:33
>> 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... 2022-01-27 01:08:34
>> calculating cor and pvalue, which may be time consuming... 2022-01-27 01:08:34
>> merging all info together... 2022-01-27 01:08:35
>> done 2022-01-27 01:08:35
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2022-01-27 01:08:35
>> merging all info together... 2022-01-27 01:08:35
>> done 2022-01-27 01:08:36
>> checking seqlevels match... 2022-01-27 01:08:36
>> 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
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region... 2022-01-27 01:08:36
>> some scan range may cross Chr bound, trimming... 2022-01-27 01:08:37
>> finding overlap peak in gene scan region... 2022-01-27 01:08:37
>> dealing with left peak not your gene scan region... 2022-01-27 01:08:37
>> merging two set peaks... 2022-01-27 01:08:38
>> calculating distance and dealing with gene strand... 2022-01-27 01:08:38
>> merging all info together ... 2022-01-27 01:08:38
>> done 2022-01-27 01:08:38
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming... 2022-01-27 01:08:40
>> merging all info together... 2022-01-27 01:08:40
>> done 2022-01-27 01:08:40
>> checking seqlevels match... 2022-01-27 01:08:40
>> 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... 2022-01-27 01:08:40
>> checking seqlevels match... 2022-01-27 01:08:40
>> 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... 2022-01-27 01:08:41
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene... 2022-01-27 01:08:42
>> checking seqlevels match... 2022-01-27 01:08:42
>> 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... 2022-01-27 01:08:43
>> calculating cor and pvalue, which may be time consuming... 2022-01-27 01:08:44
>> merging all info together... 2022-01-27 01:08:44
>> done 2022-01-27 01:08:44
Joining, by = "feature_id"
Joining, by = "feature_id"
`geom_smooth()` using formula 'y ~ x'
Joining, by = "feature_id"
Joining, by = "feature_id"
`geom_smooth()` using formula 'y ~ x'
[ FAIL 0 | WARN 0 | SKIP 0 | PASS 65 ]
>
> proc.time()
user system elapsed
114.875 2.533 117.976
FindIT2.Rcheck/FindIT2-Ex.timings
| name | user | system | elapsed | |
| TF_target_database | 0.000 | 0.000 | 0.001 | |
| calcRP_TFHit | 6.239 | 0.223 | 6.580 | |
| calcRP_coverage | 6.970 | 0.725 | 7.712 | |
| calcRP_region | 9.012 | 0.176 | 9.205 | |
| enhancerPromoterCor | 4.947 | 0.051 | 5.014 | |
| findIT_MARA | 0.628 | 0.015 | 0.645 | |
| findIT_TFHit | 1.691 | 0.021 | 1.714 | |
| findIT_TTPair | 0.212 | 0.010 | 0.222 | |
| findIT_enrichFisher | 0.308 | 0.005 | 0.313 | |
| findIT_enrichWilcox | 0.340 | 0.004 | 0.345 | |
| findIT_regionRP | 11.095 | 0.140 | 11.261 | |
| getAssocPairNumber | 3.087 | 0.023 | 3.124 | |
| integrate_ChIP_RNA | 3.514 | 0.032 | 3.551 | |
| integrate_replicates | 0.003 | 0.001 | 0.004 | |
| jaccard_findIT_TTpair | 0.247 | 0.010 | 0.257 | |
| jaccard_findIT_enrichFisher | 0.399 | 0.006 | 0.405 | |
| loadPeakFile | 0.132 | 0.003 | 0.135 | |
| mm_geneBound | 2.045 | 0.016 | 2.063 | |
| mm_geneScan | 2.083 | 0.028 | 2.113 | |
| mm_nearestGene | 1.851 | 0.027 | 1.884 | |
| peakGeneCor | 4.482 | 0.057 | 4.552 | |
| plot_annoDistance | 2.628 | 0.028 | 2.662 | |
| plot_peakGeneAlias_summary | 2.490 | 0.030 | 2.532 | |
| plot_peakGeneCor | 5.488 | 0.059 | 5.556 | |
| test_geneSet | 0.000 | 0.000 | 0.001 | |