R
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- (rev. 12)
- Hyungyong Kim
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설치 #
OS X #
$ brew install r
$ brew install r-gui
만일 문제가 있으면 다음 명령으로 관련 패키지들 모두 재설치.
$ brew reinstall $(brew deps r); brew reinstall r
OS X (구버전 설치) #
Homebrew에서는 최신버전만 가능하다. 구 버전은 별도의 디렉토리에 직접 컴파일 해야 한다. (Homebrew로 설치된 것을 지우고 해야 함)
$ brew remove r
$ ./configure --prefix=$HOME/R --with-x=no
$ make
$ make install
CentOS 사용자 홈디렉토리에 설치 #
직접 컴파일시, 의존적인 패키지들이 있을 수 있다. 홈 디렉토리에 별도의 패키지를 설치했다면 다음 처럼 컴파일해야 한다. (libz, bzip2, liblzma, pcre, libcurl) (pcre 컴파일시 --enable-utf8
옵션을 줘야하고, bzip2 설치시 Makefile CFLAG에 -fPIC 추가) 참고정보: Building R-devel on RedHat Linux 6
$ export LD_LIBRARY_PATH=$HOME/lib:$LD_LIBRARY_PATH
$ (export CFLAGS="-I$HOME/include"; export LDFLAGS="-L$HOME/lib"; ./configure --prefix=$HOME --with-cairo --with-jpeglib --with-readline --with-tcltk --with-blas --with-lapack --enable-R-profiling --enable-R-shlib --enable-memory-profiling)
관련정보 #
- R and Python cheatsheets
- The “Ten Simple Rules for Reproducible Computational Research” are easy to reach for R users
- Moving from R to Python: The Libraries You Need to Know : Python으로 넘어가기
Incoming Links #
[Codes] About (Code 0) #
Related Datasets (Dataset 1) #
Related Software Applications (SoftwareApplication 2) #
Related Articles (Article 3) #
Related Education Events (EducationEvent 4) #
Codes Written (Code 5) #
- ASCAT
- AscatNgs
- Ballgown
- Battenberg
- Biobase
- Bioconductor
- CODEX
- ChIP-PED
- ClusterCall
- DNAcopy
- DiffBind
- GeomicMating
- NarrowPeaks
- Pathview
- adegenet
- edgeR
- ngs.plot
- rrBLUP
Related Medical Scholarly Articles (MedicalScholarlyArticle 6) #
- Allele-specific copy number profiling by next-generation DNA sequencing
- SAAS-CNV: A Joint Segmentation Approach on Aggregated and Allele Specific Signals for the Identification of Somatic Copy Number Alterations with Next-Generation Sequencing Data
- Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown
Related Codes (Code 7) #
Suggested Pages #
- 0.141 Text-to-image model
- 0.101 F-statistics
- 0.083 DECIPHER
- 0.063 Anaconda
- 0.056 CBS
- 0.050 CODEX: a normalization and copy number variation detection method for whole exome sequencing
- 0.043 Kubeflow
- 0.042 Naive Bayes classifier
- 0.037 DECIPHER (database)
- 0.036 Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data
- More suggestions...