How to Install and Uninstall berkeley-express Package on Ubuntu 21.10 (Impish Indri)

Last updated: May 19,2024

1. Install "berkeley-express" package

In this section, we are going to explain the necessary steps to install berkeley-express on Ubuntu 21.10 (Impish Indri)


    
        
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                sudo apt update
            
                    
    
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            $
        

        
            
                sudo apt install
            
                        
                berkeley-express
            
                    
    
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2. Uninstall "berkeley-express" package

Please follow the guidance below to uninstall berkeley-express on Ubuntu 21.10 (Impish Indri):


    
        
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                sudo apt remove
            
                        
                berkeley-express
            
                    
    
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            $
        

        
            
                sudo apt autoclean && sudo apt autoremove
            
                    
    
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3. Information about the berkeley-express package on Ubuntu 21.10 (Impish Indri)

Package: berkeley-express
Architecture: amd64
Version: 1.5.3+dfsg-1build4
Priority: optional
Section: universe/science
Origin: Ubuntu
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Installed-Size: 742
Depends: libbamtools2.5.1 (>= 2.5.1+dfsg), libboost-filesystem1.74.0 (>= 1.74.0), libboost-program-options1.74.0 (>= 1.74.0), libboost-thread1.74.0 (>= 1.74.0), libc6 (>= 2.29), libgcc-s1 (>= 3.0), libprotobuf23 (>= 3.12.3), libstdc++6 (>= 9)
Recommends: med-config (>= 2.1)
Filename: pool/universe/b/berkeley-express/berkeley-express_1.5.3+dfsg-1build4_amd64.deb
Size: 228092
MD5sum: 7da0e7bd76ee1370317946c0e8997917
SHA1: af67864a5780a439f8c1e375927106b683276667
SHA256: d977e1fcadb1e3d48c38d30decc16df386add2d2ef349c826acb4ef487062465
SHA512: 53c6a07f1276eb5d1b9a9721f70aacf62d740e51b2b6f17a5197b6ec2ed33cba5a45dab7eab219ea1be2e31599fce5d34a1ad51c8ba6995b134d4e7b8cfd253b
Homepage: http://bio.math.berkeley.edu/eXpress/index.html
Description-en: Streaming quantification for high-throughput sequencing
eXpress is a streaming tool for quantifying the abundances of a set of
target sequences from sampled subsequences. Example applications include
transcript-level RNA-Seq quantification, allele-specific/haplotype
expression analysis (from RNA-Seq), transcription factor binding
quantification in ChIP-Seq, and analysis of metagenomic data. It is
based on an online-EM algorithm that results in space (memory)
requirements proportional to the total size of the target sequences and
time requirements that are proportional to the number of sampled
fragments. Thus, in applications such as RNA-Seq, eXpress can accurately
quantify much larger samples than other currently available tools
greatly reducing computing infrastructure requirements. eXpress can be
used to build lightweight high-throughput sequencing processing
pipelines when coupled with a streaming aligner (such as Bowtie), as
output can be piped directly into eXpress, effectively eliminating the
need to store read alignments in memory or on disk.
.
In an analysis of the performance of eXpress for RNA-Seq data, it was
observed that this efficiency does not come at a cost of accuracy.
eXpress is more accurate than other available tools, even when limited
to smaller datasets that do not require such efficiency. Moreover, like
the Cufflinks program, eXpress can be used to estimate transcript
abundances in multi-isoform genes. eXpress is also able to resolve
multi-mappings of reads across gene families, and does not require a
reference genome so that it can be used in conjunction with de novo
assemblers such as Trinity, Oases, or Trans-ABySS. The underlying model
is based on previously described probabilistic models developed for
RNA-Seq but is applicable to other settings where target sequences are
sampled, and includes parameters for fragment length distributions,
errors in reads, and sequence-specific fragment bias.
.
eXpress can be used to resolve ambiguous mappings in other
high-throughput sequencing based applications. The only required inputs
to eXpress are a set of target sequences and a set of sequenced
fragments multiply-aligned to them. While these target sequences will
often be gene isoforms, they need not be. Haplotypes can be used as the
reference for allele-specific expression analysis, binding regions for
ChIP-Seq, or target genomes in metagenomics experiments. eXpress is
useful in any analysis where reads multi-map to sequences that differ in
abundance.
Description-md5: 4d4c6aaf75f2e0fff660b1816f1f13c6