How to Install and Uninstall berkeley-express Package on Kali Linux
Last updated: December 24,2024
1. Install "berkeley-express" package
Please follow the guidance below to install berkeley-express on Kali Linux
$
sudo apt update
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$
sudo apt install
berkeley-express
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2. Uninstall "berkeley-express" package
This guide covers the steps necessary to uninstall berkeley-express on Kali Linux:
$
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 Kali Linux
Package: berkeley-express
Source: berkeley-express (1.5.3+dfsg-3)
Version: 1.5.3+dfsg-3+b2
Installed-Size: 759
Maintainer: Debian Med Packaging Team
Architecture: amd64
Depends: libbamtools2.5.2 (>= 2.5.2+dfsg), libboost-filesystem1.83.0 (>= 1.83.0), libboost-program-options1.83.0 (>= 1.83.0), libboost-thread1.83.0 (>= 1.83.0), libc6 (>= 2.34), libgcc-s1 (>= 3.0), libprotobuf32 (>= 3.21.12), libstdc++6 (>= 13.1)
Recommends: med-config
Size: 232984
SHA256: 5d15820dca8c10a3aa79b513bd0573f7690e5d1e8d1bd91b89c6b3d335f476a8
SHA1: 7778bf5685b38b0c8b6a19ffe5fdfe5fb01fce5b
MD5sum: 2490cb36149bff8af59a925b693eb430
Description: 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:
Homepage: http://bio.math.berkeley.edu/eXpress/index.html
Tag: biology::nucleic-acids, field::biology, field::biology:bioinformatics,
implemented-in::c++, interface::commandline, role::program,
works-with::biological-sequence
Section: science
Priority: optional
Filename: pool/main/b/berkeley-express/berkeley-express_1.5.3+dfsg-3+b2_amd64.deb
Source: berkeley-express (1.5.3+dfsg-3)
Version: 1.5.3+dfsg-3+b2
Installed-Size: 759
Maintainer: Debian Med Packaging Team
Architecture: amd64
Depends: libbamtools2.5.2 (>= 2.5.2+dfsg), libboost-filesystem1.83.0 (>= 1.83.0), libboost-program-options1.83.0 (>= 1.83.0), libboost-thread1.83.0 (>= 1.83.0), libc6 (>= 2.34), libgcc-s1 (>= 3.0), libprotobuf32 (>= 3.21.12), libstdc++6 (>= 13.1)
Recommends: med-config
Size: 232984
SHA256: 5d15820dca8c10a3aa79b513bd0573f7690e5d1e8d1bd91b89c6b3d335f476a8
SHA1: 7778bf5685b38b0c8b6a19ffe5fdfe5fb01fce5b
MD5sum: 2490cb36149bff8af59a925b693eb430
Description: 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:
Homepage: http://bio.math.berkeley.edu/eXpress/index.html
Tag: biology::nucleic-acids, field::biology, field::biology:bioinformatics,
implemented-in::c++, interface::commandline, role::program,
works-with::biological-sequence
Section: science
Priority: optional
Filename: pool/main/b/berkeley-express/berkeley-express_1.5.3+dfsg-3+b2_amd64.deb