How to Install and Uninstall berkeley-express-doc Package on Ubuntu 16.04 LTS (Xenial Xerus)
Last updated: November 07,2024
1. Install "berkeley-express-doc" package
Please follow the instructions below to install berkeley-express-doc on Ubuntu 16.04 LTS (Xenial Xerus)
$
sudo apt update
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$
sudo apt install
berkeley-express-doc
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2. Uninstall "berkeley-express-doc" package
Please follow the guidelines below to uninstall berkeley-express-doc on Ubuntu 16.04 LTS (Xenial Xerus):
$
sudo apt remove
berkeley-express-doc
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$
sudo apt autoclean && sudo apt autoremove
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3. Information about the berkeley-express-doc package on Ubuntu 16.04 LTS (Xenial Xerus)
Package: berkeley-express-doc
Priority: optional
Section: universe/doc
Installed-Size: 1375
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Architecture: all
Source: berkeley-express
Version: 1.5.1-1
Filename: pool/universe/b/berkeley-express/berkeley-express-doc_1.5.1-1_all.deb
Size: 790536
MD5sum: eba75205ceb420536b97b3428ac8cc53
SHA1: 79808dadce5c5c27378594418c1907ce6d0454bd
SHA256: 4be254f3cdf46d4cb74ffce635fcdab037a7d8c364ab5951a52806935c57802e
Description-en: Documentation for RNA-Seq tool eXpress
This package provides a PDF with the documentation for eXpress.
.
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: 6872981809a9528fac787c2292ad040e
Homepage: http://bio.math.berkeley.edu/eXpress/index.html
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Origin: Ubuntu
Priority: optional
Section: universe/doc
Installed-Size: 1375
Maintainer: Ubuntu Developers
Original-Maintainer: Debian Med Packaging Team
Architecture: all
Source: berkeley-express
Version: 1.5.1-1
Filename: pool/universe/b/berkeley-express/berkeley-express-doc_1.5.1-1_all.deb
Size: 790536
MD5sum: eba75205ceb420536b97b3428ac8cc53
SHA1: 79808dadce5c5c27378594418c1907ce6d0454bd
SHA256: 4be254f3cdf46d4cb74ffce635fcdab037a7d8c364ab5951a52806935c57802e
Description-en: Documentation for RNA-Seq tool eXpress
This package provides a PDF with the documentation for eXpress.
.
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: 6872981809a9528fac787c2292ad040e
Homepage: http://bio.math.berkeley.edu/eXpress/index.html
Bugs: https://bugs.launchpad.net/ubuntu/+filebug
Origin: Ubuntu