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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37796?offset=560</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38452/silix-implements-an-ultra-efficient-algorithm-for-the-clustering-of-homologous-sequences</guid>
	<pubDate>Wed, 12 Dec 2018 09:22:41 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38452/silix-implements-an-ultra-efficient-algorithm-for-the-clustering-of-homologous-sequences</link>
	<title><![CDATA[SiLiX: implements an ultra-efficient algorithm for the clustering of homologous sequences]]></title>
	<description><![CDATA[<p>The software package SiLiX implements<strong>&nbsp;an ultra-efficient algorithm for the clustering of homologous sequences</strong>, based on single transitive links (<em>single linkage</em>) with alignment coverage constraints.</p>
<p>SiLiX adopts a graph-theoretical framework to interpret similarity pairs as edges of a network. A very efficient algorithm, based on the&nbsp;<em>Disjoint Sets Data Structure</em>, allows the computation of sequence families with&nbsp;<strong>low time and space requirements</strong>.</p>
<p><strong>A parallel version</strong>&nbsp;of SiLiX, based on MPI, is also available in this package and has been proved to be scalable, so that its allows the study of&nbsp;<strong>very large datasets</strong>.</p>
<p>SiLiX is already included in the analysis pipeline for&nbsp;<a href="http://pbil.univ-lyon1.fr/databases/hogenom/acceuil.php">HOGENOM</a>.</p><p>Address of the bookmark: <a href="http://lbbe.univ-lyon1.fr/SiLiX?lang=fr" rel="nofollow">http://lbbe.univ-lyon1.fr/SiLiX?lang=fr</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/41230/curated-set-of-ribosomal-rna-rrna-reference-sequences-targeted-loci-with-verifiable-organism</guid>
	<pubDate>Sun, 23 Feb 2020 02:17:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/41230/curated-set-of-ribosomal-rna-rrna-reference-sequences-targeted-loci-with-verifiable-organism</link>
	<title><![CDATA[Curated set of ribosomal RNA (rRNA) reference sequences (targeted loci) with verifiable organism]]></title>
	<description><![CDATA[<p>MCBI have a curated set of ribosomal RNA (rRNA) reference sequences (targeted loci) with verifiable organism sources and current names. This set is critical for correctly identifying and classifying prokaryotic (bacteria and archaea) and fungal samples. To provide easy access to these sequences, we recently added a separate rRNA/ITS databases section on the nucleotide BLAST page for these targeted sequences that makes it convenient to quickly identify source organisms. The new databases are: </p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; *16S ribosomal RNA (Bacteria and Archaea)</p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; *18S ribosomal RNA sequences (SSU) from Fungi type and reference material&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; *28S ribosomal RNA sequences (LSU) from Fungi type and reference material</p><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; *Internal transcribed spacer region (ITS) from Fungi type and reference material</p><p>You can also download these from the BLAST db FTP area.&nbsp; See the <a href="https://go.usa.gov/xdEBX" target="_blank">NCBI Insights post</a> for more detail. </p><p>Useful links</p><p>-----------------</p><p><a href="https://go.usa.gov/xdEj5" target="_blank">BLAST form with rRNA/ITS databases</a></p><p><a href="https://ftp.ncbi.nlm.nih.gov/blast/db/" target="_blank">BLAST db download</a></p><p><a href="https://www.ncbi.nlm.nih.gov/refseq/targetedloci/" target="_blank">Targeted loci</a></p><p><span style="color: black;">If you have any questions or concerns, please contact <a href="mailto:blast-help@ncbi.nlm.nih.gov" target="_blank" title="Follow link">blast-help@ncbi.nlm.nih.gov<sup><span style="color: black; text-decoration: none;"><img src="https://mail.google.com/mail/u/0?ui=2&amp;ik=024a8aa0b9&amp;attid=0.1&amp;permmsgid=msg-f:1659255165855446848&amp;th=1706dbc8408bb740&amp;view=fimg&amp;sz=s0-l75-ft&amp;attbid=ANGjdJ_drW2ArYDNLoHrQh36gm6rp2Std8ZUSplCzP6bYQSQYBsQfZ_85vOujXOdTRdaLxrR7QeEBVUbyACPBJHhFUeIglX8G7Ew7TcclzhvO7fJhiz7sIdkkDgZ7QA&amp;disp=emb" alt="https://jira.ncbi.nlm.nih.gov/images/icons/mail_small.gif" width="13" height="12" style="border: 0px;"></span></sup></a></span></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43826/tiara-deep-learning-based-classification-system-for-eukaryotic-sequences</guid>
	<pubDate>Mon, 14 Mar 2022 23:02:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43826/tiara-deep-learning-based-classification-system-for-eukaryotic-sequences</link>
	<title><![CDATA[Tiara: deep learning-based classification system for eukaryotic sequences]]></title>
	<description><![CDATA[<p><span>With a large number of metagenomic datasets becoming available, eukaryotic metagenomics emerged as a new challenge. The proper classification of eukaryotic nuclear and organellar genomes is an essential step toward a better understanding of eukaryotic diversity.</span></p><p>Address of the bookmark: <a href="https://academic.oup.com/bioinformatics/article/38/2/344/6375939" rel="nofollow">https://academic.oup.com/bioinformatics/article/38/2/344/6375939</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/19087/dcgor</guid>
	<pubDate>Sat, 08 Nov 2014 14:54:28 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/19087/dcgor</link>
	<title><![CDATA[dcGOR]]></title>
	<description><![CDATA[<p>An R package for analysing ontologies and protein domain annotations has been published in PLoS Computational Biology (http://dx.doi.org/10.1371/journal.pcbi.1003929). The package is distributed as part of CRAN (http://cran.r-project.org/package=dcGOR), and also at GitHub for version control.<br /><br />The dedicated website is available in http://supfam.org/dcGOR, from which several demos are also provided:<br /><br />1. Analysing SCOP domains: http://supfam.org/dcGOR/demo-Fang.html<br /><br />2. Analysing Pfam domains: http://supfam.org/dcGOR/demo-Basu.html<br /><br />3. Analysing InterPro domains: http://supfam.org/dcGOR/demo-Customisation.html<br /><br />&nbsp;</p>]]></description>
	<dc:creator>Martin Jones</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27099/rasttk-algorithm-for-building-custom-annotation-pipelines-and-annotating-batches-of-genomes</guid>
	<pubDate>Wed, 27 Apr 2016 11:07:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27099/rasttk-algorithm-for-building-custom-annotation-pipelines-and-annotating-batches-of-genomes</link>
	<title><![CDATA[RASTtk : algorithm for building custom annotation pipelines and annotating batches of genomes]]></title>
	<description><![CDATA[<p>The RAST (Rapid Annotation using Subsystem Technology) annotation engine was built in 2008 to annotate bacterial and archaeal genomes. It works by offering a standard software pipeline for identifying genomic features (i.e., protein-encoding genes and RNA) and annotating their functions. Recently, in order to make RAST a more useful research tool and to keep pace with advancements in bioinformatics, it has become desirable to build a version of RAST that is both customizable and extensible. In this paper, we describe the RAST tool kit (RASTtk), a modular version of RAST that enables researchers to build custom annotation pipelines. RASTtk offers a choice of software for identifying and annotating genomic features as well as the ability to add custom features to an annotation job. RASTtk also accommodates the batch submission of genomes and the ability to customize annotation protocols for batch submissions. This is the first major software restructuring of RAST since its inception.</p>
<p>More at http://www.nature.com/articles/srep08365</p><p>Address of the bookmark: <a href="http://rast.nmpdr.org/" rel="nofollow">http://rast.nmpdr.org/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27430/mosaik-a-hash-based-algorithm-for-accurate-next-generation-sequencing-short-read-mapping</guid>
	<pubDate>Fri, 20 May 2016 18:53:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27430/mosaik-a-hash-based-algorithm-for-accurate-next-generation-sequencing-short-read-mapping</link>
	<title><![CDATA[MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping]]></title>
	<description><![CDATA[<p><span>MOSAIK is a stable, sensitive and open-source program for mapping second and third-generation sequencing reads to a reference genome. Uniquely among current mapping tools, MOSAIK can align reads generated by all the major sequencing technologies, including Illumina, Applied Biosystems SOLiD, Roche 454, Ion Torrent and Pacific BioSciences SMRT. Indeed, MOSAIK was the only aligner to provide consistent mappings for all the generated data (sequencing technologies, low-coverage and exome) in the 1000 Genomes Project. To provide highly accurate alignments, MOSAIK employs a hash clustering strategy coupled with the Smith-Waterman algorithm. This method is well-suited to capture mismatches as well as short insertions and deletions. To support the growing interest in larger structural variant (SV) discovery, MOSAIK provides explicit support for handling known-sequence SVs, e.g. mobile element insertions (MEIs) as well as generating outputs tailored to aid in SV discovery.</span></p><p>Address of the bookmark: <a href="http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0090581" rel="nofollow">http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0090581</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27818/gaemr</guid>
	<pubDate>Tue, 14 Jun 2016 06:18:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27818/gaemr</link>
	<title><![CDATA[GAEMR]]></title>
	<description><![CDATA[<p>The&nbsp;<span>G</span>enome&nbsp;<span>A</span>ssembly&nbsp;<span>E</span>valuation&nbsp;<span>M</span>etrics and&nbsp;<span>R</span>eporting (GAEMR) package is an assembly analysis framework composed a number of integrated modules. These modules can be executed as a single program to generate a complete analysis report, or executed individually to generate specific charts and tables. GAEMR standardizes input by converting a variety of read types to Binary Alignment Map (BAM) format, allowing a single input format to be entered into GAEMR&rsquo;s analysis pipeline, hence enabling the generation of standard reports.</p>
<p>GAEMR&rsquo;s analysis philosophy is centered on contiguity, correctness, and completeness -- how many pieces in an assembly composed of, how well those pieces accurately represent the genome sequenced, and how much of that genome is represented by those pieces. By performing over twenty different analyses based on these principles, GAEMR gives a clear picture of the condition of a genome assembly.&nbsp;</p><p>Address of the bookmark: <a href="https://www.broadinstitute.org/software/gaemr/" rel="nofollow">https://www.broadinstitute.org/software/gaemr/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30680/easybuild</guid>
	<pubDate>Fri, 27 Jan 2017 16:00:43 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30680/easybuild</link>
	<title><![CDATA[EasyBuild]]></title>
	<description><![CDATA[<p><a href="https://github.com/hpcugent/easybuild">EasyBuild</a><span>&nbsp;is a software build and installation framework that allows you to manage (scientific) software on High Performance Computing (HPC) systems in an efficient way.</span><br><span>A full list of supported software packages is available&nbsp;</span><a href="http://easybuild.readthedocs.io/en/latest/version-specific/Supported_software.html">here</a><span>.</span></p><p>Address of the bookmark: <a href="https://hpcugent.github.io/easybuild/" rel="nofollow">https://hpcugent.github.io/easybuild/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38304/lordfast-sensitive-and-fast-alignment-search-tool-for-long-noisy-read-sequencing-data</guid>
	<pubDate>Tue, 27 Nov 2018 04:43:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38304/lordfast-sensitive-and-fast-alignment-search-tool-for-long-noisy-read-sequencing-data</link>
	<title><![CDATA[lordFAST: sensitive and Fast Alignment Search Tool for LOng noisy Read sequencing Data]]></title>
	<description><![CDATA[<p><span>lordFAST is a sensitive tool for mapping long reads with high error rates. lordFAST is specially designed for aligning reads from PacBio sequencing technology but provides the user the ability to change alignment parameters depending on the reads and application.</span></p>
<p>lordFAST, a novel long-read mapper that is specifically designed to align reads generated by PacBio and potentially other SMS technologies to a reference. lordFAST not only has higher sensitivity than the available alternatives, it is also among the fastest and has a very low memory footprint.</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/vpc-ccg/lordfast" rel="nofollow">https://github.com/vpc-ccg/lordfast</a></p>]]></description>
	<dc:creator>BioJoker</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42204/g-nest-the-gene-neighborhood-scoring-tool</guid>
	<pubDate>Fri, 25 Sep 2020 20:09:18 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42204/g-nest-the-gene-neighborhood-scoring-tool</link>
	<title><![CDATA[G-NEST: The Gene NEighborhood Scoring Tool]]></title>
	<description><![CDATA[<p><span>The Gene NEighborhood Scoring Tool (G-NEST) combines genomic location, gene expression, and evolutionary sequence conservation data to score putative gene neighborhoods across all window sizes. Primary author of final code = William F. Martin. Example data files are in the separate repository.</span></p><p>Address of the bookmark: <a href="https://github.com/dglemay/G-NEST" rel="nofollow">https://github.com/dglemay/G-NEST</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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