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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/43013?offset=10</link>
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	<description><![CDATA[]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/43916/understanding-dump-files-from-ncbi-taxonomy-database</guid>
	<pubDate>Fri, 15 Jul 2022 04:29:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/43916/understanding-dump-files-from-ncbi-taxonomy-database</link>
	<title><![CDATA[Understanding DUMP files from NCBI Taxonomy database !]]></title>
	<description><![CDATA[<p>*.dmp files are bcp-like dump from GenBank taxonomy database</p><p>General information.</p><p>Field terminator is "\t|\t"</p><p>Row terminator is "\t|\n"</p><p>&nbsp;</p><p>nodes.dmp file consists of taxonomy nodes. The description for each node includes the following</p><p>fields:</p><p>tax_id -- node id in GenBank taxonomy database</p><p>&nbsp; parent tax_id -- parent node id in GenBank taxonomy database</p><p>&nbsp; rank -- rank of this node (superkingdom, kingdom, ...)&nbsp;</p><p>&nbsp; embl code -- locus-name prefix; not unique</p><p>&nbsp; division id -- see division.dmp file</p><p>&nbsp; inherited div flag&nbsp; (1 or 0) -- 1 if node inherits division from parent</p><p>&nbsp; genetic code id -- see gencode.dmp file</p><p>&nbsp; inherited GC&nbsp; flag&nbsp; (1 or 0) -- 1 if node inherits genetic code from parent</p><p>&nbsp; mitochondrial genetic code id -- see gencode.dmp file</p><p>&nbsp; inherited MGC flag&nbsp; (1 or 0) -- 1 if node inherits mitochondrial gencode from parent</p><p>&nbsp; GenBank hidden flag (1 or 0)&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; -- 1 if name is suppressed in GenBank entry lineage</p><p>&nbsp; hidden subtree root flag (1 or 0) &nbsp; &nbsp; &nbsp; -- 1 if this subtree has no sequence data yet</p><p>&nbsp; comments -- free-text comments and citations</p><p>&nbsp;</p><p>Taxonomy names file (names.dmp):</p><p>tax_id -- the id of node associated with this name</p><p>name_txt -- name itself</p><p>unique name -- the unique variant of this name if name not unique</p><p>name class -- (synonym, common name, ...)</p><p>&nbsp;</p><p>Divisions file (division.dmp):</p><p>division id -- taxonomy database division id</p><p>division cde -- GenBank division code (three characters)</p><p>division name -- e.g. BCT, PLN, VRT, MAM, PRI...</p><p>comments</p><p>&nbsp;</p><p>Genetic codes file (gencode.dmp):</p><p>genetic code id -- GenBank genetic code id</p><p>abbreviation -- genetic code name abbreviation</p><p>name -- genetic code name</p><p>cde -- translation table for this genetic code</p><p>starts -- start codons for this genetic code</p><p>&nbsp;</p><p>Deleted nodes file (delnodes.dmp):</p><p>tax_id -- deleted node id</p><p>&nbsp;</p><p>Merged nodes file (merged.dmp):</p><p>old_tax_id&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; -- id of nodes which has been merged</p><p>new_tax_id&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; -- id of nodes which is result of merging</p><p>Citations file (citations.dmp):</p><p>cit_id -- the unique id of citation</p><p>cit_key -- citation key</p><p>pubmed_id -- unique id in PubMed database (0 if not in PubMed)</p><p>medline_id -- unique id in MedLine database (0 if not in MedLine)</p><p>url -- URL associated with citation</p><p>text -- any text (usually article name and authors).</p><p>-- The following characters are escaped in this text by a backslash:</p><p>-- newline (appear as "\n"),</p><p>-- tab character ("\t"),</p><p>-- double quotes ('\"'),</p><p>-- backslash character ("\\").</p><p>taxid_list -- list of node ids separated by a single space</p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/34685/tools-for-bacterial-whole-genome-annotation</guid>
	<pubDate>Sat, 16 Dec 2017 17:37:47 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/34685/tools-for-bacterial-whole-genome-annotation</link>
	<title><![CDATA[Tools for bacterial whole genome annotation]]></title>
	<description><![CDATA[<p><a href="http://rast.nmpdr.org/">RAST</a>&nbsp;&ndash;&nbsp;Web tool (upload contigs), uses the subsystems in the SEED database and&nbsp;provides detailed annotation and pathway analysis. Takes several hours per genome but I think this is the best way to get a high quality annotation (if you have only a few genomes to annotate).</p><p><a href="http://www.vicbioinformatics.com/software.prokka.shtml">Prokka</a>&nbsp;&ndash;&nbsp;Standalone command line tool, takes just a few minutes per genome.&nbsp;This is the best way to get good quality annotation in a flash, which is particularly useful if you have loads of genomes or need to annotate a pangenome or metagenome. Note however that the quality of functional information is not as good as RAST, and you&nbsp;will need several extra steps if you want to do&nbsp;functional profiling and pathway analysis of your genome(s)&hellip; which is in-built in RAST.</p><p>NCBI Prokaryotic Genome Annotation Pipeline is designed to annotate bacterial and archaeal genomes (chromosomes and plasmids).</p><p>Genome annotation is a multi-level process that includes prediction of protein-coding genes, as well as other functional genome units such as structural RNAs, tRNAs, small RNAs, pseudogenes, control regions, direct and inverted repeats, insertion sequences, transposons and other mobile elements.</p><p><a href="https://www.ncbi.nlm.nih.gov/genome/annotation_prok/">PGAP</a>: NCBI has developed an automatic prokaryotic genome annotation pipeline that combines&nbsp;<em>ab initio</em>&nbsp;gene prediction algorithms with homology based methods. The first version of NCBI Prokaryotic Genome Automatic Annotation Pipeline (PGAAP;&nbsp;<a href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=pubmed&amp;dopt=Abstract&amp;list_uids=18416670">see Pubmed Article</a>) developed in 2005 has been replaced with an upgraded version that is capable of processing a larger data volume.&nbsp; NCBI's annotation pipeline depends on several internal databases and is not currently available for download or use outside of the NCBI environment.</p><p><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC453985">BEACON</a> (automated tool for Bacterial GEnome Annotation ComparisON), a fast tool for an automated and a systematic comparison of different annotations of single genomes. The extended annotation assigns putative functions to many genes with unknown functions. BEACON is available under GNU General Public License version 3.0 and is accessible at:&nbsp;<a href="http://www.cbrc.kaust.edu.sa/BEACON/" target="pmc_ext">http://www.cbrc.kaust.edu.sa/BEACON/</a>.</p><p><a href="http://www.kegg.jp/blastkoala/">BlastKOLA</a>: Assigns K numbers to the user's sequence data by BLAST searches, respectively, against a nonredundant set of KEGG GENES. KOALA (KEGG Orthology And Links Annotation) is KEGG's internal annotation tool for K number assignment of KEGG GENES using SSEARCH computation. Annotate Sequence in KEGG Mapper and Pathogen Checker in KEGG Pathogen are special interfaces to this server and can be executed in an interactive mode. BlastKOALA is suitable for annotating fully sequenced genomes.</p><p><a href="http://www.sanger.ac.uk/science/tools/pagit">PAGIT</a>: Provides a toolkit for improving the quality of genome assemblies created via an assembly software. PAGIT compiled four tools: (i) ABACAS which classifies and orientates contigs and estimates the sizes of gaps between them; (ii) IMAGE uses paired-end reads to extend contigs and close gaps within the scaffolds; (iii) ICORN for identifying and correcting small errors in consensus sequences and; (iv) RATT for help annotation. The software was mainly created to analyze parasite genomes of up to about 300 Mb.</p><p><a href="http://www.yandell-lab.org/software/maker.html">MAKER: </a>A portable and easily configurable genome annotation pipeline. MAKER allows smaller eukaryotic and prokaryotic genome projects to independently annotate their genomes and to create genome databases. It identifies repeats, aligns ESTs and proteins to a genome, produces ab-initio gene predictions and automatically synthesizes these data into gene annotations having evidence-based quality values. MAKER's inputs are minimal and its ouputs can be directly loaded into a Generic Model Organism Database (GMOD). They can also be viewed in the Apollo genome browser; this feature of MAKER provides an easy means to annotate, view and edit individual contigs and BACs without the overhead of a database. MAKER is available for download and can be tested online via the MAKER Web Annotation Service (MWAS).</p><p><a href="https://www.sciencedirect.com/science/article/pii/S0167701215001207">MyPro</a> is a software pipeline for high-quality prokaryotic genome assembly and annotation. It was validated on 18 oral streptococcal strains to produce submission-ready, annotated draft genomes. MyPro installed as a virtual machine and supported by updated databases will enable biologists to perform quality prokaryotic genome assembly and annotation with ease.</p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40862/alien-index-identify-potential-contaminants-or-horizontally-transferred-genes-in-transcriptomes</guid>
	<pubDate>Sun, 02 Feb 2020 13:51:31 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40862/alien-index-identify-potential-contaminants-or-horizontally-transferred-genes-in-transcriptomes</link>
	<title><![CDATA[alien_index : identify potential contaminants or horizontally transferred genes in transcriptomes.]]></title>
	<description><![CDATA[<p><span>identify potential contaminants or horizontally transferred genes in transcriptomes.</span></p>
<p><span><span>algorithm is based on alogorithm described in the following: Gladyshev, Eugene A., Matthew Meselson, and Irina R. Arkhipova. "Massive horizontal gene transfer in bdelloid rotifers." science 320.5880 (2008): 1210-1213.</span></span></p>
<p><a href="https://github.com/josephryan/alien_index">alien_index</a></p><p>Address of the bookmark: <a href="https://github.com/josephryan/alien_index" rel="nofollow">https://github.com/josephryan/alien_index</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43683/genview-a-phylogeny-based-comparative-genomics-software-to-analyze-the-genetic-environment-of-genes</guid>
	<pubDate>Tue, 28 Dec 2021 01:49:03 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43683/genview-a-phylogeny-based-comparative-genomics-software-to-analyze-the-genetic-environment-of-genes</link>
	<title><![CDATA[GEnView: A phylogeny based comparative genomics software to analyze the genetic environment of genes]]></title>
	<description><![CDATA[<p><span>A phylogeny based comparative genomics software to analyze the genetic environment of genes. The user can select one or several taxa and provide one or several reference protein(s). Genomes and plasmids (based on user choice) will be downloaded from the NCBI Assembly/NR database and searched for the respective gene. Alternatively, custom genomes can be provided. User selected stretches (20kbp by default) of the genes genetic environment are extracted, annotated and aligned between all genomes. The sequences are then visualized, enabling comparison of synteny and gene content.</span></p>
<p><span>More at&nbsp;https://pubmed.ncbi.nlm.nih.gov/34951622/</span></p><p>Address of the bookmark: <a href="https://github.com/EbmeyerSt/GEnView" rel="nofollow">https://github.com/EbmeyerSt/GEnView</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/1471/24-mb-genome-size-for-worlds-biggest-virus</guid>
	<pubDate>Thu, 08 Aug 2013 10:05:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/1471/24-mb-genome-size-for-worlds-biggest-virus</link>
	<title><![CDATA[2.4 Mb Genome Size for World's Biggest Virus]]></title>
	<description><![CDATA[<p>The genome size of new discovered Pandoraviruses have roughly twice the size of the record-holding Megavirus genomic code. Interestingly only 6 percent of its genes resembled the genes other organisms. It is assume that it may come from a different origin.</p><p>For detail : http://www.sciencemag.org/content/341/6143/281</p><p>http://www.npr.org/blogs/health/2013/07/18/203298244/worlds-biggest-virus-may-have-ancient-roots</p><p>&nbsp;</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27427/rcircos-an-r-package-for-circos-2d-track-plots</guid>
	<pubDate>Fri, 20 May 2016 11:01:13 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27427/rcircos-an-r-package-for-circos-2d-track-plots</link>
	<title><![CDATA[RCircos: an R package for Circos 2D track plots]]></title>
	<description><![CDATA[<p>RCircos package provides a simple and flexible way to make Circos 2D track plots with R and could be easily integrated into other R data processing and graphic manipulation pipelines for presenting large-scale multi-sample genomic research data. It can also serve as a base tool to generate complex Circos images.</p>
<p>More at https://bitbucket.org/henryhzhang/rcircos/src</p><p>Address of the bookmark: <a href="https://bitbucket.org/henryhzhang/rcircos/src" rel="nofollow">https://bitbucket.org/henryhzhang/rcircos/src</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28997/braker-pipeline-for-fully-automated-prediction-of-protein-coding-genes-with-genemark-eset-and-augustus-in-novel-eukaryotic-genomes</guid>
	<pubDate>Thu, 01 Sep 2016 08:02:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28997/braker-pipeline-for-fully-automated-prediction-of-protein-coding-genes-with-genemark-eset-and-augustus-in-novel-eukaryotic-genomes</link>
	<title><![CDATA[BRAKER: pipeline for fully automated prediction of protein coding genes with GeneMark-ES/ET and AUGUSTUS in novel eukaryotic genomes]]></title>
	<description><![CDATA[<p><span>Gene finding in eukaryotic genomes is notoriously difficult to automate. The task is to design a work flow with a minimal set of tools that would reach state-of-the-art performance across a wide range of species. GeneMark-ET is a gene prediction tool that incorporates RNA-Seq data into unsupervised training and subsequently generates ab initio gene predictions. AUGUSTUS is a gene finder that usually requires supervised training and uses information from RNA-Seq reads in the prediction step. Complementary strengths of GeneMark-ET and AUGUSTUS provided motivation for designing a new combined tool for automatic gene prediction.</span></p>
<p>http://www.ncbi.nlm.nih.gov/pubmed/26559507</p><p>Address of the bookmark: <a href="http://bioinf.uni-greifswald.de/bioinf/braker/" rel="nofollow">http://bioinf.uni-greifswald.de/bioinf/braker/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32379/enrichr-a-comprehensive-gene-set-enrichment-analysis</guid>
	<pubDate>Thu, 27 Apr 2017 05:42:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32379/enrichr-a-comprehensive-gene-set-enrichment-analysis</link>
	<title><![CDATA[Enrichr: a comprehensive gene set enrichment analysis]]></title>
	<description><![CDATA[<p><span>Enrichment analysis is a popular method for analyzing gene sets generated by genome-wide experiments. Here we present a significant update to one of the tools in this domain called Enrichr. Enrichr currently contains a large collection of diverse gene set libraries available for analysis and download. In total, Enrichr currently contains 180 184 annotated gene sets from 102 gene set libraries. New features have been added to Enrichr including the ability to submit fuzzy sets, upload BED files, improved application programming interface and visualization of the results as clustergrams. Overall, Enrichr is a comprehensive resource for curated gene sets and a search engine that accumulates biological knowledge for further biological discoveries. Enrichr is freely available at:&nbsp;</span><a href="http://amp.pharm.mssm.edu/Enrichr" target="">http://amp.pharm.mssm.edu/Enrichr</a><span>.</span></p>
<p>https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/gkw377</p><p>Address of the bookmark: <a href="http://amp.pharm.mssm.edu/Enrichr/" rel="nofollow">http://amp.pharm.mssm.edu/Enrichr/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30149/mypro-a-seamless-pipeline-for-automated-prokaryotic-genome-assembly-and-annotation</guid>
	<pubDate>Thu, 15 Dec 2016 05:47:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30149/mypro-a-seamless-pipeline-for-automated-prokaryotic-genome-assembly-and-annotation</link>
	<title><![CDATA[MyPro: A seamless pipeline for automated prokaryotic genome assembly and annotation]]></title>
	<description><![CDATA[<p>MyPro is an improved genomics software pipeline for prokaryotic genomes. MyPro is user-friendly and requires minimal programming skills. High-quality prokaryotic genome assembly and annotation can be obtained with ease. It performed better than de novo assemblers and contig integration software. Produces more contiguous assemblies, higher N50 values and lower number of contigs.</p>
<p>More at https://sourceforge.net/projects/sb2nhri/files/MyPro/</p><p>Address of the bookmark: <a href="http://www.sciencedirect.com/science/article/pii/S0167701215001207" rel="nofollow">http://www.sciencedirect.com/science/article/pii/S0167701215001207</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41969/shadowcaster-a-hybrid-approach-for-the-detection-of-horizontal-gene-transfer-events-in-prokaryotes</guid>
	<pubDate>Tue, 14 Jul 2020 06:42:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41969/shadowcaster-a-hybrid-approach-for-the-detection-of-horizontal-gene-transfer-events-in-prokaryotes</link>
	<title><![CDATA[ShadowCaster: a hybrid approach for the detection of horizontal gene transfer events in prokaryotes]]></title>
	<description><![CDATA[<p><span>ShadowCaster implements an evolutionary model to calculate Bayesian likelihoods for each &lsquo;alien genes&rsquo; with an unusual sequence composition according to the host genome background to detect HGT events in prokaryotes.</span></p>
<p><a href="https://www.mdpi.com/2073-4425/11/7/756/htm">https://www.mdpi.com/2073-4425/11/7/756/htm</a></p>
<p><a href="https://shadowcaster.readthedocs.io/en/latest/">https://shadowcaster.readthedocs.io/en/latest/</a></p>
<p><a href="https://github.com/dani2s/ShadowCaster_testData">https://github.com/dani2s/ShadowCaster_testData</a></p><p>Address of the bookmark: <a href="https://github.com/dani2s/ShadowCaster" rel="nofollow">https://github.com/dani2s/ShadowCaster</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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