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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/40707?offset=320</link>
	<atom:link href="https://bioinformaticsonline.com/related/40707?offset=320" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34420/rita-rapid-identification-of-high-confidence-taxonomic-assignments-for-metagenomic-data</guid>
	<pubDate>Mon, 27 Nov 2017 08:25:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34420/rita-rapid-identification-of-high-confidence-taxonomic-assignments-for-metagenomic-data</link>
	<title><![CDATA[RITA: Rapid identification of high-confidence taxonomic assignments for metagenomic data]]></title>
	<description><![CDATA[<p>RITA is a standalone software package and Web server for taxonomic assignment of metagenomic sequence reads. By combining homology predictions from BLAST or UBLAST with compositional classifications from a Naive Bayes classifier, RITA is able to achieve very high accuracy on short reads. Unlike other hybrid approaches which combine these predictions for all sequences to be classified, RITA uses a pipeline to first identify cases where both types of classifier are in agreement, which constitute the highest-confidence set. Sequences not classified in this manner are subjected to a series of downstream classification steps.</p>
<p>This work has been accepted for publication:</p>
<p>MacDonald NJ, Parks DH, and Beiko RG. Rapid identification of taxonomic assignments. Accepted to&nbsp;<em>Nucleic Acids Research</em>&nbsp;April 4, 2012.</p>
<p>If you have any questions or bug reports, please let us know at &lt;beiko@cs.dal.ca&gt;.</p><p>Address of the bookmark: <a href="http://kiwi.cs.dal.ca/Software/RITA" rel="nofollow">http://kiwi.cs.dal.ca/Software/RITA</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35272/biocircosjs-is-an-open-source-interactive-javascript-library-to-interactive-display-biological-data-on-the-web</guid>
	<pubDate>Fri, 19 Jan 2018 15:03:51 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35272/biocircosjs-is-an-open-source-interactive-javascript-library-to-interactive-display-biological-data-on-the-web</link>
	<title><![CDATA[BioCircos.js is an open source interactive Javascript library to interactive display biological data on the web]]></title>
	<description><![CDATA[<p><a href="http://bioinfo.ibp.ac.cn/biocircos/index.php">BioCircos.js</a>&nbsp;is an open source interactive&nbsp;<code>Javascript</code>&nbsp;library which provides an easy way to interactive display biological data on the web. It implements a raster-based&nbsp;<code>SVG</code>&nbsp;visualization using the open source Javascript framework jquery.js. BioCircos.js is multiplatform and works in all major internet browsers (<strong>Internet Explorer</strong>,&nbsp;<strong>Mozilla Firefox</strong>,&nbsp;<strong>Google Chrome</strong>,&nbsp;<strong>Safari</strong>,&nbsp;<strong>Opera</strong>). Its speed is determined by the client&rsquo;s hardware and internet browser. For smoothest user experience, we recommend&nbsp;<strong>Google Chrome</strong>.</p>
<p>BioCircos.js provides&nbsp;<strong>SNP</strong>,&nbsp;<strong>CNV</strong>,&nbsp;<strong>HEATMAP</strong>,&nbsp;<strong>LINK</strong>,&nbsp;<strong>LINE</strong>,&nbsp;<strong>SCATTER</strong>,&nbsp;<strong>ARC</strong>,&nbsp;<strong>TEXT</strong>, and&nbsp;<strong>HISTGRAM</strong>modules to display genome-wide genetic variations (SNPs, CNVs and chromosome rearrangement), gene expression and biomolecule interactions. BioCircos.js also provides&nbsp;<strong>BACKGROUND</strong>&nbsp;module to display background and axis circles. Tooltips showing detailed information of SVG elements are also provided.</p>
<p><a href="http://bioinfo.ibp.ac.cn/biocircos/document/demo/pages/paper01.html">Demo</a></p><p>Address of the bookmark: <a href="http://bioinfo.ibp.ac.cn/biocircos/document/index.html" rel="nofollow">http://bioinfo.ibp.ac.cn/biocircos/document/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37205/afterqc-automatic-filtering-trimming-error-removing-and-quality-control-for-fastq-data</guid>
	<pubDate>Fri, 29 Jun 2018 03:26:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37205/afterqc-automatic-filtering-trimming-error-removing-and-quality-control-for-fastq-data</link>
	<title><![CDATA[AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data]]></title>
	<description><![CDATA[Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
AfterQC can simply go through all fastq files in a folder and then output three folders: good, bad and QC folders, which contains good reads, bad reads and the QC results of each fastq file/pair.
Currently it supports processing data from HiSeq 2000/2500/3000/4000, Nextseq 500/550, MiniSeq...and other Illumina 1.8 or newer formats

The author has reimplemented this tool in C++ with multithreading support to make it much faster. The new tool is called fastp and can be found at: https://github.com/OpenGene/fastp . If you prefer a C++ based tool, please use fastp instead.

https://github.com/OpenGene/AfterQC<p>Address of the bookmark: <a href="https://github.com/OpenGene/AfterQC" rel="nofollow">https://github.com/OpenGene/AfterQC</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40546/clincnv-detection-of-copy-number-changes-in-germlinetriosomatic-contexts-in-ngs-data</guid>
	<pubDate>Thu, 16 Jan 2020 23:16:02 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40546/clincnv-detection-of-copy-number-changes-in-germlinetriosomatic-contexts-in-ngs-data</link>
	<title><![CDATA[ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data]]></title>
	<description><![CDATA[<p><span>ClinCNV detects CNVs in germline and somatic context in NGS data (targeted and whole-genome). We work in cohorts, so it makes sense to try&nbsp;</span><code>ClinCNV</code><span>&nbsp;if you have more than 10 samples (recommended amount - 40 since we estimate variances from the data). By "cohort" we mean samples sequenced with the same enrichment kit with approximately the same depth (ie 1x WGS and 30x WGS better be analysed in separate runs of ClinCNV). Of course it is better if your samples were sequenced within the same sequencing facility.</span></p><p>Address of the bookmark: <a href="https://github.com/imgag/ClinCNV" rel="nofollow">https://github.com/imgag/ClinCNV</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/41562/submit-your-sars-cov-2-sequence-data-to-genbank</guid>
	<pubDate>Thu, 09 Apr 2020 18:28:25 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/41562/submit-your-sars-cov-2-sequence-data-to-genbank</link>
	<title><![CDATA[Submit your SARS-CoV-2 sequence data to GenBank]]></title>
	<description><![CDATA[<div dir="auto">Submit your SARS-CoV-2 sequence data to GenBank and SRA with our new submission landing page. Submission is simple and streamlined *and* there&rsquo;s a rapid turnaround. <span><a href="https://l.facebook.com/l.php?u=https%3A%2F%2Fsubmit.ncbi.nlm.nih.gov%2Fsarscov2%2F%3Ffbclid%3DIwAR3p-OzZPe2yx4CZMoZxiWMF3kUQjXyVVduNQhBdehWmFTJ3cPBstsOLypI&amp;h=AT2d-umit7ciXRW-nrRYVL3gJSLKY4Hte8W8cXw8Wl94n6PGmoHmVqvvhgQj-mTo6A5lpMP9JDV_lRSq9RRLT5KeVVAAfcuRgJOeA6QhApIB2B9nFxUfDCD3sio4HYidpRwpmng&amp;__tn__=-UK-R&amp;c[0]=AT2zWGa1K5EvV4UcnB0b7HHvkBtX-wAyh7AF8_fZ9uI2y-02nOHQHT_Um3xgnto5KEZ26wRG0xNgUWTA1W-7HF0E25E23XtIL5XGOhloBXaDIcHw30AVjTCkQi7aFk4dN7aBCmVJeSbH37urtbM2kmMfyTCbdTvMU8FGlnX-DNVuCaZr4XfXnf_jvPNdxe9sBH84oXJ-uJz5kbqlHGAHDoqK" target="_blank">https://submit.ncbi.nlm.nih.gov/sarscov2/</a></span></div><div dir="auto">&nbsp;</div><div dir="auto"><span><span>Quickly and easily add your SARS-CoV-2 sequence data to the growing public archive with new, special features and support from NCBI. </span><a href="https://submit.ncbi.nlm.nih.gov/sarscov2/">new SARS-CoV-2 sequence submission landing page</a><span>&nbsp;will help you get started. GenBank submissions are accessioned and released in approximately 1-2 working days, and&nbsp;</span><a href="https://www.ncbi.nlm.nih.gov/sra" target="_blank">Sequence Read Archive</a><span>&nbsp;(SRA) submissions typically processed and released within hours. Submission is simple!</span></span></div><div><div dir="auto">&nbsp;</div><div dir="auto">More information is available on NCBI Insights. <span><a href="https://l.facebook.com/l.php?u=https%3A%2F%2Fncbiinsights.ncbi.nlm.nih.gov%2F2020%2F04%2F09%2Fsars-cov2-data-streamlined-submission-rapid-turnaround%2F%3Ffbclid%3DIwAR1OuLu3oDjz3VX4fDq5Jg316td9foTOUGNqnoN1eI2nFXTf4EBv28JiXD4&amp;h=AT0ah_epxwAc-nM6QiPBYvKSQ-kWmiPgHKO1w7SnxnnRiTI4etJJfNAWyzcR7snIdtxtcErAFRdHPBH2j0EY77gUPDdnBVnAsxnVbSgZnrrOPfnni331A37Xvytgnye0ArnUuWk&amp;__tn__=-UK-R&amp;c[0]=AT2zWGa1K5EvV4UcnB0b7HHvkBtX-wAyh7AF8_fZ9uI2y-02nOHQHT_Um3xgnto5KEZ26wRG0xNgUWTA1W-7HF0E25E23XtIL5XGOhloBXaDIcHw30AVjTCkQi7aFk4dN7aBCmVJeSbH37urtbM2kmMfyTCbdTvMU8FGlnX-DNVuCaZr4XfXnf_jvPNdxe9sBH84oXJ-uJz5kbqlHGAHDoqK" target="_blank">https://ncbiinsights.ncbi.nlm.nih.gov/2020/04/09/sars-cov2-data-streamlined-submission-rapid-turnaround/</a></span></div></div>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42806/graphunzip-phases-an-assembly-graph-using-hi-c-data-andor-long-reads</guid>
	<pubDate>Fri, 05 Feb 2021 21:22:24 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42806/graphunzip-phases-an-assembly-graph-using-hi-c-data-andor-long-reads</link>
	<title><![CDATA[GraphUnzip: Phases an assembly graph using Hi-C data and/or long reads.]]></title>
	<description><![CDATA[<p>GraphUnzip, a fast, memory-efficient and accurate tool to unzip assembly graphs into their constituent haplotypes using long reads and/or Hi-C data. As GraphUnzip only connects sequences in the assembly graph that already had a potential link based on overlaps, it yields high-quality gap-less supercontigs. To demonstrate the efficiency of GraphUnzip, we tested it on a simulated diploid Escherichia coli genome, and on two real datasets for the genomes of the rotifer Adineta vaga and the potato Solanum tuberosum. In all cases, GraphUnzip yielded highly continuous phased assemblies.</p>
<p>https://www.biorxiv.org/content/biorxiv/early/2021/02/01/2021.01.29.428779.full.pdf</p><p>Address of the bookmark: <a href="https://github.com/nadegeguiglielmoni/GraphUnzip" rel="nofollow">https://github.com/nadegeguiglielmoni/GraphUnzip</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43645/corona-virus-genome-and-data-download</guid>
	<pubDate>Sun, 12 Dec 2021 23:34:54 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43645/corona-virus-genome-and-data-download</link>
	<title><![CDATA[Corona Virus Genome and Data Download !]]></title>
	<description><![CDATA[<p>Genes and its related metadata could be found on&nbsp;https://www.ncbi.nlm.nih.gov/datasets/coronavirus/genomes/</p><p>Address of the bookmark: <a href="https://www.ncbi.nlm.nih.gov/datasets/coronavirus/genomes/" rel="nofollow">https://www.ncbi.nlm.nih.gov/datasets/coronavirus/genomes/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44252/orange-data-mining</guid>
	<pubDate>Mon, 13 Mar 2023 12:42:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44252/orange-data-mining</link>
	<title><![CDATA[Orange: Data mining]]></title>
	<description><![CDATA[<div>
<p>Open source machine learning and data visualization.</p>
<p>Build data analysis workflows visually, with a large, diverse toolbox.</p>
<p>&nbsp;</p>
</div><p>Address of the bookmark: <a href="https://orangedatamining.com/" rel="nofollow">https://orangedatamining.com/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44375/phyloherb-a-high%E2%80%90throughput-phylogenomic-pipeline-for-processing-genome-skimming-data</guid>
	<pubDate>Wed, 06 Sep 2023 00:14:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44375/phyloherb-a-high%E2%80%90throughput-phylogenomic-pipeline-for-processing-genome-skimming-data</link>
	<title><![CDATA[PhyloHerb: A high‐throughput phylogenomic pipeline for processing genome skimming data]]></title>
	<description><![CDATA[<p dir="auto"><span>Phylo</span>genomic Analysis Pipeline for&nbsp;<span>Herb</span>arium Specimens</p>
<p dir="auto"><span>What is PhyloHerb</span>: PhyloHerb is a wrapper program to process&nbsp;<span>genome skimming</span>&nbsp;data collected from plant materials. The outcomes include the plastid genome (plastome) assemblies, mitochondrial genome assemblies, nuclear ribosomal DNAs (NTS+ETS+18S+ITS1+5.8S+ITS2+28S), alignments of gene and intergenic regions, and a species tree. It is designed to be a high throughput program dealing with lower quality data. Examples include&nbsp;<span>low-coverage (5x cpDNA) plastome phylogeny, recycling plastid genes from target enrichment data, retrieving low-copy nuclear genes from medium coverage (5x nucDNA) genome skimming</span>.</p>
<p dir="auto"><span>License</span>: GNU General Public License</p>
<p dir="auto"><span>Citation</span>:</p>
<ul dir="auto">
<li>Cai, Liming, Hongrui Zhang, and Charles C. Davis. 2022. PhyloHerb: A high‐throughput phylogenomic pipeline for processing genome‐skimming data. Applications in Plant Sciences 10(3): 1&ndash;9.&nbsp;<a href="https://doi.org/10.1002/aps3.11475">https://doi.org/10.1002/aps3.11475</a></li>
</ul><p>Address of the bookmark: <a href="https://github.com/lmcai/PhyloHerb/" rel="nofollow">https://github.com/lmcai/PhyloHerb/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/21443/a-guide-for-complete-r-beginners-getting-data-into-r</guid>
	<pubDate>Tue, 24 Feb 2015 20:15:08 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/21443/a-guide-for-complete-r-beginners-getting-data-into-r</link>
	<title><![CDATA[A guide for complete R beginners :- Getting data into R]]></title>
	<description><![CDATA[<p>For a beginner this can be is the hardest part, it is also the most important to get right.</p><p>It is possible to create a vector by typing data directly into R using the combine function &lsquo;c&rsquo;</p><blockquote><p><strong>x </strong></p></blockquote><p>same as</p><blockquote><p><strong>x </strong></p></blockquote><p>creates the vector x with the numbers between 1 and 5.</p><p>You can see what is in an object at any time by typing its name;</p><blockquote><p><strong>x</strong></p></blockquote><p>will produce the output<strong> &lsquo;[1] 1 2 3 4 5&prime;</strong></p><p>Note that names need to be quoted</p><blockquote><p><strong>daysofweek </strong><strong>&larr; c(&lsquo;Monday&rsquo;, &lsquo;Tuesday&rsquo;, &lsquo;Wednesday&rsquo;, &lsquo;Thursday&rsquo;, &lsquo;Friday&rsquo;);</strong></p></blockquote><p>Usually however you want to input from a file. We have touched on the &lsquo;read.table&rsquo; function already.</p><blockquote><p><strong>mydata </strong></p></blockquote><p>Now <strong>mydata</strong> is a data frame with multiple vectors</p><p>each vector can be identified by the default syntax</p><p>#if any of these are typed it will print to screen</p><blockquote><p><strong>mydata$V1 mydata$V2 mydata$V3 </strong></p></blockquote><p>By default the function assumes certain things from the file</p><ul>
<li>The file is a plain text file (there are function to read excel files: <em>not covered here</em>)</li>
<li>columns are separated by any number of tabs or spaces</li>
<li>there is the same number of data points in each column</li>
<li>there is no header row (labels for the columns)</li>
<li>there is no column with names for the rows** [I&rsquo;ll explain].</li>
</ul><p><span style="text-decoration: underline;">If any of these are false, we need to tell that to the function</span></p><p>If it has a header column</p><blockquote><p><strong>mydata <em>header=T also works</em></strong></p></blockquote><p>Note that there is a comma between different parts of the functions arguments</p><p>If there is one less column in the header row, then R assumes that the 1<sup>st</sup> column of data after the header are the row names</p><p>Now the vectors (columns) are identified by their name</p><p>#if any of these are typed it will print to screen</p><blockquote><p><strong>mydata$A mydata$B mydata$C </strong></p></blockquote><p># Summary about the whole data frame</p><blockquote><p><strong>summary(mydata)</strong></p></blockquote><p># Summary information of column A</p><blockquote><p><strong>summary(mydata$A) </strong></p></blockquote><p>We can shortcut having to type the data frame each time by attaching it</p><blockquote><p><strong>attach(mydata)</strong></p></blockquote><p># summary of column B as &lsquo;mydata&rsquo; is attached</p><blockquote><p><strong>summary(B)</strong></p></blockquote><p><span style="text-decoration: underline;">Two other important options for </span><em><span style="text-decoration: underline;">read.table</span></em></p><p>If is is separated only by tabs and has a header</p><blockquote><p><strong>mydata </strong></p></blockquote><p>Really useful if you have spaces in the contents of some columns, so R does not mess up reading the columns . However if the columns or of an uneven length it will tell you.</p><p>If you know that the file has uneven columns</p><blockquote><p><strong>mydata </strong></p></blockquote><p>This causes R to fill empty spaces in a columns with &lsquo;NA&rsquo; .</p><p>The last two examples will still work with our file and give the same result as with only headers=T</p><p><span style="text-decoration: underline;">Graphs</span></p><p>to get an idea of what R is capable of type</p><blockquote><p><strong>demo(graphics)</strong></p></blockquote><p>steps through the examples, and the code is printed to the screen</p><p>We will work with simpler examples that have immediate use to biologists.</p><p>Remember to get more information about the options to a function type &lsquo;?function&rsquo;</p><p><span style="text-decoration: underline;">Histogram of A</span><span style="text-decoration: underline;"></span></p><blockquote><p><strong>hist(mydata$A)</strong></p></blockquote><p>If there was more data we could increase the number of vertical columns with the option, breaks=50 (or another relevant number).</p><blockquote><p><strong>boxplot(mydata)</strong></p></blockquote><p>We can get rid of the need to type the data frame each time by using the <strong>attach</strong> function</p><p># if not already done so</p><blockquote><p><strong>attach(mydata) </strong></p><p><strong>boxplot(mydata$A, mydata$B, name=c(&ldquo;Value A&rdquo;, &ldquo;Value B&rdquo;) , ylab=&ldquo;Count of Something&rdquo;)</strong></p></blockquote><p>same as</p><blockquote><p><strong>boxplot(A, B, name=c(&ldquo;Value A&rdquo;, &ldquo;Value B&rdquo;) , ylab=&ldquo;Count of Something&rdquo;)</strong></p></blockquote><p><span style="text-decoration: underline;">Scatter plot</span></p><p># if not already done so</p><blockquote><p><strong>attach(mydata) </strong></p><p><strong>plot(A,B) # or plot(mydata$A, mydata$B)</strong></p></blockquote><p><strong><span style="text-decoration: underline;">SAVING an image</span></strong></p><p>Windows users (Rgui) RIGHT click on image and select which you want.</p><p><span style="text-decoration: underline;">These instructions work for everyone.</span></p><p>You need to create a new device of the type of file you need, then send the data to that device</p><p>to save as a png file (easy to load into the likes of powerpoint, also great for web applications.</p><blockquote><p><strong>png(&lsquo;filename&rsquo;) </strong></p><p><strong>boxplot(A, B, name=c(&ldquo;Value A&rdquo;, &ldquo;Value B&rdquo;) , ylab=&ldquo;Count of Something&rdquo;)</strong></p></blockquote><p>or to save as a pdf</p><blockquote><p><strong>pdf(&lsquo;filename&rsquo;) </strong></p><p><strong>boxplot(A, B, name=c(&ldquo;Value A&rdquo;, &ldquo;Value B&rdquo;) , ylab=&ldquo;Count of Something&rdquo;)</strong></p></blockquote><p><span style="text-decoration: underline;">Note</span></p><ul>
<li>Nothing will appear on screen, the output is going to the file</li>
<li>Also it may not be saved immediately but will once the device (or R) is turned quit.</li>
</ul><p>To quit R type</p><p><strong>q() # </strong>If you save your session, next time you start R, you will have your data preloaded.</p><p>Or if you want to remain in R</p><blockquote><pre><strong>dev.off() #</strong>turns of the png (or pdf etc) device, thus forces the data to save</pre></blockquote>]]></description>
	<dc:creator>Archana Malhotra</dc:creator>
</item>

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