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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/44529?offset=50</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31139/pbsuite-software-for-long-read-sequencing-data-from-pacbio</guid>
	<pubDate>Mon, 27 Feb 2017 09:54:47 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31139/pbsuite-software-for-long-read-sequencing-data-from-pacbio</link>
	<title><![CDATA[PBSuite: Software for Long-Read Sequencing Data from PacBio]]></title>
	<description><![CDATA[<p><span>PBJelly - the genome upgrading tool.&nbsp;</span><br><span>PBHoney - the structural variation discovery tool&nbsp;</span><br><br><span>Both are contained within the PBSuite code found in downloads.</span><br><br><span>----- PBJelly -----</span><br><span>Read The Paper&nbsp;</span><br><a href="http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0047768" target="_blank">http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0047768</a><br><br><span>PBJelly is a highly automated pipeline that aligns long sequencing reads (such as PacBio RS reads or long 454 reads in fasta format) to high-confidence draft assembles. PBJelly fills or reduces as many captured gaps as possible to produce upgraded draft genomes.&nbsp;</span><br><br><span>----- PBHoney -----</span><br><span>Read The Paper</span><br><a href="http://www.biomedcentral.com/1471-2105/15/180/abstract" target="_blank">http://www.biomedcentral.com/1471-2105/15/180/abstract</a><br><br><span>PBHoney is an implementation of two variant-identification approaches designed to exploit the high mappability of long reads (i.e., greater than 10,000 bp). PBHoney considers both intra-read discordance and soft-clipped tails of long reads to identify structural variants.</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/pb-jelly/" rel="nofollow">https://sourceforge.net/projects/pb-jelly/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31375/cocacola-binning-metagenomic-contigs-using-sequence-composition-read-coverage-co-alignment-and-paired-end-read-linkage</guid>
	<pubDate>Tue, 07 Mar 2017 08:50:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31375/cocacola-binning-metagenomic-contigs-using-sequence-composition-read-coverage-co-alignment-and-paired-end-read-linkage</link>
	<title><![CDATA[COCACOLA (binning metagenomic contigs using sequence COmposition, read CoverAge, CO-alignment, and paired-end read LinkAge)]]></title>
	<description><![CDATA[<p>COCACOLA is a general framework that combines different types of information: sequence COmposition, CoverAge across multiple samples, CO-alignment to reference genomes and paired-end reads LinkAge to automatically bin contigs into OTUs. Furthermore, COCACOLA seamlessly embraces customized prior knowledge to facilitate binning accuracy.</p>
<p>News: Python version of COCACOLA is available now!</p><p>Address of the bookmark: <a href="https://github.com/younglululu/COCACOLA" rel="nofollow">https://github.com/younglululu/COCACOLA</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34475/oxford-nanopore-sequencing-hybrid-error-correction-and-de-novo-assembly-of-a-eukaryotic-genome</guid>
	<pubDate>Wed, 29 Nov 2017 05:08:53 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34475/oxford-nanopore-sequencing-hybrid-error-correction-and-de-novo-assembly-of-a-eukaryotic-genome</link>
	<title><![CDATA[Oxford Nanopore Sequencing, Hybrid Error Correction, and de novo Assembly of a Eukaryotic Genome]]></title>
	<description><![CDATA[<p><span>Monitoring the progress of DNA molecules through a membrane pore has been postulated as a method for sequencing DNA for several decades. Recently, a nanopore-based sequencing instrument, the Oxford Nanopore MinION, has become available that we used for sequencing the S. cerevisiae genome. To make use of these data, we developed a novel open-source hybrid error correction algorithm Nanocorr (</span><a href="https://github.com/jgurtowski/nanocorr">https://github.com/jgurtowski/nanocorr</a><span>) specifically for Oxford Nanopore reads, as existing packages were incapable of assembling the long read lengths (5-50kbp) at such high error rate (between ~5 and 40% error). With this new method we were able to perform a hybrid error correction of the nanopore reads using complementary MiSeq data and produce a de novo assembly that is highly contiguous and accurate: the contig N50 length is more than ten-times greater than an Illumina-only assembly (678kb versus 59.9kbp), and has greater than 99.88% consensus identity when compared to the reference. Furthermore, the assembly with the long nanopore reads presents a much more complete representation of the features of the genome and correctly assembles gene cassettes, rRNAs, transposable elements, and other genomic features that were almost entirely absent in the Illumina-only assembly.</span></p><p>Address of the bookmark: <a href="http://schatzlab.cshl.edu/data/nanocorr/" rel="nofollow">http://schatzlab.cshl.edu/data/nanocorr/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42271/mcclintock-meta-pipeline-to-identify-transposable-element-insertions-using-next-generation-sequencing-data</guid>
	<pubDate>Tue, 27 Oct 2020 00:21:18 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42271/mcclintock-meta-pipeline-to-identify-transposable-element-insertions-using-next-generation-sequencing-data</link>
	<title><![CDATA[McClintock: Meta-pipeline to identify transposable element insertions using next generation sequencing data]]></title>
	<description><![CDATA[<p><span>an integrated bioinformatics pipeline for the detection of TE insertions in whole-genome shotgun data, called McClintock (</span><a href="https://github.com/bergmanlab/mcclintock">https://github.com/bergmanlab/mcclintock</a><span>), which automatically runs and standardizes output for multiple TE detection methods. We demonstrate the utility of McClintock by evaluating six TE detection methods using simulated and real genome data from the model microbial eukaryote,&nbsp;</span><em>Saccharomyces cerevisiae</em><span>.&nbsp;</span></p><p>Address of the bookmark: <a href="https://github.com/bergmanlab/mcclintock" rel="nofollow">https://github.com/bergmanlab/mcclintock</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42826/ktrim-an-extra-fast-and-accurate-adapter-and-quality-trimmer-for-sequencing-data</guid>
	<pubDate>Thu, 11 Feb 2021 21:39:05 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42826/ktrim-an-extra-fast-and-accurate-adapter-and-quality-trimmer-for-sequencing-data</link>
	<title><![CDATA[Ktrim: an extra-fast and accurate adapter- and quality-trimmer for sequencing data]]></title>
	<description><![CDATA[<p>Ktrim&nbsp;is written in&nbsp;<code style="font-size: 13.6px; padding: 0.2em 0.4em; margin: 0px; background-color: var(--color-markdown-code-bg);">C++</code>&nbsp;for GNU Linux/Unix platforms. After uncompressing the source package, you can find an executable file&nbsp;<code style="font-size: 13.6px; padding: 0.2em 0.4em; margin: 0px; background-color: var(--color-markdown-code-bg);">ktrim</code>&nbsp;under&nbsp;<code style="font-size: 13.6px; padding: 0.2em 0.4em; margin: 0px; background-color: var(--color-markdown-code-bg);">bin/</code>&nbsp;directory compiled using&nbsp;<code style="font-size: 13.6px; padding: 0.2em 0.4em; margin: 0px; background-color: var(--color-markdown-code-bg);">g++ v4.8.5</code>&nbsp;and linked with&nbsp;<code style="font-size: 13.6px; padding: 0.2em 0.4em; margin: 0px; background-color: var(--color-markdown-code-bg);">libz v1.2.7</code>&nbsp;for Linux x86_64 system. If you could not run it (which is usually caused by low version of&nbsp;<code style="font-size: 13.6px; padding: 0.2em 0.4em; margin: 0px; background-color: var(--color-markdown-code-bg);">libc++</code>&nbsp;or&nbsp;<code style="font-size: 13.6px; padding: 0.2em 0.4em; margin: 0px; background-color: var(--color-markdown-code-bg);">libz</code>&nbsp;library) or you want to build a version optimized for your system, you can re-compile the programs:</p>
<p>user@linux$ make clean &amp;&amp; make</p><p>Address of the bookmark: <a href="https://github.com/hellosunking/Ktrim" rel="nofollow">https://github.com/hellosunking/Ktrim</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43801/smudgeplot-inference-of-ploidy-and-heterozygosity-structure-using-whole-genome-sequencing-data</guid>
	<pubDate>Fri, 25 Feb 2022 04:42:09 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43801/smudgeplot-inference-of-ploidy-and-heterozygosity-structure-using-whole-genome-sequencing-data</link>
	<title><![CDATA[Smudgeplot: Inference of ploidy and heterozygosity structure using whole genome sequencing data]]></title>
	<description><![CDATA[<p dir="auto">This tool extracts heterozygous kmer pairs from kmer count databases and performs gymnastics with them. We are able to disentangle genome structure by comparing the sum of kmer pair coverages (CovA + CovB) to their relative coverage (CovB / (CovA + CovB)). Such an approach also allows us to analyze obscure genomes with duplications, various ploidy levels, etc.</p>
<p dir="auto">Smudgeplots are computed from raw or even better from trimmed reads and show the haplotype structure using heterozygous kmer pairs. For example:</p>
<p dir="auto"><a href="https://user-images.githubusercontent.com/8181573/45959760-f1032d00-c01a-11e8-8576-ff0512c33da9.png" target="_blank"><img src="https://user-images.githubusercontent.com/8181573/45959760-f1032d00-c01a-11e8-8576-ff0512c33da9.png" alt="smudgeexample" style="border: 0px;"></a></p><p>Address of the bookmark: <a href="https://github.com/KamilSJaron/smudgeplot" rel="nofollow">https://github.com/KamilSJaron/smudgeplot</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44541/powerful-books-for-learning-data-analysis-with-r</guid>
	<pubDate>Tue, 28 May 2024 07:42:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44541/powerful-books-for-learning-data-analysis-with-r</link>
	<title><![CDATA[Powerful books for learning data analysis with R]]></title>
	<description><![CDATA[<p><span>R is powerful tool for data analysis, visualization, and machine learning. And it costs $0 to use! Here are six FREE books you can use to learn R today:</span></p>
<p><span>https://csgillespie.github.io/efficientR/</span></p>
<p><span>https://r-graphics.org/</span></p>
<p><span>https://rstudio-education.github.io/hopr/</span></p>
<p><span>https://r-pkgs.org/</span></p>
<p><span>https://r4ds.had.co.nz/</span></p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://r-graphics.org/" rel="nofollow">https://r-graphics.org/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44659/figeno-tool-for-plotting-sequencing-data-along-genomic-coordinates</guid>
	<pubDate>Tue, 17 Sep 2024 02:28:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44659/figeno-tool-for-plotting-sequencing-data-along-genomic-coordinates</link>
	<title><![CDATA[Figeno: Tool for plotting sequencing data along genomic coordinates.]]></title>
	<description><![CDATA[<p><span>Tool for plotting sequencing data along genomic coordinates.</span></p>
<div>
<pre><code>FIGENO is a
  FIGure
    GENerator
for GENOmics</code></pre>
</div>
<p dir="auto">With figeno, you can plot various types of sequencing data along genomic coordinates. Video overview:&nbsp;<a href="https://www.youtube.com/watch?v=h1cBeXoSYTA">https://www.youtube.com/watch?v=h1cBeXoSYTA</a>.</p>
<p dir="auto"><a href="https://github.com/CompEpigen/figeno/blob/main/docs/content/images/figeno.png" target="_blank"><img src="https://github.com/CompEpigen/figeno/raw/main/docs/content/images/figeno.png" alt="figeno" style="border: 0px;"></a></p><p>Address of the bookmark: <a href="https://github.com/CompEpigen/figeno" rel="nofollow">https://github.com/CompEpigen/figeno</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/10741/managing-and-analyzing-next-generation-sequence-data</guid>
	<pubDate>Sat, 10 May 2014 06:28:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/10741/managing-and-analyzing-next-generation-sequence-data</link>
	<title><![CDATA[Managing and Analyzing Next-Generation Sequence Data]]></title>
	<description><![CDATA[<p>Centralized Bioinformatics Core Facilities provide shared resources for the computational and IT requirements of the investigators in their department or institution. As such, they must be able to effectively react to new types of experimental technology. Recently faced with an unprecedented flood of data generated by the next generation of DNA sequencers, these groups found it necessary to respond quickly and efficiently to the informatics and infrastructure demands. Centralized Facilities newly facing this challenge need to anticipate time and design considerations of necessary components, including infrastructure upgrades, staffing, and tools for data analyses and management ...</p>
<p>More at http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.1000369</p><p>Address of the bookmark: <a href="http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.1000369" rel="nofollow">http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.1000369</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/33869/import-r-data</guid>
	<pubDate>Wed, 12 Jul 2017 08:30:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/33869/import-r-data</link>
	<title><![CDATA[Import R Data]]></title>
	<description><![CDATA[<p>It is often necessary to import sample textbook data into R before you start working on your homework.</p><div id="node-69"><div><p><strong>Excel File</strong></p><p>Quite frequently, the sample data is in&nbsp;<span>Excel&nbsp;</span>format, and needs to be imported into R prior to use. For this, we can use the function&nbsp;<span>read.xls&nbsp;</span>from the&nbsp;<span>gdata&nbsp;</span>package. It reads from an Excel spreadsheet and returns a&nbsp;<a href="http://www.r-tutor.com/r-introduction/data-frame">data frame</a>. The following shows how to load an Excel spreadsheet named&nbsp;<span>"mydata.xls"</span>. This method requires Perl runtime to be present in the system.</p><blockquote><div id="listing-68"><span><a></a></span>&gt;&nbsp;library(gdata)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;load&nbsp;gdata&nbsp;package&nbsp;<br /><span><a></a></span>&gt;&nbsp;help(read.xls)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;documentation&nbsp;<br /><span><a></a></span>&gt;&nbsp;mydata&nbsp;=&nbsp;read.xls("mydata.xls")&nbsp;&nbsp;#&nbsp;read&nbsp;from&nbsp;first&nbsp;sheet</div></blockquote><p>Alternatively, we can use the function&nbsp;<span>loadWorkbook&nbsp;</span>from the&nbsp;<span>XLConnect&nbsp;</span>package to read the entire workbook, and then load the worksheets with&nbsp;<span>readWorksheet</span>. The&nbsp;<span>XLConnect&nbsp;</span>package requires Java to be pre-installed.</p><blockquote><div id="listing-69"><span><a></a></span>&gt;&nbsp;library(XLConnect)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;load&nbsp;XLConnect&nbsp;package&nbsp;<br /><span><a></a></span>&gt;&nbsp;wk&nbsp;=&nbsp;loadWorkbook("mydata.xls")&nbsp;<br /><span><a></a></span>&gt;&nbsp;df&nbsp;=&nbsp;readWorksheet(wk,&nbsp;sheet="Sheet1")</div></blockquote><p>&nbsp;</p><h4><a></a>Minitab File</h4><p>If the data file is in&nbsp;<span>Minitab Portable Worksheet&nbsp;</span>format, it can be opened with the function&nbsp;<span>read.mtp&nbsp;</span>from the&nbsp;<span>foreign&nbsp;</span>package. It returns a&nbsp;<a href="http://www.r-tutor.com/r-introduction/list">list</a>&nbsp;of components in the Minitab worksheet.</p><blockquote><div id="listing-70"><span><a></a></span>&gt;&nbsp;library(foreign)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;load&nbsp;the&nbsp;foreign&nbsp;package&nbsp;<br /><span><a></a></span>&gt;&nbsp;help(read.mtp)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;documentation&nbsp;<br /><span><a></a></span>&gt;&nbsp;mydata&nbsp;=&nbsp;read.mtp("mydata.mtp")&nbsp;&nbsp;#&nbsp;read&nbsp;from&nbsp;.mtp&nbsp;file</div></blockquote><p>&nbsp;</p><h4><a></a>SPSS File</h4><p>For the data files in&nbsp;<span>SPSS&nbsp;</span>format, it can be opened with the function&nbsp;<span>read.spss&nbsp;</span>also from the&nbsp;<span>foreign&nbsp;</span>package. There is a&nbsp;<span>"to.data.frame"&nbsp;</span>option for choosing whether a data frame is to be returned. By default, it returns a list of components instead.</p><blockquote><div id="listing-71"><span><a></a></span>&gt;&nbsp;library(foreign)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;load&nbsp;the&nbsp;foreign&nbsp;package&nbsp;<br /><span><a></a></span>&gt;&nbsp;help(read.spss)&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;documentation&nbsp;<br /><span><a></a></span>&gt;&nbsp;mydata&nbsp;=&nbsp;read.spss("myfile",&nbsp;to.data.frame=TRUE)</div></blockquote><p>&nbsp;</p><h4><a></a>Table File</h4><p>A data table can resides in a text file. The cells inside the table are separated by blank characters. Here is an example of a table with 4 rows and 3 columns.</p><blockquote><div id="listing-72"><span><a></a></span>100&nbsp;&nbsp;&nbsp;a1&nbsp;&nbsp;&nbsp;b1&nbsp;<br /><span><a></a></span>200&nbsp;&nbsp;&nbsp;a2&nbsp;&nbsp;&nbsp;b2&nbsp;<br /><span><a></a></span>300&nbsp;&nbsp;&nbsp;a3&nbsp;&nbsp;&nbsp;b3&nbsp;<br /><span><a></a></span>400&nbsp;&nbsp;&nbsp;a4&nbsp;&nbsp;&nbsp;b4</div></blockquote><p>Now copy and paste the table above in a file named&nbsp;<span>"mydata.txt"&nbsp;</span>with a text editor. Then load the data into the workspace with the function&nbsp;<span>read.table</span>.</p><blockquote><div id="listing-73"><span><a></a></span>&gt;&nbsp;mydata&nbsp;=&nbsp;read.table("mydata.txt")&nbsp;&nbsp;#&nbsp;read&nbsp;text&nbsp;file&nbsp;<br /><span><a></a></span>&gt;&nbsp;mydata&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;print&nbsp;data&nbsp;frame&nbsp;<br /><span><a></a></span>&nbsp;&nbsp;&nbsp;V1&nbsp;V2&nbsp;V3&nbsp;<br /><span><a></a></span>1&nbsp;100&nbsp;a1&nbsp;b1&nbsp;<br /><span><a></a></span>2&nbsp;200&nbsp;a2&nbsp;b2&nbsp;<br /><span><a></a></span>3&nbsp;300&nbsp;a3&nbsp;b3&nbsp;<br /><span><a></a></span>4&nbsp;400&nbsp;a4&nbsp;b4</div></blockquote><p>For further detail of the function&nbsp;<span>read.table</span>, please consult the R documentation.</p><blockquote><div id="listing-74"><span><a></a></span>&gt;&nbsp;help(read.table)</div></blockquote><p>&nbsp;</p><h4><a></a>CSV File</h4><p>The sample data can also be in&nbsp;<span>comma separated values&nbsp;</span>(CSV) format. Each cell inside such data file is separated by a special character, which usually is a comma, although other characters can be used as well.</p><p>The first row of the data file should contain the column names instead of the actual data. Here is a sample of the expected format.</p><blockquote><div id="listing-75"><span><a></a></span>Col1,Col2,Col3&nbsp;<br /><span><a></a></span>100,a1,b1&nbsp;<br /><span><a></a></span>200,a2,b2&nbsp;<br /><span><a></a></span>300,a3,b3</div></blockquote><p>After we copy and paste the data above in a file named&nbsp;<span>"mydata.csv"&nbsp;</span>with a text editor, we can read the data with the function&nbsp;<span>read.csv</span>.</p><blockquote><div id="listing-76"><span><a></a></span>&gt;&nbsp;mydata&nbsp;=&nbsp;read.csv("mydata.csv")&nbsp;&nbsp;#&nbsp;read&nbsp;csv&nbsp;file&nbsp;<br /><span><a></a></span>&gt;&nbsp;mydata&nbsp;<br /><span><a></a></span>&nbsp;&nbsp;Col1&nbsp;Col2&nbsp;Col3&nbsp;<br /><span><a></a></span>1&nbsp;&nbsp;100&nbsp;&nbsp;&nbsp;a1&nbsp;&nbsp;&nbsp;b1&nbsp;<br /><span><a></a></span>2&nbsp;&nbsp;200&nbsp;&nbsp;&nbsp;a2&nbsp;&nbsp;&nbsp;b2&nbsp;<br /><span><a></a></span>3&nbsp;&nbsp;300&nbsp;&nbsp;&nbsp;a3&nbsp;&nbsp;&nbsp;b3</div></blockquote><p>In various European locales, as the comma character serves as the decimal point, the function&nbsp;<span>read.csv2&nbsp;</span>should be used instead. For further detail of the&nbsp;<span>read.csv&nbsp;</span>and&nbsp;<span>read.csv2&nbsp;</span>functions, please consult the R documentation.</p><blockquote><div id="listing-77"><span><a></a></span>&gt;&nbsp;help(read.csv)</div></blockquote><p>&nbsp;</p><h4><a></a>Working Directory</h4><p>Finally, the code samples above assume the data files are located in the R&nbsp;<span>working</span>&nbsp;<span>directory</span>, which can be found with the function&nbsp;<span>getwd</span>.</p><blockquote><div id="listing-78"><span><a></a></span>&gt;&nbsp;getwd()&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;#&nbsp;get&nbsp;current&nbsp;working&nbsp;directory</div></blockquote><p>You can select a different working directory with the function&nbsp;<span>setwd()</span>, and thus avoid entering the full path of the data files.</p><blockquote><div id="listing-79"><span><a></a></span>&gt;&nbsp;setwd("")&nbsp;&nbsp;&nbsp;#&nbsp;set&nbsp;working&nbsp;directory</div></blockquote><p>Note that the forward slash should be used as the path separator even on Windows platform.</p><blockquote><div id="listing-80"><span><a></a></span>&gt;&nbsp;setwd("C:/MyDoc")</div></blockquote></div></div>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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