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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/28290?offset=1040</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26925/reapr-a-universal-tool-for-genome-assembly-evaluation</guid>
	<pubDate>Wed, 06 Apr 2016 18:26:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26925/reapr-a-universal-tool-for-genome-assembly-evaluation</link>
	<title><![CDATA[REAPR: a universal tool for genome assembly evaluation]]></title>
	<description><![CDATA[<p>REAPR is a tool that evaluates the accuracy of a genome assembly using mapped paired end reads, without the use of a reference genome for comparison. It can be used in any stage of an assembly pipeline to automatically break incorrect scaffolds and flag other errors in an assembly for manual inspection. It reports mis-assemblies and other warnings, and produces a new broken assembly based on the error calls.</p>
<p>The software requires as input an assembly in FASTA format and paired reads mapped to the assembly in a BAM file. Mapping information such as the fragment coverage and insert size distribution is analysed to locate mis-assemblies. REAPR works best using mapped read pairs from a large insert library (at least 1000bp). Additionally, if a short insert Illumina library is also available, REAPR can combine this with the large insert library in order to score each base of the assembly.</p>
<p>http://www.sanger.ac.uk/science/tools/reapr</p><p>Address of the bookmark: <a href="https://genomebiology.biomedcentral.com/articles/10.1186/gb-2013-14-5-r47" rel="nofollow">https://genomebiology.biomedcentral.com/articles/10.1186/gb-2013-14-5-r47</a></p>]]></description>
	<dc:creator>Jitendra Prajapati</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/27046/desai-lab</guid>
  <pubDate>Thu, 21 Apr 2016 10:21:07 -0500</pubDate>
  <link></link>
  <title><![CDATA[Desai Lab]]></title>
  <description><![CDATA[
<p>Evolutionary Dynamics and Population Genetics</p>

<p>Natural selection and other evolutionary forces lead to particular patterns of evolutionary dynamics, and they leave characteristic signatures on the genetic variation within populations.  We use a combination of theory and experiments to study the dynamics and population genetics of natural selection in asexual populations such as microbes and viruses. </p>

<p>We use both theory and experiments to study evolutionary dynamics and population genetics, particularly in situations where natural selection is pervasive.</p>

<p>http://desailab.oeb.harvard.edu/home</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/27274/bioinformatics-national-certification-binc-examination-2016</guid>
  <pubDate>Wed, 11 May 2016 02:17:44 -0500</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics National Certification (BINC) Examination 2016]]></title>
  <description><![CDATA[
<p>Bioinformatics National Certification (BINC) Examination 2016</p>

<p>Department of Biotechnology, Government of India, New Delhi &amp; Pondicherry University, Puducherry</p>

<p>Starting of online submission of application : April 13, 2016</p>

<p>Last date for submission of application : May 13, 2016</p>

<p>Examination consists of two parts:</p>

<p>Part - I (Paper - I) : June 12, 2016 (10 AM -12 PM)<br />Part - II (Paper • II &amp; III) : June 26, 2016 (9 AM • 12 PM &amp; 2 PM • 4 PM)</p>

<p>Objective: Pondicherry University, on behalf of the Department of Biotechnology (DBT),<br />Government of India, will conduct the Bioinformatics National Certification (BING) examination. The objective of this examination is to identify Bioinformatics professionals<br />for further studies as well as to help potential employers in recruitment of candidates having exceptionally good Bioinformatics skills.</p>

<p>Eligibility : Bachelor degree in Life Sciences, Physical Sciences, Chemical Sciences, Mathematical Sciences, Agriculture, Veterinary, Medicine, Pharmacy, Engineering and Technology are eligible to appear for the examination. They need not have any formal training, diploma or certificate in Bioinformatics.</p>

<p>Application and syllabus : The online application can be filled from April 13, 2016 to May 13, 2016.</p>

<p>Syllabus for the examination is available online.</p>

<p>It consists of five sections:<br />Bioinformatics, Biology, Physical and Chemical Sciences, Mathematics &amp; Statistics and Computer Science &amp; Information Technology.</p>

<p>Examination : The examination fee is Rs. 600/- for general candidates, Rs. 400/- for women/OBC candidates and Rs. 200 for SC/ST candidates, and no fee for physically challenged candidates.</p>

<p>The online Part - I (Paper - I) examination is scheduled on June 12,2016 and Part- II (Paper - II and Paper- III) on June 26, 2016. The Paper- I will be of objective type and candidates scoring a minimum of 40% marks in Paper - I will be called to appear in Part II examination.</p>

<p>Part II examination consists of two papers : The Paper - II will be of short answer type questions of three hours duration while the Paper- III will be a practical examination of two hours duration to test analytical ability and programming skill of candidates.</p>

<p>Research Fellowships for all the successful candidates those who are interested and qualified in pursuing Ph.D. in India will be awarded. In addition, cash prizes will be  awarded to the top 10 successful candidates.</p>

<p>The details of examination centres, other details and submission of application, please<br />visit: http://www.pondiuni.edu.in/exams/binc/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27238/slurm</guid>
	<pubDate>Wed, 04 May 2016 05:13:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27238/slurm</link>
	<title><![CDATA[SLURM]]></title>
	<description><![CDATA[<p><a href="http://www.schedmd.com/">SLURM</a> workload manager software, a free open-source workload manager designed specifically to satisfy the demanding needs of high performance computing.</p>
<p>This page is a <em>HOWTO</em> guide for setting up a <a href="http://www.schedmd.com/">SLURM</a> installation, currently focused on a CentOS 7 Linux OS. Please send feedback to Ole.H.Nielsen /at/ fysik.dtu.dk.</p>
<p>See the <a href="http://www.schedmd.com/">SLURM</a> homepage (also <a href="https://computing.llnl.gov/linux/slurm/">https://computing.llnl.gov/linux/slurm/</a>).</p><p>Address of the bookmark: <a href="https://wiki.fysik.dtu.dk/niflheim/SLURM" rel="nofollow">https://wiki.fysik.dtu.dk/niflheim/SLURM</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/27290/scientists-post-at-monsanto</guid>
  <pubDate>Wed, 11 May 2016 07:58:44 -0500</pubDate>
  <link></link>
  <title><![CDATA[Scientists post at Monsanto]]></title>
  <description><![CDATA[
<p>Sustainable agriculture is at the core of Monsanto. We develop technologies that enable farmers to produce more crops while conserving natural resources. Monsanto scientists are conducting research and development (R&amp;D) to revolutionize plant breeding and biotechnology.</p>

<p>Monsanto is seeking a very talented Genomics Scientistto become an integral member of our Global Pipeline Analytics team with a focus on quantitative genetics. The ideal candidate will have familiarity with modeling and analysis of genetic data sets using a variety of statistical techniques.</p>

<p>Major Responsibilities:<br />- Provide guidance on experimental design for genomic-related experiments<br />- Familiarity with analysis of the following methods: GWS, QTL, eQTL, RNA-Seq<br />- Provide written and oral presentations of methods, results, conclusions, and recommendations to peer and management groups.<br />- Ensure timely delivery and clear communication of results<br />- Develop strong and successful collaborations among various Monsanto enabling teams.</p>

<p>Required Skills:</p>

<p>- PhD degree in Statistics, Biostatistics, Statistical Genetics, Quantitative Genetics, Breeding, Bioinformatics or a related field with 2 years of experience<br />- Working knowledge and experience with one of the following quantitative languages:R, Python, Perl, SAS<br />- Background in Windows and Linux operating systems<br />- Very strong problem solving skills will be required to work well as a member of a dynamic team<br />- Strong verbal and written communication skills.<br />- Demonstrated ability to deliver timely results and be results oriented.<br />- Extensive knowledge of quantitative genetics and experimental design.&nbsp;<br />- Demonstrated track record of solving challenging and complex problems.</p>

<p>Desired Skills/Experience:</p>

<p>- Excellent communication skills, with the ability to summarize complex concepts in language understandable by scientists from a variety of disciplines.<br />- Experience in agronomy and/or plant breeding in vegetables or row crops.</p>

<p>Please apply to<br />https://jobs.monsanto.com/job/st-louis/genomics-scientist/769/2081771</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/27318/sample-binc-question-paper-2016-part2</guid>
	<pubDate>Fri, 13 May 2016 03:42:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/27318/sample-binc-question-paper-2016-part2</link>
	<title><![CDATA[Sample BINC question paper 2016 - part2]]></title>
	<description><![CDATA[<p>Download the sample question paper for BINC 2016 - paer II</p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/27318" length="52024" type="application/pdf" />
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27475/polyphen-2-prediction-of-functional-effects-of-human-nssnps</guid>
	<pubDate>Mon, 23 May 2016 02:27:25 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27475/polyphen-2-prediction-of-functional-effects-of-human-nssnps</link>
	<title><![CDATA[PolyPhen-2: Prediction of functional effects of human nsSNPs]]></title>
	<description><![CDATA[<p><strong>PolyPhen-2</strong> (<strong>Poly</strong>morphism <strong>Phen</strong>otyping v<strong>2</strong>) is a tool which predicts possible impact of an amino acid substitution on the structure and function of a human protein using straightforward physical and comparative considerations.</p><p>Address of the bookmark: <a href="http://genetics.bwh.harvard.edu/pph2/" rel="nofollow">http://genetics.bwh.harvard.edu/pph2/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/27549/ra-at-university-of-hyderabad</guid>
  <pubDate>Sun, 29 May 2016 11:50:37 -0500</pubDate>
  <link></link>
  <title><![CDATA[RA at UNIVERSITY OF HYDERABAD]]></title>
  <description><![CDATA[
<p>UNIVERSITY OF HYDERABAD</p>

<p>School of Life Sciences</p>

<p>Department of Animal Biology</p>

<p>Applications are invited on a plane paper (along with copies of educational qualifications and experience) from eligible candidates for the selection of following position to work under a collaborative research project entitled “Development and application of high resolution genome conformation capture technology to investigate genome architecture in space and time” between University of Hyderabad and CR Rao advanced Institute of Mathematics, Statistics and Computer Sciences, sponsored by Department of Biotechnology, Government of India, New Delhi</p>

<p>Name and No. of positions JRF‐ONE</p>

<p>Emoluments for the position Rs. 25,000/p.m. + Eligible HRA</p>

<p>Qualifications MSc or M.Tech in any branch of biology/bioinformatics/computational biology/computer sciences/Mathematics/Physics</p>

<p>Duration Appointments are made initially for ONE year and can be extended further TWO years or until the duration of project</p>

<p>Our laboratory is interested in understanding signalling and spatiotemporal dynamics of 3‐Dimensional genome architecture and gene expression during embryonic stem cell differentiation by utilizing a combination of cellular, molecular genetics, Biochemical and computational tools in combination with next generation sequencing based chromatin structure analysing methods. Successful candidates shall pursue project related to either experimental or computational analysis of genome and Epigenomics data derived from human and mouse cells. Experience in Computational biology, bioinformatics, statistics, machine learning and algorithmic development is required. Knowledge of programming languages (e.g. C, C++, Perl, Python, Ruby etc.) and statistical framework (e.g. R, matlab, etc.) is preferable. Basic understanding of molecular biology will be an added advantage.</p>

<p>Interested candidates with the above mentioned qualification can send their curriculum vitae to   Dr. K. Sreenivasulu, Department of Animal Biology, School of Life Sciences, South campus, University of Hyderabad or via email at positionssklab@gmail.com or svksl@uohyd.ernet.in.</p>

<p>Candidates with CSIR/UGC/ICMR/DBT/BINC qualifications if interested in above mentioned area of research are welcomed to approch principal investigator for a position leading to PhD. Last date for submission of applications is 17/06/2016. Eligible candidates will be called for an interview and they should carry all original certificates of the qualifying exam. No TA/ DA will be paid for attending the interview or at the time of joining the post.</p>

<p>Advertisement: http://www.uohyd.ac.in/images/recruitment/jrf_260516.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27691/histonedb-20-%E2%80%93-with-variants</guid>
	<pubDate>Fri, 03 Jun 2016 05:06:20 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27691/histonedb-20-%E2%80%93-with-variants</link>
	<title><![CDATA[HistoneDB 2.0 – with variants]]></title>
	<description><![CDATA[<p><span>This histone database can be used to explore the diversity of histone proteins and their sequence variants in many organisms. The resource was established to better understand how sequence variation may affect functional and structural features of nucleosomes. To get started, select a histone type to explore its variants.</span></p>
<p><span>More at&nbsp;http://www.ncbi.nlm.nih.gov/projects/HistoneDB2.0/index.fcgi/browse/</span></p><p>Address of the bookmark: <a href="http://www.ncbi.nlm.nih.gov/projects/HistoneDB2.0/index.fcgi/browse/" rel="nofollow">http://www.ncbi.nlm.nih.gov/projects/HistoneDB2.0/index.fcgi/browse/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/27965/cheatsheet-for-linux</guid>
	<pubDate>Wed, 22 Jun 2016 07:55:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/27965/cheatsheet-for-linux</link>
	<title><![CDATA[Cheatsheet for Linux !!]]></title>
	<description><![CDATA[<p>Linux Commands Cheat Sheet<br /><br />&nbsp;&nbsp;&nbsp; File System<br /><br />&nbsp;&nbsp;&nbsp; ls &mdash; list items in current directory<br /><br />&nbsp;&nbsp;&nbsp; ls -l &mdash; list items in current directory and show in long format to see perimissions, size, an modification date<br /><br />&nbsp;&nbsp;&nbsp; ls -a &mdash; list all items in current directory, including hidden files<br /><br />&nbsp;&nbsp;&nbsp; ls -F &mdash; list all items in current directory and show directories with a slash and executables with a star<br /><br />&nbsp;&nbsp;&nbsp; ls dir &mdash; list all items in directory dir<br /><br />&nbsp;&nbsp;&nbsp; cd dir &mdash; change directory to dir<br /><br />&nbsp;&nbsp;&nbsp; cd .. &mdash; go up one directory<br /><br />&nbsp;&nbsp;&nbsp; cd / &mdash; go to the root directory<br /><br />&nbsp;&nbsp;&nbsp; cd ~ &mdash; go to to your home directory<br /><br />&nbsp;&nbsp;&nbsp; cd - &mdash; go to the last directory you were just in<br /><br />&nbsp;&nbsp;&nbsp; pwd &mdash; show present working directory<br /><br />&nbsp;&nbsp;&nbsp; mkdir dir &mdash; make directory dir<br /><br />&nbsp;&nbsp;&nbsp; rm file &mdash; remove file<br /><br />&nbsp;&nbsp;&nbsp; rm -r dir &mdash; remove directory dir recursively<br /><br />&nbsp;&nbsp;&nbsp; cp file1 file2 &mdash; copy file1 to file2<br /><br />&nbsp;&nbsp;&nbsp; cp -r dir1 dir2 &mdash; copy directory dir1 to dir2 recursively<br /><br />&nbsp;&nbsp;&nbsp; mv file1 file2 &mdash; move (rename) file1 to file2<br /><br />&nbsp;&nbsp;&nbsp; ln -s file link &mdash; create symbolic link to file<br /><br />&nbsp;&nbsp;&nbsp; touch file &mdash; create or update file<br /><br />&nbsp;&nbsp;&nbsp; cat file &mdash; output the contents of file<br /><br />&nbsp;&nbsp;&nbsp; less file &mdash; view file with page navigation<br /><br />&nbsp;&nbsp;&nbsp; head file &mdash; output the first 10 lines of file<br /><br />&nbsp;&nbsp;&nbsp; tail file &mdash; output the last 10 lines of file<br /><br />&nbsp;&nbsp;&nbsp; tail -f file &mdash; output the contents of file as it grows, starting with the last 10 lines<br /><br />&nbsp;&nbsp;&nbsp; vim file &mdash; edit file<br /><br />&nbsp;&nbsp;&nbsp; alias name 'command' &mdash; create an alias for a command<br />&nbsp;&nbsp;&nbsp; System<br /><br />&nbsp;&nbsp;&nbsp; shutdown &mdash; shut down machine<br /><br />&nbsp;&nbsp;&nbsp; reboot &mdash; restart machine<br /><br />&nbsp;&nbsp;&nbsp; date &mdash; show the current date and time<br /><br />&nbsp;&nbsp;&nbsp; whoami &mdash; who you are logged in as<br /><br />&nbsp;&nbsp;&nbsp; finger user &mdash; display information about user<br /><br />&nbsp;&nbsp;&nbsp; man command &mdash; show the manual for command<br /><br />&nbsp;&nbsp;&nbsp; df &mdash; show disk usage<br /><br />&nbsp;&nbsp;&nbsp; du &mdash; show directory space usage<br /><br />&nbsp;&nbsp;&nbsp; free &mdash; show memory and swap usage<br /><br />&nbsp;&nbsp;&nbsp; whereis app &mdash; show possible locations of app<br /><br />&nbsp;&nbsp;&nbsp; which app &mdash; show which app will be run by default<br />&nbsp;&nbsp;&nbsp; Process Management<br /><br />&nbsp;&nbsp;&nbsp; ps &mdash; display your currently active processes<br /><br />&nbsp;&nbsp;&nbsp; top &mdash; display all running processes<br /><br />&nbsp;&nbsp;&nbsp; kill pid &mdash; kill process id pid<br /><br />&nbsp;&nbsp;&nbsp; kill -9 pid &mdash; force kill process id pid<br />&nbsp;&nbsp;&nbsp; Permissions<br /><br />&nbsp;&nbsp;&nbsp; ls -l &mdash; list items in current directory and show permissions<br /><br />&nbsp;&nbsp;&nbsp; chmod ugo file &mdash; change permissions of file to ugo - u is the user's permissions, g is the group's permissions, and o is everyone else's permissions. The values of u, g, and o can be any number between 0 and 7.<br /><br />&nbsp;&nbsp;&nbsp; 7 &mdash; full permissions<br /><br />&nbsp;&nbsp;&nbsp; 6 &mdash; read and write only<br /><br />&nbsp;&nbsp;&nbsp; 5 &mdash; read and execute only<br /><br />&nbsp;&nbsp;&nbsp; 4 &mdash; read only<br /><br />&nbsp;&nbsp;&nbsp; 3 &mdash; write and execute only<br /><br />&nbsp;&nbsp;&nbsp; 2 &mdash; write only<br /><br />&nbsp;&nbsp;&nbsp; 1 &mdash; execute only<br /><br />&nbsp;&nbsp;&nbsp; 0 &mdash; no permissions<br /><br />&nbsp;&nbsp;&nbsp; chmod 600 file &mdash; you can read and write - good for files<br /><br />&nbsp;&nbsp;&nbsp; chmod 700 file &mdash; you can read, write, and execute - good for scripts<br /><br />&nbsp;&nbsp;&nbsp; chmod 644 file &mdash; you can read and write, and everyone else can only read - good for web pages<br /><br />&nbsp;&nbsp;&nbsp; chmod 755 file &mdash; you can read, write, and execute, and everyone else can read and execute - good for programs that you want to share<br />&nbsp;&nbsp;&nbsp; Networking<br /><br />&nbsp;&nbsp;&nbsp; wget file &mdash; download a file<br /><br />&nbsp;&nbsp;&nbsp; curl file &mdash; download a file<br /><br />&nbsp;&nbsp;&nbsp; scp user@host:file dir &mdash; secure copy a file from remote server to the dir directory on your machine<br /><br />&nbsp;&nbsp;&nbsp; scp file user@host:dir &mdash; secure copy a file from your machine to the dir directory on a remote server<br /><br />&nbsp;&nbsp;&nbsp; scp -r user@host:dir dir &mdash; secure copy the directory dir from remote server to the directory dir on your machine<br /><br />&nbsp;&nbsp;&nbsp; ssh user@host &mdash; connect to host as user<br /><br />&nbsp;&nbsp;&nbsp; ssh -p port user@host &mdash; connect to host on port as user<br /><br />&nbsp;&nbsp;&nbsp; ssh-copy-id user@host &mdash; add your key to host for user to enable a keyed or passwordless login<br /><br />&nbsp;&nbsp;&nbsp; ping host &mdash; ping host and output results<br /><br />&nbsp;&nbsp;&nbsp; whois domain &mdash; get information for domain<br /><br />&nbsp;&nbsp;&nbsp; dig domain &mdash; get DNS information for domain<br /><br />&nbsp;&nbsp;&nbsp; dig -x host &mdash; reverse lookup host<br /><br />&nbsp;&nbsp;&nbsp; lsof -i tcp:1337 &mdash; list all processes running on port 1337<br />&nbsp;&nbsp;&nbsp; Searching<br /><br />&nbsp;&nbsp;&nbsp; grep pattern files &mdash; search for pattern in files<br /><br />&nbsp;&nbsp;&nbsp; grep -r pattern dir &mdash; search recursively for pattern in dir<br /><br />&nbsp;&nbsp;&nbsp; grep -rn pattern dir &mdash; search recursively for pattern in dir and show the line number found<br /><br />&nbsp;&nbsp;&nbsp; grep -r pattern dir --include='*.ext &mdash; search recursively for pattern in dir and only search in files with .ext extension<br /><br />&nbsp;&nbsp;&nbsp; command | grep pattern &mdash; search for pattern in the output of command<br /><br />&nbsp;&nbsp;&nbsp; find file &mdash; find all instances of file in real system<br /><br />&nbsp;&nbsp;&nbsp; locate file &mdash; find all instances of file using indexed database built from the updatedb command. Much faster than find<br /><br />&nbsp;&nbsp;&nbsp; sed -i 's/day/night/g' file &mdash; find all occurrences of day in a file and replace them with night - s means substitude and g means global - sed also supports regular expressions<br />&nbsp;&nbsp;&nbsp; Compression<br /><br />&nbsp;&nbsp;&nbsp; tar cf file.tar files &mdash; create a tar named file.tar containing files<br /><br />&nbsp;&nbsp;&nbsp; tar xf file.tar &mdash; extract the files from file.tar<br /><br />&nbsp;&nbsp;&nbsp; tar czf file.tar.gz files &mdash; create a tar with Gzip compression<br /><br />&nbsp;&nbsp;&nbsp; tar xzf file.tar.gz &mdash; extract a tar using Gzip<br /><br />&nbsp;&nbsp;&nbsp; gzip file &mdash; compresses file and renames it to file.gz<br /><br />&nbsp;&nbsp;&nbsp; gzip -d file.gz &mdash; decompresses file.gz back to file<br />&nbsp;&nbsp;&nbsp; Shortcuts<br /><br />&nbsp;&nbsp;&nbsp; ctrl+a &mdash; move cursor to beginning of line<br /><br />&nbsp;&nbsp;&nbsp; ctrl+f &mdash; move cursor to end of line<br /><br />&nbsp;&nbsp;&nbsp; alt+f &mdash; move cursor forward 1 word<br /><br />&nbsp;&nbsp;&nbsp; alt+b &mdash; move cursor backward 1 word</p>]]></description>
	<dc:creator>Jit</dc:creator>
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