<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/396?offset=390</link>
	<atom:link href="https://bioinformaticsonline.com/related/396?offset=390" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	
<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/4004/33rd-annual-convention-of-indian-association-for-cancer-research-from-13th-to-15th-february-2014</guid>
  <pubDate>Tue, 27 Aug 2013 10:37:08 -0500</pubDate>
  <link></link>
  <title><![CDATA[33rd Annual Convention of Indian Association for Cancer Research from 13th to 15th February 2014]]></title>
  <description><![CDATA[
<p>RGCB is organizing the 33rd Annual Convention of Indian Association for Cancer Research from 13th to 15th February 2014 with the theme "Discovery, Innovation and Translation in Cancer Research"</p>

<p>Kindly log on to conference website http://rgcb.res.in/IACR2014 for further details and timely updates and registration. We shall truly appreciate if the same be circulated among your friends, scholars and students encouraging them to participate in the meet.</p>

<p>http://210.212.237.38/iacrconference/</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/34368/srbioinformatics-analyst-ngs-at-ocimum</guid>
  <pubDate>Fri, 17 Nov 2017 07:50:44 -0600</pubDate>
  <link></link>
  <title><![CDATA[Sr.Bioinformatics Analyst (NGS) at Ocimum]]></title>
  <description><![CDATA[
<p>JOB FUNCTIONBio Tech/R&amp;D/Scientist<br />INDUSTRYBiotechnology/Pharmaceutical/Medicine<br />SPECIALIZATIONBasic Research,Bio-Statistician,Clinical Research<br />QUALIFICATION<br />Any Post Graduate<br />BA (Arts), B.Com. (Commerce), BE/ B.Tech (Engineering), B.Pharm. (Pharmacy), B.Sc. (Science), BL/LLB, BDS (Dental Surgery), B.Ed. (Education), BHM (Hotel Management), BBA/ BBM/ BBS, B.Arch. (Architecture), BCA (Computer Application), Diploma-Other Diploma, B.Plan. (Planning), BGL, B.V.Sc. (Veterinary Science), Other School/ Graduation, BHMS (Homeopathy), BAMS (Ayurveda)<br />Job Description</p>

<p>1.  Must have basic understanding of molecular biology and Genomics.<br />2. Experience in application development or must have expertise in programming using either of Perl/Python.<br />3.  Experience in statistical programming using R/Bioconductor/Matlab.<br />4. Strong concept in statistical and mathematical modelling.<br />5.  Experience in designing and developing the bioinformatics pipeline.<br />6.  Must have minimum 2+ years of hands on experience in NSG data analysis such as RNA-Seq,Exome-Seq ,Chip-Seq and downstream analysis.<br />7. Knowledge in WGS ,WES, Targeted re-sequencing,GWAS and population genomics will be preferred.<br />8. Must have experience working on opensource software/Framework and commercial software for NGS data analysis and reporting.<br />9. Should be aware of handling big data and guiding team members on multiple projects simultaneously.<br />10. Should have experience coordinating with different groups of clinical research scientist for various project requirements.<br />11. Ability to work as team as well as independently with minimal support.</p>

<p>More at http://www3.ocimumbio.com/</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/4552/imtech-lab</guid>
  <pubDate>Sun, 15 Sep 2013 09:41:04 -0500</pubDate>
  <link></link>
  <title><![CDATA[IMTECH Lab]]></title>
  <description><![CDATA[
<p>Computer Aided Protein Structure Prediction; Identification of Vaccine<br />Candidates (T-Epitope prediction); Analysis of Nucleotide/Protein Sequences; Development of Web Server/</p>

<p>Software; Creation of Public Domain Resources in Biology<br />Present Status::</p>

<p>Developing prediction methods for gene, beta-turn, secondary structure and MHC-binding sites.<br />Area of Interest ::</p>

<p>Comparison of force field simulations. Analysis of DNA-protein interactions using molecular mechanics methods.Drug Target Identification using in silico biology.</p>

<p>More @ http://www.imtech.res.in/bic/index.php?option=com_content&amp;view=article&amp;id=65</p>

<p>PIs: http://www.imtech.res.in/bic/index.php?option=com_content&amp;view=article&amp;id=69</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/view/2023</guid>
	<pubDate>Mon, 12 Aug 2013 09:36:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/view/2023</link>
	<title><![CDATA[What is the objective of BINC examination?]]></title>
	<description><![CDATA[<p>I personally did not understand the objective behind BINC examination. Is government only try to show off that they are doing something to promote Indian bioinformatics sector?</p><p>Moreover, It looks like BINC indirectly putting&nbsp;an extra burden to bioinformatician, mentally and financially.</p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/35525/linux-commands-cheat-sheet-for-bioinformatics-and-computational-biology-professionals</guid>
	<pubDate>Mon, 05 Feb 2018 18:50:41 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/35525/linux-commands-cheat-sheet-for-bioinformatics-and-computational-biology-professionals</link>
	<title><![CDATA[Linux Commands Cheat Sheet for Bioinformatics and Computational Biology Professionals]]></title>
	<description><![CDATA[<p><span>The purpose of this cheat sheet is to introduce biologist and bioinformatician to the frequently used tools for NGS analysis as well as giving experience in writing one-liners.</span></p><ul>
<li><span></span><span><strong>File System</strong></span><span><strong><br /> </strong></span><span>ls</span><span>&nbsp;&mdash; list items in current directory</span><span><br /> </span><span>ls -l</span><span>&nbsp;&mdash; list items in current directory and show in long format to see perimissions, size, and modification date</span><span><br /> </span><span>ls -a</span><span>&nbsp;&mdash; list all items in current directory, including hidden files</span><span><br /> </span><span>ls -F</span><span>&nbsp;&mdash; list all items in current directory and show directories with a slash and executables with a star</span><span><br /> </span><span>ls dir</span><span>&nbsp;&mdash; list all items in directory dir</span><span><br /> </span><span>cd dir</span><span>&nbsp;&mdash; change directory to dir</span><span><br /> </span><span>cd ..</span><span>&nbsp;&mdash; go up one directory</span><span><br /> </span><span>cd /</span><span>&nbsp;&mdash; go to the root directory</span><span><br /> </span><span>cd ~</span><span>&nbsp;&mdash; go to to your home directory</span><span><br /> </span><span>cd -</span><span>&nbsp;&mdash; go to the last directory you were just in</span><span><br /> </span><span>pwd</span><span>&nbsp;&mdash; show present working directory</span><span><br /> </span><span>mkdir dir</span><span>&nbsp;&mdash; make directory dir</span><span><br /> </span><span>rm file</span><span>&nbsp;&mdash; remove file</span><span><br /> </span><span>rm -r dir</span><span>&nbsp;&mdash; remove directory dir recursively</span><span><br /> </span><span>cp file1 file2</span><span>&nbsp;&mdash; copy file1 to file2</span><span><br /> </span><span>cp -r dir1 dir2</span><span>&nbsp;&mdash; copy directory dir1 to dir2 recursively</span><span><br /> </span><span>mv file1 file2</span><span>&nbsp;&mdash; move (rename) file1 to file2</span><span><br /> </span><span>ln -s file link</span><span>&nbsp;&mdash; create symbolic link to file</span><span><br /> </span><span>touch file</span><span>&nbsp;&mdash; create or update file</span><span><br /> </span><span>cat file</span><span>&nbsp;&mdash; output the contents of file</span><span><br /> </span><span>less file</span><span>&nbsp;&mdash; view file with page navigation</span><span><br /> </span><span>head file</span><span>&nbsp;&mdash; output the first 10 lines of file</span><span><br /> </span><span>tail file</span><span>&nbsp;&mdash; output the last 10 lines of file</span><span><br /> </span><span>tail -f file</span><span>&nbsp;&mdash; output the contents of file as it grows, starting with the last 10 lines</span><span><br /> </span><span>vim file</span><span>&nbsp;&mdash; edit file</span><span><br /> </span><span>alias name 'command'</span><span>&nbsp;&mdash; create an alias for a command</span><span><br /> </span></li>
<li><span></span><span><strong>System</strong></span><span><strong><br /> </strong></span><span>shutdown</span><span>&nbsp;&mdash; shut down machine</span><span><br /> </span><span>reboot</span><span>&nbsp;&mdash; restart machine</span><span><br /> </span><span>date</span><span>&nbsp;&mdash; show the current date and time</span><span><br /> </span><span>whoami</span><span>&nbsp;&mdash; who you are logged in as</span><span><br /> </span><span>finger user</span><span>&nbsp;&mdash; display information about user</span><span><br /> </span><span>man command</span><span>&nbsp;&mdash; show the manual for command</span><span><br /> </span><span>df</span><span>&nbsp;&mdash; show disk usage</span><span><br /> </span><span>du</span><span>&nbsp;&mdash; show directory space usage</span><span><br /> </span><span>free</span><span>&nbsp;&mdash; show memory and swap usage</span><span><br /> </span><span>whereis app</span><span>&nbsp;&mdash; show possible locations of app</span><span><br /> </span><span>which app</span><span>&nbsp;&mdash; show which app will be run by default</span><span><br /> </span></li>
<li><span></span><span><strong>Process Management</strong></span><span><strong><br /> </strong></span><span>ps</span><span>&nbsp;&mdash; display your currently active processes</span><span><br /> </span><span>top</span><span>&nbsp;&mdash; display all running processes</span><span><br /> </span><span>kill pid</span><span>&nbsp;&mdash; kill process id pid</span><span><br /> </span><span>kill -9 pid</span><span>&nbsp;&mdash; force kill process id pid</span><span><br /> </span></li>
<li><span></span><span><strong>Permissions</strong></span><span><strong><br /> </strong></span><span>ls -l</span><span>&nbsp;&mdash; list items in current directory and show permissions</span><span><br /> </span><span>chmod ugo file</span><span>&nbsp;&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.</span><span><br /> </span><span>7</span><span>&nbsp;&mdash; full permissions</span><span><br /> </span><span>6</span><span>&nbsp;&mdash; read and write only</span><span><br /> </span><span>5</span><span>&nbsp;&mdash; read and execute only</span><span><br /> </span><span>4</span><span>&nbsp;&mdash; read only</span><span><br /> </span><span>3</span><span>&nbsp;&mdash; write and execute only</span><span><br /> </span><span>2</span><span>&nbsp;&mdash; write only</span><span><br /> </span><span>1</span><span>&nbsp;&mdash; execute only</span><span><br /> </span><span>0</span><span>&nbsp;&mdash; no permissions</span><span><br /> </span><span>chmod 600 file</span><span>&nbsp;&mdash; you can read and write - good for files</span><span><br /> </span><span>chmod 700 file</span><span>&nbsp;&mdash; you can read, write, and execute - good for scripts</span><span><br /> </span><span>chmod 644 file</span><span>&nbsp;&mdash; you can read and write, and everyone else can only read - good for web pages</span><span><br /> </span><span>chmod 755 file</span><span>&nbsp;&mdash; you can read, write, and execute, and everyone else can read and execute - good for programs that you want to share</span><span><br /> </span></li>
<li><span></span><span><strong>Networking</strong></span><span><strong><br /> </strong></span><span>wget file</span><span>&nbsp;&mdash; download a file</span><span><br /> </span><span>curl file</span><span>&nbsp;&mdash; download a file</span><span><br /> </span><span>scp user@host:file dir</span><span>&nbsp;&mdash; secure copy a file from remote server to the dir directory on your machine</span><span><br /> </span><span>scp file user@host:dir</span><span>&nbsp;&mdash; secure copy a file from your machine to the dir directory on a remote server</span><span><br /> </span><span>scp -r user@host:dir dir</span><span>&nbsp;&mdash; secure copy the directory dir from remote server to the directory dir on your machine</span><span><br /> </span><span>ssh user@host</span><span>&nbsp;&mdash; connect to host as user</span><span><br /> </span><span>ssh -p port user@host</span><span>&nbsp;&mdash; connect to host on port as user</span><span><br /> </span><span>ssh-copy-id user@host</span><span>&nbsp;&mdash; add your key to host for user to enable a keyed or passwordless login</span><span><br /> </span><span>ping host</span><span>&nbsp;&mdash; ping host and output results</span><span><br /> </span><span>whois domain</span><span>&nbsp;&mdash; get information for domain</span><span><br /> </span><span>dig domain</span><span>&nbsp;&mdash; get DNS information for domain</span><span><br /> </span><span>dig -x host</span><span>&nbsp;&mdash; reverse lookup host</span><span><br /> </span><span>lsof -i tcp:1337</span><span>&nbsp;&mdash; list all processes running on port 1337</span><span><br /> </span></li>
<li><span></span><span><strong>Searching</strong></span><span><strong><br /> </strong></span><span>grep pattern files</span><span>&nbsp;&mdash; search for pattern in files</span><span><br /> </span><span>grep -r pattern dir</span><span>&nbsp;&mdash; search recursively for pattern in dir</span><span><br /> </span><span>grep -rn pattern dir</span><span>&nbsp;&mdash; search recursively for pattern in dir and show the line number found</span><span><br /> </span><span>grep -r pattern dir --include='*.ext</span><span>&nbsp;&mdash; search recursively for pattern in dir and only search in files with .ext extension</span><span><br /> </span><span>command | grep pattern</span><span>&nbsp;&mdash; search for pattern in the output of command</span><span><br /> </span><span>find file</span><span>&nbsp;&mdash; find all instances of file in real system</span><span><br /> </span><span>locate file</span><span>&nbsp;&mdash; find all instances of file using indexed database built from the updatedb command. Much faster than find</span><span><br /> </span><span>sed -i 's/day/night/g' file</span><span>&nbsp;&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</span><span><br /> </span></li>
<li><span></span><span><strong>Compression</strong></span><span><strong><br /> </strong></span><span>tar cf file.tar files</span><span>&nbsp;&mdash; create a tar named file.tar containing files</span><span><br /> </span><span>tar xf file.tar</span><span>&nbsp;&mdash; extract the files from file.tar</span><span><br /> </span><span>tar czf file.tar.gz files</span><span>&nbsp;&mdash; create a tar with Gzip compression</span><span><br /> </span><span>tar xzf file.tar.gz</span><span>&nbsp;&mdash; extract a tar using Gzip</span><span><br /> </span><span>gzip file</span><span>&nbsp;&mdash; compresses file and renames it to file.gz</span><span><br /> </span><span>gzip -d file.gz</span><span>&nbsp;&mdash; decompresses file.gz back to file</span><span><br /> </span></li>
<li><span></span><span><strong>Shortcuts</strong></span><span><strong><br /> </strong></span><span>ctrl+a</span><span>&nbsp;&mdash; move cursor to beginning of line</span><span><br /> </span><span>ctrl+f</span><span>&nbsp;&mdash; move cursor to end of line</span><span><br /> </span><span>alt+f</span><span>&nbsp;&mdash; move cursor forward 1 word</span><span><br /> </span><span>alt+b</span><span>&nbsp;&mdash; move cursor backward 1 word</span><span><br /> </span></li>
<li></li>
</ul>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/2425/phd-fellowship-computational-biologybioinformatics-cork-ireland-cork-ireland</guid>
  <pubDate>Thu, 15 Aug 2013 14:09:00 -0500</pubDate>
  <link></link>
  <title><![CDATA[Ph.D. Fellowship (Computational Biology/Bioinformatics) : Cork, Ireland : Cork, Ireland]]></title>
  <description><![CDATA[
<p>Ph.D. Fellowship (18,000 euro/pa, plus tuition fees at the EU students rate) is available for four years to work on development of Bioinformatics resources for the analysis and visualization of ribosome profiling data. Ribosome profiling (ribo-seq) is a technology that allows mapping positions of the ribosomes on the whole transcriptome level with a nucleotide precision. The technology allows obtaining high resolution digital snapshots of gene expression in cells. The position is available starting on the 1st of October, 2013.</p>

<p>Candidate:<br />The candidate is expected to have B.S. or M.S. degree in the disciplines such as Computer Science, Statistics, Applied Mathematics, Physics or Electrical Engineering. The candidates with the backgrounds in Life Science disciplines such as Bioinformatics, Computational or Quantitative Biology will also be considered.</p>

<p>Location:<br />The position is available at LAPTI (http://lapti.ucc.ie) that is located in the Western Gate Building (http://www.stwarchitects.com/project-information.php?c=1&amp;p=09993) at University College Cork. Western Gate Building Research Complex hosts several UCC departments and provides ideal environment for interdisciplinary research. Cork (sometimes referenced as “Venice of Ireland”) is the second most populous city in the Republic. It has friendly cosmopolitan atmosphere and vibrant culture. A number of American industrial giants such as Apple , EMC and Pfizer have chosen Cork as a home for their European headquarters.</p>

<p>Application process:<br />The details of the application process are given at http://lapti.ucc.ie/jobs.html. To ensure prompt processing of your application use the subject line: ‘Ph.D. computational’. All applications received prior to August the 1st are guaranteed equal consideration. However, applications at the later dates will also be considered until the position is filled.</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/35983/some-useful-bioinformatics-links</guid>
	<pubDate>Fri, 16 Mar 2018 20:50:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/35983/some-useful-bioinformatics-links</link>
	<title><![CDATA[Some useful Bioinformatics links]]></title>
	<description><![CDATA[<p><br /> Reference-free prediction of rearrangement breakpoint reads | Bioinformatics | Oxford Academic</p><p>https://academic.oup.com/bioinformatics/article/30/18/2559/2475628<br /> Reference-free SNP detection: dealing with the data deluge</p><p>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4083407/<br /> GATB/DiscoSnp: DiscoSnp is designed for discovering all kinds of SNPs (not only isolated ones), as well as insertions and deletions, from raw set(s) of reads.</p><p>https://github.com/GATB/DiscoSnp<br /> De novo assembly | Oxford Nanopore Technologies</p><p>https://nanoporetech.com/taxonomy/term/131<br /> De novo long-read assembly of a complex animal genome | bioRxiv</p><p>https://www.biorxiv.org/content/early/2017/09/10/187054<br /> Rapid de novo assembly of the European eel genome from nanopore sequencing reads | Scientific Reports</p><p>https://www.nature.com/articles/s41598-017-07650-6.epdf?author_access_token=dktG7e98wyRJnaEEMTcPqtRgN0jAjWel9jnR3ZoTv0P7E7t-wVGo30iojNO7dICajNY_7PE5xVPv6OoLe7hn9TeUjcZ5umREOzNoPMWkfYH58RS6uxm3vm4e4BG2AA_WKW84i6egKK271NwMq-NfzA%3D%3D<br /> nanoporetech/ont-assembly-polish: ONT assembly and Illumina polishing pipeline</p><p>https://github.com/nanoporetech/ont-assembly-polish<br /> Generade-nl/TULIP: TULIP - The Uncorrected Long read Itegration Pipeline</p><p>https://github.com/Generade-nl/TULIP<br /> www.nature.com</p><p>https://www.nature.com/articles/s41598-017-03996-z<br /> Example gallery of NanoPlot &ndash; Gigabase or gigabyte</p><p>https://gigabaseorgigabyte.wordpress.com/2017/06/01/example-gallery-of-nanoplot/<br /> Tool documentation</p><p>https://broadinstitute.github.io/picard/command-line-overview.html<br /> Chromosome-scale scaffolding of de novo genome assemblies based on chromatin interactions. - PubMed - NCBI</p><p>https://www.ncbi.nlm.nih.gov/pubmed/24185095<br /> MAFFT ver.7 - a multiple sequence alignment program</p><p>https://mafft.cbrc.jp/alignment/software/algorithms/algorithms.html<br /> Measuring the distance between multiple sequence alignments | Bioinformatics | Oxford Academic</p><p>https://academic.oup.com/bioinformatics/article/28/4/495/212883<br /> The MUMmer 3 examples</p><p>http://mummer.sourceforge.net/examples/<br /> MAFFT ver.7 - a multiple sequence alignment program</p><p>https://mafft.cbrc.jp/alignment/software/tips.html<br /> Omega | Overlap-graph de novo Assembler for Metagenomics</p><p>https://omega.omicsbio.org/<br /> abiswas-odu/Disco: Multi-threaded Distributed Memory Overlap-Layout-Consensus (OLC) Metagenome Assembler</p><p>https://github.com/abiswas-odu/Disco<br /> SAGE: String-overlap Assembly of GEnomes | BMC Bioinformatics | Full Text</p><p>https://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471-2105-15-302</p><p>Fast and sensitive mapping of nanopore sequencing reads with GraphMap | Nature Communications</p><p>https://www.nature.com/articles/ncomms11307<br /> lumpy-sv/extractSplitReads_BwaMem at master &middot; arq5x/lumpy-sv</p><p>https://github.com/arq5x/lumpy-sv/blob/master/scripts/extractSplitReads_BwaMem<br /> jts/nanocorrect: Experimental pipeline for correcting nanopore reads</p><p>https://github.com/jts/nanocorrect</p><p>video - how to install flash plugin on ubuntu 14.04 LTS 64-bit version - Ask Ubuntu</p><p>https://askubuntu.com/questions/469553/how-to-install-flash-plugin-on-ubuntu-14-04-lts-64-bit-version<br /> lh3/fermi: A WGS de novo assembler based on the FMD-index for large genomes</p><p>https://github.com/lh3/fermi<br /> Multi-metagenome</p><p>http://madsalbertsen.github.io/multi-metagenome/docs/step9.html<br /> Bandage by rrwick</p><p>https://rrwick.github.io/Bandage/<br /> Codon Optimization OnLine (COOL): a web-based multi-objective optimization platform for synthetic gene design | Bioinformatics | Oxford Academic</p><p>https://academic.oup.com/bioinformatics/article/30/15/2210/2391162<br /> Genome Architecture and Evolution of a Unichromosomal Asexual Nematode - ScienceDirect</p><p>https://www.sciencedirect.com/science/article/pii/S096098221731076X?via%3Dihub#fig4<br /> How to determine chimeras in my de novo assembly? - SEQanswers</p><p>http://seqanswers.com/forums/showthread.php?t=26721<br /> samtools(1) manual page</p><p>http://www.htslib.org/doc/samtools.html<br /> How To Filter Mapped Reads With Samtools</p><p>https://www.biostars.org/p/56246/<br /> The MUMmer 3 manual</p><p>http://mummer.sourceforge.net/manual/#nucmer<br /> assembly_olc.pdf</p><p>http://www.cs.jhu.edu/~langmea/resources/lecture_notes/assembly_olc.pdf<br /> SAM and BAM filtering oneliners</p><p>https://gist.github.com/davfre/8596159<br /> Inroduction to dot-plots</p><p>http://www.code10.info/index.php%3Foption%3Dcom_content%26view%3Darticle%26id%3D64:inroduction-to-dot-plots%26catid%3D52:cat_coding_algorithms_dot-plots%26Itemid%3D76<br /> RepeatFinder Home Page</p><p>http://www.cbcb.umd.edu/software/RepeatFinder/<br /> RepeatFinderReprint.pdf</p><p>http://www.cbcb.umd.edu/software/RepeatFinder/RepeatFinderReprint.pdf<br /> https://bernatgel.github.io/karyoploter_tutorial//Tutorial/CreateIdeogram/CreateIdeogram.html</p><p>https://bernatgel.github.io/karyoploter_tutorial//Tutorial/CreateIdeogram/CreateIdeogram.html<br /> Circular Visualization in R</p><p>http://zuguang.de/circlize_book/book/introduction.html#a-qiuck-glance<br /> Creating a coverage plot using BEDTools and R</p><p>https://davetang.org/muse/2015/08/05/creating-a-coverage-plot-using-bedtools-and-r/<br /> Eval: A software package for analysis of genome annotations | BMC Bioinformatics | Full Text</p><p>https://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471-2105-4-50<br /> eval-documentation.pdf</p><p>http://mblab.wustl.edu/media/software/eval-documentation.pdf<br /> OmicCircos: A Simple-to-Use R Package for the Circular Visualization of Multidimensional Omics Data</p><p>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921174/<br /> sequence - download.tardigrades.org &gt; v1 &gt; sequence</p><p>http://download.tardigrades.org/v1/sequence/<br /> ksahlin/BESST: BESST - scaffolder for genomic assemblies</p><p>https://github.com/ksahlin/BESST<br /> reubwn/scripts: Useful scripts for various things</p><p>https://github.com/reubwn/scripts<br /> ICEberg</p><p>http://db-mml.sjtu.edu.cn/ICEberg/index.php<br /> Satsuma - Evolution and Genomics</p><p>http://evomics.org/learning/genomics/satsuma/<br /> A complete bacterial genome assembled de novo using only nanopore sequencing data | Nature Methods</p><p>https://www.nature.com/articles/nmeth.3444<br /> vezzi/FRC_align: Computes FRC from SAM/BAM file and not from afg files</p><p>https://mail.google.com/mail/u/0/#inbox<br /> Read GTF file into R - Dave Tang's blog</p><p>https://davetang.org/muse/2017/08/04/read-gtf-file-r/</p><p>https://bernatgel.github.io/karyoploter_tutorial//Tutorial/CustomGenomes/CustomGenomes.html</p><p>https://bernatgel.github.io/karyoploter_tutorial//Tutorial/CustomGenomes/CustomGenomes.html<br /> Dot: Interactive dot plot for genome-genome alignments</p><p>https://dnanexus.github.io/dot/<br /> Zoho Accounts</p><p>https://accounts.zoho.eu/signin?servicename=ZohoProjects&amp;serviceurl=https%3A%2F%2Fprojects.zoho.eu%2Fportal%2Favaga2<br /> lh3/minimap2: A versatile pairwise aligner for genomic and spliced nucleotide sequences</p><p>https://github.com/lh3/minimap2<br /> SSPACE-LongRead: scaffolding bacterial draft genomes using long read sequence information | BMC Bioinformatics | Full Text</p><p>https://bmcbioinformatics.biomedcentral.com/articles/10.1186/1471-2105-15-211<br /> Palindromic gene amplification &mdash; an evolutionarily conserved role for DNA inverted repeats in the genome | Nature Reviews Cancer</p><p>https://www.nature.com/articles/nrc2591<br /> bioinformatics - BLAST DNA Sequences Reversed - Biology Stack Exchange</p><p>https://biology.stackexchange.com/questions/8160/blast-dna-sequences-reversed<br /> LASTZ</p><p>http://www.bx.psu.edu/miller_lab/dist/README.lastz-1.02.00/README.lastz-1.02.00a.html<br /> SOGo - (1652) Inbox</p><p>https://sogo.unamur.be/SOGo/so/jnarayan/Mail/view<br /> Tetra-Nucleotide Analysis (TNA) | BIOiPLUG Help center</p><p>http://help.bioiplug.com/tetra-nucleotide-analysis-tna/</p><p>Clustering metagenomic contigs on tetranucleotide frequency &mdash; CGAT documentation</p><p>http://cgat.readthedocs.io/en/latest/recipes/metagenome_contigs_kmers.html</p><p>&nbsp;</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/2336/3rd-annual-next-generation-sequencing-asia-congress-2013-at-singapore-singapore</guid>
  <pubDate>Wed, 14 Aug 2013 09:55:04 -0500</pubDate>
  <link></link>
  <title><![CDATA[3rd Annual Next Generation Sequencing Asia Congress 2013 at Singapore, Singapore]]></title>
  <description><![CDATA[
<p>The 3rd Annual Next Generation Sequencing Asia Congress is to be held on the 22nd and 23rd of October 2013 in Singapore. Over the 2 days, the conference will provide an overview of the current options of next-generation sequencing platforms, technologies, applications and the newest computational tools for the analysis of next-generation sequencing data and analytical genomics as well as overcoming data management problems. The event will attract over 200 senior-level decision makers working in areas such as next generation sequencing, analytical genomics, computational biology, oncology, RNA profiling, molecular genomics, biomarkers, bioinformatics &amp; data management and clinical &amp; diagnostics development.</p>

<p>Dated : 22 Nov 2013 -23 Nov 2013</p>

<p>http://www.ngsasia-congress.com/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/36281/binc-bioinformatics-national-certification-examination-2018</guid>
	<pubDate>Mon, 23 Apr 2018 03:34:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/36281/binc-bioinformatics-national-certification-examination-2018</link>
	<title><![CDATA[BINC (Bioinformatics National Certification) Examination 2018]]></title>
	<description><![CDATA[<p>Bioinformatics National Certification (BINC) was instituted by Department of Biotechnology, Government of India in 2005 at Savitribai Phule Pune University, formerly University of Pune, Pune to certify bioinformatics professionals and recognizing candidate's theoretical and practical ability and fostering interdisciplinary research. Later on, it was transferred to Jawaharlal Nehru University, New Delhi and then to Pondicherry University, Puducherry. Pondicherry University conducted the BINC examination in 2015, 2016 and 2017.</p><div><p>Biotech Consortium India Limited (BCIL), New Delhi is conducting the BINC 2018 examination on behalf Department of Biotechnology, Government of India.</p></div><div><p>BINC is a certification programme for graduate and post-graduate students for recognizing their exceptional bioinformatics knowledge and skills and to improve their employment opportunities. There is a growing need for trained manpower in the area of Bioinformatics. Currently, various universities and institutions, both government and private, impart Bioinformatics education in India. The qualifying candidates will be awarded a lifetime certificate. This certification would facilitate industries and potential employers in recruitment of Bioinformatics professionals having exceptionally good bioinformatics skills.</p></div><div><p>The certification under Bioinformatics National Certification (BINC) scheme is given to the candidates after three tier selection process. The successful candidates are also eligible for availing Junior Research Fellowship (JRF) for pursuing Ph.D. in Bioinformatics at recognized Indian universities/institutes. The research fellowships of all BINC qualified Indian nationals are funded by DBT. BINC qualified candidates are called DBT certified Bioinformaticians while the individuals availing the fellowships are called as DBT-BINC Junior Research Fellows (DBT-BINC-JRF). Cash prize of 10,000/- each is awarded to the top 10 BINC qualifiers.</p></div><div><p><strong>Eligibility</strong></p></div><div><p>i) Bachelor's/Master's degree in Life Sciences, Physical Sciences, Chemical Sciences, Mathematical Sciences, Agriculture, Veterinary, Medicine, Pharmacy, Engineering and Technology.&nbsp;</p></div><div><p>ii) No formal training, diploma or certificate in bioinformatics is required.</p></div><div><p>iii) Candidates in final year of Bachelor's/ Master's degree are also eligible to apply.</p></div><div><p><strong><a href="http://bcil.nic.in/PatternofExamination.html" target="_blank">Pattern of Examination&nbsp;</a></strong></p></div><div><p><strong>Syllabus</strong>&nbsp;</p></div><div><p>The syllabus consists of six sections - Bioinformatics, Biology, Physical Science, Chemical Science, Mathematics &amp; Statistics, and Information Technology.</p></div><div><ul>
<li><a href="http://bcil.nic.in/files/BINC/BINC_SYLLABUS_for_Paper_I_2018.pdf" target="_blank">Syllabus for Paper-I (Objective)</a></li>
<li><a href="http://bcil.nic.in/files/BINC/BINC_SYLLABUS_for_Paper_II_2018.pdf" target="_blank">Syllabus for Paper-II (Short answers)</a></li>
<li><a href="http://bcil.nic.in/files/BINC/BINC_SYLLABUS_for_Paper_III_2018.pdf" target="_blank">Syllabus for Paper-III (Practical)</a></li>
</ul></div><div><p><strong>Note: Paper-III will be computer based practical and will include programming on Bioinformatics</strong></p></div><div><p><strong><a href="http://bcil.nic.in/files/BINC/Important_Dates.pdf" target="_blank">Important Dates</a></strong></p></div><div><p><strong><a href="http://bcil.nic.in/files/BINC/Examination_Centers.pdf" target="_blank">Examination Centers&nbsp;</a></strong></p></div><div><p><strong><a href="http://bcil.nic.in/files/BINC/BINC_Fellowship.pdf" target="_blank">BINC Fellowship&nbsp;</a></strong></p></div><div><p><strong><a href="http://bcil.nic.in/formanddownload.html" target="_blank">Forms &amp; Downloads&nbsp;</a></strong></p></div><div><p><strong><a href="http://bcil.nic.in/files/BINC/FAQs.pdf" target="_blank">FAQs&nbsp;</a></strong>&nbsp;</p></div><div><h3>Contact Us</h3></div><div><ul>
<li>Nisha Singh</li>
<li>Biotech Consortium India Limited</li>
<li>(CIN: U73100DL1990PLC041486)</li>
<li>5th Floor, Anuvrat Bhawan 210, Deen Dayal Upadhyaya Marg New Delhi - 110 002</li>
<li>Tel.: 011-2321 9064-67 Ext. 231, 236</li>
<li>Email - For general BINC queries:<a href="mailto:binc.dbt@biotech.co.in" target="_blank">binc.dbt@biotech.co.in</a></li>
<li>Helpline for Application submission related queries:<a href="mailto:binc.binchelpdesk@biotech.co.in" target="_blank">binchelpdesk@biotech.co.in</a></li>
<li>Website:&nbsp;<a href="http://bcil.nic.in/BINC.html" target="_blank">www.bcil.nic.in/BINC.html</a></li>
</ul></div>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/fun/view/2383/golden-rules-of-bioinformatics</guid>
	<pubDate>Wed, 14 Aug 2013 21:11:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/fun/view/2383/golden-rules-of-bioinformatics</link>
	<title><![CDATA[Golden Rules of Bioinformatics]]></title>
	<description><![CDATA[<ol>
<li>All constant are variable.</li>
<li>Copy and paste is a genetic error.</li>
<li>First solve the problem, then write the code.</li>
<li>No matter what goes wrong, it will probably look right.</li>
<li>Any simple problem can be insoluble if enough metting are held to discuss it. :P</li>
<li>Stastics is a systematic method of comming to the wrong conclusion with confidence.</li>
<li>Bug is a undocumented feature in programming languages.</li>
<li>Good biological programmer goes on summer holiday with raincoat. [because see 1]</li>
<li>Thanks god Google know python is not a python and multiplication and division are the same thing.</li>
<li>Don' be clever, complex biology will trick you.</li>
</ol>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>

</channel>
</rss>