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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/35534?offset=480</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31087/bedtools</guid>
	<pubDate>Fri, 24 Feb 2017 04:50:44 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31087/bedtools</link>
	<title><![CDATA[bedtools]]></title>
	<description><![CDATA[<p>Collectively, the&nbsp;<strong>bedtools</strong>&nbsp;utilities are a swiss-army knife of tools for a wide-range of genomics analysis tasks. The most widely-used tools enable&nbsp;<em>genome arithmetic</em>: that is, set theory on the genome. For example,&nbsp;<strong>bedtools</strong>&nbsp;allows one to<em>intersect</em>,&nbsp;<em>merge</em>,&nbsp;<em>count</em>,&nbsp;<em>complement</em>, and&nbsp;<em>shuffle</em>&nbsp;genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF. While each individual tool is designed to do a relatively simple task (e.g.,&nbsp;<em>intersect</em>&nbsp;two interval files), quite sophisticated analyses can be conducted by combining multiple bedtools operations on the UNIX command line.</p>
<p><strong>bedtools</strong>&nbsp;is developed in the&nbsp;<a href="http://quinlanlab.org/">Quinlan laboratory</a>&nbsp;at the&nbsp;<a href="http://www.utah.edu/">University of Utah</a>&nbsp;and benefits from fantastic contributions made by scientists worldwide.</p><p>Address of the bookmark: <a href="http://bedtools.readthedocs.io/en/latest/index.html" rel="nofollow">http://bedtools.readthedocs.io/en/latest/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/42921/run-bash-script-in-perl-program</guid>
	<pubDate>Sat, 27 Feb 2021 01:42:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/42921/run-bash-script-in-perl-program</link>
	<title><![CDATA[Run bash script in Perl program !]]></title>
	<description><![CDATA[<p>BioPerl is a compilation of Perl modules that can be used to build bioinformatics-related Perl scripts. It is used, for example, in the development of source codes, standalone software/tools, and algorithms in bioinformatics programmes. Different modules are easy to instal and include, making it easier to perform different functions. Despite the fact that Python is commonly favoured over Perl, some bioinformatics software, such as the standalone version of 'alienomics', is written in Perl. Often it's a major problem for beginners to execute certain Unix/shell commands in Perl script, so it's hard to determine which feature is unique to a situation.</p><div style="background-color: white;">Perl provides various features and operators for the execution of external commands (described as follows), which are unique in their own way.</div><div style="background-color: white;">&nbsp;</div><div style="background-color: white;">They vary slightly from one another, making it difficult for Perl beginners to choose between them.</div><div style="background-color: white;">&nbsp;</div><div style="background-color: white;"><strong>1. IPC::Open2</strong></div><p>More at https://bioinformaticsonline.com/snippets/view/42919/perl-ipcopen2-module</p><p><strong>2. exec&rdquo;&rdquo;</strong></p><p><em>&nbsp;syntax:&nbsp;</em><code>exec "command";</code></p><div style="background-color: #edfbff;">It's a Perl function (perlfunc) that executes a command but never returns, similar to a function's return statement.</div><div style="background-color: white;">While running the command, it keeps processing the script and does not wait until it finishes first, returns false when the command is not found, but never returns true.</div><p><strong>3. Backticks &ldquo; or qx//</strong></p><p><em>syntax:&nbsp;</em><code>`command`;</code></p><p><em>syntax:&nbsp;</em><code>qx/command/;</code></p><div style="background-color: white;">It's a Perl operator (perlop) that executes a command and then resumes the Perl script once the command has ended, but the return value is the command's STDOUT.</div><p><strong>4. IPC::Open3</strong></p><p><em>syntax:&nbsp;</em><code>$output =&nbsp;open3(\*CHLD_IN, \*CHLD_OUT, \*CHLD_ERR,&nbsp;'command arg1 arg2', 'optarg',...);</code></p><p style="text-align: justify;"><code></code>It is very similar to <code>IPC::Open2</code> with the capability to capture all three file handles of the process, i.e., STDIN, STDOUT, and STDERR. It can also be used with or without the shell. You can read about it more in the documentation: <a href="https://perldoc.perl.org/IPC/Open3.html" target="_blank">IPC::Open3</a>.</p><p><code>$output = open3(my $o ut,&nbsp;my $in, 'command arg1 arg2');</code></p><p>OR without using the shell</p><p><code>$output = open3(my $out,&nbsp;my $in, 'command', 'arg1', 'arg2');</code></p><p><strong>5.a2p</strong></p><p><em>syntax:&nbsp;</em><code>a2p [options] [awkscript]</code></p><p>There is a Perl utility known as <code>a2p</code> which translates <code>awk</code> command to Perl. It takes awk script as input and generates a comparable Perl script as the output. Suppose, you want to execute the following <code>awk</code> statement</p><p><code>awk '{$1 = ""; $2 = ""; print}' f1.txt</code></p><p>This statement gives error sometimes even after escaping the variables (\$1, \$2) but by using <code>a2p</code> it can be easily converted to Perl script:</p><p>For further information, you can read it&rsquo;s documentation: <code><a href="https://perldoc.perl.org/a2p.html" target="_blank">a2p</a></code></p><p>More help at https://bioinformaticsonline.com/snippets/view/42920/perl-script-to-run-awk-inside-perl</p><p><strong>6. system()</strong></p><p><em>syntax:&nbsp;</em><code>system( "command" );</code></p><p>It is also a Perl function (<a href="https://perldoc.perl.org/functions/system.html" target="_blank">perlfunc</a>) that executes a command and waits for it to get finished first and then resume the Perl script. The return value is the exit status of the command. It can be called in two ways:</p><p><code>system( "command arg1 arg2" );</code></p><p>OR</p><p><code>system( "command", "arg1", "arg2" );</code></p><p>HELP</p><p>Here are some useful Perl cheat sheets that can be used as a quick reference guide.--&nbsp;<a href="https://www.pcwdld.com/perl-cheat-sheet" target="_blank">https://www.pcwdld.com/perl-cheat-sheet</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31137/finishersc-a-repeat-aware-and-scalable-tool-for-upgrading-de-novo-assembly-using-long-reads</guid>
	<pubDate>Mon, 27 Feb 2017 09:49:45 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31137/finishersc-a-repeat-aware-and-scalable-tool-for-upgrading-de-novo-assembly-using-long-reads</link>
	<title><![CDATA[FinisherSC: a repeat-aware and scalable tool for upgrading de novo assembly using long reads]]></title>
	<description><![CDATA[<p><span>FinisherSC, a repeat-aware and scalable tool for upgrading&nbsp;</span><em>de novo</em><span>&nbsp;assembly using long reads. Experiments with real data suggest that FinisherSC can provide longer and higher quality contigs than existing tools while maintaining high concordance.</span></p><p>Address of the bookmark: <a href="http://kakitone.github.io/finishingTool/" rel="nofollow">http://kakitone.github.io/finishingTool/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/14302/bioinformatician-at-work</guid>
	<pubDate>Sat, 23 Aug 2014 04:44:55 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/14302/bioinformatician-at-work</link>
	<title><![CDATA[Bioinformatician at work !!!]]></title>
	<description><![CDATA[<p>Yet another peep up view of a bioinformatician research laboratory ...</p>]]></description>
	<dc:creator>Neel</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/14302" length="232751" type="image/png" />
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/31258/bioinformatics-walk-in-interview-at-tezpur-university</guid>
  <pubDate>Thu, 02 Mar 2017 04:24:46 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics walk-in-interview at Tezpur University]]></title>
  <description><![CDATA[
<p>A walk-in-interview will be held on 09 March, 2017, 11.15 a.m. at the office of the Head, Department of Computer Science and Engineering, Tezpur University for one (01) temporary position of Junior Research Fellow (JRF) in the DBT, Govt. of India sponsored project entitled “Integrating genome scale metabolic analysis of model plant pathogen Ralstonia solanacearum with RNAseq and fluxomics” under Dr. Siddhartha Sankar Satapathy (ssankar@tezu.ernet.in), Associate Professor, Department of Computer Science and Engineering, Tezpur University.<br /> <br />Interested candidates may appear before the interview board with original documents from 10th standard onwards and photocopies of mark sheets, certificates, testimonials, caste certificate (if applicable), experience certificate certificates of NET/GATE/BET or similar examination qualifications, any other testimonials and a copy of recent curriculum vitae (CV) on the day of interview.<br /> <br />Essential qualification: M.Tech. in CSE/IT (With specialization in Computational Biology/Bioinformatics) or M.Sc. in Bioinformatics/Biosciences/Molecular Biology Biotechnology preferably with NET/GATE/BET.<br /> <br />Candidates should have minimum 55 % mark both in 10th and 10+2 Science examinations and mathematics at 10+2 Science.<br /> <br />Desirable: Preference will be given to the candidates having experience in computational analysis of genome sequences or similar projects.<br /> <br />Remuneration: Rs. 25,000/- (Rupees twenty five thousand) only + HRA as admissible per month for the 1st two years and Rs. 28,000/- (Rupees twenty eight thousand) only + HRA as admissible per month for the 3rd year for SRF and applicable to the candidate having post graduate degree in Basic Science with NET/GATE/BET qualification or post graduate degree in professional course. Rs. 12,000/- (Rupees twelve thousand) only + HRA as admissible per month for the 1st two years and Rs. 14,000/- (Rupees fourteen thousand) only + HRA as admissible per month for the 3 rd year for SRF, for the candidate without NET/GATE/BET qualification. HRA will not be provided if campus accommodation is availed.<br /> <br />Age: Candidate shall not be more than 28 years of age on the date of interview. Upper age limit may be relaxed up to 5 years in the case of candidate belonging to SC/ST/ OBC/Women/Differently abled.<br /> <br />Duration: Three (03) years or till completion of the project or until further order, whichever is earlier.<br /> <br />N.B. No TA/DA will be paid to the candidates for attending the interview. For further details please contact: Dr. S. S. Satapathy Associate Professor Department of Computer Science and Engineering Tezpur University, Napaam-784028 Email: ssankar@tezu.ernet.in Contact no.: +91-9435979648<br /> <br />More Info:  www.tezu.ernet.in/ProjectWalkin/Advt-DoRD-CSE-SSS-20-295-188-A.pdf</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/42803/bioinformatician-purdue-cancer-center</guid>
  <pubDate>Wed, 03 Feb 2021 22:54:14 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatician - Purdue Cancer Center]]></title>
  <description><![CDATA[
<p>The Center for Cancer Research is an NCI-designated cancer center. The center is a catalyst for collaborative cancer research around Purdue University. In this role, the selected individual will have the opportunity to cooperate with Purdue faculty and students in performing cutting-edge research and analyses, with opportunities for professional development, and the possibility of co-authorship in faculty research publications. <br />Projects will be challenging, including various model organisms, and we are looking for an individual who is excited about interacting with multi-disciplinary cancer research groups and the development of new tools, techniques, and workflows. Independently perform both routine and project-specific analyses, advise faculty on the design of experiments, writing manuscripts for publication, and writing grant proposals. Interact and collaborate with bioinformatics services (i.e. Statistical Consulting Center to provide relevant services to the campus research community), where applicable. Support all of the bioinformatics activities of the Center for Cancer Research at Purdue University<br />Required:</p>

<p>Master's degree in bioinformatics, computer science, molecular biology, or related field<br />One year of experience in analyzing RNA-Seq data <br />In lieu of a degree, consideration will be given to an equivalent combination of related education and required work experience.<br />Understanding of molecular biology, biochemistry, and genetics<br />Proficiency in writing scripts using Perl, Python, Java, or equivalent languages<br />Proficiency in R and UNIX/LINUX <br />Knowledge of genomics, alignment, annotation, bioinformatics, concepts of sequence assembly<br />Highly motivated and detail-oriented<br />Ability, interest, and curiosity to learn new skills<br />Must possess strong communication skills to work effectively with users across disciplines<br />Ability to work independently and as part of a multi-disciplinary team<br />Strong visual, verbal, and written communication skills<br />Excellent time organizational skills<br />Preferred:</p>

<p>Experience writing software or building software pipelines<br />Experience with oncology-specific public databases including TCGA<br />Experience with deploying and/or running software on high-performance computational systems<br />Statistical and experimental design knowledge<br />Additional Information: </p>

<p>This position is contingent on the availability of funding<br />Purdue will not sponsor employment authorization for this position  <br />A background check will be required for employment in this position<br />FLSA: Exempt (Not Eligible For Overtime)<br />Retirement Eligibility: Defined Contribution Waiting Period <br />Purdue University is an EOE/AA employer. All individuals, including minorities, women, individuals with disabilities, and veterans are encouraged to apply</p>

<p>More at https://careers.purdue.edu/job/West-Lafayette-Bioinformatician-Purdue-Cancer-Center-IN-47906/686617600/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31343/metabat-an-efficient-tool-for-accurately-reconstructing-single-genomes-from-complex-microbial-communities</guid>
	<pubDate>Mon, 06 Mar 2017 03:44:34 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31343/metabat-an-efficient-tool-for-accurately-reconstructing-single-genomes-from-complex-microbial-communities</link>
	<title><![CDATA[MetaBAT:  An Efficient Tool for Accurately Reconstructing Single Genomes from Complex Microbial Communities]]></title>
	<description><![CDATA[<p>MetaBAT, An Efficient Tool for Accurately Reconstructing Single Genomes from Complex Microbial Communities</p>
<p>Grouping large genomic fragments assembled from shotgun metagenomic sequences to deconvolute complex microbial communities, or metagenome binning, enables the study of individual organisms and their interactions. Here we developed an automated metagenome binning software, called MetaBAT, which integrates empirical probabilistic distances of genome abundance and tetranucleotide frequency. Tested on both synthetic and real metagenome datasets, MetaBAT outperforms alternative methods in both accuracy and computational efficiency. Applying MetaBAT to an assembly from 1,704 human gut samples formed 1,634 genome bins (&gt;200kb) in 3 hours, where 621 genome bins are &gt;50% complete with &lt;5% contamination from other species. Further analysis shows that the quality of these genome bins approaches manually curated genomes.</p><p>Address of the bookmark: <a href="https://bitbucket.org/berkeleylab/metabat" rel="nofollow">https://bitbucket.org/berkeleylab/metabat</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/23119/senior-statistician-manchester-or-belfast-uk</guid>
  <pubDate>Fri, 03 Jul 2015 08:06:04 -0500</pubDate>
  <link></link>
  <title><![CDATA[Senior Statistician - Manchester or Belfast UK]]></title>
  <description><![CDATA[
<p>The Role</p>

<p>My client provide innovative biomarker discovery and development services to the pharmaceutical industry.  They partner with the pharmaceutical industry to develop and implement biomarker strategies, providing a full range of biomarker services from pre-clinical biomarker discovery, assay development, right through to the delivery of clinical tests in their CLIA lab.</p>

<p>As a Senior Statistician you would support this effort and be responsible for the management of technical experimental study design and data handling processes required for the discovery, development and commercial delivery of multiplex clinical diagnostic assays; You will:</p>

<p>Develop analytical experimental designs for multiplex clinical diagnostic assays in accordance with regulatory requirements (e.g. CLIA, FDA)<br />Lead and coordinate the evaluation of analytical studies including characterization, verification, and validation studies<br />Lead specification setting and specification alterations<br />Ensure DOE methodology is routinely used in analytical studies.<br />Work with the Operations Department to ensure robust, reproducible and precise assay development<br />Provide expertise of general aspects for Statistical Process Control<br />Provide statistical expertise for R&amp;D, Quality, and Manufacturing<br />You will work in a fast-paced, project orientated environment and the ability to plan and execute objectives under tight timelines is a must. This is a unique opportunity suited for a qualified statistician with an interest in working to deliver first class data analysis support and solutions in a clinical setting.</p>

<p>Requirements</p>

<p>MSc or PhD in statistics or a related discipline<br />In depth knowledge of DOE methods to analytically validate, monitor and trouble shoot multiplex clinical diagnostic assays, ideally in a commercial/industrial setting<br />Experienced in the analysis of statistical technology evaluation, independent data and dependent data analysis, medical diagnostic accuracy, statistical graphics and reproducible reporting.<br />Excellent interpersonal, communication (including written and spoken English)<br />Ability to independently manage multiple projects and to deliver results on time per project deadlines<br />Proficient programming and analysis skills in one or more statistical package (e.g. R, Stata, SAS)<br />The following skills, while not mandatory, are highly desirable:</p>

<p>Development and validation of predictive models<br />Experience of clinical epidemiology, survival analysis, biomarker research, Bayesian methods, quantifying predictive accuracy.<br />Knowledge of regulatory standards for CLIA and/or FDA IVD tests<br />Reward</p>

<p>An attractive remuneration package will reflect the importance of this role and will include 6.8 weeks annual leave (pro rata, including fixed closure days), company pension scheme, enhanced sick pay and maternity entitlements, healthcare plan and opportunities for learning and development, as well as access to a company restaurant and parking facilities</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31371/phenogram</guid>
	<pubDate>Tue, 07 Mar 2017 08:35:12 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31371/phenogram</link>
	<title><![CDATA[PhenoGram]]></title>
	<description><![CDATA[<p><span>With PhenoGram researchers can create chomosomal ideograms annotated with lines in color at specific base-pair locations, or colored base-pair to base-pair regions, with or without other annotation. PhenoGram allows for annotation of chromosomal locations and/or regions with shapes in different colors, gene identifiers, or other text. PhenoGram also allows for creation of plots showing expanded chromosomal locations, providing a way to show results for specific chromosomal regions in greater detail.</span></p><p>Address of the bookmark: <a href="http://ritchielab.psu.edu/software/phenogram-downloads" rel="nofollow">http://ritchielab.psu.edu/software/phenogram-downloads</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/31520/research-associate-openings-at-iasri-india</guid>
  <pubDate>Fri, 10 Mar 2017 03:53:03 -0600</pubDate>
  <link></link>
  <title><![CDATA[Research Associate openings at IASRI, India]]></title>
  <description><![CDATA[
<p>Research Associate (RA) Two (2) </p>

<p>Ph.D. in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent or Master’s in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent with 4 years or 5 years of Bachelor’s degree having 1st Division or 60% marks or equivalent overall grade point average, with at least two years of research experience as evidenced from fellowship/ associateship/ training/ other engagements. </p>

<p>Knowledge in System Biology/ Statistical and computational Genomics/ Bioinformatics <br />Knowledge in computer programming, LINUX OS. <br />Expertise in use of R/other Bioinformatics software </p>

<p>More at http://iasri.res.in/employment/2017/cabin_advertisement_RA_SRF_YP_Mar2017.pdf</p>

<p>Phenomics of Moisture Deficit Stress Tolerance and Nitrogen Use December 31, 2019 </p>

<p>Research Associate (RA) Two (2) </p>

<p>Ph.D. in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent or System Administrator/ Computer expert for database development, development of phenome data bank and virtual phenomics facility, data archiving and Efficiency in Rice and Wheat-Phase II (Funded by National Agricultural Science Fund, ICAR) Master’s in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent with 4 years or 5 years of Bachelor’s degree having 1st Division or 60% marks or equivalent overall grade point average, with at least two years of research experience as evidenced from fellowship/ associateship/ training/ other engagements. maintenance; Development of image analysis algorithms, APIs and IAPs. </p>

<p>Knowledge in System Biology/ Statistical and computational Genomics/ Bioinformatics <br />Knowledge of programming in LINUX/R/Perl/JAVA/PHP/JSP and use of various software &amp; tools. <br />December 31, 2019 </p>

<p>Ph.D. in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science / Computer Application or equivalent or Master’s in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent with 4 years or 5 years of Bachelor’s degree having 1st Division or 60% marks or equivalent overall grade point average, with at least two years of research experience as evidenced from fellowship/ associateship/ training/ other engagements. </p>

<p>Knowledge of Statistical and Computational Genomics/ Bioinformatics. <br />Knowledge of programming in LINUX/R/Perl/JAVA/PHP/JSP and use of various software &amp; tools. <br />March 31, 2020</p>
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