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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/29912?offset=1070</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/24264/cancer-research-database</guid>
	<pubDate>Tue, 01 Sep 2015 17:36:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/24264/cancer-research-database</link>
	<title><![CDATA[Cancer research database]]></title>
	<description><![CDATA[<p>Researchers in Andhra Pradesh have developed a database to identify genes that are common in tumours to provide their colleagues with easy access to insights into the genetic alterations in cancer.<br /> &nbsp;<br /> The database, hosted at the Sri Venkateswara University (SVU) in Tirupati, will integrate information on cancer genes and markers with experimental data.<br /> &nbsp;<br /> The <a href="http://cgmd.in/" target="_blank">Cancer Gene Markers Database</a> (CGMD) is meant to help scientists better understand tumour genes and markers at a molecular level by combining data with literature on treatment regimen and recent advances in cancer therapy.<br /> <br /> The database is free to access, and already includes 309 genes and 206 markers that correspond to 40 different human cancers. Accompanying literature comes from databases such as the United States&rsquo; <a href="http://www.ncbi.nlm.nih.gov/" target="_blank">National Center for Biotechnology Information</a> and the <a href="http://www.genome.jp/kegg/" target="_blank">Kyoto Encyclopedia of Genes and Genomes</a>. It also includes experimental data from <a href="http://www.ncbi.nlm.nih.gov/pubmed" target="_blank">PubMed</a>.<br /> <br /> In a paper <a href="http://dx.doi.org/10.1038/srep12035" target="_blank">published</a> last month in <em>Nature Scientific Reports</em>, the researchers from SVU&rsquo;s department of animal biotechnology, describes the need for a database for different genes and markers along with their molecular characteristics and pathway associations.</p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41046/iseqqc-a-tool-for-expression-based-quality-control-in-rna-sequencing</guid>
	<pubDate>Sun, 16 Feb 2020 08:47:17 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41046/iseqqc-a-tool-for-expression-based-quality-control-in-rna-sequencing</link>
	<title><![CDATA[iSeqQC: a tool for expression-based quality control in RNA sequencing]]></title>
	<description><![CDATA[<p><span>iSeqQC, an expression-based QC tool that detects outliers either produced due to variable laboratory conditions or due to dissimilarity within a phenotypic group. iSeqQC implements various statistical approaches including unsupervised clustering, agglomerative hierarchical clustering and correlation coefficients to provide insight into outliers.</span></p>
<p><a href="http://cancerwebpa.jefferson.edu/iSeqQC/">http://cancerwebpa.jefferson.edu/iSeqQC/</a></p>
<p><a href="https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-020-3399-8">https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-020-3399-8</a></p><p>Address of the bookmark: <a href="https://github.com/gkumar09/iSeqQC" rel="nofollow">https://github.com/gkumar09/iSeqQC</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/24363/walk-in-interview-for-srf-jrf-posts-at-national-research-centre-on-plant-biotechnology-new-delhi-110012</guid>
  <pubDate>Thu, 10 Sep 2015 15:58:55 -0500</pubDate>
  <link></link>
  <title><![CDATA[Walk-in-interview for SRF, JRF posts at NATIONAL RESEARCH CENTRE ON PLANT BIOTECHNOLOGY New Delhi-110012]]></title>
  <description><![CDATA[
<p>NATIONAL RESEARCH CENTRE ON PLANT BIOTECHNOLOGY New Delhi-110012</p>

<p>Eligible candidates may appear in Walk-in-interview for the positions of Senior Research Fellow in ICAR funded projects as follows</p>

<p>ICAR Network Project on Transgenics in Crops- Amelioration of cold induced sweetening in potato.</p>

<p>PI: Dr Debasis Pattanayak </p>

<p>SRF</p>

<p>Rs.25000/‐+ 30% HRA</p>

<p>September 29, 2015</p>

<p>Essential: Master’s Degree in Bioinformatics /Biotechnology/ Biochemistry/ life sciences with four years Bachelor’s Degree (or) Master’s Degree in Bioinformatics /Biotechnology/Biochemistry/ life sciences with NET qualification. .</p>

<p>Desirable: Experience in Bioinformatics and programming.</p>

<p>Age Limit: 35 years max. (5 years relaxation for SC/ST/OBC and woman candidates as per ICAR rules).</p>

<p>The post is purely temporary in nature and is co-terminus with the project. The interview will be held on September 29, 2015 at 10 AM at NRCPB, LBS Building, Pusa Campus, and New Delhi-110012. The candidates must bring four copies of biodata, original certificates, attested photocopies of each of the certificates and an attested copy of recent passport size photograph.</p>

<p>No TA/DA would be given for the appearance in interview. Only the candidates having essential qualifications would be entertained for the interviews </p>

<p>http://www.nrcpb.org/sites/default/files/NPTC%20walk%20in%20interview%20September%202015%20for%20NRCPB%20webpage%20D%20%20%20Pattanayak.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42530/shovill-assemble-bacterial-isolate-genomes-from-illumina-paired-end-reads</guid>
	<pubDate>Sat, 02 Jan 2021 07:05:36 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42530/shovill-assemble-bacterial-isolate-genomes-from-illumina-paired-end-reads</link>
	<title><![CDATA[shovill: Assemble bacterial isolate genomes from Illumina paired-end reads]]></title>
	<description><![CDATA[<p><span>Shovill is a pipeline which uses SPAdes at its core, but alters the steps before and after the primary assembly step to get similar results in less time. Shovill also supports other assemblers like SKESA, Velvet and Megahit, so you can take advantage of the pre- and post-processing the Shovill provides with those too.</span></p><p>Address of the bookmark: <a href="https://github.com/tseemann/shovill" rel="nofollow">https://github.com/tseemann/shovill</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/24464/guest-faculty-job-vacancies-in-pondicherry-university</guid>
  <pubDate>Tue, 22 Sep 2015 23:50:16 -0500</pubDate>
  <link></link>
  <title><![CDATA[Guest Faculty Job vacancies in Pondicherry University]]></title>
  <description><![CDATA[
<p>Guest Faculty Job vacancies in Pondicherry University<br />Qualification : M.Phil. / M.Tech. / M.Sc. in Computer Science / Master of Computer Applications with a minimum of 55% of marks. Candidates with Ph.D. degree and NET/SLET qualification will be given preference as per UGC norms.</p>

<p>Desirable : Research or teaching experience in Bioinformatics and Computational Biology.<br />Honorarium : Rs. 1,000/- per lecture (subject to a maximum of 25,000/- per month)<br />How to apply</p>

<p>Interested eligible candidates may attend the 'walk-in' interview along with all original certificates and testimonials with a copy of their bio-data. Walk-in-interview will be held on 28.09.2015 (Monday), 03:00 P.M. at the office of the Dean, School of Life Sciences, Science Block — I, Pondicherry University, Puducherry — 605 014. Candidates reporting after 03:00 P.M. will not be entertained.</p>

<p>More at http://www.pondiuni.edu.in/news/walk-interview-guest-faculty-centre-bioinformatics</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/34702/run-miniasm-assembler-on-nanopore-reads</guid>
	<pubDate>Mon, 18 Dec 2017 04:07:50 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/34702/run-miniasm-assembler-on-nanopore-reads</link>
	<title><![CDATA[Run miniasm assembler on nanopore reads !]]></title>
	<description><![CDATA[<p>Miniasm is a very fast OLC-based&nbsp;<em>de novo</em>&nbsp;assembler for noisy long reads. It takes all-vs-all read self-mappings (typically by&nbsp;<a href="https://github.com/lh3/minimap">minimap</a>) as input and outputs an assembly graph in the&nbsp;<a href="https://github.com/pmelsted/GFA-spec/blob/master/GFA-spec.md">GFA</a>&nbsp;format. Different from mainstream assemblers, miniasm does not have a consensus step. It simply concatenates pieces of read sequences to generate the final&nbsp;<a href="http://wgs-assembler.sourceforge.net/wiki/index.php/Celera_Assembler_Terminology">unitig</a>&nbsp;sequences. Thus the per-base error rate is similar to the raw input reads.</p><p>Find the detail of the reads repeats:</p><blockquote><p>fq2fa ONT_A.fastq ONT_A.fasta&nbsp;<br /><br />minimap2 -xava-ont ONT_A.fasta ONT_A.fasta -t10 -X &gt; AONT.paf&nbsp;<br /><br />awk '{if($1==$6){print}}' AONT.paf &gt; AONTself.paf&nbsp;<br /><br />awk '$5=="-"' AONTself.paf | awk '{print $1}'| sort|uniq &gt; invertedrepeat.list</p></blockquote><p>Generated a few palindrome and repeats plots (highlighting only repeats largest than 10, 20 and 30 kb)</p><blockquote><p>minidot -f 5 -m 30000 AONTself.paf &gt; AONTself30000.eps&nbsp;<br />sed 's/_template_pass_FAH31515//' AONTself30000.eps &gt; AONTself30000final.eps&nbsp;<br /><br />minidot -f 5 -m 20000 AONTself.paf &gt; AONTself20000.eps&nbsp;<br />sed 's/_template_pass_FAH31515//' AONTself20000.eps &gt; AONTself20000final.eps&nbsp;<br /><br />minidot -f 5 -m 10000 AONTself.paf &gt; AONTself10000.eps&nbsp;<br />sed 's/_template_pass_FAH31515//' AONTself10000.eps &gt; AONTself10000final.eps&nbsp;</p></blockquote><p>Assemble with miniasm:</p><blockquote><p>miniasm -f ONT_A.fasta AONT.paf &gt; AONT.gfa&nbsp;</p><p>grep '^S' AONT.gfa |awk '{print "&gt;"$2"\n"$3}' &gt; AONT_miniasm.fasta&nbsp;<br /><br />minimap2 -xasm10 AONT_miniasm.fasta AONT_miniasm.fasta -t1 -X &gt; AONT_miniasm.paf&nbsp;<br /><br />awk '{if($1==$6){print}}' AONT_miniasm.paf &gt; AONT_miniasm_self.paf&nbsp;<br /><br />minidot -f 5 -m 10000 AONT_miniasm_self.paf &gt; AONT_miniasm_self10000.eps&nbsp;</p></blockquote><p>Njoy the assembly !</p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25252/bioinformatics-faculty-at-university-of-pune</guid>
  <pubDate>Fri, 13 Nov 2015 03:06:00 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics Faculty at University of Pune]]></title>
  <description><![CDATA[
<p>SAVITRIBAI PHULE PUNE UNIVERSITY<br />(Formerly University of Pune)<br />(APPOINTMENT OF TEACHING POSTS)</p>

<p>Accompaniment to the Advertisement No. 52 dated 10.11.2015 for various Teaching Positions purely on contract basis for a maximum period of five years in the various Departments/Centre of the University.</p>

<p>Last date for receipt of application in the University Office is 04.12.2015.</p>

<p>Associate Professor</p>

<p>    Environmental Science</p>

<p>    Institute of Bioinformatics &amp; Biotechnology (IBB)</p>

<p>    Microbiology</p>

<p>Assistant Professor</p>

<p>    Biotechnology</p>

<p>    Institute of Bioinformatics &amp; Biotechnology (IBB)</p>

<p>    Microbiology</p>

<p>More Info : http://collegecirculars.unipune.ac.in/sites/documents/Job%20Openings/advt-no-52-dt-10-11-2015-contract-positions.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36607/tarean-a-computational-tool-for-identification-and-characterization-of-satellite-dna-from-unassembled-short-reads</guid>
	<pubDate>Tue, 15 May 2018 02:53:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36607/tarean-a-computational-tool-for-identification-and-characterization-of-satellite-dna-from-unassembled-short-reads</link>
	<title><![CDATA[TAREAN: A computational tool for identification and characterization of satellite DNA from unassembled short reads]]></title>
	<description><![CDATA[<p><strong>TA</strong>ndem&nbsp;<strong>RE</strong>peat&nbsp;<strong>AN</strong>alyzer -TAREAN &ndash; is a computational pipeline for&nbsp;<strong>unsupervised identification of satellite repeats</strong>&nbsp;from unassembled sequence reads. The pipeline uses low-pass whole genome sequence reads and performs their graph-based clustering. Resulting clusters, representing all types of repeats, are then examined for the presence of circular structures and putative satellite repeats are reported.</p>
<p><em><strong>How to use TAREAN</strong></em>:</p>
<ul>
<li>Install a local instance of the pipeline using its source code available from&nbsp;<a href="https://bitbucket.org/petrnovak/repex_tarean" target="_blank" title="TAREAN source code">bitbucket repository</a>.</li>
<li>Use&nbsp; public Galaxy-based server at&nbsp;<a href="https://repeatexplorer-elixir.cerit-sc.cz/" target="_blank">https://repeatexplorer-elixir.cerit-sc.cz/</a>. The server is provided in frame of the&nbsp;<a href="https://www.elixir-czech.cz/" target="_blank">Elixir CZ project</a>&nbsp;and is maintained by&nbsp;<a href="https://www.cesnet.cz/" target="_blank">CESNET</a>&nbsp;and&nbsp;<a href="https://www.cerit-sc.cz/en/index.html" target="_blank">CERIT-SC</a>. Simple registration is required to use this service.</li>
</ul>
<p>Development of TAREAN was supported by&nbsp;<a href="https://www.elixir-czech.cz/" target="_blank" title="ELIXIR-CZ">ELIXIR CZ</a>&nbsp;research infrastructure project (MEYS Grant No: LM2015047).</p>
<p><strong><em>References</em></strong></p>
<p>Novak, P., Avila Robledillo, L., Koblizkova, A., Vrbova, I., Neumann, P., Macas, J. (2017) &ndash;&nbsp;<a href="https://academic.oup.com/nar/article/3574061/" target="_blank">TAREAN: a computational tool for identification and characterization of satellite DNA from unassembled short reads</a>.&nbsp;<em>Nucleic Acids Res.</em>, doi:10.1093/nar/gkx257</p><p>Address of the bookmark: <a href="https://bitbucket.org/petrnovak/repex_tarean" rel="nofollow">https://bitbucket.org/petrnovak/repex_tarean</a></p>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/24923/postdoctoral-positions-are-available-at-the-faryabi-lab</guid>
  <pubDate>Sun, 11 Oct 2015 03:36:18 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral positions are available at the Faryabi Lab]]></title>
  <description><![CDATA[
<p>Postdoctoral positions are available at the Faryabi Lab located in the Department of Pathology and the Center for Personalized Diagnostics at the University of Pennsylvania.</p>

<p>A qualified candidate will be strongly motivated individual with following qualifications: a Ph.D. in computational sciences, engineering, physics, bioinformatics, or related field. Ability to program in Python/Perl and R in Unix environment, knowledge of C++, Java, and SQL is a plus. Demonstrated applied bioinformatics/computational proficiency as evidenced by relevant publications in peer-reviewed journals. Experience with cancer genomics is a plus.</p>

<p>The primary research focus of the Faryabi Lab is on developing novel computational methods to study mechanisms involved in genome instability and elucidate their roles in tumorigenesis. In addition the position provides collaborative opportunities with both basic and translational scientists across the Perelman School of Medicine, one of the top 5 medical research universities in the nation.<br />. a Ph.D. degree in either physical or computational sciences<br />. solid programming skills ( Python/Perl, Java, C/C++, R, SQL)<br />. computational genomics experience ( high throughput sequence analysis)<br />. excellent spoken and written communication and interaction skills<br />. publications in English in relevant areas of research in peer-reviewed journals.<br />. Previous experience or interest in data visualization design is a plus.</p>

<p>More at <br />University of Pennsylvania<br />Pathology and Laboratory Medicine<br />Robert B. Faryabi<br />faryabiPenn@gmail.com<br />http://faryabib.github.io/<br />How To Apply:	email CV and contacts of 3 references to faryabiPenn@gmail.com</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36895/npscarf-real-time-scaffolder-using-spades-contigs-and-nanopore-sequencing-reads</guid>
	<pubDate>Mon, 11 Jun 2018 05:14:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36895/npscarf-real-time-scaffolder-using-spades-contigs-and-nanopore-sequencing-reads</link>
	<title><![CDATA[npScarf: real-time scaffolder using SPAdes contigs and Nanopore sequencing reads]]></title>
	<description><![CDATA[npScarf (jsa.np.npscarf) is a program that connect contigs from a draft genomes to generate sequences that are closer to finish. These pipelines can run on a single laptop for microbial datasets. In real-time mode, it can be integrated with simple structural analyses such as gene ordering, plasmid forming.<p>Address of the bookmark: <a href="http://japsa.readthedocs.io/en/latest/tools/jsa.np.npscarf.html" rel="nofollow">http://japsa.readthedocs.io/en/latest/tools/jsa.np.npscarf.html</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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