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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/31568?offset=1520</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41148/pbmm2a-minimap2-frontend-for-pacbio-native-data-formats</guid>
	<pubDate>Tue, 18 Feb 2020 03:36:22 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41148/pbmm2a-minimap2-frontend-for-pacbio-native-data-formats</link>
	<title><![CDATA[pbmm2:A minimap2 frontend for PacBio native data formats]]></title>
	<description><![CDATA[<p><em>pbmm2</em> is a SMRT C++ wrapper for <a href="https://github.com/lh3/minimap2">minimap2</a>'s C API. Its purpose is to support native PacBio in- and output, provide sets of recommended parameters, generate sorted output on-the-fly, and postprocess alignments. Sorted output can be used directly for polishing using GenomicConsensus, if BAM has been used as input to <em>pbmm2</em>. Benchmarks show that <em>pbmm2</em> outperforms BLASR in sequence identity, number of mapped bases, and especially runtime. <em>pbmm2</em> is the official replacement for BLASR.</p><p>Address of the bookmark: <a href="https://github.com/PacificBiosciences/pbmm2" rel="nofollow">https://github.com/PacificBiosciences/pbmm2</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25251/m-d-university-rohtak-is-looking-for-the-post-of-research-associate</guid>
  <pubDate>Fri, 13 Nov 2015 02:56:48 -0600</pubDate>
  <link></link>
  <title><![CDATA[M. D. University, Rohtak is looking for the post of Research Associate]]></title>
  <description><![CDATA[
<p>M. D. University, Rohtak - Rohtak, Haryana<br />M. D. University, Rohtak is looking vacancies for the post of Research Associate</p>

<p>Project entitled: "Establish of Bioinformatics Facility for biology teaching through bioinformatics"</p>

<p>Name of post: Research Associate /Trainees</p>

<p>Number of post: 03</p>

<p>Educational Qualification and Experience: Candidates should have Ph D in relevant subjects with experience in handling computational biology resources and software</p>

<p>Selection mode: Walk in interview</p>

<p>How to apply?<br />Interested and eligible candidates may appear for a walk-in interview on 14th November 2015 at 11.00 am, in the office of Director, Centre for Bioinformatics along with CV and attested copies of all testimonials and additional qualifications.</p>

<p>Recruitment reference: http://www.mdurohtak.ac.in/pdf/career/adv_research_asso_dbt_bioinfo.pdf</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25253/scientist-e-ii-or-f-in-bioinformatics-computational-biology-at-rajiv-gandhi-centre-for-biotechnology</guid>
  <pubDate>Fri, 13 Nov 2015 03:10:32 -0600</pubDate>
  <link></link>
  <title><![CDATA[Scientist E-II or F in Bioinformatics &amp; Computational Biology at Rajiv Gandhi Centre for Biotechnology]]></title>
  <description><![CDATA[
<p>Advt. No.RGCB Advt./SCI 2015/1</p>

<p>Rajiv Gandhi Centre for Biotechnology (RGCB) invites applications for the following three faculty scientist positions:</p>

<p>    Scientist G in any of the following disciplines of disease biology: Cancer Research/Cardiovascular Biology/Diabetes Biology/Pathogen Biology<br />    Scientist E-II or F in Bioinformatics &amp; Computational Biology<br />    Scientist E-I or E-II in Cancer Research with special emphasis on Human Papillomavirus Research</p>

<p>More at http://rgcb.res.in/wp-content/uploads/2015/11/APPLICATION-FORMAT-FOR-SCIENTISTS.docx</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/38277/understating-pacbio-reads-name</guid>
	<pubDate>Fri, 23 Nov 2018 07:36:46 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/38277/understating-pacbio-reads-name</link>
	<title><![CDATA[Understating pacbio reads name !]]></title>
	<description><![CDATA[<pre>m140415_143853_42175_c100635972550000001823121909121417_s1_p0/553/3100_11230 0.99 24
└1┘└─────2─────┘└──3─┘└────────────────4────────────────┘└5┘└6┘└7┘└────8────┘└─9─┘└10┘
</pre><ol>
<li>"<code>m</code>" =&nbsp;<em>movie</em></li>
<li>Time of Run Start (<code>yymmdd_hhmmss</code>)</li>
<li>Instrument Serial Number</li>
<li>SMRT Cell Barcode</li>
<li>Set Number (a.k.a. "Look Number". Deprecated field, used in earlier version of RS)</li>
<li>Part Number (usually "<code>p0</code>", "<code>X0</code>" when using expired reagents)</li>
<li>ZMW hole number</li>
<li>Subread Region (<code>start_stop</code>&nbsp;using polymerase read coordinates)</li>
<li>readScore</li>
<li>barcodeScore</li>
</ol>]]></description>
	<dc:creator>BioJoker</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/42955/post-doctoral-position-scientist-mfd-in-bioinformatics</guid>
  <pubDate>Mon, 15 Mar 2021 11:34:23 -0500</pubDate>
  <link></link>
  <title><![CDATA[Post-doctoral position / Scientist (m/f/d) in Bioinformatics]]></title>
  <description><![CDATA[
<p>The Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V. in Dortmund is looking for a Post-doctoral position / Scientist (m/f/d) in Bioinformatics</p>

<p>More at</p>

<p>https://www.isas.de/files/redaktion/jobs/2021/18.60.1_Postdoc_deNBI_06_21_AS.pdf</p>

<p>https://www.isas.de/en/news/062021-post-doctoral-position-scientist-mfd-in-bioinformatics</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34445/inc-seq-accurate-single-molecule-reads-using-nanopore-sequencing</guid>
	<pubDate>Mon, 27 Nov 2017 10:38:56 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34445/inc-seq-accurate-single-molecule-reads-using-nanopore-sequencing</link>
	<title><![CDATA[INC-Seq: accurate single molecule reads using nanopore sequencing]]></title>
	<description><![CDATA[<p><span>INC-Seq reads enabled accurate species-level classification, identification of species at 0.1&nbsp;% abundance and robust quantification of relative abundances, providing a cheap and effective approach for pathogen detection and microbiome profiling on the MinION system.</span></p><p>Address of the bookmark: <a href="https://github.com/CSB5/INC-Seq" rel="nofollow">https://github.com/CSB5/INC-Seq</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25308/traineeship-at-biomedical-informatics-centre-pgimer-chandigarh</guid>
  <pubDate>Sun, 29 Nov 2015 03:04:27 -0600</pubDate>
  <link></link>
  <title><![CDATA[Traineeship at Biomedical Informatics Centre  PGIMER  Chandigarh]]></title>
  <description><![CDATA[
<p>Biomedical Informatics Centre</p>

<p>PGIMER</p>

<p>Chandigarh</p>

<p>invites application for a project dissertation program for students who have completed their first year of M.Sc. in Bioinformatics.</p>

<p>This is an exciting opportunity for Master's students to train in modern methods in Bioinformatics. The duration of the training will be four to six months, starting from January 2016.</p>

<p>Education: Pursuing M.Sc. Bioinformatics</p>

<p>Essential: Post graduate applicants should have completed their first year and should be in the third semester or first half of the second year.</p>

<p>Only students who are willing to spend a minimum period of 4 months to a maximum of six months, without any break, would be eligible for the program.</p>

<p>How to Apply: Candidates interested in the above project dissertation program should apply online. Send your CV, Scanned copy of letter of recommendation from Head of Institution along with Registration form in the given format should be sent to: info@bicpgi.org</p>

<p>Please mention clearly “Project dissertation &amp; your Name” in the Subject.</p>

<p>The last date for application is December 23, 2015</p>

<p>Note: Selected candidates may please note that the program is free of cost and would not provide any financial aid for transport and stay. Name of the selected candidates would be posted on the centre website by December 31, 2015.</p>

<p>Incomplete applications will be rejected.</p>

<p>For more information visit our website: http://bic-pgi.org/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36512/hisat2-a-fast-and-sensitive-alignment-program-for-mapping-next-generation-sequencing-reads</guid>
	<pubDate>Tue, 08 May 2018 04:27:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36512/hisat2-a-fast-and-sensitive-alignment-program-for-mapping-next-generation-sequencing-reads</link>
	<title><![CDATA[HISAT2: a fast and sensitive alignment program for mapping next-generation sequencing reads]]></title>
	<description><![CDATA[<p><strong>HISAT2</strong><span>&nbsp;is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) to a population of human genomes (as well as to a single reference genome). Based on an extension of BWT for graphs&nbsp;</span><a href="http://dl.acm.org/citation.cfm?id=2674828">[Sir&eacute;n et al. 2014]</a><span>, we designed and implemented a graph FM index (GFM), an original approach and its first implementation to the best of our knowledge. In addition to using one global GFM index that represents a population of human genomes, HISAT2 uses a large set of small GFM indexes that collectively cover the whole genome (each index representing a genomic region of 56 Kbp, with 55,000 indexes needed to cover the human population). These small indexes (called local indexes), combined with several alignment strategies, enable rapid and accurate alignment of sequencing reads. This new indexing scheme is called a Hierarchical Graph FM index (HGFM).&nbsp;</span></p>
<p><span>more at&nbsp;https://ccb.jhu.edu/software/hisat2/index.shtml</span></p><p>Address of the bookmark: <a href="https://github.com/infphilo/hisat2" rel="nofollow">https://github.com/infphilo/hisat2</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25302/ra-bioinformatics-at-jamia-hamdard</guid>
  <pubDate>Sat, 28 Nov 2015 03:37:36 -0600</pubDate>
  <link></link>
  <title><![CDATA[RA Bioinformatics at Jamia Hamdard]]></title>
  <description><![CDATA[
<p>Research Associate, Bioinformatics Facility<br />Jamia Hamdard - New Delhi, Delhi<br />Research Associate, Bioinformatics Facility, Jamia Hamdard.<br />Emoluments: Rs. 22,000 + HRA 30%<br />Qualification: PhD or equivalent or having 3 years of research, teaching and design and development experience after M. Pharm./M.VSc./M.E./M.Tech. PhD in life sciences and related areas with experience in Bioinformatics may apply. Company Info.<br />Jamia Hamdard</p>

<p>Jamia Hamdard New Delhi - 110062 Additional Information States &amp; U.T State &amp; Union Territories Delhi How To Apply Apply Details<br />Last date of application: December 5, 2015 Web/Notification URL http://www.jamiahamdard.ac.in/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36800/genomemapper-simultaneous-alignment-of-short-reads-against-multiple-genomes</guid>
	<pubDate>Fri, 25 May 2018 09:29:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36800/genomemapper-simultaneous-alignment-of-short-reads-against-multiple-genomes</link>
	<title><![CDATA[GenomeMapper: Simultaneous alignment of short reads against multiple genomes]]></title>
	<description><![CDATA[GenomeMapper is a short read mapping tool designed for accurate read alignments. It quickly aligns millions of reads either with ungapped or gapped alignments. It can be used to align against multiple genomes simulanteously or against a single reference. If you are unsure which one is the appropriate GenomeMapper, you might want to use the latter

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768987/<p>Address of the bookmark: <a href="http://1001genomes.org/software/genomemapper.html" rel="nofollow">http://1001genomes.org/software/genomemapper.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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