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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/31568?offset=980</link>
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<item>
  <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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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35899/reference-free-prediction-of-rearrangement-breakpoint-reads</guid>
	<pubDate>Thu, 08 Mar 2018 05:05:25 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35899/reference-free-prediction-of-rearrangement-breakpoint-reads</link>
	<title><![CDATA[Reference-free prediction of rearrangement breakpoint reads]]></title>
	<description><![CDATA[<p><span>lideSort-BPR (&nbsp;</span><span>b</span><span>&nbsp;reak&nbsp;</span><span>p</span><span>&nbsp;oint&nbsp;</span><span>r</span><span>&nbsp;eads) is based on a fast algorithm for all-against-all comparisons of short reads and theoretical analyses of the number of neighboring reads. When applied to a dataset with a sequencing depth of 100&times;, it finds &sim;88% of the breakpoints correctly with no false-positive reads. Moreover, evaluation on a real prostate cancer dataset shows that the proposed method predicts more fusion transcripts correctly than previous approaches, and yet produces fewer false-positive reads. To our knowledge, this is the first method to detect breakpoint reads without using a reference genome.</span></p>
<p><span>https://github.com/ewijaya/slidesort-bpr</span></p><p>Address of the bookmark: <a href="https://code.google.com/archive/p/slidesort-bpr/" rel="nofollow">https://code.google.com/archive/p/slidesort-bpr/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

<item>
  <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>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/36630/frequent-paired-end-reads-pe-2x100-mapping-command-lines</guid>
	<pubDate>Tue, 15 May 2018 08:59:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/36630/frequent-paired-end-reads-pe-2x100-mapping-command-lines</link>
	<title><![CDATA[Frequent Paired-end reads (PE 2x100) mapping command lines]]></title>
	<description><![CDATA[
<p>bowtie2 -x hs37m -X 650 -q -1 r1.fq -2 r2.fq -S r12.bowtie2.sam  </p>

<p>bwa aln hs37m.fa r1.fq &gt; r1.sai &amp;&amp; bwa aln hs37m.fa r2.fq &gt; r2.sai \  <br />    &amp;&amp; bwa sampe hs37m r1.sai r2.sai r1.fq r2.fq &gt; r12.bwa.sam  </p>

<p>bwa bwasw ../index/bwa/hs37m.fa r12.fq &gt; r12.bwasw.sam  </p>

<p>gsnap -A sam -d hs37m r1.fq r2.fq &gt; r12.gsnap.sam  </p>

<p>novoalign -r Random -o SAM -f r1.fq r2.fq -i 500 50 -d hs37m-k14s3.novo &gt; r12.novo.sam  </p>

<p>smalt map -f samsoft -i 650 -o r12.smalt-k20s13.sam hs37m-k20s13 r1.fq r2.fq  </p>

<p>stampy.py -g hs37m -h hs37m -o r12.stampy.sam -M r1.fq,r2.fq  </p>

<p>soap -D hs37m.fa.index -a r1.fq -b r2.fq -l 32 -g 3 -u dummy -2 dummy -o r12.soap</p>
]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25249/research-associatesresearch-fellow-school-of-agricultural-biotechnology-last-date-17-11-2015-and-interview-on-26-11-2015-at-1100-am</guid>
  <pubDate>Fri, 13 Nov 2015 02:46:59 -0600</pubDate>
  <link></link>
  <title><![CDATA[Research Associates/Research Fellow - School of Agricultural Biotechnology (Last Date 17-11-2015 and Interview on 26-11-2015 at 11.00 AM)]]></title>
  <description><![CDATA[
<p>PAU Recruitment November 2015, Punjab</p>

<p>Job notification in Punjab Agricultural University (PAU) for research Associate/ Research Fellow posts for different projects. Eligible candidates may apply in prescribed application format on or before 17-11-2015 from 09:00 am to 05:00 pm.</p>

<p>Vacancies:<br />Research Associate/ Research Fellow-03<br />Qualification:<br />Candidates should possess B.Sc. with minimum 50% marks, M.Sc. in Bioinformatics/ Biotechnology/ Genetics/ Plant Breeding/ Plant Breeding &amp; Genetics/ Plant Breeding, Genetics &amp; Biotechnology/ Microbiology/ Biochemistry/ Botany with 65% marks.<br />Selection Process:<br />Selection will be based on interview.<br />How to Apply:<br />Eligible candidates may send their applications along with attested copies of certificates, fee to the Director, School of Agricultural Biotechnology, PAU, Ludhiana on or before 17-11-2015 from 09:00 am to 05:00 pm<br />Last Date:<br />17-11-2015 </p>

<p>More at http://web.pau.edu/content/banner/1349.pdf</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36921/breakpointer-using-local-mapping-artifacts-to-support-sequence-breakpoint-discovery-from-single-end-reads</guid>
	<pubDate>Tue, 12 Jun 2018 12:41:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36921/breakpointer-using-local-mapping-artifacts-to-support-sequence-breakpoint-discovery-from-single-end-reads</link>
	<title><![CDATA[Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads]]></title>
	<description><![CDATA[Breakpointer is a fast tool for locating sequence breakpoints from the alignment of single end reads (SE) produced by next generation sequencing (NGS). It adopts a heuristic method in searching for local mapping signatures created by insertion/deletions (indels) or more complex structural variants(SVs).<p>Address of the bookmark: <a href="https://github.com/ruping/Breakpointer" rel="nofollow">https://github.com/ruping/Breakpointer</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25095/jrf-bioinformatics</guid>
  <pubDate>Mon, 02 Nov 2015 03:24:50 -0600</pubDate>
  <link></link>
  <title><![CDATA[JRF Bioinformatics]]></title>
  <description><![CDATA[
<p>JRF Bioinformatics</p>

<p>Eligibility : ME/M.Tech, MSc(Bio-Chemistry, Bio-Informatics, Bio-Tech, Microbiology), BE/B.Tech</p>

<p>Location : Gandhinagar</p>

<p>Last Date : 05 Nov 2015</p>

<p>Hiring Process : Face to Face Interview</p>

<p>Junior Research Fellow (JRF) Job vacancies in Gujarat State Biotechnology Mission (GSBTM)</p>

<p>Project : “Establishing a network in computational and system biology”</p>

<p>No. of Post : 01</p>

<p>Qualification : MSc. /M.Tech. /B.E. /B.Tech. in Biotechnology/Bioinformatics /Life Sciences /Microbiology /Biochemistry /Genetics from recognized University. Preference would be given to the candidates having NET/GATE.</p>

<p>Fellowship : Rs. 12,000 + 20% HRA<br />How to apply</p>

<p>Applications should be filled Online. The last date for submission of application is 5th November, 2015.</p>

<p>More at http://btm.gujarat.gov.in/btm/recruitment2.htm</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37576/lrcstats-a-tool-for-evaluating-long-reads-correction-methods</guid>
	<pubDate>Wed, 22 Aug 2018 11:05:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37576/lrcstats-a-tool-for-evaluating-long-reads-correction-methods</link>
	<title><![CDATA[LRCstats: a tool for evaluating long reads correction methods]]></title>
	<description><![CDATA[<p><span>LRCstats is an open-source pipeline for benchmarking DNA long read correction algorithms for long reads outputted by third generation sequencing technology such as machines produced by Pacific Biosciences. The reads produced by third generation sequencing technology, as the name suggests, are longer in length than reads produced by next generation sequencing technologies, such as those produced by Illumina. However, long reads are plagued by high error rates, which can cause issues in downstream analysis. Long read correction algorithms reduce the error rate of long reads either through self-correcting methods or using accurate, short reads outputted by next generation sequencing technologies to correct long reads.</span></p><p>Address of the bookmark: <a href="https://github.com/cchauve/lrcstats" rel="nofollow">https://github.com/cchauve/lrcstats</a></p>]]></description>
	<dc:creator>Aaryan Lokwani</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25149/project-assistant-ii-job-vacancies-in-national-institute-of-oceanography-nio-goa</guid>
  <pubDate>Fri, 06 Nov 2015 01:33:22 -0600</pubDate>
  <link></link>
  <title><![CDATA[Project Assistant-II job vacancies in National Institute of Oceanography (NIO Goa)]]></title>
  <description><![CDATA[
<p>Vacancy no : GAP0423/1509-15</p>

<p>Project Assistant-II job vacancies in National Institute of Oceanography (NIO Goa)</p>

<p>Project Title and Code : Biotechnology Information System. -- GAP0423</p>

<p>Qualification : M.Sc Bioinformatics / Zoology / Botany / Environmental Science. Desirable : Basic understanding of biodiversity concept is desirable</p>

<p>No. of Post : 01</p>

<p>Age : 28 Years</p>

<p>Place of Posting : Goa</p>

<p>Consolidated Stipend Per Month : Rs.16000/-</p>

<p>Job Requirement : Collection and handling of biodiversity data as assigned by the scientists and working with in-house biodiversity data management applications and software<br />How to apply</p>

<p>Candidates satisfying requirements may attend the Walk-in-interview on 12.11.2015, 10.00 AM at NIO Dona Paula, Goa-403004 along with their bio-data, attested copies of certificates &amp; mark lists in proof of qualification (SSC onwards), age, experience and testimonials. Candidates should bring a photo identity proof at the time of registration</p>

<p>More at http://www.nio.org/index/option/com_vacgoa/task/show/title/Goa/tid/6/sid/28/thid/64</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39671/flye-fast-and-accurate-de-novo-assembler-for-single-molecule-sequencing-reads</guid>
	<pubDate>Sat, 06 Jul 2019 03:48:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39671/flye-fast-and-accurate-de-novo-assembler-for-single-molecule-sequencing-reads</link>
	<title><![CDATA[Flye: Fast and accurate de novo assembler for single molecule sequencing reads]]></title>
	<description><![CDATA[<p><span>Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The package represents a complete pipeline: it takes raw PB / ONT reads as input and outputs polished contigs. Flye also includes a special mode for metagenome assembly.</span></p><p>Address of the bookmark: <a href="https://github.com/fenderglass/Flye" rel="nofollow">https://github.com/fenderglass/Flye</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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