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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/29912?offset=1350</link>
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<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>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33461/graphmap-a-highly-sensitive-and-accurate-mapper-for-long-error-prone-reads</guid>
	<pubDate>Wed, 07 Jun 2017 04:18:16 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33461/graphmap-a-highly-sensitive-and-accurate-mapper-for-long-error-prone-reads</link>
	<title><![CDATA[GraphMap - A highly sensitive and accurate mapper for long, error-prone reads]]></title>
	<description><![CDATA[<p>GraphMap - A highly sensitive and accurate mapper for long, error-prone reads http://www.nature.com/ncomms/2016/160415/ncomms11307/full/ncomms11307.html<br><br><strong>Features</strong><br><br>&nbsp;&nbsp;&nbsp; Mapping position agnostic to alignment parameters.<br>&nbsp;&nbsp;&nbsp; Consistently very high sensitivity and precision across different error profiles, rates and sequencing technologies even with default parameters.<br>&nbsp;&nbsp;&nbsp; Circular genome handling to resolve coverage drops near ends of the genome.<br>&nbsp;&nbsp;&nbsp; E-value.<br>&nbsp;&nbsp;&nbsp; Meaningful mapping quality.<br>&nbsp;&nbsp;&nbsp; Various alignment strategies (semiglobal bit-vector and Gotoh, anchored).<br>&nbsp;&nbsp;&nbsp; Overlapping of reads for de novo assembly.<br>&nbsp;&nbsp;&nbsp; Transcriptome mapping through internal construction of a transcriptome from a given genomic reference and a GTF file.<br>&nbsp;&nbsp;&nbsp; ...and much more.<br><br>GraphMap is also used as an overlapper in a new de novo genome assembly project called Ra (https://github.com/mariokostelac/ra-integrate).<br>Ra attempts to create de novo assemblies from raw nanopore and PacBio reads without requiring error correction, for which a highly sensitive overlapper is required.<br><br>Currently, development of a new spliced-alignment mode for mapping RNA-seq reads is under way.<br>Description of the current effort as well as how to reach the experimental implementation can be found here: doc/rnaseq.md.</p><p>Address of the bookmark: <a href="https://github.com/isovic/graphmap" rel="nofollow">https://github.com/isovic/graphmap</a></p>]]></description>
	<dc:creator>Jit</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>
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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/bookmarks/view/36755/minialign-fast-and-accurate-alignment-tool-for-pacbio-and-nanopore-long-reads</guid>
	<pubDate>Thu, 24 May 2018 08:33:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36755/minialign-fast-and-accurate-alignment-tool-for-pacbio-and-nanopore-long-reads</link>
	<title><![CDATA[minialign: fast and accurate alignment tool for PacBio and Nanopore long reads]]></title>
	<description><![CDATA[Minialign is a little bit fast and moderately accurate nucleotide sequence alignment tool designed for PacBio and Nanopore long reads. It is built on three key algorithms, minimizer-based index of the minimap overlapper, array-based seed chaining, and SIMD-parallel Smith-Waterman-Gotoh extension.<p>Address of the bookmark: <a href="https://github.com/ocxtal/minialign" rel="nofollow">https://github.com/ocxtal/minialign</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25293/srfjrf-bioinformatics-at-national-bureau-of-animal-genetic-resources</guid>
  <pubDate>Thu, 26 Nov 2015 01:54:07 -0600</pubDate>
  <link></link>
  <title><![CDATA[SRF/JRF Bioinformatics at National Bureau of Animal Genetic Resources]]></title>
  <description><![CDATA[
<p>National Bureau of Animal Genetic Resources </p>

<p>SRF Job vacancies in National Bureau of Animal Genetic Resources (NBAGR) on contractual basis</p>

<p>No. of Posts : 03</p>

<p>Qualifications : Master degree in any one of discipline/ Subjects Biotechnology/Bioinformatics/Life Sciences/ Computer Applications with 4 years/5 years of Bachelor’s degree. Candidates having post graduate degree in above mentioned subjects with 3 years Bachelor’s degree should be NET qualified.</p>

<p>Note : i. The Ph.D. Degree holders are eligible for the posts. ii. The Master’s degree holders with the integrated degrees like B.Tech. &amp; M. Tech. (5 years) are eligible. iii. Graduates with three years Bachelor’s degree, who have acquired professional Master’s degree (3 years) like M.Sc. (Ag.), Masters in Computer Applications, M. Tech., etc., are eligible.</p>

<p>Desirable : The candidates should have zeal to work in R environment and NGS data analysis</p>

<p>Emolument : Rs. 28,000/- </p>

<p>Age Limit : 35 year for Men and 40 years for Women in case of SRF on the date of Interview.<br />How to apply</p>

<p>Walk-in-Interview is proposed to be held at National Bureau of Animal Genetic Resources, Karnal (Haryana)-132 001 at 10:30 AM on 02.12.2015. Interested candidates may attend Walk-in-Interview at 10:30 AM on 02.12.2015 alongwith original certificates and typed bio-data with one set of attested copies of each their certificates with passport size photograph.</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37241/remilo-reference-assisted-misassembly-detection-algorithm-using-short-and-long-reads</guid>
	<pubDate>Fri, 06 Jul 2018 04:27:49 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37241/remilo-reference-assisted-misassembly-detection-algorithm-using-short-and-long-reads</link>
	<title><![CDATA[ReMILO: reference assisted misassembly detection algorithm using short and long reads.]]></title>
	<description><![CDATA[ReMILO, a reference assisted misassembly detection algorithm that uses both short reads and PacBio SMRT long reads. ReMILO aligns the initial short reads to both the contigs and reference genome, and then constructs a novel data structure called red-black multipositional de Bruijn graph to detect misassemblies. In addition, ReMILO also aligns the contigs to long reads and find their differences from the long reads to detect more misassemblies.<p>Address of the bookmark: <a href="https://github.com/songc001/remilo" rel="nofollow">https://github.com/songc001/remilo</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25303/ciab-recruits-scientist-engineer-informatics-officer</guid>
  <pubDate>Sat, 28 Nov 2015 03:40:28 -0600</pubDate>
  <link></link>
  <title><![CDATA[CIAB Recruits Scientist, Engineer, Informatics Officer]]></title>
  <description><![CDATA[
<p>Center of Innovative and Applied Bioprocessing (CIAB) - Punjab</p>

<p>Center of Innovative and Applied Bioprocessing (CIAB) invites applications to recruit on vacant posts of Scientist, Associate Plant Manager/ Plant Engineer, Informatics Officer. Applications against these Government Jobs can be submitted on or before 7th January 2016.<br />CIAB Vacancy 2015 Details</p>

<p>9. Research &amp; Development – Informatics Officer<br />Qualification: M. Tech or M.E. in computer science or information technology or bioinformatics with 4 years of R&amp;D experience (after Master’s Degree) in an R&amp;D organization with work profile of large data assembly, analysis.<br />Age Limit: 45 years<br />How to Apply : Duly filled-in applications in prescribed application format along with copies of required documents should be reach to: Chief Exec</p>
]]></description>
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<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/researchlabs/view/26827/kamaleshwar-singh-lab</guid>
  <pubDate>Fri, 25 Mar 2016 10:46:49 -0500</pubDate>
  <link></link>
  <title><![CDATA[Kamaleshwar Singh Lab]]></title>
  <description><![CDATA[
<p>The focus of Dr. Singh’s research and teaching is on the molecular mechanistic basis for environmental carcinogen-induced genetic (DNA damage) and epigenetic changes, and susceptibility to human cancer development</p>

<p>More at http://www.tiehh.ttu.edu/dr.-kamaleshwar-singh.html</p>
]]></description>
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