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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/11249?offset=860</link>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/24462/icar-project-ra-position-institute-of-bioinformatics-iob-bangalore</guid>
  <pubDate>Tue, 22 Sep 2015 23:41:31 -0500</pubDate>
  <link></link>
  <title><![CDATA[ICAR project RA position @ Institute of Bioinformatics (IOB) Bangalore]]></title>
  <description><![CDATA[
<p>Applications are invited for the post of Research Associate (RA) in the ICAR project on "Lactation stress associated postpartum anestrus SNP array in buffaloes". We are looking for a motivated candidate for handling Next Generation sequencing data analysis with a strong background in bioinformatics and programming.</p>

<p>The position is open for immediate appointment and available for two years and then extendable for additional one year. The applicant will be appointed as Research Associate based on qualifications as detailed below:</p>

<p>Research Associate:</p>

<p>-Master’s degree with bioinformatics with at least 2 years of research experience in Next Generation sequencing data analysis as evidence from Fellowship/ Associateship / Training / other engagements.</p>

<p>-Familiarity with bioinformatics tools, database development, programming skills</p>

<p>-Minimum 1 publication in any peer reviewed journal</p>

<p>Salary will be as per ICAR rules and guidelines. Application will be shortlisted based on CV, reference letters from mentors and telephonic interview. Candidates will be called for a personal interview at Bangalore before appointment. No travel expense will be provided for attending interview at Bangalore.</p>

<p>Interested candidates may send a Letter of Interest and CV by email to: keshav@ibioinformatics.org before September 29, 2015.</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40754/understanding-your-reads-and-mapping</guid>
	<pubDate>Wed, 29 Jan 2020 06:29:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40754/understanding-your-reads-and-mapping</link>
	<title><![CDATA[Understanding your reads and mapping !]]></title>
	<description><![CDATA[<p>One of the best tutorial for beginners ...</p>
<p>https://bioinformatics-core-shared-training.github.io/cruk-summer-school-2017/Day1/Session4-seqIntro.html</p><p>Address of the bookmark: <a href="https://bioinformatics-core-shared-training.github.io/cruk-summer-school-2017/Day1/Session4-seqIntro.html" rel="nofollow">https://bioinformatics-core-shared-training.github.io/cruk-summer-school-2017/Day1/Session4-seqIntro.html</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/24463/project-fellow-at-indian-institute-of-chemical-biology-iicb</guid>
  <pubDate>Tue, 22 Sep 2015 23:47:35 -0500</pubDate>
  <link></link>
  <title><![CDATA[Project Fellow at Indian Institute of Chemical Biology (IICB)]]></title>
  <description><![CDATA[
<p>Advertisement No. : R&amp;C/CD/427/2015  ,Vacancy Code: 4271501    </p>

<p>Project Fellow Bioinformatics recruitment in Indian Institute of Chemical Biology (IICB) purely temporary </p>

<p>Name of the Project:  "Genomics and Informatics Solutions for Integrating Biology(Genesis)".     </p>

<p>No. of Vacancies: 1     </p>

<p>Qualification required : M.Sc in Bioinformatics with 55% Marks. </p>

<p>Experience (Desirable): Candidate should be well versed with sequencing data analysis,assembly and annotation of whole genome sequence. Experience in transcriptional data analysis is also preferred.</p>

<p>Age Limit : 28 Years   <br />  <br />Stipend : Rs.16000<br />How to apply<br />Interested candidates may appear for the walk-in-interview to be held on 28.09.2015 from 11.00 a.m. in the Red Carpet Room with the following documents self attested copy - (1) Matriculation Certificate in support of your date of birth, (2) Degree/Diploma Certificate, (3) Original reprints of all testimonials regarding educational qualification, (4) No Objection Certificate from the employer if employed, (5) Final Mark Sheet of M.Sc. Examination, (6) One Passport size photograph.</p>

<p>http://www.career.iicb.res.in/Recruitment%20Notice.php</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</guid>
	<pubDate>Thu, 29 Aug 2013 15:05:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</link>
	<title><![CDATA[Sequencing Solutions to World Health]]></title>
	<description><![CDATA[<p>"<em>New technology that quickly, easily and economically reveals the genomes of viruses and pathogens transforms public health and medicine."</em></p>
<p><strong>Source</strong>: Life technologies</p><p>Address of the bookmark: <a href="http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264" rel="nofollow">http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/2726/comparison-of-short-read-de-novo-alignment-algorithms</guid>
	<pubDate>Wed, 21 Aug 2013 07:56:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/2726/comparison-of-short-read-de-novo-alignment-algorithms</link>
	<title><![CDATA[Comparison of Short Read De Novo Alignment Algorithms]]></title>
	<description><![CDATA[<p>Excellent article to introduce different sequencing methods along with tools for de novo assembly of sequencing reads and their relevant references.</p>
<p>Title:&nbsp;<strong>Comparison of Short Read De Novo Alignment Algorithms&nbsp;</strong></p>
<p>Author<strong>: Nikhil Gopal</strong></p><p>Address of the bookmark: <a href="http://biochem218.stanford.edu/Projects%202011/Gopal%202011.pdf" rel="nofollow">http://biochem218.stanford.edu/Projects%202011/Gopal%202011.pdf</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/6896/dna-tale-of-3-to-4-years-old-serbia-boy</guid>
	<pubDate>Tue, 26 Nov 2013 17:34:00 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/6896/dna-tale-of-3-to-4-years-old-serbia-boy</link>
	<title><![CDATA[DNA tale of 3 to 4 years old Serbia boy]]></title>
	<description><![CDATA[<p><span>The genome of a young boy found underground at Mal&rsquo;ta near Lake Baikal of eastern Siberia around 24,000 years ago came out as close relative of Europeans and Native Indians.</span></p><p><span>Link:</span></p><p><span><a href="http://www.nytimes.com/2013/11/21/science/two-surprises-in-dna-of-boy-found-buried-in-siberia.html?_r=0">http://www.nytimes.com/2013/11/21/science/two-surprises-in-dna-of-boy-found-buried-in-siberia.html?_r=0</a></span></p><p>&nbsp;</p><p><a href="http://www.nature.com/nature/journal/vaop/ncurrent/full/nature12736.html">http://www.nature.com/nature/journal/vaop/ncurrent/full/nature12736.html</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10237/genome-of-rainbow-trout-sequenced</guid>
	<pubDate>Fri, 25 Apr 2014 10:36:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10237/genome-of-rainbow-trout-sequenced</link>
	<title><![CDATA[Genome of Rainbow Trout Sequenced]]></title>
	<description><![CDATA[<p>Major finding:</p><p><span>&ldquo;In humans and most vertebrates the duplication events were older so there are fewer duplicated genes still present. Most of the duplicated genes get lost or modified so much that they are no longer recognizable as duplicates over time. In the trout and salmon we can see an earlier stage in the process and many duplicated genes are still present,&rdquo; said Dr Gary Thorgaard of Washington State University, a co-author of the paper published in the journal Nature Communications.</span></p><p><span>Source:</span></p><p><span>http://www.sci-news.com/genetics/science-genome-rainbow-trout-01877.html</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10378/real-time-sequencing</guid>
	<pubDate>Sun, 04 May 2014 18:16:42 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10378/real-time-sequencing</link>
	<title><![CDATA[Real time Sequencing]]></title>
	<description><![CDATA[<p><span>&ldquo;... we now know we can do high-throughput sequencing at any location on Earth,&rdquo; Moroz said.</span></p><p><span>Source:</span></p><p><span>http://news.ufl.edu/2014/04/28/real-time-genome-sequencing-at-sea/</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/13415/genomics-and-sequencing-approach-for-identification-of-biomarkers-to-assess-the-efficacy-of-tgf-%CE%B2ri-inhibitors-of-liver-cancer-in-vivo</guid>
	<pubDate>Tue, 05 Aug 2014 13:55:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/13415/genomics-and-sequencing-approach-for-identification-of-biomarkers-to-assess-the-efficacy-of-tgf-%CE%B2ri-inhibitors-of-liver-cancer-in-vivo</link>
	<title><![CDATA[Genomics and sequencing approach for identification of biomarkers to assess the efficacy of TGF-βRI inhibitors (of liver cancer) in vivo]]></title>
	<description><![CDATA[<p>Liver cancer is third leading cause of deaths and fourth most frequent occuring cancer worldwide. There are multiple signaling pathways responsible for causing cancer amongst which TGFb is most important cytokine whose signaling pathway promote cancer. However, main problem is to cure this cancer at late stage where we still have no treatment strategy to tackle this deadly cancer. &nbsp;Hence we need to find out new therapeutic target. One way is to look the relationships between mRNA, methylation and miRNA data of patients with different pathological conditions (cancer vs control either with inhibitor/not). MiRNA is small RNA molecules known to inhibit mRNA expression of particular gene by binding improperly to 3'UTR region of a gene and hence block binding of TF /translation of gene. CpG regions is known to located at promoter region of gene (5' UTR) and usually hypomethylated which allow to gene to transcribe and translate however sometime this region become hyper-methylated thats prevent expression of host gene. Thus , integration of these three data reveal new targets and pathways important for causing or preventing cancer and also reveal biomarker thats check the effects of inhibitor on signaling pathway underlying liver cancer.</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/13415" length="26423" type="image/jpeg" />
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34470/simngs-and-simlibrary-%E2%80%93-software-for-simulating-next-gen-sequencing-data</guid>
	<pubDate>Tue, 28 Nov 2017 06:49:11 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34470/simngs-and-simlibrary-%E2%80%93-software-for-simulating-next-gen-sequencing-data</link>
	<title><![CDATA[simNGS and simLibrary – Software for Simulating Next-Gen Sequencing Data]]></title>
	<description><![CDATA[<p>simNGS is software for simulating observations from Illumina sequencing machines using the statistical models behind the AYB base-calling software. By default, observations only incorporate noise due to sequencing and do not incorporate effects from more esoteric sources of noise that may be present in real data ("dust", bubbles, merged clusters, sequence-heterogeneous clusters, etc). Many of these additional sources may optionally applied.</p>
<p>simNGS takes fasta format sequences and a file describing the covariance of noise between bases and cycles observed in an actual run of the machine, randomly generates noisy intensities representing the signals for the sequence at each cycle and calculates likelihoods for all possible base calls.</p><p>Address of the bookmark: <a href="https://www.ebi.ac.uk/goldman-srv/simNGS/" rel="nofollow">https://www.ebi.ac.uk/goldman-srv/simNGS/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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