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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/22920?offset=1130</link>
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	<description><![CDATA[]]></description>
	
	
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/39695/nbri-research-recruitment-2019</guid>
  <pubDate>Thu, 11 Jul 2019 01:11:34 -0500</pubDate>
  <link></link>
  <title><![CDATA[NBRI Research Recruitment 2019]]></title>
  <description><![CDATA[
<p>NBRI Recruitment 2019: National Botanical Research Institute (NBRI) has issued the Recruitment Notification of Principal Scientist, Senior Principal Scientist, Senior Scientist, Scientist Jobs for 12 Vacancies. The organization has invited Offline applications for NBRI Recruitment 2019. This is a good opportunity for the candidates who are waiting to find an employment opportunity in Govt Sectors. Job Seekers must focus on all the Latest Job Vacancies available in the NBRI. So Applicants who have qualified in Ph.D. in any Science Subject are eligible for these posts given in the Official Notification can apply Offline by downloading the Application form of NBRI and apply on or before 31st July 2019.</p>

<p>More at https://www.nbri.res.in/uploads/new/Advt.%2001%20of%202019.pdf</p>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43788/fulbright-kalam-postdoctoral-research-scholarships-for-indians</guid>
  <pubDate>Tue, 15 Feb 2022 04:27:22 -0600</pubDate>
  <link></link>
  <title><![CDATA[Fulbright-Kalam Postdoctoral Research Scholarships for Indians]]></title>
  <description><![CDATA[
<p>These fellowships are designed for Indian faculty and researchers who are in the early stages of their research careers in India. Fulbright-Kalam Climate Fellowships will provide opportunities to talented faculty and researchers to strengthen their research capacities. Postdoctoral fellows will have access to some of the finest resources in their areas of interest and will help build long-term collaborative relationships with U.S. faculty and institutions. These fellowships are for eight to 24 months.</p>

<p>Affiliation<br />The selected candidate will be affiliated to one U.S. host institution.</p>

<p>USIEF strongly recommends all applicants to identify institutions with which they wish to be affiliated, and to correspond, in advance, with potential host institutions. If the applicant has secured a letter of invitation from a U.S. institution, it should be included as a part of the online application. The letter of invitation should indicate the duration of visit, preferably with dates.</p>

<p>Grant Benefits</p>

<p>These fellowships provide J-1 visa support, a monthly stipend, Accident and Sickness Program for Exchanges per U.S. Government guidelines, round-trip economy class air travel between India and the U.S., a modest settling-in allowance, and a professional allowance.</p>

<p>Subject to availability of funds, a dependent allowance and international travel may be provided for one accompanying eligible dependent provided the dependent is with the grantee in the U.S. for at least 80 per cent of the grant period. Flex grantees are not eligible for dependent benefits.</p>

<p>Eligibility Requirements</p>

<p>In addition to the General Prerequisites:</p>

<p>Applicants must have a Ph.D. degree within the past four years. S/he must have obtained a Ph.D. degree between September 15, 2018 and September 14, 2022. The applicants are required to upload his/her Ph.D. degree certificate/provisional Ph.D. certificate on the online application;<br />Applicants must have a publication in reputed journals and demonstrate evidence of superior academic and professional achievement. S/he must upload a recent significant publication (copy of paper/article) on the online application (not exceeding 30 pages); and<br />If applicant is employed, please follow the instructions carefully regarding employer’s endorsement. If applicable, obtain the endorsement from the appropriate administrative authority on the Letter of Support from Home Institution. The employer must indicate that leave will be granted for the fellowship period. The applicant can download the Letter of Support from Home Institution from the USIEF website. Candidates working under government-funded projects are also required to get endorsement from their affiliating institutions in India.</p>

<p>How to Apply</p>

<p>Applications must be submitted online at: https://apply.iie.org/fvsp2023/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/34912/list-of-cancer-genomics-research-web-resources</guid>
	<pubDate>Wed, 27 Dec 2017 20:33:09 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/34912/list-of-cancer-genomics-research-web-resources</link>
	<title><![CDATA[List of cancer genomics research web resources !]]></title>
	<description><![CDATA[<p>Major web resources for cancer genomics research</p><p>CGHub <br />https://cghub.ucsc.edu/ <br />Comprehensive data repository; huge data size</p><p>EGA <br />https://www.ebi.ac.uk/ega/ <br />Comprehensive data repository; huge data size</p><p>COSMIC <br />http://cancer.sanger.ac.uk <br />Largest somatic mutation database; genome sequencing paper curation</p><p>CPRG <br />http://www.broadinstitute.org/software/cprg <br />Interface for cancer program resources</p><p>GDAC <br />http://gdac.broadinstitute.org/ <br />Data analysis; automatic pipelines; user-friendly reports</p><p>SNP500Cancer <br />http://snp500cancer.nci.nih.gov <br />Sequence and genotype verification of SNPs</p><p>canEvolve <br />www.canevolve.org/ <br />Comprehensive analysis of tumor profile; Data from 90 studies involving more than 10,000 patients</p><p>MethyCancer <br />http://methycancer.psych.ac.cn <br />Relationship among DNA methylation, gene expression and cancer</p><p>SomamiR <br />http://compbio.uthsc.edu/SomamiR/ <br />Correlation between somatic mutation and microRNA; genome-wide displaying</p><p>cBioPortal <br />http://www.cbioportal.org/public-portal/ <br />Graphical summaries; gene alteration; processed data; visualization</p><p>UCSC Cancer Genomics Browser <br />https://genome-cancer.soe.ucsc.edu/ <br />Clinical information; gene expression; copy number variation; visualization</p><p>CGWB <br />https://cgwb.nci.nih.gov/ <br />Visualization; gene mutation and variation; automated analysis pipeline</p><p>GDSC <br />http://www.cancerrxgene.org <br />Drug sensitivity information; drug response information</p><p>canSAR <br />https://cansar.icr.ac.uk/ <br />Multidisciplinary information; drug discovery</p><p>NONCODE <br />http://www.noncode.org/ ncRNAs; <br />lncRNAs; up-to-date and comprehensive resource</p>]]></description>
	<dc:creator>biogeek</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/43092/where-to-aproach-for-rd-funds-in-india</guid>
	<pubDate>Thu, 24 Jun 2021 01:04:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/43092/where-to-aproach-for-rd-funds-in-india</link>
	<title><![CDATA[Where to Aproach for R&amp;D Funds in India ?]]></title>
	<description><![CDATA[<p>Companies and governments do research and development (R&amp;D/ R'n'D/ R+D) to promote innovation in order to produce new goods or services and/or enhance existing product lines. R&amp;D covers all actions inside an organization aimed at boosting innovation, such as creating incubators, assisting innovators in scaling up their ideas, and cultivating an innovation culture.</p><p>Here are the list of all the research and development funding agencies in India.</p>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/43092" length="73912" type="application/pdf" />
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40479/wos-c-women-scientist-scheme-kiran-ipr</guid>
	<pubDate>Fri, 27 Dec 2019 20:51:15 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40479/wos-c-women-scientist-scheme-kiran-ipr</link>
	<title><![CDATA[WOS-C Women Scientist Scheme KIRAN-IPR]]></title>
	<description><![CDATA[<p>Women Scientist Scheme WOS-C is one among the most coveted programs that Women Scientists in India apply for. It is an initiative started by the Government of India, Department of Science &amp; Technology (DST) to help women scientists in India to return to the field of mainstream science with a special focus on Intellectual Property Rights (IPR).</p>
<p>WOS-C Women Scientist Scheme aims to train women from a myriad of scientific backgrounds for a year, this, in turn, allows them to even work from home and maintain a good work and home life balance. This call opens once a year and is one of the most sought after schemes.</p>
<p><span>The selection process for the WOS-C Women Scientist Scheme is via an online examination and interview. Only shortlisted applicants will be called to appear for the online examination.</span></p>
<p><span>More at&nbsp;<a href="http://115.112.95.114/wosc/online/Control.do?_main=488t3s">http://115.112.95.114/wosc/online/Control.do?_main=488t3s</a></span></p><p>Address of the bookmark: <a href="http://115.112.95.114/wosc/online/Control.do?_main=488t3s" rel="nofollow">http://115.112.95.114/wosc/online/Control.do?_main=488t3s</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42321/updated-science-wide-author-databases-of-standardized-citation-indicators</guid>
	<pubDate>Mon, 16 Nov 2020 03:39:19 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42321/updated-science-wide-author-databases-of-standardized-citation-indicators</link>
	<title><![CDATA[Updated science-wide author databases of standardized citation indicators]]></title>
	<description><![CDATA[<p><span>There was great interest in the databases of standardized citation metrics across all scientists and scientific disciplines [</span><a href="https://journals.plos.org/plosbiology/article?id=10.1371%2Fjournal.pbio.3000918#pbio.3000918.ref001">1</a><span>], and many scientists urged us to provide updates of the databases. Accordingly, we have provided updated analyses that use citations from Scopus with data freeze as of May 6, 2020, assessing scientists for career-long citation impact up until the end of 2019 (Table-S6-career-2019) and for citation impact during the single calendar year 2019 (Table-S7-singleyr-2019). Updated databases and code are freely available in Mendeley (</span><a href="https://dx.doi.org/10.17632/btchxktzyw">https://dx.doi.org/10.17632/btchxktzyw</a><span>). The original database (version 1) can also be found in&nbsp;</span><a href="https://data.mendeley.com/datasets/btchxktzyw/1">https://data.mendeley.com/datasets/btchxktzyw/1</a><span>, the updated (version 2) can also be found in&nbsp;</span><a href="https://data.mendeley.com/datasets/btchxktzyw/2">https://data.mendeley.com/datasets/btchxktzyw/2</a><span>, and any subsequent updates that might appear in the future will be generally accessible in&nbsp;</span><a href="https://dx.doi.org/10.17632/btchxktzyw">https://dx.doi.org/10.17632/btchxktzyw</a><span>.</span></p><p>Address of the bookmark: <a href="https://journals.plos.org/plosbiology/article?id=10.1371%2Fjournal.pbio.3000918" rel="nofollow">https://journals.plos.org/plosbiology/article?id=10.1371%2Fjournal.pbio.3000918</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/12883/breaking-chromosomes-to-study-cancer</guid>
	<pubDate>Fri, 18 Jul 2014 05:42:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/12883/breaking-chromosomes-to-study-cancer</link>
	<title><![CDATA[Breaking chromosomes to study cancer !!!]]></title>
	<description><![CDATA[<p>Chromosomes are present in every cell of our body and they contain the information the body needs to develop and function properly. This information is carried in genes that are arranged along the chromosomes. There are usually 46 chromosomes in every cell. These chromosomes come in pairs, one from our mother and one from our father. The chromosomes can be sorted into 23 pairs by looking at them down a microscope.</p><p>Most people who have a balanced translocation have the right amount of chromosome material but it has been rearranged in some way. This may happen if two chromosomes swap pieces (a reciprocal translocation). In other cases two whole chromosomes may become stuck together (a Robertsonian translocation). This page describes what happens when someone has a reciprocal translocation. <br /><br />Reciprocal chromosomal translocations occur following double-strand breaks (DSBs) in DNA when a section of one chromosome is exchanged with that of another, non-homologous chromosome. These exchanges may produce a dysfunctional fusion gene that disrupts cell growth and survival pathways, such as the translocations seen in leukemia and childhood sarcomas. <br /><br />Chromosomal translocations have been well studied in cancer cell lines which are associated with two types of cancer, acute myeloid leukemia and Ewing's sarcoma, but determining how they contribute to cancer development is complicated by additional mutations and altered gene expression profiles in these cultured cells. Now, Juan Carlos Ramirez, head of the Viral Vector Facility at the Fundacion Centro Nacional de Investigaciones Cardiovasculares (CNIC) and his colleagues Raul Torres at CNIC and Sandra Rodriguez-Peralez at the Spanish National Cancer Center (CNIO) in Madrid, Spain have used a new genome editing tool, CRISPR-Cas9, to induce chromosomal translocations for the first time in a human cell line and in primary cells. The study's authors conclude by stating that the use of this technology will allow for the clarification of how and why chromosomal translocation occurs, which without doubt will allow new anti-cancer therapeutic strategies to be tackled.</p><p>Using RNA-Guided Endonuclease (RGEN) technology or CRISPR/Cas9 genome engineering technology, CNIO and CNIC researchers have shown that it is possible to obtain such chromosomal translocations. The CRISPR-Cas9 system is extremely simple to introduce a cut at the desired locus, easier to design, and cheaper than many other systems. Using the CRISPR-Cas9 system, Ramirez and his colleagues reproduced the translocations observed in Ewing&rsquo;s Sarcoma (ES) and Acute Myeloid Leukemia (AML) patient cell lines in HEK293 cells and also generated the ES translocation in human mesenchymal stem cells and the AML translocation in umbilical cord blood cells.</p><p>By focusing on chromosomal translocation without the confounding characteristics of established cell lines, these new cells lines should help answer the fundamental question of what causes a cell to become cancerous. Ramirez and his team now look forward to modeling other chromosome translocations in a variety of cell types.</p><p>Reference:</p><p>http://en.wikipedia.org/wiki/Chromosomal_translocation</p><p>http://www.nature.com/ncomms/2014/140603/ncomms4964/abs/ncomms4964.html<br /><br /></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43892/choosing-the-right-ngs-sequencing-instrument-for-your-study</guid>
	<pubDate>Wed, 15 Jun 2022 00:37:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43892/choosing-the-right-ngs-sequencing-instrument-for-your-study</link>
	<title><![CDATA[Choosing the Right NGS Sequencing Instrument for Your Study]]></title>
	<description><![CDATA[<p>The right sequencing instrument for your study depends on your project goal. Setting aside turnaround time and price, it essentially comes down to the numbers of reads and read length you need for your experiment. Below, we've described and compared metrics for each of the instruments available. If you&rsquo;re new to high-throughput sequencing and have questions about how you should design your sequencing run, fill out our&nbsp;<a href="https://genohub.com/ngs-consultation/"><span>free consultation form</span></a>&nbsp;and we'll get in touch with you to help.</p>
<p>More at&nbsp;https://genohub.com/ngs-instrument-guide/</p><p>Address of the bookmark: <a href="https://genohub.com/ngs-instrument-guide/" rel="nofollow">https://genohub.com/ngs-instrument-guide/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42012/phewas-r-package-is-designed-to-provide-an-accessible-interface-to-the-phenome-wide-association-study</guid>
	<pubDate>Thu, 30 Jul 2020 22:06:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42012/phewas-r-package-is-designed-to-provide-an-accessible-interface-to-the-phenome-wide-association-study</link>
	<title><![CDATA[PheWAS: R package is designed to provide an accessible interface to the phenome wide association study]]></title>
	<description><![CDATA[<p>The PheWAS R package is designed to provide an accessible interface to the phenome wide association study. For a description of the methods available and some simple examples, please see the&nbsp;<a href="https://github.com/PheWAS/PheWAS/blob/master/inst/doc/PheWAS-package.pdf?raw=true">package vignette</a>&nbsp;or the R documentation. For installation help, see below. ##Installing the PheWAS Package The PheWAS package can be installed using the devtools package. The following code when executed in R will get you started:</p>
<pre><code>install.packages("devtools")
#It may be necessary to install required as not all package dependencies are installed by devtools:
install.packages(c("dplyr","tidyr","ggplot2","MASS","meta","ggrepel","DT"))
devtools::install_github("PheWAS/PheWAS")
library(PheWAS)</code></pre><p>Address of the bookmark: <a href="https://github.com/PheWAS/PheWAS" rel="nofollow">https://github.com/PheWAS/PheWAS</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/17504/postdoc-scientist-bioinformatics-at-ccmb</guid>
  <pubDate>Fri, 26 Sep 2014 19:58:41 -0500</pubDate>
  <link></link>
  <title><![CDATA[PostDoc Scientist Bioinformatics at CCMB]]></title>
  <description><![CDATA[
<p>1. Project Assistant/Junior Research Fellow/ Project Fellow [PA_JRF_PF]</p>

<p>a) M.Sc/or equivalent in biological sciences/related areas [Position Code: PA_JRF_PF_a]<br />b) B.E/B.Tech/ M.Sc in biotechnology/bioinformatics/computer science/Chemistry/Physics or MCA [Position Code: PA_JRF_PF_b]<br />c) M.Sc/or equivalent in wildlife sciences/ecology/environmental sciences or MBBS/BVSc/MVSc. [Position Code: PA_JRF_PF_c]</p>

<p>(Candidates with result awaited are NOT eligible to apply)</p>

<p>Upper Age limit 28years</p>

<p>Rs.12000 / Rs.16000 (as sanctioned by the funding agency)</p>

<p>2. Post Doctoral Fellow/Research Associate in multiple research areas [PDF_RA]</p>

<p>Ph.D. (submitted/awarded) in any branch of biological Sciences. Candidates with Ph.D. in other sciences are also encouraged to apply.</p>

<p>Experience in molecular biology, biochemistry, structural biology, cell biology, infectious disease, conservation genetics, veterinary science, reproductive biology, and molecular diagnostics is desired but not mandatory.</p>

<p>[Position Code: PDF_RA]</p>

<p>UpperAge limit 35years</p>

<p>Rs. 22000- 26000 (as sanctioned by the funding agency)</p>

<p>3. Post Doctoral Scientist Fellow [PDSF]</p>

<p>Ph.D in any of the following areas: bioinformatics, next generation sequencing, high throughput data analysis, proteomics, bio-statistics, computer science, information technology, computer hardware and networking/clustering, parallel processing.<br />[Position Code: PDSF]</p>

<p>Upper Age limit 40 years</p>

<p>Rs. 40000 consolidated (as sanctioned by the funding agency)</p>

<p>Download Application: Last date for apply online: 09th Oct 2014</p>

<p>Advertisement: www.ccmb.res.in//index.php?view=notifications&amp;mid=0&amp;id=71&amp;nid=38</p>

<p>Apply online http://www.ccmb.res.in/positions/temp_notif/online_form.html</p>

<p>More at http://www.ccmb.res.in//index.php?view=notifications&amp;mid=0&amp;id=71&amp;nid=38</p>
]]></description>
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