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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/28891?offset=800</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41009/genomics-public-data-links</guid>
	<pubDate>Thu, 13 Feb 2020 00:20:00 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41009/genomics-public-data-links</link>
	<title><![CDATA[genomics public data links !]]></title>
	<description><![CDATA[<p>List of publically available databases on google server.</p>
<p>More at <a href="https://software.broadinstitute.org/gatk/download/bundle">https://software.broadinstitute.org/gatk/download/bundle</a></p>
<p><a href="ftp://ftp.ncbi.nlm.nih.gov/snp/organisms/human_9606/VCF/GATK/">ftp://ftp.ncbi.nlm.nih.gov/snp/organisms/human_9606/VCF/GATK/</a>.</p>
<p><a href="ftp://ftp.broadinstitute.org/bundle/hg38/hg38bundle/">ftp://ftp.broadinstitute.org/bundle/hg38/hg38bundle/</a></p><p>Address of the bookmark: <a href="https://console.cloud.google.com/storage/browser/genomics-public-data/resources/broad/hg38/v0?pli=1" rel="nofollow">https://console.cloud.google.com/storage/browser/genomics-public-data/resources/broad/hg38/v0?pli=1</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/20471/bioinformatics-scripts</guid>
	<pubDate>Thu, 22 Jan 2015 22:29:39 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/20471/bioinformatics-scripts</link>
	<title><![CDATA[Bioinformatics Scripts]]></title>
	<description><![CDATA[<p>Some of the useful bioinformatics scripts.</p>
<p>For example ... contig-stats.pl is a Perl script that will automatically describe features of a sequence assembly.</p>
<p>http://milkweedgenome.org/?q=scripts</p><p>Address of the bookmark: <a href="http://milkweedgenome.org/?q=scripts" rel="nofollow">http://milkweedgenome.org/?q=scripts</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39187/distruct-a-program-for-the-graphical-display-of-population-structure</guid>
	<pubDate>Mon, 25 Mar 2019 03:33:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39187/distruct-a-program-for-the-graphical-display-of-population-structure</link>
	<title><![CDATA[DISTRUCT: a program for the graphical display of population structure]]></title>
	<description><![CDATA[<p><em>distruct</em><span>&nbsp;is a program that can be used to graphically display results produced by the genetic clustering program&nbsp;</span><em><a href="http://pritch.bsd.uchicago.edu/">structure</a></em><span>&nbsp;or by other similar programs. The figures produced by&nbsp;</span><em>distruct</em><span>display individual membership coefficients in the same form as used in&nbsp;</span><a href="https://rosenberglab.stanford.edu/papers/popstruct.pdf">"Genetic structure of human populations"&nbsp;<em>Science</em>&nbsp;298: 2381-2385 (2002)</a><span>. Various options enable the user to control left-to-right printing order of populations, bottom-to-top printing order of clusers, colors, and other graphical details. [</span><a href="https://rosenberglab.stanford.edu/distructExample.html">Example</a><span>]</span></p>
<p>[<a href="https://rosenberglab.stanford.edu/distructForms/distructRegistration.html">Download software package (includes the manual)</a>] (you will be directed first to a registration page and we would very much appreciate if you register)&nbsp;<br>[<a href="https://rosenberglab.stanford.edu/software/distructManual.pdf">Download manual</a>]&nbsp;<br>[<a href="https://rosenberglab.stanford.edu/papers/distructNote.pdf">Download software note from&nbsp;<em>Molecular Ecology Notes</em>&nbsp;4: 137-138 (2004)</a>]</p>
<p>To use the UNIX versions, unzip and untar the files in an appropriate directory using</p>
<pre>gunzip filename.tar.gz; tar xvf filename.tar</pre>
<p><span>where "filename.tar.gz" is the downloaded file. Winzip will unzip the Windows version. Run the program by typing</span></p>
<pre>./distruct</pre>
<p><span>in UNIX or</span></p>
<pre>distruct</pre>
<p><span>from a Dos prompt in Windows. It will produce a figure using the data that are represented in the Central/South Asia&nbsp;</span><em>K=5</em><span>&nbsp;plot in&nbsp;</span><em>Science</em><span>&nbsp;298: 2381-2385 (2002).</span></p>
<p>Please send comments or problems with&nbsp;<em>distruct</em>&nbsp;to Noah Rosenberg.</p>
<h4><em>October 15, 2014 &mdash; Users of Distruct may also find&nbsp;<a href="https://rosenberglab.stanford.edu/clumpp.html">CLUMPP</a>&nbsp;and&nbsp;<a href="http://clumpak.tau.ac.il/">CLUMPAK</a>&nbsp;of interest.</em></h4><p>Address of the bookmark: <a href="https://rosenberglab.stanford.edu/distruct.html" rel="nofollow">https://rosenberglab.stanford.edu/distruct.html</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/20504/chromevol</guid>
	<pubDate>Sun, 25 Jan 2015 00:33:11 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/20504/chromevol</link>
	<title><![CDATA[ChromEvol]]></title>
	<description><![CDATA[<p>Chromosome number is a remarkably dynamic feature of eukaryotic evolution. Chromosome numbers can change by a duplication of the whole genome (a process termed polyploidy), or by single chromosome changes (ascending dysploidy via, e.g., chromosome fission or descending dysploidy via, e.g., chromosome fusion).<br> Of the various mechanisms of chromosome number change, polyploidy has received significant attention because of the impact such an event may have on the organism.<br> ChromEvol implements a series of likelihood models for the evolution of chromosome numbers. By comparing the fit of the different models to biological data, it may be possible to gain insight regarding the pathways by which the evolution of chromosome number proceeds. For each model, the program estimates the rates for the possible transitions assumed by the model, infers the set of ancestral chromosome numbers, and estimates the location along the tree for which polyploidy events (and other chromosome number changes) occurred. For further methodological details, see the publications and manual on the Downloads page.</p>
<p>http://www.tau.ac.il/~itaymay/cp/chromEvol/about.html</p><p>Address of the bookmark: <a href="http://www.tau.ac.il/~itaymay/cp/chromEvol/downloads.html" rel="nofollow">http://www.tau.ac.il/~itaymay/cp/chromEvol/downloads.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43904/jasmine-jointly-accurate-sv-merging-with-intersample-network-edges</guid>
	<pubDate>Sat, 02 Jul 2022 11:41:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43904/jasmine-jointly-accurate-sv-merging-with-intersample-network-edges</link>
	<title><![CDATA[JASMINE: Jointly Accurate Sv Merging with Intersample Network Edges]]></title>
	<description><![CDATA[<p><span>This tool is used to merge structural variants (SVs) across samples. Each sample has a number of SV calls, consisting of position information (chromosome, start, end, length), type and strand information, and a number of other values. Jasmine represents the set of all SVs across samples as a network, and uses a modified minimum spanning forest algorithm to determine the best way of merging the variants such that each merged variants represents a set of analogous variants occurring in different samples.</span></p><p>Address of the bookmark: <a href="https://github.com/mkirsche/Jasmine" rel="nofollow">https://github.com/mkirsche/Jasmine</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/20672/jrfra-structuralcomputational-biology-at-icgeb</guid>
  <pubDate>Thu, 29 Jan 2015 11:52:40 -0600</pubDate>
  <link></link>
  <title><![CDATA[JRF/RA Structural/Computational Biology at ICGEB]]></title>
  <description><![CDATA[
<p>Research Associate and JRF positions in the Structural and Computational Biology Group starting 1st March 2015. Collaborative projects include work on:</p>

<p>a) bioinformatics, systems and computational biology <br />b) malaria <br />c) drug discovery <br />d) genomics <br />e) microbiology <br />f) metabolic disorders <br />g) molecular medicine</p>

<p>Eligibility: Applicants must have one of the following :</p>

<p>1) INSPIRE award for undertakig either PhD or Postdoctoral research; <br />2) SPM award for PhD; <br />3) JRF for pursuing PhD from CSIR/DBT/ICMR</p>

<p>Interest and experience in Biochemistry/Bioinformatics/Biophysics/ Chemistry/Genomics/Molecular Biology/ is essential.</p>

<p>Submit curriculum vitae to sb.icgeb@gmail.com by 20 February 2015</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40711/vg-variation-graph-data-structures-interchange-formats-alignment-genotyping-and-variant-calling-methods</guid>
	<pubDate>Tue, 28 Jan 2020 03:53:24 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40711/vg-variation-graph-data-structures-interchange-formats-alignment-genotyping-and-variant-calling-methods</link>
	<title><![CDATA[VG: variation graph data structures, interchange formats, alignment, genotyping, and variant calling methods]]></title>
	<description><![CDATA[<p><em>Variation graphs</em>&nbsp;provide a succinct encoding of the sequences of many genomes. A variation graph (in particular as implemented in vg) is composed of:</p>
<ul>
<li><em>nodes</em>, which are labeled by sequences and ids</li>
<li><em>edges</em>, which connect two nodes via either of their respective ends</li>
<li><em>paths</em>, describe genomes, sequence alignments, and annotations (such as gene models and transcripts) as walks through nodes connected by edges</li>
</ul><p>Address of the bookmark: <a href="https://github.com/vgteam/vg" rel="nofollow">https://github.com/vgteam/vg</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/21538/senior-research-fellow-at-all-india-institute-of-medical-sciences-aiims-delhi-delhi-delhi</guid>
  <pubDate>Wed, 11 Mar 2015 03:06:10 -0500</pubDate>
  <link></link>
  <title><![CDATA[SENIOR RESEARCH FELLOW at All India Institute of Medical Sciences (AIIMS Delhi) - Delhi, Delhi]]></title>
  <description><![CDATA[
<p>Applications are invited from eligible candidates for the following temporary post in an ICMR funded Research Project entitle “An Investigation to find out reasons for Phenotypic Heterogeneity/Variability in 22q11.2 Microdeletion Syndrome” in Department of Reproductive Biology, AIIMS, New Delhi PI: Dr. Ashutosh Halder, Professor, Department of Reproductive Biology </p>

<p>Name of the post: Senior Research Fellow (SRF) <br />Duration: 2 year <br />Salary: Rs. 28000/- per month + 30% HRA <br />Eligibility: MSc (life sciences) with 2 years research experience, NET/GATE qualified <br />Desirable: Experience in the field of Genomics, Epigenomics &amp; Bioinformatics <br />SELECTION PROCEDURE FOR ALL INDIA INSTITUTE OF MEDICAL SCIENCES (AIIMS DELHI) – SENIOR RESEARCH FELLOW POST: </p>

<p>Candidates can apply on or before 15/03/2015 <br />No Detailed information about the selection process is mentioned in the recruitment notification <br />HOW TO APPLY FOR SENIOR RESEARCH FELLOW VACANCY IN ALL INDIA INSTITUTE OF MEDICAL SCIENCES (AIIMS DELHI): </p>

<p>Deadline: 15.03.15 Submit your C.V in Room No. 2099 (Molecular Cytogenetics Lab), 2nd floor, Reproductive Biology, All India Institute of Medical Sciences, New Delhi-110029 or Email CV to: ashutoshhalder@gmail.com Your CV should include the details of your work experience &amp; degrees along with two references with e-mail and contact number Only 10 shortlisted (on merit) candidates will be invited for interview. No TA/DA will be applicable for the same</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/20959/research-associate-and-jrf-positions-in-the-structural-and-computational-biology-group-at-icgeb</guid>
  <pubDate>Mon, 02 Feb 2015 23:00:37 -0600</pubDate>
  <link></link>
  <title><![CDATA[Research Associate and JRF positions in the Structural and Computational Biology Group at ICGEB]]></title>
  <description><![CDATA[
<p>Research Associate and JRF positions in the Structural and Computational Biology Group starting 1st March 2015. Collaborative projects include work on:</p>

<p>a) bioinformatics, systems and computational biology <br />b) malaria <br />c) drug discovery <br />d) genomics <br />e) microbiology <br />f) metabolic disorders <br />g) molecular medicine</p>

<p>Eligibility: Applicants must have one of the following :</p>

<p>1) INSPIRE award for undertakig either PhD or Postdoctoral research; <br />2) SPM award for PhD; <br />3) JRF for pursuing PhD from CSIR/DBT/ICMR</p>

<p>Interest and experience in Biochemistry/Bioinformatics/Biophysics/ Chemistry/Genomics/Molecular Biology/ is essential.</p>

<p>Submit curriculum vitae to sb.icgeb@gmail.com by 20 February 2015</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/21064/jrf-project-assistant-recruitment-at-shillong-%E2%80%93-bioinformatics-centre-dic</guid>
  <pubDate>Sat, 07 Feb 2015 06:00:23 -0600</pubDate>
  <link></link>
  <title><![CDATA[JRF / Project Assistant Recruitment at Shillong – Bioinformatics Centre (DIC)]]></title>
  <description><![CDATA[
<p>3 Vacancies at Bioinformatics Centre (DIC) For M.Tech/M.Sc. Degree Candidates. Apply Before 15th February,2015</p>

<p>Bioinformatics Centre (DIC) invites applications for the following posts:</p>

<p>Job Number: 01<br />Job Designation: Junior Research Fellow (JRF)<br />Number of Vacancy: 02 (Two)<br />Educational Qualification:<br />M.Tech/M.Sc. in Life Sciences/Botany/Zoology/Biochemistry/Biotechnology/Bioinformatics.<br />Desirable Qualification:<br />Aptitude for Bioinformatics and Computer Programming/Next generation sequencing data analysis.</p>

<p>Job Number: 02<br />Job Designation: Project Assistant<br />Number of Vacancy: 01 (One)<br />Educational Qualification:<br />Graduation in Science.<br />Desirable Qualification:<br />Experience of working in a Life Science/Plant Biotechnology Lab.</p>

<p>Place of Work: Shillong</p>

<p>How To Apply For Opening:<br />The applications through email bicnehu@gmail.com or post must reach the undersigned within 15 days from the date of publication of this advertisement.</p>

<p>Last Date To Apply: 15th February,2015</p>

<p>Contact Address: Bioinformatics Centre (DIC),Shillong-793022</p>

<p>Advertisement Details: Employment News (31 January – 6 February) Page 28</p>
]]></description>
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