<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/29210?offset=1010</link>
	<atom:link href="https://bioinformaticsonline.com/related/29210?offset=1010" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<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/37746/funannotate-eukaryotic-genome-annotation-pipeline</guid>
	<pubDate>Wed, 19 Sep 2018 07:47:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37746/funannotate-eukaryotic-genome-annotation-pipeline</link>
	<title><![CDATA[funannotate: Eukaryotic Genome Annotation Pipeline]]></title>
	<description><![CDATA[<p><span>Funannotate is a genome prediction, annotation, and comparison software package. It was originally written to annotate fungal genomes (small eukaryotes ~ 30 Mb genomes), but has evolved over time to accomodate larger genomes. The impetus for this software package was to be able to accurately and easily annotate a genome for submission to NCBI GenBank. Existing tools (such as Maker) require significant manually editing to comply with GenBank submission rules, thus funannotate is aimed at simplifying the genome submission process.</span></p><p>Address of the bookmark: <a href="https://github.com/nextgenusfs/funannotate" rel="nofollow">https://github.com/nextgenusfs/funannotate</a></p>]]></description>
	<dc:creator>Jit</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>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/36405/earth-biogenome-project</guid>
	<pubDate>Wed, 25 Apr 2018 07:48:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/36405/earth-biogenome-project</link>
	<title><![CDATA[Earth BioGenome Project]]></title>
	<description><![CDATA[<p><span>The central goal of the Earth BioGenome Project is to understand the evolution and organization of life on our planet by sequencing and functionally annotating the genomes of 1.5 million known species of eukaryotes, a massive group that includes plants, animals, fungi and other organisms whose cells have a nucleus that houses their chromosomal DNA. To date, the genomes of less than 0.2 percent of eukaryotic species have been sequenced.&nbsp;</span></p><p><span>More at&nbsp;https://www.ucdavis.edu/news/earth-biogenome-project-aims-sequence-dna-all-complex-life</span></p>]]></description>
	<dc:creator>Jit</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/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/bookmarks/view/36950/salsa-a-tool-to-scaffold-long-read-assemblies-with-hi-c</guid>
	<pubDate>Fri, 15 Jun 2018 04:01:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36950/salsa-a-tool-to-scaffold-long-read-assemblies-with-hi-c</link>
	<title><![CDATA[SALSA: A tool to scaffold long read assemblies with Hi-C]]></title>
	<description><![CDATA[This code is used to scaffold your assemblies using Hi-C data. This version implements some improvements in the original SALSA algorithm. If you want to use the old version, it can be found in the old_salsa branch.

To use the latest version, first run the following commands:

  cd SALSA
  make
To run the code, you will need Python 2.7, BOOST libraries and Networkx(version lower than 1.2).

If you consider using this tool, please cite our publication which describes the methods used for scaffolding.

Ghurye, J., Pop, M., Koren, S., Bickhart, D., &amp; Chin, C. S. (2017). Scaffolding of long read assemblies using long range contact information. BMC genomics, 18(1), 527. Link

Ghurye, J., Rhie, A., Walenz, B.P., Schmitt, A., Selvaraj, S., Pop, M., Phillippy, A.M. and Koren, S., 2018. Integrating Hi-C links with assembly graphs for chromosome-scale assembly. bioRxiv, p.261149 Link

For any queries, please either ask on github issue page or send an email to Jay Ghurye (jayg@cs.umd.edu).<p>Address of the bookmark: <a href="https://github.com/machinegun/SALSA" rel="nofollow">https://github.com/machinegun/SALSA</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</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/news/view/37927/you-cant-hide-from-genome-hackers</guid>
	<pubDate>Sat, 13 Oct 2018 14:17:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/37927/you-cant-hide-from-genome-hackers</link>
	<title><![CDATA[You can't hide from Genome Hackers]]></title>
	<description><![CDATA[<p><span>Young computational biologist named Yaniv Erlich shocked the research world by showing it was possible to&nbsp;</span><a href="https://www.wired.com/2013/01/your-genome-could-reveal-your-identity/">unmask the identities</a><span>&nbsp;of people listed in anonymous genetic databases using&nbsp;</span><a href="http://science.sciencemag.org/content/339/6117/321" target="_blank">only an Internet connection</a></p><p>Paper: http://science.sciencemag.org/content/early/2018/10/10/science.aau4832</p><p>More at&nbsp;https://www.wired.com/story/genome-hackers-show-no-ones-dna-is-anonymous-anymore/</p>]]></description>
	<dc:creator>Neel</dc:creator>
</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>
</item>

</channel>
</rss>