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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/28844?offset=880</link>
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	<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/bookmarks/view/33847/omega2-metagenome-assembly-pipeline</guid>
	<pubDate>Mon, 10 Jul 2017 05:56:07 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33847/omega2-metagenome-assembly-pipeline</link>
	<title><![CDATA[Omega2: metagenome assembly pipeline]]></title>
	<description><![CDATA[<p><span>Omega found overlaps between reads using a prefix/suffix hash table. The overlap graph of reads was simplified by removing transitive edges and trimming short branches. Unitigs were generated based on minimum cost flow analysis of the overlap graph and then merged to contigs and scaffolds using mate-pair information. In comparison with three de Bruijn graph assemblers (SOAPdenovo, IDBA-UD and MetaVelvet), Omega provided comparable overall performance on a HiSeq 100-bp dataset and superior performance on a MiSeq 300-bp dataset. In comparison with Celera on the MiSeq dataset, Omega provided more continuous assemblies overall using a fraction of the computing time of existing overlap-layout-consensus assemblers. This indicates Omega can more efficiently assemble longer Illumina reads, and at deeper coverage, for metagenomic datasets.</span></p><p>Address of the bookmark: <a href="http://omega.omicsbio.org/" rel="nofollow">http://omega.omicsbio.org/</a></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/bookmarks/view/34525/hic-pro-an-optimized-and-flexible-pipeline-for-hi-c-data-processing</guid>
	<pubDate>Wed, 06 Dec 2017 01:05:21 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34525/hic-pro-an-optimized-and-flexible-pipeline-for-hi-c-data-processing</link>
	<title><![CDATA[HiC-Pro: an optimized and flexible pipeline for Hi-C data processing]]></title>
	<description><![CDATA[<p><span>HiC-Pro was designed to process Hi-C data, from raw fastq files (paired-end Illumina data) to the normalized contact maps. Since version 2.7.0, HiC-Pro supports the main Hi-C protocols, including digestion protocols as well as protocols that do not require restriction enzyme such as DNase Hi-C. In practice, HiC-Pro can be used to process dilution Hi-C, in situ Hi-C, DNase Hi-C, Micro-C, capture-C, capture Hi-C or HiChip data.</span></p>
<p>&nbsp;</p>
<p>http://nservant.github.io/HiC-Pro/</p><p>Address of the bookmark: <a href="http://nservant.github.io/HiC-Pro/" rel="nofollow">http://nservant.github.io/HiC-Pro/</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/bookmarks/view/38666/mcat-motif-combining-and-association-tool</guid>
	<pubDate>Sun, 13 Jan 2019 06:27:28 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38666/mcat-motif-combining-and-association-tool</link>
	<title><![CDATA[MCAT: Motif Combining and Association Tool]]></title>
	<description><![CDATA[<p>This is a pipeline for finding motifs in fasta files.<br>It can be run from the command line as follows:</p>
<p>usage: orange_pipeline_refine.py [-h] [-w W] [--nmotifs NMOTIFS] [--iter ITER] [-c C]<br>[-s S] [-d] [-ff] [-v V]<br>positive_seq negative_seq</p>
<p>positional arguments:<br>positive_seq the fasta file for the positive sequences<br>negative_seq the fasta file for the negative sequences</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/yanshen43/MCAT" rel="nofollow">https://github.com/yanshen43/MCAT</a></p>]]></description>
	<dc:creator>Neel</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/bookmarks/view/40409/haplotypo-a-variant-calling-pipeline-for-phased-genomes</guid>
	<pubDate>Thu, 19 Dec 2019 07:33:40 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40409/haplotypo-a-variant-calling-pipeline-for-phased-genomes</link>
	<title><![CDATA[HaploTypo: a variant-calling pipeline for phased genomes]]></title>
	<description><![CDATA[<p>An increasing number of phased (i.e. with resolved haplotypes) reference genomes are available. However, most genetic variant calling tools do not explicitly account for haplotype structure. Here, we present HaploTypo, a pipeline tailored to resolve haplotypes in genetic variation analyses. HaploTypo infers the haplotype correspondence for each heterozygous variant called on a phased reference genome.</p>
<div>Availability and Implementation</div>
<p>HaploTypo is implemented in Python 2.7 and Python 3.5, and is freely available at&nbsp;<a href="https://github.com/gabaldonlab/haplotypo" target="">https://github.com/gabaldonlab/haplotypo</a>, and as a Docker image.</p><p>Address of the bookmark: <a href="https://github.com/gabaldonlab/haplotypo" rel="nofollow">https://github.com/gabaldonlab/haplotypo</a></p>]]></description>
	<dc:creator>Jit</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>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41893/sunbeam-a-robust-extensible-metagenomics-pipeline</guid>
	<pubDate>Thu, 18 Jun 2020 06:58:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41893/sunbeam-a-robust-extensible-metagenomics-pipeline</link>
	<title><![CDATA[sunbeam: A robust, extensible metagenomics pipeline]]></title>
	<description><![CDATA[<p><span>Sunbeam is a pipeline written in&nbsp;</span><a href="http://snakemake.readthedocs.io/">snakemake</a><span>&nbsp;that simplifies and automates many of the steps in metagenomic sequencing analysis. It uses&nbsp;</span><a href="http://conda.io/">conda</a><span>&nbsp;to manage dependencies, so it doesn't have pre-existing dependencies or admin privileges, and can be deployed on most Linux workstations and clusters. To read more, check out&nbsp;</span><a href="https://microbiomejournal.biomedcentral.com/articles/10.1186/s40168-019-0658-x">our paper in Microbiome</a><span>.</span></p>
<p><span><a href="https://sunbeam.readthedocs.io/en/latest/">https://sunbeam.readthedocs.io/en/latest/</a></span></p><p>Address of the bookmark: <a href="https://github.com/sunbeam-labs/sunbeam" rel="nofollow">https://github.com/sunbeam-labs/sunbeam</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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