<?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/26999?offset=730</link>
	<atom:link href="https://bioinformaticsonline.com/related/26999?offset=730" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34720/meraculous-haplotype-sensitive-assembly-of-highly-heterozygous-genomes</guid>
	<pubDate>Wed, 20 Dec 2017 18:59:42 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34720/meraculous-haplotype-sensitive-assembly-of-highly-heterozygous-genomes</link>
	<title><![CDATA[Meraculous: Haplotype-sensitive Assembly of Highly Heterozygous genomes.]]></title>
	<description><![CDATA[<p><span>Meraculous is a whole genome assembler for Next Generation Sequencing data geared for large genomes. It is a hybrid k-mer/read-based assembler that capitalizes on the high accuracy of Illumina sequence by eschewing an explicit error correction step which we argue to be redundant with the assembly process. Meraculous achieves high performance with large datasets by utilizing lightweight data structures and multi-threaded parallelization, allowing to assemble human-sized genomes on commodity clusters in under a day. The process pipeline implements a highly transparent and portable model of job control and monitoring where different assembly stages can be executed and re-executed separately or in unison on a wide variety of architectures.</span></p>
<p><span>https://jgi.doe.gov/data-and-tools/meraculous/</span></p>
<p><span>https://arxiv.org/ftp/arxiv/papers/1703/1703.09852.pdf</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/meraculous20/" rel="nofollow">https://sourceforge.net/projects/meraculous20/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/32629/bienko-and-crosetto-labs</guid>
  <pubDate>Fri, 12 May 2017 07:42:15 -0500</pubDate>
  <link></link>
  <title><![CDATA[Bienko and Crosetto Labs]]></title>
  <description><![CDATA[
<p>We are two groups of scientists doing frontier research in quantitative biology and biomedicine. The Bienko group is interested in exploring the fundamental design principles controlling how DNA is packed in the eukaryotic nucleus and its relation to gene expression regulation. The Crosetto group engineers new molecular methods for single-cell and spatially resolved omic measurements of DNA, RNA, and proteins, with a strong focus on tumor heterogeneity. By sharing ideas and resources, we work synergistically towards a more quantitative understanding of life’s processes in healthy and diseased conditions.</p>

<p>https://bienkocrosettolabs.org/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36476/flye-fast-and-accurate-de-novo-assembler-for-single-molecule-sequencing-reads</guid>
	<pubDate>Fri, 04 May 2018 19:16:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36476/flye-fast-and-accurate-de-novo-assembler-for-single-molecule-sequencing-reads</link>
	<title><![CDATA[Flye: Fast and accurate de novo assembler for single molecule sequencing reads]]></title>
	<description><![CDATA[<p><span>Flye is a de novo assembler for long and noisy reads, such as those produced by PacBio and Oxford Nanopore Technologies. The algorithm uses an A-Bruijn graph to find the overlaps between reads and does not require them to be error-corrected. After the initial assembly, Flye performs an extra repeat classification and analysis step to improve the structural accuracy of the resulting sequence. The package also includes a polisher module, which produces the final assembly of high nucleotide-level quality.</span></p><p>Address of the bookmark: <a href="https://github.com/fenderglass/Flye" rel="nofollow">https://github.com/fenderglass/Flye</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/32822/phd-positions-in-genova-at-dibris-univ-of-genoa-italy</guid>
  <pubDate>Thu, 18 May 2017 00:04:07 -0500</pubDate>
  <link></link>
  <title><![CDATA[PhD positions in Genova at DIBRIS - Univ. of Genoa, Italy]]></title>
  <description><![CDATA[
<p>PhD positions in Genova at DIBRIS - Univ. of Genoa (Italy)</p>

<p>http://www.disi.unige.it/person/MasulliF/ricerca/PhDinGenova2017.html</p>

<p>The call for some funded positions for  the 3 years PhD studies  at the Department of Informatics, Bioengineering, Robotics and System Engineering (DIBRIS) in Genova is available at</p>

<p>http://www.studenti.unige.it/postlaurea/dottorati/XXXIII/ENG/</p>

<p>The deadline for applications is June13, 2017 and the PhD courses and fellowships should start on Nov 2017.</p>

<p>Details for the application to the  PhD Program in Computer Science and Systems Engineering (CODICE 6608) are at http://phd.dibris.unige.it/csse/index.php/how-to-apply</p>

<p>The research activity of my research group is focused on Computational Intelligence, Machine Learning, Bioinformatics, Systems Biology, and Positive Technology as described at http://www.disi.unige.it/person/MasulliF/ricerca/index.html</p>

<p>The research themes proposed by me and Prof. Stefano Rovetta are:</p>

<p>- Computational Intelligence and Machine Learning (see http://www.disi.unige.it/person/MasulliF/ricerca/Phd2017-T1.html)</p>

<p>- Computational Intelligence and Health and Wellbeing Support( see http://www.disi.unige.it/person/MasulliF/ricerca/Phd2017-T3.html)</p>

<p>You can also propose a different research theme belonging to the research activity of my group.</p>

<p>Looking for self-motivated PhD candidates, interested to the mathematical aspects of their research and to the development of new algorithms for intelligent data analysis, and skilled in programming and   in  thorough experimental data analysis. They will be part of my research group and will collaborate to our research projects and publications.</p>

<p>Italian and international students interested to work are invited  to send their cv  and the name/email-addresses of 3 referees to my email address francesco.masulli@unige.it A.S.A.P.</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/33966/ra-bioinformatics-at-national-institute-of-biomedical-genomics-india</guid>
  <pubDate>Wed, 26 Jul 2017 03:49:52 -0500</pubDate>
  <link></link>
  <title><![CDATA[RA Bioinformatics at NATIONAL INSTITUTE OF BIOMEDICAL GENOMICS,  INDIA]]></title>
  <description><![CDATA[
<p>NATIONAL INSTITUTE OF BIOMEDICAL GENOMICS<br />(An Autonomous Institution of the Government of India) <br />P.O.: N.S.S., Kalyani 741251, West Bengal</p>

<p>Advertisement No. 137/ESTB/NIBMG/17-18 </p>

<p>Position available Project Description: Several positions are available for the project titled: “A unified web-portal for analysis, integration and visualization of multi-omics data”. The goal of this project is to develop a user-accessible resource for integrated analysis and visualization of multi-OMICs data sets (including gene expression, genotype, methylation, microRNA, etc.). Data sets generated on various platforms shall be maintained in a stable database, accessed through standard querying mechanisms, and the results shall be displayed via user-friendly interface. The analysis engine shall run on open-source software (such as R/Bioconductor) developed in-house. All positions are contractual. </p>

<p>Appointment will be initially given for a period of one year which is extendable depending upon performance, availability of funds and requirements of the institute. </p>

<p>Project Code: 20275 Position: (No. of positions available) </p>

<p>Research Associate (3)</p>

<p>Position 1: Ph.D. or equivalent in statistics, computer science, mathematics, bioinformatics, or related subject. <br />Position 1: Those with experience in database management shall be preferred. Experience with UNIX or GNU/Linux operating system. <br />Position 1: Creation and maintenance of a database for population- and diseaseassociated variation resource. Development of programmatic interface for querying the database, filtering of the results and identification of genes of interest. </p>

<p>Rs. 36000/- + 10% HRA </p>

<p>Please apply online via web link http://apply.nibmg.ac.in/ (no other form of application will be accepted). The last date of application is 14-08-2017. All letters to attend screening test and /or interview will be sent only to the short-listed candidates by Email only. No correspondence will be made with applicants who are not shortlisted /not called for screening test and /or interview. No TA/DA will be paid for attending the screening test and /or interview.<br />Detail information at http://www.nibmg.ac.in/academic/Advt_20275.pdf</p>

<p>More Info: http://www.nibmg.ac.in/?q=Project%20Linked%20Personnel</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34479/bioinformatics-lectures</guid>
	<pubDate>Wed, 29 Nov 2017 05:39:54 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34479/bioinformatics-lectures</link>
	<title><![CDATA[Bioinformatics lectures !]]></title>
	<description><![CDATA[<div>
<div>
<div>Computational Biology is a&nbsp;<em style="font-size: 12.8px; font-weight: normal;">huge</em>&nbsp;field of study, that touches upon many distinct algorithmic and biological areas of study. What we are able to cover in this course will depend, in part, on the pace at which we move, which I will attempt to adjust as appropriate. However, here is a tentative list of topics I hope to cover this semester (not necessarily in order).
<ul>
<li>Optimal sequence alignment (global, local, and glocal alignment &amp;mdash with constant &amp; affine gap penalties</li>
<li>Algorithms and data structures for efficient text indexing and&nbsp;<em>exact</em>&nbsp;search</li>
<li>Heuristics for read&nbsp;<em>alignment</em>&nbsp;and&nbsp;<em>mapping</em>&nbsp;&amp;mdash mapping DNA-seq and RNA-seq reads</li>
<li>Genome assembly &amp;mdash k-mers, De Brujin graph construction and representation, long-read technology and read-overlap graph assembly</li>
<li>Motif finding via Gibbs sampling</li>
<li>Gene finding &amp;mdash statistical models for&nbsp;<em>ab initio</em>&nbsp;and evidence-guided prediction of genes</li>
<li>RNA-seq and transcriptomics &amp;mdash transcript assembly, abundance estimation and differential expression testing</li>
<li>Phylogenetics &amp;mdash The small and large phylogeny problem; parsimony, maximum likelihood and Bayesian methods</li>
</ul>
</div>
</div>
</div><p>Address of the bookmark: <a href="https://rob-p.github.io/CSE549F16/lectures/" rel="nofollow">https://rob-p.github.io/CSE549F16/lectures/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/35125/eugene-v-koonin-lab</guid>
  <pubDate>Tue, 09 Jan 2018 05:01:15 -0600</pubDate>
  <link></link>
  <title><![CDATA[Eugene V. Koonin Lab]]></title>
  <description><![CDATA[
<p>Interested in understanding the evolution of life. To obtain glimpses of such understanding, we employ existing and new methods of computational biology to perform research in several major areas.</p>

<p>https://www.ncbi.nlm.nih.gov/research/groups/koonin/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39269/ragoo-fast-reference-guided-scaffolding-of-genome-assembly-contigs</guid>
	<pubDate>Wed, 17 Apr 2019 19:45:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39269/ragoo-fast-reference-guided-scaffolding-of-genome-assembly-contigs</link>
	<title><![CDATA[RaGOO: Fast Reference-Guided Scaffolding of Genome Assembly Contigs]]></title>
	<description><![CDATA[<p>Alonge M, Soyk S, Ramakrishnan S, Wang X, Goodwin S, Sedlazeck FJ, Lippman ZB, Schatz MC:&nbsp;<a href="https://www.biorxiv.org/content/early/2019/01/13/519637">Fast and accurate reference-guided scaffolding of draft genomes</a>.&nbsp;<em>bioRxiv</em>&nbsp;2019.</p>
<p>RaGOO is a tool for coalescing genome assembly contigs into pseudochromosomes via minimap2 alignments to a closely related reference genome. The focus of this tool is on practicality and therefore has the following features:</p>
<ol>
<li>Good performance. On a MacBook Pro using Arabidopsis data, pseudochromosome construction takes less than a minute and the whole pipeline with SV calling takes ~2 minutes.</li>
<li>Intact ordering and orienting of contigs.</li>
<li><a href="https://github.com/malonge/RaGOO/wiki/Breaking-Chimeric-Contigs">Chimeric contig correction</a></li>
<li><a href="https://github.com/malonge/RaGOO/wiki/GFF-File-Lift-Over">GFF lift-over</a></li>
<li><a href="https://github.com/malonge/RaGOO/wiki/Calling-Structural-Variants">Structural variant calling with and integrated version of Assemblytics</a></li>
<li>Confidence scores associated with the grouping, localization, and orientation for each contig.</li>
</ol><p>Address of the bookmark: <a href="https://github.com/malonge/RaGOO" rel="nofollow">https://github.com/malonge/RaGOO</a></p>]]></description>
	<dc:creator>BioJoker</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/35563/bioinformatics-postdoctoral-position-at-instem</guid>
  <pubDate>Tue, 13 Feb 2018 03:18:54 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics postdoctoral position at inStem]]></title>
  <description><![CDATA[
<p>One postdoctoral position is available in the area of Bioinformatics. This position is available through a highly collaborative project involving multiple labs. </p>

<p>The primary focus here would be to analyse and integrate high throughput data from various aspects of translation regulation including non-coding RNAs, mRNAs and modification of ribosomal RNA. We request the interested candidates to approach either</p>

<p>Dasaradhi Palakodeti (dasaradhip@instem.res.in)<br />Or<br />Ravi Muddashetty (ravism@instem.res.in)</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41452/apollo-a-sequencing-technology-independent-scalable-and-accurate-assembly-polishing-algorithm</guid>
	<pubDate>Mon, 16 Mar 2020 10:09:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41452/apollo-a-sequencing-technology-independent-scalable-and-accurate-assembly-polishing-algorithm</link>
	<title><![CDATA[Apollo: A Sequencing-Technology-Independent, Scalable, and Accurate Assembly Polishing Algorithm]]></title>
	<description><![CDATA[<p><span>Apollo is an assembly polishing algorithm that attempts to correct the errors in an assembly. It can take multiple set of reads in a single run and polish the assemblies of genomes of any size. Described by Firtina et al. (preliminary version at&nbsp;</span><a href="https://arxiv.org/pdf/1902.04341.pdf">https://arxiv.org/pdf/1902.04341.pdf</a></p>
<p>More at&nbsp;<a href="https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/btaa179/5804978?rss=1">https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/btaa179/5804978?rss=1</a></p><p>Address of the bookmark: <a href="https://github.com/CMU-SAFARI/Apollo" rel="nofollow">https://github.com/CMU-SAFARI/Apollo</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

</channel>
</rss>