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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/28842?offset=1020</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43722/crossmap-program-for-genome-coordinates-conversion-between-different-assemblies</guid>
	<pubDate>Tue, 25 Jan 2022 17:59:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43722/crossmap-program-for-genome-coordinates-conversion-between-different-assemblies</link>
	<title><![CDATA[CrossMap: program for genome coordinates conversion between different assemblies]]></title>
	<description><![CDATA[<p><span>CrossMap is a program for genome coordinates conversion between&nbsp;</span><em>different assemblies</em><span>&nbsp;(such as&nbsp;</span><a href="http://www.ncbi.nlm.nih.gov/assembly/2928/">hg18 (NCBI36)</a><span>&nbsp;&lt;=&gt;&nbsp;</span><a href="http://www.ncbi.nlm.nih.gov/assembly/2758/">hg19 (GRCh37)</a><span>). It supports commonly used file formats including&nbsp;</span><a href="https://samtools.github.io/hts-specs/SAMv1.pdf">BAM</a><span>,&nbsp;</span><a href="https://en.wikipedia.org/wiki/CRAM_(file_format)">CRAM</a><span>,&nbsp;</span><a href="https://en.wikipedia.org/wiki/SAM_(file_format)">SAM</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/goldenPath/help/wiggle.html">Wiggle</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/goldenPath/help/bigWig.html">BigWig</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/FAQ/FAQformat.html#format1">BED</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/FAQ/FAQformat.html#format3">GFF</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/FAQ/FAQformat.html#format4">GTF</a><span>,&nbsp;</span><a href="https://docs.gdc.cancer.gov/Data/File_Formats/MAF_Format/">MAF</a><span>&nbsp;</span><a href="https://samtools.github.io/hts-specs/VCFv4.2.pdf">VCF</a><span>, and&nbsp;</span><a href="https://sites.google.com/site/gvcftools/home/about-gvcf">gVCF</a><span>.</span></p><p>Address of the bookmark: <a href="http://crossmap.sourceforge.net/" rel="nofollow">http://crossmap.sourceforge.net/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/10394/bioinformatics-protocols</guid>
	<pubDate>Mon, 05 May 2014 10:21:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/10394/bioinformatics-protocols</link>
	<title><![CDATA[Bioinformatics Protocols]]></title>
	<description><![CDATA[<h2><span> RNA Seq </span></h2>
<p><strong> Basic Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/pub?id=1KbTiBHtvHLfPRZ39AY3uriazrINA8TJzgjjwn1zPP7Y">RNA-Seq tutorial</a> based on <a href="http://www.nature.com/protocolexchange/protocols/2327">Trapnell et al. (2012)</a> <em>Nature Protocols</em></li>
</ul>
<dl><dd>In this tutorial we cover the concepts of <a href="http://en.wikipedia.org/wiki/RNA-Seq">RNA-Seq</a> differential gene expression (DGE) analysis using a very small synthetic dataset from a well studied organism.</dd></dl>
<p><strong> Advanced Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1fQ1XfeOKhezJUDTzMXtZVY20c3RGoHe-HLvFOGzqU4s/pub">RNA-Seq (Advanced) Tutorial</a></li>
</ul>
<dl><dd>In this tutorial we compare the performance of three statistically-based differential expression tools:</dd><dd>* CuffDiff</dd><dd>* EdgeR</dd><dd>* DESeq2</dd></dl>
<p><strong> Advanced Command Line Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1ayJXtgBP1OXtnV7o7lq4QHKMNk5SdPHFq4hGkqndBtI/pub">Graphical Output with CummeRbund</a> introduces some basic commands using the cummeRbund package of the R programming language</li>
</ul>
<dl><dd>You will need to install R, RStudio and cummeRbund on your PC (explained in the Tutorial). You will learn how to produce graphical output from RNA-Seq analysis previously done using a Cuffdiff analysis.</dd></dl>
<h2><span> Variant Detection </span></h2>
<p><strong> Basic Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/pub?id=1ZRzrjjOCvtAu3m-IKL-rbJ1f4On60dDL_IEwG7oejdI">Variant Detection tutorial</a></li>
</ul>
<dl><dd>In this tutorial we cover the concepts of detecting small variants (SNVs and indels) in human genomic DNA using a small set of reads from chromosome 22.</dd></dl>
<p><strong>Advanced Galaxy Tutorial</strong></p>
<ul>
<li><a href="https://docs.google.com/document/pub?id=1CuKkKylVDb03tnN7RSWl5EUzleetn0ctjmvaidPKLxM">Variant Detection (Advanced) Tutorial</a></li>
</ul>
<dl><dd>In this tutorial we compare the performance of three statistically-based variant detection tools:</dd><dd>* SAMtools: Mpileup</dd><dd>* GATK: Unified Genotyper</dd><dd>* FreeBayes</dd><dd>Each of these tools takes as its input a BAM file of aligned reads and generates a list of likely variants in VCF format</dd></dl>
<p><strong>Pipelines</strong> are for those who are comfortable with using the UNIX command line; and often allow more control over branching and iteration logic.</p>
<ul>
<li><a href="https://github.com/claresloggett/variant_calling_pipeline">WGS/exome GATK-based variant calling pipeline</a></li>
</ul>
<dl><dd>This is a basic variant-calling and annotation pipeline developed at the Victorian Life Sciences Computation Initiative (VLSCI), University of Melbourne. It is based around BWA, GATK and ENSEMBL and was originally designed for human (or similar) data. The master branch is configured for WGS data; there is an exome branch configured for variant calling in exome data.</dd><dd>To run the pipeline you will need Rubra: <a href="https://github.com/bjpop/rubra">https://github.com/bjpop/rubra</a>. Rubra uses the python Ruffus library: <a href="http://www.ruffus.org.uk/">http://www.ruffus.org.uk/</a>.</dd></dl>
<p><strong>Protocols</strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1lfDYNzHjfDA1pHTHd-0w3xHhg7L4TipT1gRfzgiV8es/pub">Familial Variant Calling</a></li>
</ul>
<dl><dd>In this protocol we discuss and outline the process of calling familial related mutations.</dd></dl>
<ul>
<li><a href="https://docs.google.com/document/d/1PIhm8NrFGaSK0hxpDcp8wUOz11ZkOaHIrpnJshMgDec/pub">Somatic Variant Calling</a></li>
</ul>
<dl><dd>In this protocol we discuss and outline the process of identifying somatic variants or mutations.</dd></dl>
<h2><span> Assembly </span></h2>
<p><strong> Basic Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/pub?id=1N3AB9ptISUu4zULqe1kXpVF0BDyGb5f5yzxWSJd_WNM">Genome assembly tutorial</a></li>
</ul>
<dl><dd>In this tutorial we carry out de novo assembly of a microbial genome. We have also written a <a href="https://docs.google.com/document/d/1xs-TI5MejQARqo0pcocGlymsXldwJbJII890gnmjI0o/pub">De novo Genome Assembly for Illumina Data</a> Protocol for a more generic description of the method.</dd></dl>
<p><strong> Protocol </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1xs-TI5MejQARqo0pcocGlymsXldwJbJII890gnmjI0o/pub">De novo Genome Assembly for Illumina Data</a></li>
</ul>
<dl><dd>In this protocol we discuss and outline the process of de novo assembly for small to medium sized genomes. Use our <a href="https://docs.google.com/document/pub?id=1N3AB9ptISUu4zULqe1kXpVF0BDyGb5f5yzxWSJd_WNM">Genome assembly tutorial</a> to learn a specific case of using Galaxy to carry out de novo assembly of a microbial genome.</dd></dl>
<h2><span> Small RNAs </span></h2>
<p><strong> Basic Galaxy Tutorial </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1WAObJr7M0m8U-2ku-0Y0Sdt_IHmqd1h8WaJHPhnJ1lM/pub">Quality control for small RNA</a></li>
</ul>
<dl><dd>This tutorial covers initial steps of the workflow for analysis of short RNA expression such as a quality control of the raw reads, processing of the raw reads for the subsequent analysis and initial quality assessment of the library.</dd></dl>
<h2><span> ChIP Seq </span></h2>
<p><strong> Protocol </strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1UPJC8dsiDeP5R9MH9U0IvoDgPF2Q3EOstAuzS3e6WCE/pub">ChIP-Seq</a></li>
</ul>
<dl><dd>In this protocol we discuss ChIP-Seq: a method to analyze the interaction between proteins and DNA.</dd></dl>
<h2><span> Amplicons </span></h2>
<p><strong>Protocol</strong></p>
<ul>
<li><a href="https://docs.google.com/document/d/1uW7JzxG86QzS92hTyeuNsLhX_d1XFbaZPSjh7jWxcSg/pub">Amplicon Alignment</a></li>
</ul>
<dl><dd>In this protocol we discuss and outline the process of aligning custom amplicons using primers for high precision.</dd></dl>
<h2><span> Learn Galaxy </span></h2>
<p><a href="https://docs.google.com/document/d/1wsdJDYfjZVg2uJxm9AHi_j0mY3X1M1F4gB-elkuYL7c/pub">Introduction to Galaxy,</a> for those who are very new to Galaxy.</p>
<p><a href="https://docs.google.com/document/d/1t7vVqa3mdeZYPv5-8hiHBFBYhNiynV_3mWByno9-wUM/pub">Using Histories and Workflows,</a> for those with some Galaxy knowledge.</p>
<p>The Galaxy project website has many <a href="http://wiki.galaxyproject.org/Learn">tutorials</a> and <a href="http://wiki.galaxyproject.org/Learn/Screencasts">screencasts</a> about using Galaxy and the tools, and developing new tools.</p><p>Address of the bookmark: <a href="https://genome.edu.au/wiki/Learn" rel="nofollow">https://genome.edu.au/wiki/Learn</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43791/comparative-genomics-visualisation-tools</guid>
	<pubDate>Thu, 17 Feb 2022 05:37:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43791/comparative-genomics-visualisation-tools</link>
	<title><![CDATA[Comparative genomics visualisation tools !]]></title>
	<description><![CDATA[<p>Comparative genomics visualisation tools !</p><p>Address of the bookmark: <a href="https://cmdcolin.github.io/awesome-genome-visualization/?latest=true&amp;selected=%23BRIG&amp;tag=Comparative" rel="nofollow">https://cmdcolin.github.io/awesome-genome-visualization/?latest=true&amp;selected=%23BRIG&amp;tag=Comparative</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/10457/assistant-professor-bio-informatics-at-health-and-family-welfare-department-medical-education-in-raipur</guid>
  <pubDate>Wed, 07 May 2014 00:08:38 -0500</pubDate>
  <link></link>
  <title><![CDATA[Assistant Professor (Bio-Informatics) at Health and Family Welfare Department (Medical Education) in Raipur]]></title>
  <description><![CDATA[
<p>Advertisement No.05/2014/ Exam/Dated 17/04/2014</p>

<p>No of vacancies: 01</p>

<p>Pay scale:Rs. 15600 – 39100 + 6600/-</p>

<p>Essential Academic Qualifications / Experience : Good academic record as defined by the concerned university with at least 55% marks (or an equivalent grade in a point scale wherever grading system is followed) at the Master's Degree level in a relevant subject from an Indian University, or an equivalent degree from an accredited foreign university.</p>

<p>Besides fulfilling the above qualifications, the candidate must have cleared the National Eligibility Test (NET) conducted by the UGC, CSIR or similar test accredited by the UGC like SLET/ SET.</p>

<p>Notwithstanding anything contained in sub-clauses (a) and (b) to this Clause, candidates, who are, or have been awarded a Ph.D. Degree in accordance with the University Grants Commission (Minimum Standards and Procedure for Award of Ph.D. Degree) Regulations, 2009, shall be exempted from the requirement of the minimum eligibility condition of NET/SLET/SET for recruitment and appointment of Assistant Professor or equivalent positions in Universities/Colleges/Institutions.</p>

<p>NET/SLET/SET shall also not be required for such Masters Programmes in disciplines for which NET/SLET/SET is not conducted.</p>

<p>Apply online: http://www.psc.cg.gov.in/htm/OA_ME2014.html</p>

<p>Last Date for Online Registration: 22/05/2014</p>

<p>For more details: http://www.psc.cg.gov.in/pdf/Advertisement/ADV_ME2014.pdf</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43867/genomeqc-a-quality-assessment-tool-for-genome-assemblies-and-gene-structure-annotations</guid>
	<pubDate>Thu, 19 May 2022 04:29:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43867/genomeqc-a-quality-assessment-tool-for-genome-assemblies-and-gene-structure-annotations</link>
	<title><![CDATA[GenomeQC: a quality assessment tool for genome assemblies and gene structure annotations]]></title>
	<description><![CDATA[<p><span>The GenomeQC web application is implemented in R/Shiny version 1.5.9 and Python 3.6 and is freely available at&nbsp;</span><a href="https://genomeqc.maizegdb.org/">https://genomeqc.maizegdb.org/</a><span>&nbsp;under the GPL license. All source code and a containerized version of the GenomeQC pipeline is available in the GitHub repository&nbsp;</span><a href="https://github.com/HuffordLab/GenomeQC">https://github.com/HuffordLab/GenomeQC</a><span>.</span></p>
<p>https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-020-6568-2</p><p>Address of the bookmark: <a href="https://github.com/HuffordLab/GenomeQC" rel="nofollow">https://github.com/HuffordLab/GenomeQC</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/10659/gps-dna-tracking-university-of-sheffield</guid>
	<pubDate>Sat, 10 May 2014 04:33:28 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/10659/gps-dna-tracking-university-of-sheffield</link>
	<title><![CDATA[GPS DNA tracking - University of Sheffield]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/Aap-s1kle4Q" frameborder="0" allowfullscreen></iframe>University of Sheffield geneticist and bioinformatics expert Dr Eran Elhaik demonstrates the power of his new DNA research, which allows people to discover their genetic homeland from 1000 years ago. Find out more about our biological research here http://www.sheffield.ac.uk/aps]]></description>
	
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44373/mitohifi-a-python-pipeline-for-mitochondrial-genome-assembly-from-pacbio-high-fidelity-reads</guid>
	<pubDate>Tue, 05 Sep 2023 07:31:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44373/mitohifi-a-python-pipeline-for-mitochondrial-genome-assembly-from-pacbio-high-fidelity-reads</link>
	<title><![CDATA[MitoHiFi: a python pipeline for mitochondrial genome assembly from PacBio high fidelity reads]]></title>
	<description><![CDATA[<p dir="auto">MitoHiFi v3.2 is a python pipeline distributed under&nbsp;<a href="https://github.com/marcelauliano/MitoHiFi/blob/master/LICENSE">MIT License</a>&nbsp;!</p>
<p dir="auto">MitoHiFi was first developed to assemble the mitogenomes for a wide range of species in the Darwin Tree of Life Project (DToL)</p>
<p dir="auto">https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-023-05385-y&nbsp;</p>
<p dir="auto"><a href="https://github.com/marcelauliano/MitoHiFi/blob/master/docs/dtol-logo-round-300x132.png" target="_blank"><img src="https://github.com/marcelauliano/MitoHiFi/raw/master/docs/dtol-logo-round-300x132.png" alt="" style="border: 0px; border: 0px;"></a></p><p>Address of the bookmark: <a href="https://github.com/marcelauliano/MitoHiFi" rel="nofollow">https://github.com/marcelauliano/MitoHiFi</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44549/quartet-a-telomere-to-telomere-toolkit-for-gap-free-genome-assembly-and-centromeric-repeat-identification</guid>
	<pubDate>Sat, 08 Jun 2024 15:54:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44549/quartet-a-telomere-to-telomere-toolkit-for-gap-free-genome-assembly-and-centromeric-repeat-identification</link>
	<title><![CDATA[quarTeT: a telomere-to-telomere toolkit for gap-free genome assembly and centromeric repeat identification.]]></title>
	<description><![CDATA[<p><span>quarTeT is a collection of tools for T2T genome assembly and basic analysis in automatic workflow.</span><br><br><span>Task include:</span></p>
<ul>
<li><a href="http://www.atcgn.com:8080/quarTeT/docuWeb.html#AssemblyMapper">AssemblyMapper</a>&nbsp;: reference-guided genome assembly</li>
<li><a href="http://www.atcgn.com:8080/quarTeT/docuWeb.html#GapFiller">GapFiller</a>&nbsp;: long-reads based gap filling</li>
<li><a href="http://www.atcgn.com:8080/quarTeT/docuWeb.html#TeloExplorer">TeloExplorer</a>&nbsp;: telomere identification</li>
<li><a href="http://www.atcgn.com:8080/quarTeT/docuWeb.html#CentroMiner">CentroMiner</a>&nbsp;: centromere candidate prediction</li>
</ul>
<p>https://academic.oup.com/hr/article/10/8/uhad127/7197191?login=false&nbsp;</p><p>Address of the bookmark: <a href="http://www.atcgn.com:8080/quarTeT/home.html" rel="nofollow">http://www.atcgn.com:8080/quarTeT/home.html</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/12593/visiting-scientist-computational-genomics-two-positions</guid>
  <pubDate>Mon, 07 Jul 2014 22:53:41 -0500</pubDate>
  <link></link>
  <title><![CDATA[Visiting Scientist - Computational Genomics (two positions)]]></title>
  <description><![CDATA[
<p>Scientific/Managerial &amp; International Recruitment</p>

<p>ICRISAT seeks applications from Indian nationals Visiting Scientist-Computational Genomics (2 positions), to be part of a team of Centre of Excellence in Genomics (CEG), (www.icrisat.org/ceg) to work on legume genomics projects.  The positions will be based at ICRISAT’s Headquarters in Patancheru, Hyderabad, India.</p>

<p>ICRISAT is a non-profit, non-political organization that conducts agricultural research for development in Asia and sub-Saharan Africa with a wide array of partners throughout the world. Covering 6.5 million square kilometers of land in 55 countries, the semi-arid tropics is home to over 2 billion people, with 650 million of these are the poorest of the poor. ICRISAT and its partners help empower those living in the semi-arid tropics, especially smallholder farmers, to overcome poverty, hunger, malnutrition and a degraded environment through more efficient and profitable agriculture. ICRISAT is headquartered in Greater Hyderabad, Andhra Pradesh, India and belongs to the Consortium of Centers supported by the Consultative Group on International Agricultural Research (CGIAR).</p>

<p>The Job: Responsibilities for these positions include:</p>

<p>    Analyzing and handling large-scale next generation sequencing DNA and RNA data<br />    Data mining and development of pipelines and troubleshooting<br />    Genome diversity analysis such as SNPs, Indels, Structural Variations, population structure<br />    Genome wide association study (GWAS) related analysis- LD analysis, hapmap and trait mapping<br />    Expression analysis based on RNA-Seq data, annotation, gene ontology and metabolic pathway analysis<br />    Epigenome analysis, small RNA identification<br />    Gene family analysis, sequence level protein analysis, orthology/paralogy and molecular modelling<br />    Compiling and analysis of results, writing reports and research papers</p>

<p>The Person:  Ph.D. or MSc/MTech/PGDCA with two years research experience in Biotechnology, Computational biology, Agricultural/ Plant Biotechnology, Genetics, Molecular Biology or related discipline. Good knowledge of programming/scripting in at least two of following languages: Perl, C, C++, R, Shell Scripting and Python is plus.</p>

<p>How to apply: Please apply latest by 20 July 2014.  The application should include the name of the position applied for, a letter of motivation, a full Curriculum Vita (CV), and the names and contact information of three references that are knowledgeable of the candidate’s professional qualifications and work experience. Technical details and more information about these positions can be obtained from R.K.VARSHNEY@CGIAR.ORG. All applications will be acknowledged, however only short listed candidates will be contacted.</p>

<p>Apply here https://recruit.zoho.com/ats/Portal.na?digest=T642sgLYWZOStExJ77cPrcM*sIMGZETWw4yPxngbmHA-</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/view/982</guid>
	<pubDate>Wed, 17 Jul 2013 15:25:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/view/982</link>
	<title><![CDATA[Is reference genome necessary for gene expression study in transcriptome sequencing or for variant discovery in genome sequencing?]]></title>
	<description><![CDATA[<p><span>Like in case of plant genomes where nature of genome is too complex and huge in size to accomplish complete<em> de novo</em> assembly by current sequencing technology. What would be alternate solution? Can we live in reference free world?</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

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