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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/30212?offset=770</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38792/nxrepair-error-correction-in-de-novo-assemblies-using-nextera-mate-pair-reads</guid>
	<pubDate>Thu, 24 Jan 2019 10:35:12 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38792/nxrepair-error-correction-in-de-novo-assemblies-using-nextera-mate-pair-reads</link>
	<title><![CDATA[NxRepair: error correction in de novo assemblies using Nextera Mate Pair Reads]]></title>
	<description><![CDATA[<p>NxRepair is a python module that automatically detects large structural errors in de novo assemblies using Nextera mate pair reads. The decector will break a contig at the site of an identified misassembly and will generate a new fasta file containing both the corrected contigs and the correct, unaffected contigs.</p>
<p>https://nxrepair.readthedocs.io/en/latest/tutorial.html</p>
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<pre>nxrepair aligned_matepairs.bam assemblyfasta.fasta error_locations.csv new_fasta.fasta</pre>
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<div>&nbsp;</div><p>Address of the bookmark: <a href="https://github.com/rebeccaroisin/nxrepair" rel="nofollow">https://github.com/rebeccaroisin/nxrepair</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32184/metagenomics-assembly-workshop</guid>
	<pubDate>Tue, 18 Apr 2017 04:28:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32184/metagenomics-assembly-workshop</link>
	<title><![CDATA[Metagenomics assembly workshop !!]]></title>
	<description><![CDATA[<div>
<div>
<div id="welcome-to-metagenomics-workshop">
<p>Welcome to the one-day metagenomics assembly workshop. This tutorial will guide you through the typical steps of metagenome assembly and binning.</p>
<div>
<ul>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/data.html">The Tutorial Data Set</a></li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/qc/index.html">FastQC Quality Control</a></li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/assembly/index.html">Assembly</a>
<ul>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/assembly/velvet.html">Velvet Assembly</a></li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/assembly/megahit.html">MEGAHIT Assembly</a></li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/assembly/idba_ud.html">IDBA-UD Assembly</a></li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/assembly/ray.html">Ray Assembly</a></li>
</ul>
</li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/geneprediction/index.html">Gene Prediction</a></li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/evaluation/index.html">Assembly Evaluation</a>
<ul>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/evaluation/mapping.html">Read Mapping</a></li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/evaluation/metaquast.html">MetaQUAST</a></li>
</ul>
</li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/binning/index.html">Binning</a>
<ul>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/binning/maxbin.html">MaxBin Binning</a></li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/binning/metabat.html">MetaBAT Binning</a></li>
</ul>
</li>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/classification/index.html">Classification</a>
<ul>
<li><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/classification/kraken.html">Kraken Taxonomic Sequence Classification System</a></li>
</ul>
</li>
</ul>
</div>
</div>
</div>
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<div><a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/data.html" title="The Tutorial Data Set">Next&nbsp;<span></span></a>
<p>&nbsp;</p>
</div><p>Address of the bookmark: <a href="http://denbi-metagenomics-workshop.readthedocs.io/en/latest/index.html" rel="nofollow">http://denbi-metagenomics-workshop.readthedocs.io/en/latest/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39098/sda-long-read-sequence-and-assembly-of-segmental-duplications</guid>
	<pubDate>Tue, 05 Mar 2019 10:00:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39098/sda-long-read-sequence-and-assembly-of-segmental-duplications</link>
	<title><![CDATA[SDA: Long-read sequence and assembly of segmental duplications]]></title>
	<description><![CDATA[<p><span><span>Segmental Duplication Assembler (SDA; https://github.com/mvollger/SDA) constructs graphs in which paralogous sequence variants define the nodes and long-read sequences provide attraction and repulsion edges, enabling the partition and assembly of long reads corresponding to distinct paralogs.<br></span></span></p>
<p><span><span>https://github.com/mvollger/SDA</span></span></p><p>Address of the bookmark: <a href="https://www.nature.com/articles/s41592-018-0236-3" rel="nofollow">https://www.nature.com/articles/s41592-018-0236-3</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32376/diamond</guid>
	<pubDate>Thu, 27 Apr 2017 04:21:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32376/diamond</link>
	<title><![CDATA[DIAMOND]]></title>
	<description><![CDATA[<p><span>DIAMOND is a sequence aligner for protein and translated DNA searches and functions as a drop-in replacement for the NCBI BLAST software tools. It is suitable for protein-protein search as well as DNA-protein search on short reads and longer sequences including contigs and assemblies, providing a speedup of BLAST ranging up to x20,000.</span></p>
<p><span>More at&nbsp;file:///home/urbe/Downloads/diamond_manual.pdf</span></p>
<p><span>http://www.nature.com/nmeth/journal/v12/n1/full/nmeth.3176.html</span></p><p>Address of the bookmark: <a href="https://github.com/bbuchfink/diamond" rel="nofollow">https://github.com/bbuchfink/diamond</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40099/contiguator</guid>
	<pubDate>Fri, 04 Oct 2019 01:27:58 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40099/contiguator</link>
	<title><![CDATA[CONTIGuator !]]></title>
	<description><![CDATA[<p><span>CONTIGuator is a Python script for Linux environments whose purpose is to speed-up the bacterial genome assembly process and to obtain a first insight of the genome structure using the well-known artemis comparison tool (ACT).</span></p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/contiguator/" rel="nofollow">https://sourceforge.net/projects/contiguator/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/32496/bioinformatician-at-23andme</guid>
  <pubDate>Sat, 06 May 2017 17:57:39 -0500</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatician at 23andMe]]></title>
  <description><![CDATA[
<p>23andMe’s mission is to help people access, understand, and benefit<br />from the human genome. We are a group of passionate individuals excited<br />to push the boundaries of what’s possible to help turn genetic insight<br />into better health and personal understanding.</p>

<p>Our Research Team prides itself on driving cutting edge, industrial-scale<br />science to make an impact that belies the team’s size, in an environment<br />and culture that fosters creativity, innovation, collaboration, and fun.</p>

<p>More than 80% of our customers consent to participate in research, and as<br />a result of their participation, we have one of the largest recontactable,<br />genotyped, and phenotyped research cohorts in the world. The scope and<br />breadth of our vision means that most of the methods and tools necessary<br />to unlock the potential of this unique resource for discovery have yet<br />to be developed.</p>

<p>Our science has garnered the respect of many members of the<br />broader scientific community. For a list of our publications, see<br />www.23andme.com/publications/for-scientists/.</p>

<p>Join us! Visit our Careers page (www.23andMe.com/careers) to learn more<br />about these open positions:</p>

<p>•	Scientist, Research Communications<br />•	Bioinformaticist<br />•	Computational Biologist, Ancestry R&amp;D<br />•	Scientist/Senior Scientist, Statistical Genetics<br />•	Scientist/Senior Scientist, Survey Methodology<br />•	Scientist/Senior Scientist, Health R&amp;D<br />•	Senior Computational Biologist<br />•	Biostatistician</p>

<p>pfontanillas@23andme.com</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/32716/jrfsrf-project-assistant-ii-recruitment-in-national-agri-food-biotechnology-institute-nabi</guid>
  <pubDate>Mon, 15 May 2017 05:37:52 -0500</pubDate>
  <link></link>
  <title><![CDATA[JRF/SRF / Project Assistant-II recruitment in National Agri-Food Biotechnology Institute (NABI)]]></title>
  <description><![CDATA[
<p>National Agri-Food Biotechnology Institute<br />ADVT. No: 2017-Researcher (02)</p>

<p>JRF/SRF / Project Assistant-II recruitment in National Agri-Food Biotechnology Institute (NABI)</p>

<p>Essential Qualification: According to the DST (DST OM No.SR/S9/Z-09/2012 dated 21.10.2014) Post Graduate degree in basic science(M.Sc) in Bioinformatics/Computational Biology/Systems Biology/Information Technology with NET or Graduate degree in professional course with NET or Post Graduate Degree (M.Tech) in professional course in Bioinformatics/Computational Biology/Systems Biology/Information Technology. Desirable qualification/skills: 1) Should be proficient in programming in Perl/Python/R language etc. 2) Should have knowledge and skills for data mining in biological sequence database . sequence analysis tools/packages, NGS Analysis . 3) Should have knowledge and skills to work in linux environment and write shell scripts.</p>

<p>Age : 28 years</p>

<p>Hiring Process : Written-test<br />Job Role : Research/JRF/SRF<br />How to apply</p>

<p>Application should be sent to Administrative officer, National Agri-Food Biotechnology Institute, Knowledge City, Sector-81, Mohali so as to reach latest by 30.05.2017 before 5:30 pm.</p>

<p>More at http://www.nabi.res.in/Vacancies/NABI/ResearchFellowships/JRFSRFRA/2017/ADVT.%20No%202017Researcher%20(02)/ApplicationForm.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/33741/diya-a-bacterial-annotation-pipeline-for-any-genomics-lab</guid>
	<pubDate>Fri, 30 Jun 2017 08:48:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/33741/diya-a-bacterial-annotation-pipeline-for-any-genomics-lab</link>
	<title><![CDATA[DIYA: a bacterial annotation pipeline for any genomics lab]]></title>
	<description><![CDATA[<p><span>DIY Genomics is an open source bioinformatics consortium intended to bring a collection of tools and libraries into the hands of small scale genomics labs for the process of sequence assembly and annotation. Projects include DIYA, MGAP, CRISPR, and DIYGV</span></p>
<p><span>http://gmod.org/wiki/Diya</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/diyg/" rel="nofollow">https://sourceforge.net/projects/diyg/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/34368/srbioinformatics-analyst-ngs-at-ocimum</guid>
  <pubDate>Fri, 17 Nov 2017 07:50:44 -0600</pubDate>
  <link></link>
  <title><![CDATA[Sr.Bioinformatics Analyst (NGS) at Ocimum]]></title>
  <description><![CDATA[
<p>JOB FUNCTIONBio Tech/R&amp;D/Scientist<br />INDUSTRYBiotechnology/Pharmaceutical/Medicine<br />SPECIALIZATIONBasic Research,Bio-Statistician,Clinical Research<br />QUALIFICATION<br />Any Post Graduate<br />BA (Arts), B.Com. (Commerce), BE/ B.Tech (Engineering), B.Pharm. (Pharmacy), B.Sc. (Science), BL/LLB, BDS (Dental Surgery), B.Ed. (Education), BHM (Hotel Management), BBA/ BBM/ BBS, B.Arch. (Architecture), BCA (Computer Application), Diploma-Other Diploma, B.Plan. (Planning), BGL, B.V.Sc. (Veterinary Science), Other School/ Graduation, BHMS (Homeopathy), BAMS (Ayurveda)<br />Job Description</p>

<p>1.  Must have basic understanding of molecular biology and Genomics.<br />2. Experience in application development or must have expertise in programming using either of Perl/Python.<br />3.  Experience in statistical programming using R/Bioconductor/Matlab.<br />4. Strong concept in statistical and mathematical modelling.<br />5.  Experience in designing and developing the bioinformatics pipeline.<br />6.  Must have minimum 2+ years of hands on experience in NSG data analysis such as RNA-Seq,Exome-Seq ,Chip-Seq and downstream analysis.<br />7. Knowledge in WGS ,WES, Targeted re-sequencing,GWAS and population genomics will be preferred.<br />8. Must have experience working on opensource software/Framework and commercial software for NGS data analysis and reporting.<br />9. Should be aware of handling big data and guiding team members on multiple projects simultaneously.<br />10. Should have experience coordinating with different groups of clinical research scientist for various project requirements.<br />11. Ability to work as team as well as independently with minimal support.</p>

<p>More at http://www3.ocimumbio.com/</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41734/supernova-generates-phased-whole-genome-de-novo-assemblies-from-a-chromium-prepared-library</guid>
	<pubDate>Sun, 31 May 2020 01:59:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41734/supernova-generates-phased-whole-genome-de-novo-assemblies-from-a-chromium-prepared-library</link>
	<title><![CDATA[Supernova: generates phased, whole-genome de novo assemblies from a Chromium-prepared library.]]></title>
	<description><![CDATA[<p>Supernova generates phased, whole-genome&nbsp;<em>de novo</em>&nbsp;assemblies from a Chromium-prepared library.</p>
<p>Please see&nbsp;<a href="https://support.10xgenomics.com/de-novo-assembly/guidance/doc/achieving-success-with-de-novo-assembly">Achieving Success with De Novo Assembly</a>&nbsp;and&nbsp;<a href="https://support.10xgenomics.com/de-novo-assembly/software/overview/system-requirements">System Requirements</a>&nbsp;<em>before</em>&nbsp;creating your Chromium libraries for assembly.</p>
<p>Supernova should be run using 38-56x coverage of the genome.<br>&bull; Somewhat higher coverage is&nbsp;<em>sometimes</em>&nbsp;advantageous.<br>&bull; Supernova will exit if it finds that coverage is far from the recommended range.<br>&bull; Note that at most 2.14 billion reads are allowed.<br>&bull; Please note that we have not extensively tested genomes larger than human, and any genome above approximately 4 GB should be considered experimental and is not supported.</p><p>Address of the bookmark: <a href="https://support.10xgenomics.com/de-novo-assembly/software/pipelines/latest/using/running" rel="nofollow">https://support.10xgenomics.com/de-novo-assembly/software/pipelines/latest/using/running</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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