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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/39612?offset=1290</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28141/csbb-v10</guid>
	<pubDate>Wed, 29 Jun 2016 07:33:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28141/csbb-v10</link>
	<title><![CDATA[CSBB-v1.0]]></title>
	<description><![CDATA[<p>CSBB is a command line based bioinformatics suite to analyze biological data acquired through varied avenues of biological experiments. CSBB is implemented in Perl, while it also leverages the use of R and python in background for specific modules. Major focus of CSBB is to allow users from biology and bioinformatics community, to get benefited by performing down-stream analysis tasks while eliminating the need to write programming code. CSBB is currently available on Linux, UNIX, MAC OS and Windows platforms.</p>
<p>Currently CSBB provides 13 modules focused on analytical tasks like performing upper-quantile normalization on expression data or convert genome wide gene expression to z-scores when comparing expression data from different platforms.</p>
<p>More at&nbsp;https://github.com/skygenomics/CSBB-v1.0</p><p>Address of the bookmark: <a href="https://github.com/skygenomics/CSBB-v1.0" rel="nofollow">https://github.com/skygenomics/CSBB-v1.0</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28417/wisescaffolder</guid>
	<pubDate>Wed, 13 Jul 2016 08:08:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28417/wisescaffolder</link>
	<title><![CDATA[WiseScaffolder]]></title>
	<description><![CDATA[<p>Function</p>
<p>WiseScaffolder is a stand-alone semi-automatic application for genome scaffolding of pre-assembled contigs using mate-pair data. It also produces editable scaffold maps, allowing either to build gapped scaffolds or usable as a common thread for the manual improvement of scaffolds.</p>
<p>Description&nbsp;</p>
<p>WiseScaffolder includes 4 subcommands: dumpconfig generates a configuration file that notably specifies the average insert size of the mate-pair library preprocess allows the detection and correction of chimerae, the estimation of contigs copy number and produces valuable outputs for the manual improvement of scaffolds scaffold constitutes the central scaffold-builder and comprises two modules:</p>
<p>i) the interative_scaffold_extender, which works with big, unambiguous contigs, or when they run out, single copy contigs, and</p>
<p>ii) the small_contig_inserter, which inserts the small contigs within scaffolds buildfasta converts the scaffold(s) map(s) into Fasta sequences.</p><p>Address of the bookmark: <a href="http://abims.sb-roscoff.fr/wisescaffolder" rel="nofollow">http://abims.sb-roscoff.fr/wisescaffolder</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/28564/dbt-%E2%80%93-bioinformatics-industrial-training-programme-biitp-2016-%E2%80%93-17</guid>
	<pubDate>Wed, 27 Jul 2016 04:09:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/28564/dbt-%E2%80%93-bioinformatics-industrial-training-programme-biitp-2016-%E2%80%93-17</link>
	<title><![CDATA[DBT – Bioinformatics Industrial Training Programme (BIITP) 2016 – 17]]></title>
	<description><![CDATA[<p>BIITP is a programme of Department of Biotechnology (DBT), Ministry of Science and Technology, Government of India, managed by Biotech Consortium India Limited (BCIL).The objective of BIITP is to provide an opportunity to bioinformatics students to acquire practical skills and experience by working on projects alongside industry experts as well as to provide an opportunity for the industry to identify potential employees.</p><p><strong>DBT Invites online applications from the bioinformatics&nbsp;students and requisitions from biotech/bioinformatics companies.</strong></p><p><strong>Biotech Industry</strong>&nbsp;:</p><p>Biotech/Bioinformatics companies interested to provide hands on industrial training to the students of Bioinformatics under BIITP may apply online. The companies would have no obligation towards any payments to trainees. The companies would be paid bench fee to cover expenses towards training. Trainees would be provided to companies subject to availability.</p><p><strong>Attn: Bioinformatics Students</strong></p><p>Bioinformatics students interested in training in biotech / bioinformatics companies may apply online.&nbsp;<strong>Stipend of Rs. 10,000/- per month</strong>&nbsp;will be paid to candidates placed for training. The candidates will be selected for training through an interview.</p><p><strong>Eligiblity</strong>&nbsp;:</p><p>a) B.E /B.Tech./M.Sc./M.Tech./Advanced Post Graduate Diploma in Bioinformatics from an Indian recognized university with minimum 55% marks or equivalent grade at highest degree/diploma completed in the year 2015 or 2016 are only eligible to apply.</p><p>b) The Advanced Post Graduate diploma should be of at least one year duration after graduation.</p><p>c)&nbsp; Students whose result of last semester/final year is not declared can also apply mentioning their marks upto the semester/year upto which result declared. The final result with original mark sheet(s) of all the semesters/years will have to be produced at the time of interview.</p><p><strong>Application Procedure</strong>&nbsp;:</p><p>The online application form is available below :</p><p><strong><a href="https://www.biotecnika.org/2016/07/dbt-bioinformatics-industrial-training-programme-biitp-2016-17/?xurl=%3A%2F%2Fwww.bcil.nic.in%2Fbiitp2016-17%2Fregistration1.asp" target="_blank">Application Form For Students (New User)</a></strong></p><p><strong><a href="https://www.biotecnika.org/2016/07/dbt-bioinformatics-industrial-training-programme-biitp-2016-17/?xurl=%3A%2F%2Fwww.bcil.nic.in%2Fbiitp2016-17%2Fregistration.asp%3FT1%3DCompany" target="_blank">Requisition form for companies (New User)</a></strong></p><p><strong><a href="https://www.biotecnika.org/2016/07/dbt-bioinformatics-industrial-training-programme-biitp-2016-17/?xurl=%3A%2F%2Fwww.bcil.nic.in%2Fbiitp2016-17%2Findex1.asp" target="_blank">Already registered User Click Here</a></strong></p><p>The following documents are to be sent to Mr. Manoj Gupta, Manager, Biotech Consortium India Limited, 5th floor, Anuvrat Bhawan, 210, Deen Dayal UpadhyayaMarg, New Delhi-110002.</p><p>More at&nbsp;http://www.bcil.nic.in/biitp2016-17/index.asp</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28884/tgnet</guid>
	<pubDate>Wed, 24 Aug 2016 05:36:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28884/tgnet</link>
	<title><![CDATA[TGNet]]></title>
	<description><![CDATA[<p><span>Recent technological progress has greatly facilitated&nbsp;</span><em>de novo</em><span>&nbsp;genome sequencing. However,&nbsp;</span><em>de novo</em><span>&nbsp;assemblies consist in many pieces of contiguous sequence (contigs) arranged in thousands of scaffolds instead of small numbers of chromosomes. Confirming and improving the quality of such assemblies is critical for subsequent analysis.&nbsp;</span></p>
<p>Visualization and quality assessment of de novo genome assemblies</p>
<p>Citation</p>
<p>This software is fully described in the paper:<br>Riba-Grognuz, Keller, Falquet, Xenarios &amp; Wurm (2011) Visualization and quality assessment of de novo genome assemblies.</p>
<p>In brief, our scripts create Cytoscape files to visualize transcript evidence that suggests adjacency between scaffolds and contigs.</p>
<p>Software requirements</p>
<p>BLAT (tested with Standalone BLAT v. 32&times;1). Source Binaries .<br>Cytoscape (tested with versions 2.7.0, 2.8.2)<br>a UNIX machine (tested on Mac OS X 10.6 and CentOS 4.6)</p><p>Address of the bookmark: <a href="https://github.com/ksanao/TGNet" rel="nofollow">https://github.com/ksanao/TGNet</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28906/gene-finding-and-predictions</guid>
	<pubDate>Fri, 26 Aug 2016 07:26:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28906/gene-finding-and-predictions</link>
	<title><![CDATA[Gene Finding and Predictions]]></title>
	<description><![CDATA[<p><span>In this exercise, a previously annotated gene will be used to measure the accuracy of different gene finding approaches. GRAIL, GENSCAN,&nbsp;</span><tt>geneid</tt><span>, FGENESH, GenomeScan, GrailEXP and GENEWISE will be used to annotate the sequence. Both search by signal, content and homology (protein and cDNA sequences) methods will be employed in order to improve the ab initio results. Weak conservation of Start codons will lead to wrong prediction of initial exons in most cases.</span></p>
<p>http://genome.crg.es/courses/Bioinformatics2003_genefinding/</p><p>Address of the bookmark: <a href="http://genome.crg.es/courses/Bioinformatics2003_genefinding/" rel="nofollow">http://genome.crg.es/courses/Bioinformatics2003_genefinding/</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28937/sushi-an-rbioconductor-package-for-visualizing-genomic-data</guid>
	<pubDate>Wed, 31 Aug 2016 08:29:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28937/sushi-an-rbioconductor-package-for-visualizing-genomic-data</link>
	<title><![CDATA[Sushi: An R/Bioconductor package for visualizing genomic data]]></title>
	<description><![CDATA[<p>Sushi: An R/Bioconductor package for visualizing genomic data</p><p>Address of the bookmark: <a href="https://www.bioconductor.org/packages/devel/bioc/vignettes/Sushi/inst/doc/Sushi.pdf" rel="nofollow">https://www.bioconductor.org/packages/devel/bioc/vignettes/Sushi/inst/doc/Sushi.pdf</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29004/r-chie</guid>
	<pubDate>Thu, 01 Sep 2016 11:47:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29004/r-chie</link>
	<title><![CDATA[R-chie]]></title>
	<description><![CDATA[<p><strong>R-chie</strong><span>&nbsp;allows you to make arc diagrams of RNA secondary structures, allowing for easy comparison and overlap of two structures, rank and display basepairs in colour and to also visualize corresponding multiple sequence alignments and co-variation information.</span><br><strong>R4RNA</strong><span>&nbsp;is the R package powering R-chie, available for&nbsp;</span><a href="http://www.e-rna.org/r-chie/download.cgi">download</a><span>&nbsp;and local use for more customized figures and scripting.</span></p>
<p>http://www.e-rna.org/r-chie/plot.cgi?eg=single</p><p>Address of the bookmark: <a href="http://www.e-rna.org/r-chie/plot.cgi?eg=single" rel="nofollow">http://www.e-rna.org/r-chie/plot.cgi?eg=single</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/29108/assembly-tutorial-ppt</guid>
	<pubDate>Wed, 07 Sep 2016 03:12:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/29108/assembly-tutorial-ppt</link>
	<title><![CDATA[Assembly tutorial PPT]]></title>
	<description><![CDATA[<p>Saved Cornell University assembly workshop PPT.</p><p>Reference:&nbsp;</p><p>http://cbsu.tc.cornell.edu/lab/doc/assembly_workshop_20150420_lecture1.pdf</p>]]></description>
	<dc:creator>Jit</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/29108" length="1617402" type="application/pdf" />
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29142/opera-optimal-paired-end-read-assembler</guid>
	<pubDate>Fri, 09 Sep 2016 05:28:58 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29142/opera-optimal-paired-end-read-assembler</link>
	<title><![CDATA[OPERA : Optimal Paired-End Read Assembler]]></title>
	<description><![CDATA[<p>OPERA (Optimal Paired-End Read Assembler) is a sequence assembly program (<a href="http://en.wikipedia.org/wiki/Sequence_assembly">http://en.wikipedia.org/wiki/Sequence_assembly</a>). It uses information from paired-end/mate-pair/long reads to order and orient the intermediate contigs/scaffolds assembled in a genome assembly project, in a process known as Scaffolding. OPERA is based on an exact algorithm that is guaranteed to minimize the discordance of scaffolds with the information provided by the paired-end/mate-pair/long reads (for further details see Gao et al, 2011).</p>
<p>Note that since the original publication, we have made significant changes to OPERA (v1.0 onwards) including refinements to its basic algorithm (to reduce local errors, improve efficiency etc.) and incorporated features that are important for scaffolding large genomes (multi-library support, better repeat-handling etc.), in addition to other scalability and usability improvements (bam and gzip support, smaller memory footprint). We therefore encourage you to download and use our latest version: OPERA-LG. In our benchmarks, it has significantly improved corrected N50 and reduced the number of scaffolding errors. Furthermore, our latest release contains the wrapper script OPERA-long-read that enables scaffolding with long-reads from third-generation sequencing technologies (PacBio or Oxford Nanopore). The manuscript describing the new features and algorithms is available at&nbsp;<a href="https://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-0951-y">Genome Biology</a>. We look forward to getting your feedback to improve it further.</p><p>Address of the bookmark: <a href="https://sourceforge.net/p/operasf/wiki/The%20OPERA%20wiki/" rel="nofollow">https://sourceforge.net/p/operasf/wiki/The%20OPERA%20wiki/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29274/strudel</guid>
	<pubDate>Fri, 30 Sep 2016 09:47:02 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29274/strudel</link>
	<title><![CDATA[Strudel]]></title>
	<description><![CDATA[<p>Strudel is our graphical tool for visualizing genetic and physical maps of genomes for comparative purposes. The application aims to let the user examine their data at a variety of different levels of resolution, from entire maps to individual markers, and explore syntenic relationships between genomes. All browsing and interaction with Strudel happens in real-time &ndash; there is no need to wait while the maps are generated. It is built using Java 1.6 and ships with its own JRE, so there is no need for users to install or update Java.</p><p>Address of the bookmark: <a href="https://ics.hutton.ac.uk/strudel/" rel="nofollow">https://ics.hutton.ac.uk/strudel/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
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