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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/1956?offset=10</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36833/bfc-a-standalone-high-performance-tool-for-correcting-sequencing-errors-from-illumina-sequencing-data</guid>
	<pubDate>Thu, 31 May 2018 09:35:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36833/bfc-a-standalone-high-performance-tool-for-correcting-sequencing-errors-from-illumina-sequencing-data</link>
	<title><![CDATA[BFC: a standalone high-performance tool for correcting sequencing errors from Illumina sequencing data]]></title>
	<description><![CDATA[BFC is a standalone high-performance tool for correcting sequencing errors from Illumina sequencing data. It is specifically designed for high-coverage whole-genome human data, though also performs well for small genomes.

The BFC algorithm is a variant of the classical spectrum alignment algorithm introduced by Pevzner et al (2001). It uses an exhaustive search to find a k-mer path through a read that minimizes a heuristic objective function jointly considering penalties on correction, quality and k-mer support. This algorithm was first implemented in my fermi assembler and then refined a few times in fermi, fermi2 and now in BFC. In the k-mer counting phase, BFC uses a blocked bloom filter to filter out most singleton k-mers and keeps the rest in a hash table (Melsted and Pritchard, 2011). The use of bloom filter is how BFC is named, though other correctors such as Lighter and Bless actually rely more on bloom filter than BFC.

https://github.com/lh3/bfc<p>Address of the bookmark: <a href="https://github.com/lh3/bfc" rel="nofollow">https://github.com/lh3/bfc</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35286/alfred-bam-statistics-and-feature-counting</guid>
	<pubDate>Tue, 23 Jan 2018 05:28:38 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35286/alfred-bam-statistics-and-feature-counting</link>
	<title><![CDATA[Alfred: BAM Statistics and Feature Counting]]></title>
	<description><![CDATA[<p>The easiest way to get Alfred is to download a statically linked binary from the&nbsp;<a href="https://github.com/tobiasrausch/alfred/releases/">Alfred github release page</a>. Alternatively, you can build Alfred from source. Alfred dependencies are included as submodules so you need to do a recursive clone.</p>
<p><code>git clone --recursive https://github.com/tobiasrausch/alfred.git</code></p>
<p><code>cd alfred/</code></p>
<p><code>make all</code></p>
<p>https://github.com/tobiasrausch/alfred/</p><p>Address of the bookmark: <a href="https://gear.embl.de/alfred" rel="nofollow">https://gear.embl.de/alfred</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28168/sam-flags</guid>
	<pubDate>Wed, 29 Jun 2016 15:38:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28168/sam-flags</link>
	<title><![CDATA[SAM flags]]></title>
	<description><![CDATA[<p>Decoding SAM flags</p>
<p>This utility makes it easy to identify what are the properties of a read based on its SAM flag value, or conversely, to find what the SAM Flag value would be for a given combination of properties.</p>
<p>To decode a given SAM flag value, just enter the number in the field below. The encoded properties will be listed under Summary below, to the right.</p><p>Address of the bookmark: <a href="https://broadinstitute.github.io/picard/explain-flags.html" rel="nofollow">https://broadinstitute.github.io/picard/explain-flags.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</guid>
	<pubDate>Thu, 29 Aug 2013 15:05:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</link>
	<title><![CDATA[Sequencing Solutions to World Health]]></title>
	<description><![CDATA[<p>"<em>New technology that quickly, easily and economically reveals the genomes of viruses and pathogens transforms public health and medicine."</em></p>
<p><strong>Source</strong>: Life technologies</p><p>Address of the bookmark: <a href="http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264" rel="nofollow">http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/2518/genome-browsers</guid>
	<pubDate>Fri, 16 Aug 2013 19:04:47 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/2518/genome-browsers</link>
	<title><![CDATA[Genome Browsers]]></title>
	<description><![CDATA[<p>Genome Browser is the platform/database used for searching and retreiving sequences and annotation of genomes belong to various eukaryotes, prokaryotes, etc.</p><p>Following are the weblink for different available browsers:</p><p><a href="http://www.ensembl.org/index.html">http://www.ensembl.org/index.html</a></p><p><a href="http://ensemblgenomes.org/">http://ensemblgenomes.org/</a></p><p><a href="http://genome.ucsc.edu/">http://genome.ucsc.edu/</a></p><p><a href="http://www.ncbi.nlm.nih.gov/genome">http://www.ncbi.nlm.nih.gov/genome</a></p><p><a href="http://www.ebi.ac.uk/genomes/">http://www.ebi.ac.uk/genomes/</a></p><p><a href="http://flybase.org/">http://flybase.org/</a></p><p><a href="http://cmr.jcvi.org/tigr-scripts/CMR/CmrHomePage.cgi">http://cmr.jcvi.org/tigr-scripts/CMR/CmrHomePage.cgi</a></p><p><a href="http://www.sanger.ac.uk/resources/databases/">http://www.sanger.ac.uk/resources/databases/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/4164/two-major-breakthrough</guid>
	<pubDate>Mon, 02 Sep 2013 10:18:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/4164/two-major-breakthrough</link>
	<title><![CDATA[Two major breakthrough!!]]></title>
	<description><![CDATA[<p>"Scientists in Uruguay in colloboration with European partners sequenced the genome of the high-value Tannat grape, from which "the most healthy of red wines" are fermented.</p><p>A quick, $1 syphilis&nbsp;test in development by researchers from UNU-BIOLAC."</p><p><strong>Source</strong>:</p><p><a href="http://www.sciencedaily.com/releases/2013/09/130902101846.htm">http://www.sciencedaily.com/releases/2013/09/130902101846.htm</a></p><p><a href="http://www.eurekalert.org/pub_releases/2013-09/tca-ssg082613.php">http://www.eurekalert.org/pub_releases/2013-09/tca-ssg082613.php</a></p><p>&nbsp;</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/9032/encode-sequencing-data-freely-available-to-download-and-use-for-academic-means</guid>
	<pubDate>Thu, 13 Mar 2014 18:18:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/9032/encode-sequencing-data-freely-available-to-download-and-use-for-academic-means</link>
	<title><![CDATA[Encode sequencing data freely available to download and use for academic means]]></title>
	<description><![CDATA[<p>In <span style="text-decoration: underline;"><strong>Encode</strong></span>,&nbsp;<span>regulatory elements investigated via DNA hypersensitivity assays, assays of DNA methylation, and chromatin immunoprecipitation (ChIP) of proteins that interact with DNA, including modified histones and transcription factors, followed by sequencing (ChIP-Seq).</span></p>
<p><span>More information:</span></p>
<p><span>https://genome.ucsc.edu/ENCODE/pilot.html</span></p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://genome.ucsc.edu/ENCODE/" rel="nofollow">https://genome.ucsc.edu/ENCODE/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10238/tsetse-fly-genome-sequenced</guid>
	<pubDate>Fri, 25 Apr 2014 10:48:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10238/tsetse-fly-genome-sequenced</link>
	<title><![CDATA[Tsetse Fly Genome sequenced]]></title>
	<description><![CDATA[<p><span><span>As it&nbsp;</span><a href="http://www.sciencemag.org/content/344/6182/380" target="_blank">reported online today</a><span>&nbsp;in&nbsp;</span><em>Science</em><span>, the team used several sequencing approaches to tackle the tsetse fly's 366 million base genome.</span></span></p><p><span>The current study, and companion articles slated to appear in&nbsp;</span><em>PLOS One</em><span>,&nbsp;</span><em>PLOS Genetics</em><span>, and&nbsp;</span><em>PLOS Neglected Tropic Diseases</em><span>, are the result of &nbsp;nearly 150 researchers based in 18 countries.</span></p><p><span>Source:</span></p><p><span>http://www.genomeweb.com/sequencing/international-team-sequences-tsetse-fly-genome</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/10739/science-for-life-laboratory-scilifelab-sweden</guid>
  <pubDate>Sat, 10 May 2014 06:22:30 -0500</pubDate>
  <link></link>
  <title><![CDATA[Science for Life Laboratory (SciLifeLab)-Sweden]]></title>
  <description><![CDATA[
<p>Science for Life Laboratory (SciLifeLab) is a national center for molecular biosciences with focus on health and environmental research. The center combines frontline technical expertise with advanced knowledge of translational medicine and molecular bioscience. SciLifeLab is a national resource and a collaboration between four universities: Karolinska Institutet, KTH Royal Institute of Technology, Stockholm University and Uppsala University.</p>

<p>Webpage : https://www.scilifelab.se/about-us/<br />Opportunity: https://www.scilifelab.se/about-us/career/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/11644/mirna-database-and-tools</guid>
	<pubDate>Mon, 09 Jun 2014 07:58:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/11644/mirna-database-and-tools</link>
	<title><![CDATA[miRNA database and tools]]></title>
	<description><![CDATA[<p>Since few years miRNA has shown to play important role in therapeutic related research and also known to play vital role in controlling gene expression specifically at transcriptional and post-transcription levels. Here are some important DBs and tools related with miRNA:</p><p><strong>miRNA Sequencing data analysis</strong> :&nbsp;http://tools.genxpro.net/omiras/</p><p><strong>miRNApath( R based tool)&nbsp;</strong>: &nbsp;<a href="http://www.bioconductor.org/packages/release/bioc/html/miRNApath.html">http://www.bioconductor.org/packages/release/bioc/html/miRNApath.html</a></p><p><strong>miRWalk DB</strong> :&nbsp;http://www.umm.uni-heidelberg.de/apps/zmf/mirwalk/</p><p><strong>TargetScanHuman</strong> :&nbsp;http://www.targetscan.org/</p><p><strong>RNAhybrid</strong> :&nbsp;http://bibiserv.techfak.uni-bielefeld.de/rnahybrid/welcome.html</p><p><strong>RNA22 predictor</strong> :&nbsp;http://cbcsrv.watson.ibm.com/rna22.html</p><p><strong>miRNA predictor</strong> :&nbsp;http://www.microrna.org/microrna/home.do</p><p><strong>Plant miRNA DB</strong> :http://bioinformatics.cau.edu.cn/PMRD/</p><p><strong>miRBASE DB</strong>:&nbsp;http://www.mirbase.org/</p><p><strong>Plant RNA predictor</strong> : http://plantgrn.noble.org/psRNATarget/</p><p><strong>miRNA Interaction DB</strong> :&nbsp;http://starbase.sysu.edu.cn/</p><p><strong>Sequencing based miRNA DB</strong> :&nbsp;http://mirgator.kobic.re.kr/</p><p><strong>predicted A-to-I edited miRNA DB </strong>:&nbsp;http://microrna.osumc.edu/mireditar/</p><p><strong>Animal, plant and virus miRNA DB</strong> :&nbsp;http://lemur.amu.edu.pl/share/php/mirnest/</p><p><strong>Atlantic Salmon&nbsp;miRNAs DB </strong>:<strong>&nbsp;</strong>http://www.molgenv.com/ssa_mirnas_db_home.php</p><p><strong>miRNA prediction on UTRs</strong> :&nbsp;http://genie.weizmann.ac.il/pubs/mir07/mir07_prediction.html</p><p><span style="text-decoration: underline;"><strong>Idea of analysing miRNA Sequencing data</strong></span> :</p><p>http://www.illumina.com/applications/epigenetics/small_rna_analysis.ilmn</p><p><strong>More:</strong></p><p><a href="http://www.bioconductor.org/help/search/index.html?q=miRNA+target">http://www.bioconductor.org/help/search/index.html?q=miRNA+target</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

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