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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/41493?offset=190</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34549/kraken-a-universal-genomic-coordinate-translator-for-comparative-genomics</guid>
	<pubDate>Thu, 07 Dec 2017 04:45:43 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34549/kraken-a-universal-genomic-coordinate-translator-for-comparative-genomics</link>
	<title><![CDATA[kraken: A universal genomic coordinate translator for comparative genomics]]></title>
	<description><![CDATA[<p><span>If you planning on conducting a study involving dozens of large genomes, then you do not have to run all pairwise synteny alignments .. simply try&nbsp;kraken: A universal genomic coordinate translator for comparative genomics</span></p><p>Address of the bookmark: <a href="https://github.com/nedaz/kraken" rel="nofollow">https://github.com/nedaz/kraken</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40476/libsdyogen-libibrary-for-comparative-genomics</guid>
	<pubDate>Wed, 25 Dec 2019 01:32:39 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40476/libsdyogen-libibrary-for-comparative-genomics</link>
	<title><![CDATA[LibsDyogen: Libibrary for comparative genomics]]></title>
	<description><![CDATA[<p>Library of usual classes and functions written in python and used in the Dyogen team for comparative genomics applications.</p>
<p>Collaborative python library used in the<span>&nbsp;</span><a href="http://www.ibens.ens.fr/?rubrique43&amp;lang=fr">DYOGEN team</a>for studying the evolution of gene order in vertebrates.</p>
<p><a href="http://www.ibens.ens.fr/?rubrique43&amp;lang=fr">http://www.ibens.ens.fr/?rubrique43&amp;lang=fr</a></p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/DyogenIBENS/LibsDyogen" rel="nofollow">https://github.com/DyogenIBENS/LibsDyogen</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43046/postdoctoral-fellow-for-a-large-scale-microbial-comparative-genomics</guid>
  <pubDate>Thu, 29 Apr 2021 08:44:53 -0500</pubDate>
  <link></link>
  <title><![CDATA[postdoctoral fellow for a large-scale microbial comparative genomics !]]></title>
  <description><![CDATA[
<p>Asaf Levy hiring a postdoctoral fellow for a large-scale microbial comparative genomics project at the Hebrew University of Jerusalem (Israel). <br />The project is a continuation of Levy Asaf et al. Nature Genetics 2018 paper.<br />Requirements: <br />1.Experience with programming in at least one programming language, preferably Python.<br />2.A PhD in bioinformatics/computational biology<br />3.At least one first authorship publication in a good journal, preferably more.<br />4.Good communication skills in English <br />5.Ability to enter and study in Israel (not applicable for Pakistani people, for example). <br />6.Ability to work in a team.<br />Please send CV to alevy@mail.huji.ac.il</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44661/lovis4u-locus-visualisation-tool-for-comparative-genomics</guid>
	<pubDate>Tue, 17 Sep 2024 02:30:57 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44661/lovis4u-locus-visualisation-tool-for-comparative-genomics</link>
	<title><![CDATA[LoVis4u: Locus Visualisation tool for comparative genomics]]></title>
	<description><![CDATA[<p dir="auto"><a href="https://github.com/art-egorov/lovis4u/blob/main/docs/img/lovis4u_logo.png" target="_blank"><img src="https://github.com/art-egorov/lovis4u/raw/main/docs/img/lovis4u_logo.png" alt="image" width="300" style="border: 0px; border: 0px;"></a></p>
<div dir="auto">
<h2 dir="auto">Description</h2>
<a href="https://github.com/art-egorov/lovis4u#description"></a></div>
<p dir="auto"><span>LoVis4u</span>&nbsp;is a bioinformatics tool for&nbsp;<span>Lo</span>ci&nbsp;<span>Vis</span>ualisation.</p>
<p dir="auto"><span>LoVis4u, a command-line tool and Python API designed for highly customizable and fast visualisation of multiple genomic loci. LoVis4u generates vector images in PDF format based on annotation data from GenBank or GFF files. It is capable of visualising entire genomes of bacteriophages as well as plasmids and user-defined regions of longer prokaryotic genomes. Additionally, LoVis4u offers optional data processing steps to identify and highlight accessory and core genes in input sequences.</span></p>
<p dir="auto">https://art-egorov.github.io/lovis4u/</p>
<p dir="auto">&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/art-egorov/lovis4u" rel="nofollow">https://github.com/art-egorov/lovis4u</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/2423/cancers-origins-revealed</guid>
	<pubDate>Thu, 15 Aug 2013 13:06:56 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/2423/cancers-origins-revealed</link>
	<title><![CDATA[Cancer's origins revealed]]></title>
	<description><![CDATA[<p>Researchers have provided the first comprehensive compendium of mutational processes that drive tumour development. Together, these mutational processes explain most mutations found in 30 of the most common cancer types. This new understanding of cancer development could help to treat and prevent a wide-range of cancers.<br /><br />More at &gt;&gt; http://www.sanger.ac.uk/about/press/2013/130814.html</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42965/nucl2vec-local-alignment-of-dna-sequences-using-distributed-vector-representation</guid>
	<pubDate>Tue, 16 Mar 2021 05:45:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42965/nucl2vec-local-alignment-of-dna-sequences-using-distributed-vector-representation</link>
	<title><![CDATA[Nucl2Vec: Local alignment of DNA sequences using Distributed Vector Representation]]></title>
	<description><![CDATA[<p><span>We demonstrate a novel approach for</span><span>local alignment of DNA reads with respect to reference genome.</span><span>For this process we have used Skip-gram model for creating</span><span>encoding(Nucl2Vec) and k-nearest neighbor for the alignment.</span><span>With our new approach we have reduced computation cost for</span><span>local alignment , while achieving accuracy comparable to existing</span><span>defacto standard BWA-MEM tool.</span> </p>
<p><em>https://prakharg24.github.io/papers/401851.full.pdf</em></p><p>Address of the bookmark: <a href="https://prakharg24.github.io/papers/401851.full.pdf" rel="nofollow">https://prakharg24.github.io/papers/401851.full.pdf</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34543/acana-an-accurate-and-consistent-alignment-tool-for-dna-sequences</guid>
	<pubDate>Wed, 06 Dec 2017 09:45:29 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34543/acana-an-accurate-and-consistent-alignment-tool-for-dna-sequences</link>
	<title><![CDATA[ACANA: An accurate and consistent alignment tool for DNA sequences]]></title>
	<description><![CDATA[<p><span>ACANA is an accurate and consistent alignment tool for DNA sequences. ACANA is specifically designed for aligning sequences that share only some moderately conserved regions and/or have a high frequency of long insertions or deletions. It attempts to combine the best of local and global alignments algorithms in searching for evolutionarily related regions of sequences in order to achieve the best alignment. ACANA is also robust to the small changes of alignment parameters, particularly the gap extension score. As an accurate alignment tool, ACANA is particularly useful in comparative sequence analysis for identifying conserved functional regulatory elements.</span></p><p>Address of the bookmark: <a href="https://www.niehs.nih.gov/research/resources/software/biostatistics/acana/index.cfm" rel="nofollow">https://www.niehs.nih.gov/research/resources/software/biostatistics/acana/index.cfm</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37987/ropebwt2-incremental-construction-of-fm-index-for-dna-sequences</guid>
	<pubDate>Thu, 25 Oct 2018 04:48:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37987/ropebwt2-incremental-construction-of-fm-index-for-dna-sequences</link>
	<title><![CDATA[RopeBWT2: Incremental construction of FM-index for DNA sequences]]></title>
	<description><![CDATA[<p><span>RopeBWT2 is an tool for constructing the FM-index for a collection of DNA sequences. It works by incrementally inserting one or multiple sequences into an existing pseudo-BWT position by position, starting from the end of the sequences. This algorithm can be largely considered a mixture of&nbsp;</span><a href="http://dx.doi.org/10.1007/978-3-642-21458-5_20">BCR</a><span>&nbsp;and&nbsp;</span><a href="http://dfmi.sourceforge.net/">dynamic FM-index</a><span>. Nonetheless, ropeBWT2 is unique in that it may&nbsp;</span><em>implicitly</em><span>sort the input into reverse lexicographical order (RLO) or reverse-complement lexicographical order (RCLO) while building the index.</span></p><p>Address of the bookmark: <a href="https://github.com/lh3/ropebwt2" rel="nofollow">https://github.com/lh3/ropebwt2</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45244/the-ghost-ancestors-hidden-in-our-dna</guid>
	<pubDate>Tue, 18 Aug 2026 22:16:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45244/the-ghost-ancestors-hidden-in-our-dna</link>
	<title><![CDATA[The Ghost Ancestors Hidden in Our DNA]]></title>
	<description><![CDATA[<p>Imagine standing in a museum of human evolution.</p><p>There are Neanderthal bones. Denisovan remains. Fossils from ancient relatives of our species. Each specimen gives us another piece of the story of how Homo sapiens came to be.</p><p>But now imagine that one of the most important characters in that story has left behind no fossil, no skull, no bone, and no genome.</p><p>Nothing that a paleontologist could put behind glass.</p><p>And yet, somehow, that ancient population is still speaking.</p><p>It is speaking through us.</p><p>A fascinating new study published in Science (https://www.science.org/doi/10.1126/science.aef8874?) introduces a computational method called TRACE, which allows scientists to search modern human genomes for genetic traces of ancient populations that have never been directly identified.</p><p>For years, scientists have known that our ancestors interacted with Neanderthals and Denisovans. Their DNA still survives in modern human populations. But these may not have been the only ancient humans who crossed paths with our ancestors.</p><p>Using TRACE, researchers found evidence of an unknown archaic population that contributed DNA to the ancestors of modern humans before humans spread beyond Africa.</p><p>Even more surprisingly, they found evidence of a much older lineage&mdash;possibly around 1.8 million years old&mdash;whose genetic legacy may have reached some modern humans indirectly through Denisovans.</p><p>The extraordinary part is that researchers did not need DNA from these mysterious populations to detect them. Instead, they studied the ancestry of modern genomes and looked for genetic patterns that revealed unusually ancient branches of our family history.</p><p>It is almost like finding the footprints of someone who disappeared thousands of years ago&mdash;without ever finding the person themselves.</p><p>These discoveries suggest that human evolution was far more complicated than a simple family tree. Ancient human populations repeatedly separated, migrated, met and exchanged genes. Some eventually disappeared, but pieces of their genetic legacy survived.</p><p>And that means our DNA is more than a biological instruction manual.</p><p>It is also an archive of human history.</p><p>Some of the people recorded in that archive may never have a name or a fossil. But thanks to methods like TRACE, their genetic echoes are finally becoming visible.</p><p>The next big discovery about our ancient past may not come from a fossil in the ground.</p><p>It may already be inside us.</p><p>Reference: Zhang et al., &ldquo;Recovering signatures of archaic hominin introgression using ancestral recombination graphs,&rdquo; Science (2026), DOI: 10.1126/science.aef8874. Detail paper @&nbsp;https://www.science.org/doi/10.1126/science.aef8874?</p><p><br />The TRACE repository (https://github.com/YulinZhang9806/trace) contains the Python package and command-line tools used to infer archaic admixture tracts from ancestral recombination graphs.</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/914/welch-lab</guid>
  <pubDate>Mon, 15 Jul 2013 18:21:13 -0500</pubDate>
  <link></link>
  <title><![CDATA[Welch Lab]]></title>
  <description><![CDATA[
<p>They are based in the Department of Genetics at the University of Cambridge. </p>

<p>The research covers diverse areas of evolutionary biology, and molecular evolution in particular. It combines theoretical and empirical approaches, and particularly evolutionary inference from genome sequence data.</p>

<p>Links @ http://www.gen.cam.ac.uk/research/welch/GroupPage/Home.html</p>
]]></description>
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