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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/36476?offset=410</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43850/merfin-improved-variant-filtering-assembly-evaluation-and-polishing-via-k-mer-validation</guid>
	<pubDate>Sun, 03 Apr 2022 20:35:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43850/merfin-improved-variant-filtering-assembly-evaluation-and-polishing-via-k-mer-validation</link>
	<title><![CDATA[Merfin: improved variant filtering, assembly evaluation and polishing via k-mer validation]]></title>
	<description><![CDATA[<p><span>Merfin, a&nbsp;</span><em>k</em><span>-mer based variant-filtering algorithm for improved accuracy in genotyping and genome assembly polishing. Merfin evaluates each variant based on the expected&nbsp;</span><em>k</em><span>-mer multiplicity in the reads, independently of the quality of the read alignment and variant caller&rsquo;s internal score. Merfin increased the precision of genotyped calls in several benchmarks, improved consensus accuracy and reduced frameshift errors when applied to human and nonhuman assemblies built from Pacific Biosciences HiFi and continuous long reads or Oxford Nanopore reads, including the first complete human genome. Moreover, we introduce assembly quality and completeness metrics that account for the expected genomic copy numbers.</span></p>
<p><span>More at&nbsp;https://www.nature.com/articles/s41592-022-01445-y</span></p>
<p><img src="https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41592-022-01445-y/MediaObjects/41592_2022_1445_Fig1_HTML.png" alt="image" style="border: 0px; border: 0px;"></p><p>Address of the bookmark: <a href="https://github.com/arangrhie/merfin" rel="nofollow">https://github.com/arangrhie/merfin</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44768/tritex-a-computational-pipeline-for-chromosome-scale-assembly-of-plant-genomes</guid>
	<pubDate>Fri, 14 Feb 2025 10:53:48 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44768/tritex-a-computational-pipeline-for-chromosome-scale-assembly-of-plant-genomes</link>
	<title><![CDATA[TRITEX, a computational pipeline for chromosome-scale assembly of plant genomes]]></title>
	<description><![CDATA[<p><span>This is the documentation of TRITEX, a computational pipeline for chromosome-scale assembly of plant genomes. It was developed in the research group Domestication Genomics at the Leibniz Institute of Plant Genetics and Crop Research (IPK) Gatersleben.</span></p><p>Address of the bookmark: <a href="https://tritexassembly.bitbucket.io/" rel="nofollow">https://tritexassembly.bitbucket.io/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26303/maker</guid>
	<pubDate>Sun, 07 Feb 2016 15:59:24 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26303/maker</link>
	<title><![CDATA[MAKER]]></title>
	<description><![CDATA[<p>MAKER is a portable and easily configurable genome annotation pipeline.Its purpose is to allow smaller eukaryotic and prokaryotic genome projects to independently annotate their genomes and to create genome databases. MAKER identifies repeats, aligns ESTs and proteins to a genome, produces ab-initio gene predictions and automatically synthesizes these data into gene annotations having evidence-based quality values.</p>
<p>More at http://www.yandell-lab.org/software/maker.html</p><p>Address of the bookmark: <a href="http://www.yandell-lab.org/software/maker.html" rel="nofollow">http://www.yandell-lab.org/software/maker.html</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26325/crossmap</guid>
	<pubDate>Mon, 08 Feb 2016 15:47:00 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26325/crossmap</link>
	<title><![CDATA[CrossMap]]></title>
	<description><![CDATA[<p>CrossMap is a program for convenient conversion of genome coordinates (or annotation files) between <em>different assemblies</em> (such as Human <a href="http://www.ncbi.nlm.nih.gov/assembly/2928/">hg18 (NCBI36)</a> &lt;&gt; <a href="http://www.ncbi.nlm.nih.gov/assembly/2758/">hg19 (GRCh37)</a>, Mouse <a href="http://www.ncbi.nlm.nih.gov/assembly/165668/">mm9 (MGSCv37)</a> &lt;&gt; <a href="http://www.ncbi.nlm.nih.gov/assembly/327618/">mm10 (GRCm38)</a>).</p>
<p>It supports most commonly used file formats including SAM/BAM, Wiggle/BigWig, BED, GFF/GTF, VCF.</p>
<p>CrossMap is designed to liftover genome coordinates between assemblies. It&rsquo;s <em>not</em> a program for aligning sequences to reference genome.</p>
<p>We <em>do not</em> recommend using CrossMap to convert genome coordinates between species.</p>
<p>More at http://crossmap.sourceforge.net/</p><p>Address of the bookmark: <a href="http://crossmap.sourceforge.net/" rel="nofollow">http://crossmap.sourceforge.net/</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27110/easyfig</guid>
	<pubDate>Fri, 29 Apr 2016 05:49:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27110/easyfig</link>
	<title><![CDATA[Easyfig]]></title>
	<description><![CDATA[<p>Easyfig has moved to github, for newer releases of Easyfig please visit our new webpage - https://mjsull.github.io/Easyfig.&nbsp; Easyfig is a Python application for creating linear comparison figures of multiple genomic loci with an easy-to-use graphical user interface (GUI).</p>
<p>More at http://easyfig.sourceforge.net/</p><p>Address of the bookmark: <a href="http://easyfig.sourceforge.net/" rel="nofollow">http://easyfig.sourceforge.net/</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26923/quast-quality-assessment-tool-for-genome-assemblies</guid>
	<pubDate>Wed, 06 Apr 2016 18:23:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26923/quast-quality-assessment-tool-for-genome-assemblies</link>
	<title><![CDATA[QUAST: quality assessment tool for genome assemblies]]></title>
	<description><![CDATA[<p><span>QUAST evaluates genome assemblies. For metagenomes, please see&nbsp;<a href="http://bioinf.spbau.ru/metaquast">MetaQUAST</a>&nbsp;project.</span><br><span>It can works both with and without a given reference genome.</span><br><span>The tool accepts multiple assemblies, thus is suitable for comparison.</span></p>
<p><span>More at&nbsp;http://bioinf.spbau.ru/quast</span></p>
<p><span>http://bioinformatics.oxfordjournals.org/content/early/2013/03/09/bioinformatics.btt086.long</span></p><p>Address of the bookmark: <a href="http://bioinformatics.oxfordjournals.org/content/early/2013/03/09/bioinformatics.btt086.long" rel="nofollow">http://bioinformatics.oxfordjournals.org/content/early/2013/03/09/bioinformatics.btt086.long</a></p>]]></description>
	<dc:creator>Jitendra Prajapati</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27257/busco-assessing-genome-assembly-and-annotation-completeness-with-benchmarking-universal-single-copy-orthologs</guid>
	<pubDate>Tue, 10 May 2016 07:46:24 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27257/busco-assessing-genome-assembly-and-annotation-completeness-with-benchmarking-universal-single-copy-orthologs</link>
	<title><![CDATA[BUSCO: Assessing genome assembly and annotation completeness with Benchmarking Universal Single-Copy Orthologs]]></title>
	<description><![CDATA[<ul>
<li><span>High-throughput genomics has revolutionized biological research, however, while the number of sequenced genomes grows by the day, quality assessment of the resulting assembled sequences remains complicated and mostly limited to technical measures like N50.&nbsp;</span></li>
<li></li>
<li><span>BUSCO provides measures for quantitative assessment of genome assembly, gene set, and transcriptome completeness based on evolutionarily informed expectations of gene content from near-universal single-copy orthologs selected from&nbsp;</span><a href="http://orthodb.org/">OrthoDB</a><span>.&nbsp;</span></li>
<li></li>
<li><span>BUSCO assessments are implemented in open-source software, with comprehensive lineage-specific sets of Benchmarking Universal Single-Copy Orthologs for arthropods, vertebrates, metazoans, fungi, eukaryotes, and bacteria.&nbsp;</span></li>
<li></li>
<li><span>These conserved orthologs are ideal candidates for large-scale phylogenomics studies, and the annotated BUSCO gene models built during genome assessments provide a comprehensive gene predictor training set for use as part of genome annotation pipelines.&nbsp;</span></li>
<li></li>
<li><span>BUSCO assessments offer intuitive metrics, based on evolutionarily informed expectations of gene content from hundreds of species, to gauge completeness of rapidly accumulating genomic data and satisfy an Iberian's quest for quality - "Busco calidad/qualidade".</span></li>
</ul><p>Address of the bookmark: <a href="http://busco.ezlab.org/" rel="nofollow">http://busco.ezlab.org/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27806/blobology</guid>
	<pubDate>Mon, 13 Jun 2016 10:18:33 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27806/blobology</link>
	<title><![CDATA[Blobology]]></title>
	<description><![CDATA[<p><span>Tools for making blobplots or Taxon-Annotated-GC-Coverage plots (TAGC plots) to visualise the contents of genome assembly data sets as a QC step</span></p>
<p>Blaxter Lab, Institute of Evolutionary Biology, University of Edinburgh</p>
<p><span>Goal</span>: To create blobplots or Taxon-Annotated-GC-Coverage plots (TAGC plots) to visualise the contents of genome assembly data sets as a QC step.</p>
<p>This repository accompanies the paper:<br><span>Blobology: exploring raw genome data for contaminants, symbionts and parasites using taxon-annotated GC-coverage plots.</span>&nbsp;<em>Sujai Kumar, Martin Jones, Georgios Koutsovoulos, Michael Clarke, Mark Blaxter</em><br>(submitted 2013-10-01 to&nbsp;<em>Frontiers in Bioinformatics and Computational Biology special issue : Quality assessment and control of high-throughput sequencing data</em>).</p>
<p>It contains bash/perl/R scripts for running the analysis presented in the paper to create a preliminary assembly, and to create and collate GC content, read coverage and taxon annotation for the preliminary assembly, which can be visualised, such as Figure 2a from the paper showing TAGC plots/blobplots for&nbsp;<em>Caenorhabditis</em>&nbsp;sp. 5:&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/blaxterlab/blobology" rel="nofollow">https://github.com/blaxterlab/blobology</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28999/redundans</guid>
	<pubDate>Thu, 01 Sep 2016 08:28:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28999/redundans</link>
	<title><![CDATA[Redundans]]></title>
	<description><![CDATA[<p>Redundans pipeline assists&nbsp;<span>an assembly of heterozygous genomes</span>.<br>Program takes as input&nbsp;<span>assembled contigs</span>,&nbsp;<span>paired-end and/or mate pairs sequencing libraries</span>&nbsp;and returns&nbsp;<span>scaffolded homozygous genome assembly</span>, that should be&nbsp;<span>less fragmented</span>&nbsp;and with total&nbsp;<span>size smaller</span>&nbsp;than the input contigs. In addition, Redundans will automatically&nbsp;<span>close the gaps</span>&nbsp;resulting from genome assembly or scaffolding&nbsp;<a href="https://github.com/Gabaldonlab/redundans/blob/master/test#redundans-pipeline">more details</a>.</p>
<p>The pipeline consists of three steps/modules:</p>
<ul>
<li><span>redundancy reduction</span>: detection and selectively removal of redundant contigs from an initial&nbsp;<em>de novo</em>&nbsp;assembly</li>
<li><span>scaffolding</span>: joining of genome fragments using paired-end and/or mate-pairs reads</li>
<li><span>gap closing</span></li>
</ul>
<p>Redundans is:</p>
<ul>
<li><span>fast</span>&nbsp;&amp;&nbsp;<span>lightweight</span>, multi-core support and memory-optimised, so it can be run even on the laptop for small-to-medium size genomes</li>
<li><span>flexible</span>&nbsp;toward many sequencing technologies (Illumina, 454 or Sanger) and library types (paired-end, mate pairs, fosmids)</li>
<li><span>modular</span>: every step can be ommited or replaced by another tools</li>
</ul><p>Address of the bookmark: <a href="https://github.com/Gabaldonlab/redundans" rel="nofollow">https://github.com/Gabaldonlab/redundans</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29995/hga</guid>
	<pubDate>Tue, 29 Nov 2016 07:25:53 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29995/hga</link>
	<title><![CDATA[HGA]]></title>
	<description><![CDATA[<p>HGA tool version 1.0 This tool helps to apply the Hierarchical Genome Assembly (HGA) method. The tool will apply: 1. Partitioning a given reads dataset into a given number of partitions. 2. Assembling each partitions using a pre-specified assembler (Velvet or SPAdes in this version) and using a given kmer size. 3. Merging all the assemblies of the partition. 4. Combining all the assemblies of the partition (using velvet with kmer value of 31). 5. Finaly, re-assembling the whole dataset with the merged contigs or the combined contigs, using a given kmer size.</p>
<p>https://github.com/aalokaily/Hierarchical-Genome-Assembly-HGA</p><p>Address of the bookmark: <a href="https://github.com/aalokaily/Hierarchical-Genome-Assembly-HGA" rel="nofollow">https://github.com/aalokaily/Hierarchical-Genome-Assembly-HGA</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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