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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/38625?offset=50</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40214/gooey-turn-almost-any-python-command-line-program-into-a-full-gui-application-with-one-line</guid>
	<pubDate>Fri, 01 Nov 2019 00:29:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40214/gooey-turn-almost-any-python-command-line-program-into-a-full-gui-application-with-one-line</link>
	<title><![CDATA[Gooey: Turn (almost) any Python command line program into a full GUI application with one line]]></title>
	<description><![CDATA[<p><span>Turn (almost) any Python command line program into a full GUI application with one line</span></p>
<p>The easiest way to install Gooey is via&nbsp;<code>pip</code></p>
<pre><code>pip install Gooey 
</code></pre>
<p>Alternatively, you can install Gooey by cloning the project to your local directory</p>
<pre><code>git clone https://github.com/chriskiehl/Gooey.git
</code></pre>
<p>run&nbsp;<code>setup.py</code></p>
<pre><code>python setup.py install</code></pre><p>Address of the bookmark: <a href="https://github.com/chriskiehl/Gooey" rel="nofollow">https://github.com/chriskiehl/Gooey</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43722/crossmap-program-for-genome-coordinates-conversion-between-different-assemblies</guid>
	<pubDate>Tue, 25 Jan 2022 17:59:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43722/crossmap-program-for-genome-coordinates-conversion-between-different-assemblies</link>
	<title><![CDATA[CrossMap: program for genome coordinates conversion between different assemblies]]></title>
	<description><![CDATA[<p><span>CrossMap is a program for genome coordinates conversion between&nbsp;</span><em>different assemblies</em><span>&nbsp;(such as&nbsp;</span><a href="http://www.ncbi.nlm.nih.gov/assembly/2928/">hg18 (NCBI36)</a><span>&nbsp;&lt;=&gt;&nbsp;</span><a href="http://www.ncbi.nlm.nih.gov/assembly/2758/">hg19 (GRCh37)</a><span>). It supports commonly used file formats including&nbsp;</span><a href="https://samtools.github.io/hts-specs/SAMv1.pdf">BAM</a><span>,&nbsp;</span><a href="https://en.wikipedia.org/wiki/CRAM_(file_format)">CRAM</a><span>,&nbsp;</span><a href="https://en.wikipedia.org/wiki/SAM_(file_format)">SAM</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/goldenPath/help/wiggle.html">Wiggle</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/goldenPath/help/bigWig.html">BigWig</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/FAQ/FAQformat.html#format1">BED</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/FAQ/FAQformat.html#format3">GFF</a><span>,&nbsp;</span><a href="https://genome.ucsc.edu/FAQ/FAQformat.html#format4">GTF</a><span>,&nbsp;</span><a href="https://docs.gdc.cancer.gov/Data/File_Formats/MAF_Format/">MAF</a><span>&nbsp;</span><a href="https://samtools.github.io/hts-specs/VCFv4.2.pdf">VCF</a><span>, and&nbsp;</span><a href="https://sites.google.com/site/gvcftools/home/about-gvcf">gVCF</a><span>.</span></p><p>Address of the bookmark: <a href="http://crossmap.sourceforge.net/" rel="nofollow">http://crossmap.sourceforge.net/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44789/kallisto-vs-salmon-choosing-the-right-tool-for-rna-seq-quantification</guid>
	<pubDate>Fri, 02 May 2025 06:28:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44789/kallisto-vs-salmon-choosing-the-right-tool-for-rna-seq-quantification</link>
	<title><![CDATA[Kallisto vs Salmon: Choosing the Right Tool for RNA-Seq Quantification]]></title>
	<description><![CDATA[<p>In the world of transcriptomics, quantifying gene and transcript expression accurately and efficiently is crucial. With the explosion of RNA-Seq data, researchers have turned to fast, alignment-free tools that streamline the quantification process without compromising accuracy. Two leading tools in this space are&nbsp;<span>Kallisto</span>&nbsp;and&nbsp;<span>Salmon</span>. Both tools are highly efficient and widely used in the bioinformatics community, but they differ in subtle yet important ways. If you're unsure which one to use for your next RNA-Seq project, this post is for you.</p><h2>What Are Kallisto and Salmon?</h2><p>At their core, both&nbsp;<span>Kallisto</span>&nbsp;and&nbsp;<span>Salmon</span>&nbsp;are tools for&nbsp;<span>quantifying transcript abundance</span>&nbsp;from RNA-Seq reads. They bypass traditional alignment-based methods, replacing them with&nbsp;<span>pseudoalignment</span>&nbsp;or&nbsp;<span>quasi-mapping</span>, which drastically speeds up the process.</p><ul>
<li><span>Kallisto</span>&nbsp;was developed by Lior Pachter&rsquo;s lab and introduced the concept of&nbsp;<em>pseudoalignment</em>&nbsp;using a de Bruijn graph.</li>
<li><span>Salmon</span>, developed by Rob Patro&rsquo;s group, builds on this idea with&nbsp;<em>quasi-mapping</em>&nbsp;and offers additional features like advanced bias correction.</li>
</ul><h2>Head-to-Head Comparison</h2><h3>1. Algorithm</h3><ul>
<li><span>Kallisto</span>&nbsp;uses&nbsp;<em>pseudoalignment</em>, focusing on matching k-mers from reads to a transcriptome index.</li>
<li><span>Salmon</span>&nbsp;uses&nbsp;<em>quasi-mapping</em>, which adds more flexibility and can also work with aligned reads (BAM files).</li>
</ul><h3>2. Input and Flexibility</h3><ul>
<li><span>Kallisto</span>&nbsp;works with raw FASTQ reads and requires a custom transcriptome index.</li>
<li><span>Salmon</span>&nbsp;accepts FASTQ or pre-aligned BAM files, giving you more workflow options.</li>
</ul><h3>3. Bias Correction</h3><p>One of Salmon&rsquo;s major advantages is its sophisticated bias correction system. It corrects for:</p><ul>
<li>Sequence-specific bias</li>
<li>Positional bias</li>
<li>GC-content bias</li>
</ul><p>Kallisto offers basic sequence bias correction but lacks the comprehensive models found in Salmon.</p><h3>4. Speed and Resources</h3><ul>
<li><span>Kallisto</span>&nbsp;is blazing fast and slightly more memory-efficient.</li>
<li><span>Salmon</span>&nbsp;is still very fast, but the added features can come at a small computational cost.</li>
</ul><h3>5. Output and Downstream Analysis</h3><ul>
<li>Both tools provide transcript-level quantifications and support bootstrapping for variance estimation.</li>
<li><span>Salmon</span>&nbsp;can also summarize counts at the gene level if provided with a mapping file (<code>--geneMap</code>).</li>
<li>Kallisto integrates seamlessly with&nbsp;<span>Sleuth</span>&nbsp;for differential expression analysis.</li>
<li>Salmon works well with&nbsp;<span>tximport</span>,&nbsp;<span>DESeq2</span>,&nbsp;<span>edgeR</span>, and other Bioconductor tools.</li>
</ul><h2>Choosing the Right Tool</h2><table>
<thead>
<tr><th>Goal</th><th>Recommended Tool</th></tr>
</thead>
<tbody>
<tr>
<td>Maximum speed</td>
<td>Kallisto</td>
</tr>
<tr>
<td>Advanced bias correction</td>
<td>Salmon</td>
</tr>
<tr>
<td>Use BAM files</td>
<td>Salmon</td>
</tr>
<tr>
<td>Transcript-level quantification with Sleuth</td>
<td>Kallisto</td>
</tr>
<tr>
<td>Integration with DESeq2/edgeR</td>
<td>Salmon</td>
</tr>
</tbody>
</table><h2>Example Command Lines</h2><p><span>Kallisto</span>&nbsp;(paired-end):</p><pre><code>kallisto quant -i transcriptome.idx -o output -b 100 sample_R1.fastq sample_R2.fastq
</code></pre><p><span>Salmon</span>&nbsp;(paired-end, bias correction):</p><pre><code>salmon quant -i salmon_index -l A -1 sample_R1.fastq -2 sample_R2.fastq \
  -p 8 --validateMappings --seqBias --gcBias -o output
</code></pre><h2>Conclusion</h2><p>Both Kallisto and Salmon are exceptional tools that have transformed RNA-Seq analysis. Your choice largely depends on your priorities&mdash;whether it's speed, accuracy, flexibility, or compatibility with downstream tools.</p><p>For many users,&nbsp;<span>Salmon</span>&nbsp;offers a more complete and flexible solution, especially when bias correction and gene-level outputs are essential. However,&nbsp;<span>Kallisto</span>&nbsp;remains a favorite for quick, accurate quantification, especially when paired with the&nbsp;<span>Sleuth</span>&nbsp;pipeline.</p>]]></description>
	<dc:creator>BioStar</dc:creator>
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