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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37993?offset=440</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44508/a-web-based-tool-for-sequence-alignment-statistics-and-innovative-visualization</guid>
	<pubDate>Thu, 04 Apr 2024 01:44:50 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44508/a-web-based-tool-for-sequence-alignment-statistics-and-innovative-visualization</link>
	<title><![CDATA[A web-based tool for sequence alignment statistics and innovative visualization]]></title>
	<description><![CDATA[<p>AlignStatPlot, a new R package and online tool that is well-documented and easy-to usefor MSA and post-MSA analysis. This tool performs both traditional and cutting-edge analy-ses on sequencing data and generates new visualisation methods for MSA results. Whencompared to currently available tools, AlignStatPlot provides a robust ability to handle andvisualise diversity data, while the online version will save time and encourage researchersto focus on explaining their findings. It is a simple tool that can be used in conjunction withpopulation genetics software (PDF) AlignStatPlot: An R package and online tool for robust sequence alignment statistics and innovative visualization of big data.</p><p>Address of the bookmark: <a href="https://bioinformatics.um6p.ma/AlignStatPlot/" rel="nofollow">https://bioinformatics.um6p.ma/AlignStatPlot/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/1720/postdoctoral-associate-bioinformatics-at-duke-university-medical-center</guid>
  <pubDate>Sat, 10 Aug 2013 18:38:38 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral Associate - Bioinformatics  at Duke University Medical Center]]></title>
  <description><![CDATA[
<p>The Department of Biostatistics and Bioinformatics at Duke University Medical Center is seeking a Postdoctoral Associate for a one year appointment to work on several high-dimensional research projects. The specific goals of the project are to identify genes or molecular markers that are predictive of clinical outcomes in renal and prostate cancer.</p>

<p>Candidates must have: a PhD degree in statistics, biostatistics or bioinformatics, extensive experience in analyzing high-dimensional data (microarray, SNP, CNVs) and of validation approaches. In addition, experience in penalized regression methods, data base manipulation; and strong programming skills in order to conduct Monte Carlo studies and applications (R). Candidate must have excellent communication skills (verbal, written and presentation), a strong proficiency in Linux system.</p>

<p>This position is available immediately and will be filled as soon as possible. Appointment could be extended beyond the first year based on additional funding.</p>

<p>For more information about the Department of Biostatistics and Bioinformatics, please visit our website: http://www.biostat.duke.edu.</p>

<p>For more info: http://biostat.duke.edu/sites/biostat.duke.edu/files/Halabi%20-%20Postdoc%20Job%20Posting%202013%20updated.pdf</p>

<p>Duke University is an Equal Opportunity/Affirmative Action Employer.</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/6302/a-allele-of-slc24a5-gene-is-found-to-be-responsible-for-variation-in-skin-color-of-south-east-asians-and-europeans</guid>
	<pubDate>Tue, 12 Nov 2013 21:02:27 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/6302/a-allele-of-slc24a5-gene-is-found-to-be-responsible-for-variation-in-skin-color-of-south-east-asians-and-europeans</link>
	<title><![CDATA[A-allele of SLC24A5 gene is found to be responsible for variation in skin color of South-East Asians and Europeans]]></title>
	<description><![CDATA[<p><strong>Key finding</strong>:</p><ol>
<li><span>rs1426654 SNP of <em>SLC24A5</em>&nbsp;gene is decider of skin pigmentation variation in South Asia</span></li>
<li><span><span>rs1426654-A allele is widely spread throughout the Indian subcontinent&nbsp;</span></span></li>
<li><span>Skin pigmentation is also account by the combination of processes like selection and demographic history of populations affected by their language and origin</span></li>
<li><span><span>Sign of positive selection in Europeans, Middle East, Pakistan, Central Asia and North India but not in South India</span></span></li>
<li><span><span>In European , A-allele is almost reached to fixation</span></span></li>
</ol><p><span><span><strong>Paper</strong>:</span></span></p><p><span><span><a href="http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1003912">http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1003912</a></span></span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44675/variant-calling-pipeline</guid>
	<pubDate>Sat, 19 Oct 2024 12:23:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44675/variant-calling-pipeline</link>
	<title><![CDATA[Variant Calling Pipeline]]></title>
	<description><![CDATA[<p dir="auto">The&nbsp;<a href="https://github.com/Tom-Jenkins/maerl-wgs-pipelines/blob/main/src/variantcalling.nf"><code>variantcalling.nf</code></a>&nbsp;nextflow script will take any number of samples with paired-end reads in FASTQ format, map reads using Bowtie2, process BAM files, and finally call variants using BCFtools v1.21 and/or Freebayes v1.3.6. If part of the pipeline is unsuccessful for a sample then these errors are ignored.</p>
<p dir="auto">Pipeline flowchart:</p>
<div dir="auto">
<div dir="auto">
<div>&nbsp;</div>
<div></div>
</div>
<div>&nbsp;</div>
<div dir="auto">
<h2 dir="auto">Dependencies (version tested)</h2>
<a href="https://github.com/Tom-Jenkins/nextflow-pipelines/blob/main/docs/variant-calling.md#dependencies-version-tested"></a></div>
<ul dir="auto">
<li>Nextflow (24.04.4)</li>
<li>Java (18.0.2.1)</li>
<li>Python (3.10)</li>
<li>Perl (5.32.1)</li>
<li>Bowtie2 (2.5.3)</li>
<li>SAMtools (1.19.2)</li>
<li>GATK4 (4.5)</li>
<li>BCFtools (1.21)</li>
<li>Freebayes (1.3.6)</li>
</ul>
</div><p>Address of the bookmark: <a href="https://github.com/Tom-Jenkins/nextflow-pipelines/blob/main/docs/variant-calling.md" rel="nofollow">https://github.com/Tom-Jenkins/nextflow-pipelines/blob/main/docs/variant-calling.md</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40705/malva-genotyping-by-mapping-free-allele-detection-of-known-variants</guid>
	<pubDate>Tue, 28 Jan 2020 03:39:22 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40705/malva-genotyping-by-mapping-free-allele-detection-of-known-variants</link>
	<title><![CDATA[MALVA: Genotyping by Mapping-free ALlele Detection of Known VAriants]]></title>
	<description><![CDATA[<p id="p0010">MALVA is able to genotype multi-allelic SNPs and indels without mapping reads</p>
<p id="p0015">MALVA calls correctly more indels than the most widely adopted genotyping pipelines</p>
<p id="p0020">Mapping-free approaches are as accurate as alignment-based ones, while being faster</p>
<p>More at&nbsp;<a href="https://www.sciencedirect.com/science/article/pii/S2589004219302366">https://www.sciencedirect.com/science/article/pii/S2589004219302366</a></p>
<p><a href="https://www.sciencedirect.com/science/article/pii/S2589004219302366">https://www.sciencedirect.com/science/article/pii/S2589004219302366</a></p><p>Address of the bookmark: <a href="https://github.com/AlgoLab/malva" rel="nofollow">https://github.com/AlgoLab/malva</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/13226/you-and-your-friend-have-similar-dna</guid>
	<pubDate>Sun, 27 Jul 2014 20:44:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/13226/you-and-your-friend-have-similar-dna</link>
	<title><![CDATA[You and your friend have similar DNA !!!]]></title>
	<description><![CDATA[<p>New research out of Massachusetts claims that people often choose friends that are similar to them in genetics and they are more accurate than you might suppose. A study published on PNAS&nbsp;http://www.pnas.org/content/111/Supplement_3/10796.full found that people are apt to pick friends who are genetically similar to themselves - so much so that friends tend to be as alike at the genetic level as a person's fourth cousin.</p><div style="text-align: center;"><img src="http://i.kinja-img.com/gawker-media/image/upload/s--CwLwHa43--/18fbmlokxcmqcjpg.jpg" alt="image" width="300" height="271" style="border: 0px; border: 0px;"></div><p>Scientists with a long-running Framingham Heart Study looked at 1,932 people (examination of about 1.5 million markers of genetic variations), comparing unrelated friends to unrelated strangers. They found that friends shared about 1% of their genes &mdash; a percentage much higher than those shared with strangers.This new findings made it clear that people have more DNA in common with those who are selected as friends than with strangers in the same population.&nbsp;</p><p>The genes that lined up the most were olfactory genes, which deal with smell. The ones that lined up the least were immune system genes. The researchers weren't sure why that happened :/. Olfactory genes might be a straightforward explanation: People who like the same smells tend to be drawn to similar environments, where they meet others with the same tendencies.</p><p>Reference:</p><p>http://www.pnas.org/content/111/Supplement_3/10796.full</p><p>Image : http://i.kinja-img.com</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/43607/classification-of-sars-cov2-variant</guid>
	<pubDate>Fri, 26 Nov 2021 12:53:12 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/43607/classification-of-sars-cov2-variant</link>
	<title><![CDATA[Classification of SARS-CoV2 Variant !]]></title>
	<description><![CDATA[<p>The scientists established some guidelines for determining whether a variant is a legitimate branch of an existing lineage:</p><p>The variant should be transmitted from its original location to another "geographically distinct population"&mdash;say, another country or a province of a large and populous country.<br />It should differ from its ancestor by at least one nucleotide.<br />At least 95% of its genetic code should have been sequenced at least five times from different samples.</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38004/vcfr-a-package-to-manipulate-and-visualize-vcf-data-in-r</guid>
	<pubDate>Thu, 25 Oct 2018 09:05:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38004/vcfr-a-package-to-manipulate-and-visualize-vcf-data-in-r</link>
	<title><![CDATA[vcfR:  a package to manipulate and visualize VCF data in R]]></title>
	<description><![CDATA[<p><span>VcfR is an R package intended to allow easy manipulation and visualization of variant call format (VCF) data. Functions are provided to rapidly read from and write to VCF files. Once VCF data is read into R a parser function extracts matrices from the VCF data for use with typical R functions. This information can then be used for quality control or other purposes. Additional functions provide visualization of genomic data. Once processing is complete data may be written to a VCF file or converted into other popular R objects (e.g., genlight, DNAbin). VcfR provides a link between VCF data and the R environment connecting familiar software with genomic data.</span></p><p>Address of the bookmark: <a href="https://github.com/knausb/vcfR" rel="nofollow">https://github.com/knausb/vcfR</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<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/37259/epiviz-an-interactive-visualization-tool-for-functional-genomics-data</guid>
	<pubDate>Mon, 09 Jul 2018 05:27:39 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37259/epiviz-an-interactive-visualization-tool-for-functional-genomics-data</link>
	<title><![CDATA[Epiviz: an interactive visualization tool for functional genomics data.]]></title>
	<description><![CDATA[<p><span>Epiviz is an interactive visualization tool for functional genomics data. It supports genome navigation like other genome browsers, but allows multiple visualizations of data within genomic regions using scatterplots, heatmaps and other user-supplied visualizations. It also includes data from the&nbsp;</span><a href="http://barcode.luhs.org/" target="_blank">Gene Expression Barcode project</a><span>&nbsp;for transcriptome visualization. It has a flexible plugin framework so users can add</span><a href="http://d3js.org/" target="_blank">d3</a><span>&nbsp;visualizations. You can see a video tour&nbsp;</span><a href="http://youtu.be/099c4wUxozA" target="_blank">here</a><span>.</span></p>
<p><span>https://bioconductor.org/packages/release/bioc/html/epivizr.html</span></p>
<p><span>https://github.com/epiviz</span></p>
<p><span>https://github.com/epiviz/epiviz</span></p><p>Address of the bookmark: <a href="https://epiviz.github.io/" rel="nofollow">https://epiviz.github.io/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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