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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/44267?</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43362/machine-learning-for-genomics</guid>
	<pubDate>Thu, 09 Sep 2021 11:26:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43362/machine-learning-for-genomics</link>
	<title><![CDATA[Machine Learning for Genomics]]></title>
	<description><![CDATA[<h3>Module 1: Statistics for genomics (2-8 August 2021)</h3>
<ul>
<li>A simple intro to statistical distributions</li>
<li>hypothesis testing</li>
<li>linear models.</li>
</ul>
<p>reading:&nbsp;<a href="http://compgenomr.github.io/book/stats.html">http://compgenomr.github.io/book/stats.html</a></p>
<p>slides:&nbsp;<a href="https://github.com/BIMSBbioinfo/compgen2021/tree/main/week1/compgen2021_stats.pdf">https://github.com/BIMSBbioinfo/compgen2021/tree/main/week1/compgen2021_stats.pdf</a></p>
<p>exercises+code:&nbsp;<a href="https://github.com/BIMSBbioinfo/compgen2021/tree/main/week1/">https://github.com/BIMSBbioinfo/compgen2021/tree/main/week1/</a></p>
<h3><a href="https://github.com/BIMSBbioinfo/compgen2021#module-2-unsupervised-learning-for-genomics-9-15-august-2021"></a>Module 2: Unsupervised learning for genomics (9-15 August 2021)</h3>
<ul>
<li>Understanding basic intuition behind machine learning approaches.</li>
<li>Using unsupervised learning to cluster and visualise data points</li>
<li>Dimension reduction techniques for visualisation and as input to clustering methods</li>
</ul>
<p>reading:&nbsp;<a href="http://compgenomr.github.io/book/unsupervisedLearning.html">http://compgenomr.github.io/book/unsupervisedLearning.html</a></p>
<p>slides:&nbsp;<a href="https://github.com/BIMSBbioinfo/compgen2021/tree/main/week2/compgen2021_unsupervisedLearning.pdf">https://github.com/BIMSBbioinfo/compgen2021/tree/main/week2/compgen2021_unsupervisedLearning.pdf</a></p>
<p>exercises+code:&nbsp;<a href="https://github.com/BIMSBbioinfo/compgen2021/tree/main/week2/">https://github.com/BIMSBbioinfo/compgen2021/tree/main/week2/</a></p>
<h3><a href="https://github.com/BIMSBbioinfo/compgen2021#module-3-supervised-learning-for-genomics-16-22-august-2021"></a>Module 3: Supervised learning for genomics (16-22 August 2021)</h3>
<ul>
<li>Understanding and using supervised learning methods for predictive purposes</li>
<li>How to measure prediction performance</li>
<li>Understand and use cross-validation and related concepts</li>
</ul>
<p>reading:&nbsp;<a href="http://compgenomr.github.io/book/supervisedLearning.html">http://compgenomr.github.io/book/supervisedLearning.html</a></p>
<p>slides:&nbsp;<a href="https://github.com/BIMSBbioinfo/compgen2021/tree/main/week3/compgen2021_supervisedLearning.pdf">https://github.com/BIMSBbioinfo/compgen2021/tree/main/week3/compgen2021_supervisedLearning.pdf</a></p>
<p>exercises+code:&nbsp;<a href="https://github.com/BIMSBbioinfo/compgen2021/tree/main/week3/">https://github.com/BIMSBbioinfo/compgen2021/tree/main/week3/</a></p>
<p>https://github.com/BIMSBbioinfo/compgen2021</p><p>Address of the bookmark: <a href="https://github.com/BIMSBbioinfo/compgen2021" rel="nofollow">https://github.com/BIMSBbioinfo/compgen2021</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44770/nvidia-and-arc-institute-unveil-evo-2-a-breakthrough-ai-for-dna-design</guid>
	<pubDate>Fri, 21 Feb 2025 10:39:47 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44770/nvidia-and-arc-institute-unveil-evo-2-a-breakthrough-ai-for-dna-design</link>
	<title><![CDATA[NVIDIA and Arc Institute Unveil Evo 2: A Breakthrough AI for DNA Design]]></title>
	<description><![CDATA[<p>NVIDIA and the Arc Institute have introduced <strong style="font-size: 12.8px;">Evo 2</strong>, a groundbreaking AI model designed to <strong style="font-size: 12.8px;">understand, predict, and generate DNA sequences</strong>. This marks a major advancement in computational biology, offering scientists an unprecedented tool to decode the genetic blueprint of life and even design entirely new biological systems.</p><h3><strong>The Power of Evo 2: AI Meets DNA</strong></h3><p>Evo 2 is <strong>the largest AI model for biology ever created</strong>, trained on an astonishing <strong>9.3 trillion DNA "letters"</strong> (nucleotides) carefully selected from genomes spanning the entire tree of life. This massive dataset ensures that Evo 2 can recognize patterns and relationships in genetic sequences at an unparalleled scale.</p><p>For the first time, scientists can <strong>design DNA with AI</strong>, moving beyond simple sequence analysis to active DNA generation. Evo 2 enables researchers to <strong>predict, modify, and even create entire genetic sequences</strong>, opening new possibilities in medicine, agriculture, and synthetic biology.</p><h3><strong>Decoding the Dark Genome</strong></h3><p>One of the biggest challenges in genetics is understanding the <strong>non-coding regions</strong> of DNA&mdash;vast stretches of the genome that do not code for proteins but play crucial roles in regulating gene expression. These regions control when and how genes are activated, influencing everything from development to disease.</p><p>Evo 2 is designed to <strong>decode these non-coding elements</strong>, helping researchers uncover their functions and use this knowledge to develop gene-based therapies, synthetic life forms, and precision agriculture solutions.</p><h3><strong>From Reading DNA to Writing It</strong></h3><p>To put Evo 2&rsquo;s impact into perspective:</p><ul>
<li><strong>Previous AI models could "read" DNA</strong> like a book, analyzing genetic sequences and identifying patterns.</li>
<li><strong>Evo 2 can "write" entirely new DNA</strong>, designing functional genes, chromosomes, and even full genomes from scratch.</li>
</ul><p>This means scientists can now <strong>engineer biological systems with AI</strong>, designing new proteins, metabolic pathways, and genetic circuits to address real-world challenges.</p><h3><strong>A Step Toward Generative Biology</strong></h3><p>The Arc Institute describes Evo 2 as a major step toward <strong>"generative biology"</strong>&mdash;a revolutionary approach where AI is used to create <strong>novel biological structures</strong> rather than just analyzing existing ones. This could lead to breakthroughs such as:</p><ul>
<li><strong>New medicines</strong>: AI-generated enzymes and proteins tailored for targeted therapies.</li>
<li><strong>Disease-resistant crops</strong>: Genetically optimized plants for higher yield and climate resilience.</li>
<li><strong>Synthetic organisms</strong>: Custom-designed microbes for bioremediation, biofuel production, and industrial applications.</li>
</ul><h3><strong>An Open-Source Revolution</strong></h3><p>Unlike many proprietary AI models, <strong>Evo 2 is open source</strong>, making its capabilities accessible to researchers worldwide. This democratization of AI-driven biology means that scientists from different disciplines can <strong>collaborate, experiment, and innovate</strong>, accelerating discoveries in genetic engineering and synthetic biology.</p><p>With Evo 2, the boundaries of what&rsquo;s possible in <strong>DNA design, genetic engineering, and biological innovation</strong> are being redrawn. The future of life sciences is no longer just about understanding life&rsquo;s code&mdash;it&rsquo;s about writing it.</p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/43008/list-of-useful-machine-ai-learning-resources</guid>
	<pubDate>Tue, 30 Mar 2021 08:56:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/43008/list-of-useful-machine-ai-learning-resources</link>
	<title><![CDATA[List of useful machine / ai learning resources !]]></title>
	<description><![CDATA[<p>ML&nbsp;cheatsheet !</p><p>https://github.com/remicnrd/ml_cheatsheet</p><p>Visual AI / ML</p><p>https://setosa.io/ev/</p><p>Simple and efficient tools for predictive data analysis</p><p><span>https://scikit-learn.org/stable/</span></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/45216/the-best-free-crash-course-on-large-language-models-llms-ive-come-across</guid>
	<pubDate>Tue, 04 Aug 2026 04:57:00 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/45216/the-best-free-crash-course-on-large-language-models-llms-ive-come-across</link>
	<title><![CDATA[The Best Free Crash Course on Large Language Models (LLMs) I&#039;ve Come Across]]></title>
	<description><![CDATA[<div><div><div><div><div><div><div><div dir="auto"><div><div><p><strong>Stanford CME 295: Transformers &amp; Large Language Models</strong> course by Afshine Amidi and Shervine Amidi. The official course website contains the syllabus, slides, and links to all lecture recordings.</p><h3>Official course</h3><ul>
<li><a href="https://cme295.stanford.edu/?utm_source=chatgpt.com" target="_blank">Stanford CME 295 &ndash; Transformers &amp; Large Language Models</a></li>
</ul><h3>Official YouTube playlist</h3><ul>
<li><a href="https://www.youtube.com/playlist?list=PLoROMvodv4rOCXd21gf0CF4xr35yINeOy&amp;utm_source=chatgpt.com" target="_blank">Stanford Online &ndash; CME 295 Playlist</a></li>
</ul><h3>Course schedule</h3><ol>
<li><strong>Transformer</strong> &ndash; Tokenization, embeddings, attention, Transformer architecture</li>
<li><strong>Transformer-Based Models &amp; Tricks</strong> &ndash; RoPE, MQA/GQA, BERT variants</li>
<li><strong>Large Language Models</strong> &ndash; GPT, MoE, prompting, Chain-of-Thought</li>
<li><strong>LLM Training</strong> &ndash; Pretraining, SFT, LoRA, optimization</li>
<li><strong>LLM Tuning</strong> &ndash; RLHF, DPO, preference tuning</li>
<li><strong>LLM Reasoning</strong> &ndash; Reasoning models, GRPO, scaling</li>
<li><strong>Agentic LLMs</strong> &ndash; RAG, tool calling, ReAct, agents</li>
<li><strong>LLM Evaluation</strong> &ndash; LLM-as-a-Judge, benchmarks, biases</li>
<li><strong>Current Trends &amp; Recap</strong> &ndash; Vision Transformers, diffusion-based LLMs, future directions</li>
</ol><p>If you're looking for a <strong>research-level understanding</strong> of LLMs (beyond prompt engineering), this is one of the best freely available university courses currently available. It pairs particularly well with:</p><ul>
<li><a href="https://huggingface.co/learn/nlp-course?utm_source=chatgpt.com" target="_blank">Hugging Face NLP Course</a></li>
<li><a href="https://www.deeplearning.ai/courses/how-transformer-llms-work?utm_source=chatgpt.com" target="_blank">DeepLearning.AI &ndash; How Transformer LLMs Work</a></li>
<li><a href="https://developers.google.com/machine-learning/crash-course/llm/transformers?utm_source=chatgpt.com" target="_blank">Google Machine Learning Crash Course &ndash; LLMs</a></li>
</ul></div></div></div></div></div></div></div></div></div></div>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/43227/project-associate-i-project-associate-ii-senior-project-associate-igib</guid>
  <pubDate>Thu, 05 Aug 2021 16:11:32 -0500</pubDate>
  <link></link>
  <title><![CDATA[Project Associate-I | Project Associate-II | Senior Project Associate @ IGIB]]></title>
  <description><![CDATA[
<p>Experience in Next Generation Sequencing (NGS) application and interest in Genomics/ Clinical / Translational Applications. OR Good computational programming skills and deep interest in working on interface of Genomics and Clinical application. </p>

<p>Project Scientist-I <br />Experimental / Computation analysis experience in highthroughput genomics/ clinical application.</p>

<p>Project Manager <br />Experience in handling large biological projects involving high-throughput genomics/ clinical application.</p>

<p>Scientific Administrative Assistant <br />Lab Work. </p>

<p>More at https://vinodscaria.genomes.in/positionsopen</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/39939/automatic-predictive-model-constructor-apmc</guid>
	<pubDate>Mon, 16 Sep 2019 09:43:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/39939/automatic-predictive-model-constructor-apmc</link>
	<title><![CDATA[Automatic Predictive Model Constructor - APMC]]></title>
	<description><![CDATA[<div><div><div><div><div><div><div><div><div><div><div><div><div><div><div>I would like to invite everyone interested in the subject of machine learning in life science, to test <strong>APMC</strong> module,</div><div>it`s a fully automatic tool (created by students) to simply create and develop supervised machine learning models</div><div>for classification and regression purposes. Links to tool, instruction and documentation bellow:</div><div><span style="font-size: 12.8px;"></span></div><ul>
<li><span style="font-size: 12.8px;">APMC:&nbsp;</span><a href="https://gene-calc.pl/apmc?fbclid=IwAR1j51l7qXsL3BuMPb-P5yQhwkmDCiVdoP-qodeCrbu2DbWtxtihRJ0n9-g" target="_blank">https://gene-calc.pl/apmc</a></li>
<li><span>How to use:&nbsp;</span><a href="https://l.facebook.com/l.php?u=https%3A%2F%2Fgene-calc.pl%2Fapmc%2Fhow-to-use%3Ffbclid%3DIwAR3tCwJiegeuVn_ZZ-YPD7lB7UrqGWaab_zItU30MvFKZiuheSEiGUxyZ9Y&amp;h=AT1x8z09NwNUiLjTgNw8Vzg9OLsEjnpHESvjOescfLF-mzjMMqTBnkh5AqHRkOaXwjVHetdQtQO7mgstwke6ivUz-hzT-ifo5TrMBuMm8XMTmvhz7nyDdKmQZ38yyXW942J_47Oj5YxYxWaMDreugIU2ytT2yvxvgKi-FgNo4N7mvYoj_1A5eCuNxHWuGA3voYn0GAWSSR96ZK4gsj3pvqBcCK9Zi2Fo8IoBNK9JZIbtnV9fdvZLMEUryCoWEceZkMX-76jmGinOXss5L3AGp_6oSUr_aFus73B4q5PXMbKubUoU4inr-0kVoO0werx5YNPWdgXtpiyD6TKXQIhI6lDtyi2jx645A5CKqW-nARPqKwa-Iwtt-KGoNyHvcSnhvfLPK9n4Lhs8W6PK9ZeobOqHwm4y1C1my-N4dvlmvGBWTgSj_E31e0GIhYxvI9Uk3nREVnMw3lfD20BTmwL-wfhSidm8Lue_Akn1Flpfcl0jP1DBpkcwJ3OMxDVA82bL4lcsGmyLGedXjrpKAiVGF3R_e57r9EeI5bWyrbYZGTaHJdOGJBQSvplDir_AfH9Pr5NSRVZOStr13e6XxUIXhCiR58Qua_yuQOsNYBKGN5OP7XAL0DeFIKmI" target="_blank">https://gene-calc.pl/apmc/how-to-use</a></li>
<li><span>Documentation:&nbsp;</span><a href="https://gene-calc.pl/apmc/documentation?fbclid=IwAR1_2agQ8vnqDw0DudUI5UJq3_ip0EFwWR3zyccOynaDlbzkfFmYXnPtFXI" target="_blank">https://gene-calc.pl/apmc/documentation</a></li>
</ul></div></div></div></div></div></div></div></div></div></div></div></div></div></div>]]></description>
	<dc:creator>Jan Bińkowski</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/4882/detect-the-sequence-pattern-and-its-location-in-fasta-file-with-match-and-mismatches-information</guid>
	<pubDate>Thu, 26 Sep 2013 15:02:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/4882/detect-the-sequence-pattern-and-its-location-in-fasta-file-with-match-and-mismatches-information</link>
	<title><![CDATA[Detect the sequence pattern and its location in fasta file with match and mismatches information.]]></title>
	<description><![CDATA[<p>This script is one of my old script to detect some centromeric pattern in chromosomes. User can also control the number of mismatches allowed through command line ..</p><p>To run:</p><p>perl centro.pl</p>]]></description>
	<dc:creator>Jit</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/4882" length="3596" type="text/x-perl" />
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/11175/next-generation-sequencingngs-books</guid>
	<pubDate>Fri, 30 May 2014 04:48:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/11175/next-generation-sequencingngs-books</link>
	<title><![CDATA[Next generation sequencing(NGS) books]]></title>
	<description><![CDATA[<p>Employing different technologies, the purpose of NGS platform is to decode the identity or modification on the nucleotides. NGS platforms evolve quickly and capture the main stream.</p>
<p>This bookmark is created to provide NGS online books links.</p><p>Address of the bookmark: <a href="http://en.wikibooks.org/wiki/Next_Generation_Sequencing_%28NGS%29/Print_version" rel="nofollow">http://en.wikibooks.org/wiki/Next_Generation_Sequencing_%28NGS%29/Print_version</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44871/10-books-to-kickstart-and-level-up-your-bioinformatics-journey</guid>
	<pubDate>Tue, 12 Aug 2025 03:50:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44871/10-books-to-kickstart-and-level-up-your-bioinformatics-journey</link>
	<title><![CDATA[10 Books to Kickstart (and Level Up) Your Bioinformatics Journey]]></title>
	<description><![CDATA[<p>If you&rsquo;re starting out in bioinformatics or looking to sharpen your computational biology skills, having the right learning resources makes all the difference.<br />Here&rsquo;s my curated list of 10 must-read books &mdash; from beginner-friendly introductions to advanced computational genomics.</p><p>1️⃣ Data Analysis for the Life Sciences<br />A fantastic starting point to learn statistics, R programming, and exploratory data analysis in the context of biology. The best part? It&rsquo;s available free online from HarvardX.</p><p>2️⃣ Practical Computing for Biologists<br />The very first book I picked up when I started learning computational biology. It&rsquo;s beginner-friendly and focuses on essential computing skills every biologist needs.</p><p>3️⃣ A Primer for Computational Biology<br />An open-access, hands-on introduction to computational biology concepts and coding techniques. Perfect if you want to learn through real examples.</p><p>4️⃣ Computational Genomics with R<br />For those who already know R and want to dive deeper into genome-scale data analysis, from sequence alignment to gene expression.</p><p>5️⃣ The Biologist&rsquo;s Guide to Computing<br />Bridges the gap between biological problems and computational thinking, making it easier for life scientists to approach programming and data analysis.</p><p>6️⃣ Bioinformatics Data Skills<br />A must-read to sharpen your bioinformatics toolkit &mdash; from command-line skills to reproducible research workflows. Ideal once you&rsquo;ve covered the basics.</p><p>7️⃣ Bioinformatics Workbook<br />A practical tutorial series to help scientists design bioinformatics projects, analyze data, and understand best practices.</p><p>8️⃣ Modern Statistics for Modern Biology<br />An essential guide to modern statistical methods applied to biology, blending theory with hands-on examples in R.</p><p>9️⃣ Algorithms on Strings, Trees, and Sequences by Dan Gusfield<br />A classic reference for anyone wanting to understand the algorithms behind sequence alignment, genome assembly, and biological data structures.</p><p></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/41496/new-machine-learning-packages-in-r</guid>
	<pubDate>Fri, 27 Mar 2020 12:11:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/41496/new-machine-learning-packages-in-r</link>
	<title><![CDATA[New Machine Learning Packages in R]]></title>
	<description><![CDATA[<h3 id="machine-learning">Machine Learning</h3><p><a href="https://cran.r-project.org/package=autokeras">autokeras</a>&nbsp;v1.0.1: Implements an interface to&nbsp;<a href="https://autokeras.com/">AutoKeras</a>, an open source software library for automated machine learning. See&nbsp;<a href="https://cran.r-project.org/web/packages/autokeras/readme/README.html">README</a>&nbsp;for an example.</p><p><a href="https://cran.r-project.org/package=MTPS">MTPS</a>&nbsp;v0.1.9: Implements functions to predict simultaneous multiple outcomes based on revised stacking algorithms as described in&nbsp;<a href="denied:doi:10.1093/bioinformatics/btz531">Xing et al. (2019)</a>. See the&nbsp;<a href="https://cran.r-project.org/web/packages/MTPS/vignettes/Guide.html">vignette</a>&nbsp;to get started.</p><p><a href="https://cran.r-project.org/package=quanteda.textmodels">quanteda.textmodels</a>&nbsp;v0.9.1: Implements methods for scaling models and classifiers based on sparse matrix objects representing textual data. It includes implementations of the&nbsp;<a href="denied:doi:10.1017/S0003055403000698">Laver et al. (2003)</a>&nbsp;wordscores model, the&nbsp;<a href="denied:arxiv:1710.08963">Perry &amp; Benoit&rsquo;s (2017)</a>&nbsp;class affinity scaling model, and the&nbsp;<a href="denied:doi:10.1111/j.1540-5907.2008.00338.x">Slapin &amp; Proksch (2008)</a>&nbsp;wordfish model. See the&nbsp;<a href="https://cran.r-project.org/web/packages/quanteda.textmodels/vignettes/textmodel_performance.html">vignette</a>&nbsp;to get started.</p><p><a href="https://cran.r-project.org/package=SeqDetect">SeqDetect</a>&nbsp;v1.0.7: Implements the automaton model found in&nbsp;<a href="https://ieeexplore.ieee.org/document/8910574">Krleža, Vrdoljak &amp; Brčić (2019)</a>&nbsp;to detect and process sequences. See the&nbsp;<a href="https://cran.r-project.org/web/packages/SeqDetect/vignettes/SequentialDetector.pdf">vignette</a>&nbsp;for examples and theory.</p><p><a href="https://cran.r-project.org/package=studyStrap">studyStrap</a>&nbsp;v1.0.0: Implements multi-Study Learning algorithms such as Merging, Study-Specific Ensembling (Trained-on-Observed-Studies Ensemble), the Study Strap, and the Covariate-Matched Study Strap. and offers over 20 similarity measures. See&nbsp;<a href="denied:doi:10.1101/856385">Kishida, et al. (2019)</a>&nbsp;for background and the&nbsp;<a href="https://cran.r-project.org/web/packages/studyStrap/vignettes/vignette.html">vignette</a>&nbsp;for how to use the package.</p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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