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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37498?offset=40</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38634/eyechrom-visualizing-chromosome-count-data-from-plants</guid>
	<pubDate>Tue, 08 Jan 2019 10:20:54 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38634/eyechrom-visualizing-chromosome-count-data-from-plants</link>
	<title><![CDATA[EyeChrom: Visualizing Chromosome Count Data From Plants]]></title>
	<description><![CDATA[<p><span>It's goal is to show chromosmal data per genus. Select the genus, and the plot will show the records found for it in the Chromosome Counts Database. note: Report an issue via Gihub: github.com/roszenil/CCDBcurator and github.com/RodrigoRivero/EyeChrom</span></p>
<p>https://bsapubs.onlinelibrary.wiley.com/doi/pdf/10.1002/aps3.1207</p><p>Address of the bookmark: <a href="http://eyechrom.com:3838/EyeChrom/" rel="nofollow">http://eyechrom.com:3838/EyeChrom/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41328/deephic-a-generative-adversarial-network-for-enhancing-hi-c-data-resolution</guid>
	<pubDate>Tue, 03 Mar 2020 01:12:47 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41328/deephic-a-generative-adversarial-network-for-enhancing-hi-c-data-resolution</link>
	<title><![CDATA[DeepHiC: A Generative Adversarial Network for Enhancing Hi-C Data Resolution]]></title>
	<description><![CDATA[<p><strong>DeepHiC</strong> is a GAN-based model for enhancing Hi-C data resolution. We developed this server for helping researchers to enhance their own low-resolution data by a few steps of clicks. <em>Ab initio</em> training could be performed according to our published <a href="https://github.com/omegahh/DeepHiC">code</a>. We provided trained models for various depth of low-coverage sequencing Hi-C data. The depth of input data is estimated by its distribution comparing with those of the downsampled Hi-C data we used in training</p><p>Address of the bookmark: <a href="http://sysomics.com/deephic" rel="nofollow">http://sysomics.com/deephic</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43374/reference-sequence-resource</guid>
	<pubDate>Wed, 15 Sep 2021 21:15:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43374/reference-sequence-resource</link>
	<title><![CDATA[Reference Sequence Resource!]]></title>
	<description><![CDATA[<p><span>The ENCODE project uses Reference Genomes from&nbsp;</span><a href="http://www.ncbi.nlm.nih.gov/genome/browse/reference/">NCBI</a><span>&nbsp;or&nbsp;</span><a href="http://hgdownload.cse.ucsc.edu/downloads.html">UCSC</a><span>&nbsp;to provide a consistent framework for mapping high-throughput sequencing data.&nbsp;In general, ENCODE data are mapped consistently to 2 human (GRCH38, hg19) and 2 mouse (mm9/mm10) genomes for historical comparability.&nbsp;</span><em>Drosophia melanogaster</em><span>&nbsp;experiments are mapped to either dm3 or dm6 and&nbsp;</span><em>Caenorhabdilis elegans&nbsp;</em><span>experiments are mapped to ce10 or ce11.&nbsp;T</span></p><p>Address of the bookmark: <a href="https://www.encodeproject.org/data-standards/reference-sequences/" rel="nofollow">https://www.encodeproject.org/data-standards/reference-sequences/</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/44751/large-language-models-in-bioinformatics-transforming-data-analysis-and-interpretation</guid>
	<pubDate>Thu, 02 Jan 2025 11:26:29 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/44751/large-language-models-in-bioinformatics-transforming-data-analysis-and-interpretation</link>
	<title><![CDATA[Large Language Models in Bioinformatics: Transforming Data Analysis and Interpretation]]></title>
	<description><![CDATA[<p>The integration of artificial intelligence (AI) into bioinformatics has ushered in a new era of computational biology. Among the most transformative advancements are large language models (LLMs), such as GPT and BERT, which leverage deep learning to process and interpret vast amounts of text data. These models are reshaping bioinformatics by enhancing data analysis, hypothesis generation, and literature mining.</p><h3>Understanding Large Language Models</h3><p>LLMs are AI systems trained on extensive datasets of natural language. Their ability to model context, identify patterns, and generate coherent language has proven invaluable across domains, including bioinformatics. By fine-tuning these models on biological datasets, researchers can unlock insights into molecular biology, systems biology, and beyond.</p><h3>Key Applications of LLMs in Bioinformatics</h3><h4>1. <strong>Annotating Biological Data</strong></h4><p>Annotating genomic and proteomic data is fundamental yet labor-intensive. LLMs streamline this process by extracting functional annotations from literature and databases, predicting gene and protein functions, and providing automated insights.</p><h4>2. <strong>Mining Scientific Literature</strong></h4><p>The exponential growth of publications presents a challenge for researchers to stay updated. LLMs can process large volumes of text to extract key findings, summarize papers, and identify trends, thereby facilitating efficient literature reviews.</p><h4>3. <strong>Predicting Gene and Protein Functions</strong></h4><p>By leveraging sequence data and annotations, LLMs can predict the functions of uncharacterized genes and proteins. This capability is particularly useful for studying non-model organisms and orphan genes.</p><h4>4. <strong>Drug Discovery and Repurposing</strong></h4><p>LLMs enable pattern recognition across chemical, genomic, and clinical datasets, identifying novel drug candidates and repurposing existing drugs for new therapeutic targets. They can simulate interactions between drugs and biological molecules, accelerating the discovery pipeline.</p><h4>5. <strong>Generating Hypotheses for Research</strong></h4><p>LLMs analyze complex datasets to propose testable hypotheses. For example, they can predict protein-protein interactions, identify regulatory motifs, or model evolutionary processes in genomes.</p><h3>Advantages of LLMs in Bioinformatics</h3><ul>
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<p><strong>Scalability:</strong> LLMs process massive datasets rapidly, reducing the time required for data analysis.</p>
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<p><strong>Versatility:</strong> These models adapt to diverse bioinformatics tasks, from genomic annotation to network analysis.</p>
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<p><strong>Contextual Insights:</strong> By synthesizing information across disparate datasets, LLMs provide integrative insights into biological systems.</p>
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</ul><h3>Challenges in Applying LLMs</h3><p>Despite their promise, LLMs face limitations:</p><ul>
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<p><strong>Data Quality and Bias:</strong> Inaccurate or biased datasets can affect model predictions, necessitating rigorous data curation.</p>
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<p><strong>Interpretability:</strong> Understanding the decision-making process of LLMs remains a critical challenge, especially in high-stakes fields like genomics and medicine.</p>
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<p><strong>Resource Intensity:</strong> Training and deploying LLMs require substantial computational power, which can limit accessibility.</p>
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<p><strong>Ethical Concerns:</strong> Handling sensitive genomic data raises privacy and security issues, emphasizing the need for ethical guidelines.</p>
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</ul><h3>Future Prospects</h3><p>The continued development of LLMs tailored for bioinformatics promises exciting advancements. Specialized models trained on omics data, open-access platforms, and interdisciplinary collaborations will expand the utility of LLMs. Moreover, integrating LLMs with other AI technologies, such as graph neural networks and reinforcement learning, can unlock deeper biological insights.</p><h3>Conclusion</h3><p>Large language models are revolutionizing bioinformatics by addressing longstanding challenges in data annotation, literature mining, and function prediction. Their ability to analyze complex biological datasets efficiently positions them as indispensable tools for modern research. As bioinformatics embraces AI, the synergy between LLMs and biological sciences holds the potential to unravel the complexities of life with unprecedented precision and scale.</p>]]></description>
	<dc:creator>LEGE</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36403/ngmlr-long-read-mapper-designed-to-align-pacbio-or-oxford-nanopore</guid>
	<pubDate>Wed, 25 Apr 2018 07:30:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36403/ngmlr-long-read-mapper-designed-to-align-pacbio-or-oxford-nanopore</link>
	<title><![CDATA[NGMLR: long-read mapper designed to align PacBio or Oxford Nanopore]]></title>
	<description><![CDATA[<p><span>CoNvex Gap-cost alignMents for Long Reads (ngmlr) is a long-read mapper designed to sensitively align PacBilo or Oxford Nanopore to (large) reference genomes. It was designed to quickly and correctly align the reads, including those spanning (complex) structural variations. Ngmlr uses an SV aware k-mer search to find approximate mapping locations for a read and then a banded Smith-Waterman alignment algorithm to compute the final alignment. Ngmlr uses a convex gap cost model that penalizes gap extensions for longer gaps less than for shorter ones to compute precise alignments. The gap model allows ngmlr to account for both the sequencing error and real genomic variations at the same time and makes it especially effective at more precisely identifying the position of breakpoints stemming from structural variations. The k-mer search helps to detect and split reads that cannot be aligned linearly, enabling ngmlr to reliably align reads to a wide range of different structural variations including nested SVs (e.g. inversions flanked by deletions).</span></p><p>Address of the bookmark: <a href="https://github.com/philres/ngmlr" rel="nofollow">https://github.com/philres/ngmlr</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39098/sda-long-read-sequence-and-assembly-of-segmental-duplications</guid>
	<pubDate>Tue, 05 Mar 2019 10:00:57 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39098/sda-long-read-sequence-and-assembly-of-segmental-duplications</link>
	<title><![CDATA[SDA: Long-read sequence and assembly of segmental duplications]]></title>
	<description><![CDATA[<p><span><span>Segmental Duplication Assembler (SDA; https://github.com/mvollger/SDA) constructs graphs in which paralogous sequence variants define the nodes and long-read sequences provide attraction and repulsion edges, enabling the partition and assembly of long reads corresponding to distinct paralogs.<br></span></span></p>
<p><span><span>https://github.com/mvollger/SDA</span></span></p><p>Address of the bookmark: <a href="https://www.nature.com/articles/s41592-018-0236-3" rel="nofollow">https://www.nature.com/articles/s41592-018-0236-3</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/989/bioinformatics-approach-to-boar-taint</guid>
	<pubDate>Wed, 17 Jul 2013 15:50:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/989/bioinformatics-approach-to-boar-taint</link>
	<title><![CDATA[Bioinformatics approach to Boar Taint]]></title>
	<description><![CDATA[<p><span>Meat products obtained from intact male pigs often produce offensive smell or odour which is recognized as a complex genetic trait called boar taint.Androstenone and Skatole&nbsp;in the fat primarily cause boar taint. Metabolism of androstenone and sex steroids share a common pathway which makes removal of boar taint a very challenging task. Castration is a traditional solution to remove boar taint but it also results in bad quality of meat due to low level of steroids which is objectionable to many consumers. Detected functional variant(s) underlying boar taint compounds can be used as genetic markers in selection of male pigs with reduced boar taint levels. Resequencing of a total of 47 samples belong to Norwegian Landrace (NL) and Duroc (D) pigs with varied boar taint levels were done in Illumina HiSeq2000 to &gt;10X average coverage. Short reads generated from these samples mapped to&nbsp;<em>Sus Scrofa</em>&nbsp;version 10.2 reference assembly using Bowtie2. Alignment file then used for calling SNPs and InDels inside previousy identified QTL regions on SSC5,13, and 7 with the aid of FreeBayes , a variant caller tool. A final list of SNPs was prepared after filtering SNPs on the basis of SNP quality, coverage of SNP allele, functional and structural annotation, and repeats, etc. Selected SNPs will be genotyped in sample population for validation and then used for constructing SNPs haplotypes in close linkage disequilibrium with QTLs and fine mapping of QTLs through association mapping of genotyped SNPs.</span><span>&nbsp;</span></p><p><span>&nbsp;</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/989" length="19688" type="image/jpeg" />
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	<guid isPermaLink="true">https://bioinformaticsonline.com/view/1926</guid>
	<pubDate>Sun, 11 Aug 2013 11:42:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/view/1926</link>
	<title><![CDATA[Want to Know which genome assembler rule the world ?]]></title>
	<description><![CDATA[<p><span><strong>Assemblathon 2</strong>: evaluating de novo methods of genome assembly&nbsp;</span></p><p><span><a href="http://www.gigasciencejournal.com/content/2/1/10/abstract">http://www.gigasciencejournal.com/content/2/1/10/abstract</a></span></p><p><span><a href="http://blogs.nature.com/news/2013/07/genome-assembly-contest-prompts-soul-searching.html">http://blogs.nature.com/news/2013/07/genome-assembly-contest-prompts-soul-searching.html</a></span></p><p><a href="http://assemblathon.org/post/44431915644/feedback-and-analysis-of-the-assemblathon-2-p">http://assemblathon.org/post/44431915644/feedback-and-analysis-of-the-assemblathon-2-p</a></p><p>&nbsp;</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/4195/barber-pole-worm-sheep-pathogen-sequenced</guid>
	<pubDate>Tue, 03 Sep 2013 16:32:18 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/4195/barber-pole-worm-sheep-pathogen-sequenced</link>
	<title><![CDATA[Barber pole worm , sheep pathogen sequenced !!!]]></title>
	<description><![CDATA[<p>Haemonchus contortus is a highly pathogenic parasitic nematode of that can infect a large number of wild and domesticated ruminant species and is the most economically important parasite of sheep and goats worldwide. Scientists at the Wellcome Trust Sanger Institute have sequenced the genome of the barber's pole worm (Haemonchus contortus), which will help to explore the this tropical parasite which&nbsp;been disseminated around the world by livestock movement.&nbsp;</p><p>H. contortus is a member of the superfamily trichostrongyloidea (Strongylida) which contains most of the economically important parasitic nematodes of grazing livestock. These parasites cost the global livestock industry billions of dollars per annum in lost production and drug costs.&nbsp;A common type of clover may be a preventative or palliative for the disease. However, some particular breeds of sheep, such as the Gulf Coast Native from the Southern United States, have been shown to have developed special resistance to H. contortus.</p><p>Getting the full genome can help to tackle the problem and understand the resistance mechanism with an ease. Moreover, the genome could now provide a comprehensive understanding of how treatments against parasitic worms work and point to further new treatments and vaccines.&nbsp;By comparing the genome of the barber's pole worm with those of worms that have acquired drug resistance, researchers expect to reveal information about how and why resistance has occurred. Till now, researchers have uncovered essential information in the fight against drug resistance in worms.</p><p>Reference:</p><p><a href="http://www.fwi.co.uk/articles/28/08/2013/140758/researchers-close-in-on-worm-resistance-in-sheep.htm">http://www.fwi.co.uk/articles/28/08/2013/140758/researchers-close-in-on-worm-resistance-in-sheep.htm</a></p><p><a href="http://www.sciencedaily.com/releases/2013/08/130828103351.htm?utm_source=feedburner&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+sciencedaily%2Fplants_animals+(ScienceDaily%3A+Plants+%26+Animals+News)">http://www.sciencedaily.com/releases/2013/08/130828103351.htm?utm_source=feedburner&amp;utm_medium=feed&amp;utm_campaign=Feed%3A+sciencedaily%2Fplants_animals+(ScienceDaily%3A+Plants+%26+Animals+News)</a></p><p>Image source: Wikipedia</p><p><img src="http://upload.wikimedia.org/wikipedia/commons/8/8e/Haemonchus_contortus.jpg" alt="image" width="800" height="533" style="border: 0px; border: 0px;"></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/6896/dna-tale-of-3-to-4-years-old-serbia-boy</guid>
	<pubDate>Tue, 26 Nov 2013 17:34:00 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/6896/dna-tale-of-3-to-4-years-old-serbia-boy</link>
	<title><![CDATA[DNA tale of 3 to 4 years old Serbia boy]]></title>
	<description><![CDATA[<p><span>The genome of a young boy found underground at Mal&rsquo;ta near Lake Baikal of eastern Siberia around 24,000 years ago came out as close relative of Europeans and Native Indians.</span></p><p><span>Link:</span></p><p><span><a href="http://www.nytimes.com/2013/11/21/science/two-surprises-in-dna-of-boy-found-buried-in-siberia.html?_r=0">http://www.nytimes.com/2013/11/21/science/two-surprises-in-dna-of-boy-found-buried-in-siberia.html?_r=0</a></span></p><p>&nbsp;</p><p><a href="http://www.nature.com/nature/journal/vaop/ncurrent/full/nature12736.html">http://www.nature.com/nature/journal/vaop/ncurrent/full/nature12736.html</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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