Treatise of Computer Science and Bioinformatics
@ReseaproTCSB
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An open access journal where the world of Computer Science and Bioinformatics shakes their hand. Published by @ReseaproJ
Bhubaneswar, Odisha
Joined July 2023
Advanced bioinformatics tool tests approach for the identification of cancer genes.📷#tcsbjournallaunch #ResearchInnovation #journallaunch #computerscience #ScientificDiscovery #bioinformatics #reseapro #reseaprojournals #cancergenes
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AstraZeneca and Benchling have developed FRAGLER, an open-source DNA assembly framework that reduces plasmid construction time from months to 3 weeks and saves 50-90% in costs. Thanks to @AstraZeneca @benchling.#DNAassembly #drugdiscovery #syntheticbiology #automation
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De novo sequencing, QTL mapping (Quantitative Trait Locus), WGS, and lcWGS drive agrigenomics breakthroughs! 🌱 Unveiling genes, traits, and variations for smarter breeding. Let's revolutionize agriculture sustainably! 🚀🧬🌾 #Agrigenomics #Breakthroughs #MedEd @CruzRamirezLab1
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Yet, our adventure continues as we strive to conquer the enigmatic Y chromosome, which remained elusive in this study. Stay tuned for more updates! #humangenomeproject #genome #sequencing #genetics #science #nextgensequencing #humangenomeassembly #gaplessgenome #t2tchm1.
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By sequencing fragments up to 20k and 1 mil. base pairs long, they've triumphantly filled in the remaining gaps of 8 %, revealing the awe-inspiring T2T-CHM13 genome. With approximately 200 million base pairs and an estimated 115 genes, scientific progress is a true marvel.
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Back in 2003, the Human Genome Project achieved a groundbreaking 92% completion, showcasing the ingenuity of the time. But now, armed with cutting-edge long-read sequencing- technologies like PacBio HiFi and Oxford Nanopore, T2T has taken us even further. #dna #chromosome #gene.
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The Telomere to Telomere (T2T) consortium, led by NIH researchers, has embarked on an incredible quest to complete the human genome. #humangenome #genomeassembly #longreadsequencing #pacbio #nanopore #t2t #chm13 #geneticresearch #scientificprogress #breakthrough #Marvel
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🚀 Embark on a journey through the epigenetic code's impact on development, diseases, and more, guided by the synergy of epigenetics and bioinformatics. Let's explore this incredible frontier together! 🌟🧪 #JourneyToTheEpigenome #BioinformaticsAdventures.
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🗄️ Tame the torrent of epigenetic data with the organizational prowess of bioinformatics! Seamlessly manage and integrate data from different studies and platforms, unlocking new levels of understanding. 🗃️💡 #DataHarmonization #BioinformaticsControlTower.
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⚙️ Unlock the intricate web of gene interactions and epigenetic tweaks using network analysis powered by bioinformatics. See the intricate dance of genes and regulatory elements like never before! 🕸️🧬 #GeneNetworksRevealed #BioinformaticsInsight.
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🔍 Detecting epigenetic changes has never been easier! Unearth specific epigenetic patterns across the genome with the wizardry of bioinformatics tools. Let the digital magnifying glass unveil the hidden marks! 🔬🧬 #EpigeneticTreasureHunt #BioinformaticsSleuth.
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🌐 Merge the worlds of epigenetics and omics data through bioinformatics alchemy! Blend epigenetic insights with gene expression and DNA variations to paint a holistic picture of gene control. 🧪🧬📊 #OmicsIntegration #BioinformaticsAlchemy.
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📊 Let bioinformatics be your guide in decoding epigenetic mysteries! Analyzing heaps of epigenomic data? No problem! These tools ensure precision and reliability in unraveling gene expression puzzles. 💻🧬 #DataDrivenDiscovery #BioinformaticsWizardry.
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🧬 Dive into the captivating realm of epigenetics with the help of bioinformatics! Uncover the secrets of gene regulation beyond DNA sequences and discover the power of epigenetic modifications. 🧪🔬 #EpigeneticsUnveiled #BioinformaticsMagic
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Step 7: Saving and Downloading the Alignment.Capture your alignment masterpiece by downloading it in your preferred file format, such as FASTA or Clustal. This allows you to use the alignment for further analysis, share it with collaborators, or proudly showcase your work!.
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Step 6: Refining and Editing the Alignment.Fine-tune your alignment using the available tools and options. Remove unwanted gaps, trim sequences, or adjust the display settings to optimize the visualization. Mold it to perfection! #bioinformaticscareers.#bioinformaticseducation.
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Step 5: Analyzing the Results.Once the alignment is complete, immerse yourself in the results page. Marvel at the visual representation of the multiple sequence alignment (MSA), showcasing the aligned sequences and their similarities. Discover the patterns hidden within!.
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Step 4: Running the Alignment.Hit that Submit button and let Clustal Omega work its magic! Depending on the size and complexity of your sequences, the alignment process may take a few moments. Be patient, and the alignment will soon be revealed! #bioinformaticsjobs.
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