BioCode: Learning Bioinformatics
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Exploring the vast universe of molecules with PubChem: Where every compound tells a story of potential and possibility 🧪🔍 From drug discovery to environmental research, PubChem serves as a beacon of knowledge, guiding scientists towards groundbreaking discoveries and innovative solutions. #PubChem #ChemicalDatabase #Research #Science
We are working on a very large project to identify ncRNAs for therapeutic purposes #bioinformatics
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Unlock the full potential of ATAC-Seq with our expert-led live training sessions starting the 10th February at BioCode! Whether you're diving into Chromatin Accessibility, Nucleosomes, or Histones, our comprehensive curriculum and interactive learning platform will empower you with the skills needed for cutting-edge research.
🔬 ATAC-Seq Live Training Highlights:
✨ Expert-Led Sessions: Join seasoned instructors with hands-on experience in ATAC-Seq methodologies. Gain insights into the latest techniques, best practices, and troubleshooting tips.
📚 Comprehensive Curriculum: Dive deep into the world of ATAC-Seq with our carefully curated training, covering sample preparation, data analysis, and everything in between.
🌐 Interactive Learning Platform: Engage with instructors and fellow participants in a collaborative online environment. Ask questions, participate in discussions, and enhance your understanding through real-time interactions.
🎓 Certificate of Completion: Successfully complete the training and receive a prestigious Certificate of Completion from BioCode, validating your expertise in ATAC-Seq.
🚀 Take Your Research to New Heights: Whether you're a seasoned researcher or just starting with ATAC-Seq, our live training is designed to elevate your skills and accelerate your research projects.
Key Lectures:
In-depth Introduction to ATAC-Seq Data Analysis and Its Biology (Chromatin Accessibility, Nucleosomes, Histones)
Selection and Retrieval of Raw ATAC-Seq Reads
Understanding Raw Reads & FASTQ Files
Introduction to Linux for ATAC-Seq Analysis
In-depth Theory: Quality Control
Hands-on: Preprocess Raw Reads Using FASTQC, FASTP, Trimmomatic & Cutadapt
In-depth Theory: Mapping (Alignment of Raw Reads)
Hands-on: Mapping Preprocessed Reads Against a Reference Genome Using BOWTIE2, BWA-MEM
Hands-on: Deduplication and Post-Alignment Processing
In-depth Theory: Read Counts & Peak Calling (Chromatin Accessibility Identification)
In-depth Theory: MACS2 & HOMER
Hands-on: Peak Calling Using MACS
Hands-on: Differential Peak Calling Using HOMER
Theory: Downstream Functional Enrichment Analysis
Hands-on: Gene Ontology Analysis Using topGO & enrichR
Hands-on: Pathways Analysis Using KEGG, PANTHER, Reactome
Don't miss out on this opportunity to enhance your skills and make breakthroughs in your research. Secure your spot now for the live training sessions!
📅 Date: 20th February 2024
📍 Location: Online
Network analysis, hub genes and transcription factors identification - available!
Get fastest molecular docking services for your ligands and proteins
• RNA-Seq course: A course that teaches how to use RNA-Seq, a next-generation sequencing method, to identify genes and pathways related to diseases or conditions.
• Course content: The course covers the basics of NGS, the RNA-Seq workflow, data preparation, quality control, mapping, quantification, differential expression analysis, visualization, and gene ontology and pathway analysis.
• Course benefits: The course provides an in-demand skill for analyzing high-throughput sequencing data, which is useful for researchers in various fields of biology and medicine.
• Course enrollment: The course is open for anyone who is interested in learning RNA-Seq, especially students and researchers who want to enhance their career prospects.
