Sequencing DNA with Linux Cores and Nanopores
Explore real-time DNA sequencing using the Oxford Nanopore MinION device, from sample preparation to data analysis, showcasing the power of portable genomics and open-source software.
A Voyage of DNA, Genes and the Sea
Explore genomics pioneer Craig Venter's groundbreaking expedition to map ocean biodiversity, uncovering millions of genes and revolutionizing our understanding of marine life and DNA.
Reconstructing Every Haplotype with De Novo Assembly
Discover advanced techniques for haplotype-resolved de novo genome assembly, focusing on phased assembly graphs and innovative methods for diploid and polyploid genome reconstruction.
Sequence Data - Part 2
Explore advanced techniques for analyzing and interpreting sequence data, enhancing your bioinformatics skills and research capabilities.
Sequence Data - Part 1
Explore fundamental concepts and techniques for analyzing sequence data in bioinformatics, focusing on DNA and protein sequences.
rhAmpSeq CRISPR Analysis Tool Tutorial
Learn to analyze CRISPR experiments using IDT's rhAmpSeq™ tool. Explore features for efficient data interpretation and result visualization in genome editing projects.
M2GEN's ORIEN Avatar Program: Accelerating Oncology Research with Custom xGen Exome Research Panel
Accelerate oncology research using M2GEN's ORIEN Avatar program and IDT's xGen Exome Panel. Learn about sequencing metrics and use cases.
Automated IDT xGen Hybridization Capture of DNA Libraries on Biomek i7 Hybrid Genomics Workstation
Automate IDT xGen™ hybridization capture for uniform coverage and robust performance. Learn to generate reproducible targeted NGS libraries using Biomek i7 automation for efficiency and consistency.
The History and Future of Whole Exome Sequencing at the McDonnell Genome Institute
Explore the evolution and impact of whole exome sequencing at MGI, including applications, read depth, CNV detection, and gene fusion identification.
The Future of Personalized Genomics: Advancing Hematology Research with NGS
Explore next-generation sequencing's role in advancing hematology research and personalized genomics for improved patient outcomes.
Deciphering the Mysteries of Human Genomes
Explore the intersection of biology, technology, and medicine in rare genetic disease research. Discover how Python aids in unraveling genomic mysteries and advancing healthcare.
Applied Functional Programming in Computational Genomics
Explore functional programming solutions for computational genomics algorithms, focusing on the "read alignment problem" in next-gen DNA sequencing.
Uni-alignment: A Parameter-free Framework for Fast and Accurate Sequence Alignment
Discover a parameter-free framework for fast sequence alignment through UniAligner, exploring innovative approaches to computational genomics and bioinformatics analysis.
DNA Data Storage: Introduction and Future Storage Solutions
Discover how DNA data storage revolutionizes traditional systems with unparalleled density and efficiency, exploring its processes, standards development, and future potential for petabyte-scale storage solutions.
DNA Data Storage: A Decade of Coding and Decoding Progress
Explore the evolution of DNA data storage technology over the past decade, examining coding algorithms, mapping schemes, error correction methods, and key achievements in this revolutionary storage medium.
Computational Deconvolution of Cancer Genomes and Transcriptomes - CGSI 2022
Explore computational methods for deconvoluting cancer genomes and transcriptomes. Learn advanced techniques to analyze tumor heterogeneity and uncover molecular phenotypes shaping clinical outcomes in cancer research.
A Practical Guide to Performing Genome-Wide Analyses of Tandem Repeats
Explore genome-wide tandem repeat analysis techniques. Learn practical tools and methods for identifying, profiling, and interpreting repetitive DNA sequences across entire genomes.
Large Language Models for Computational Biology - A Primer
Explore large language models in computational biology, covering transformers, pretraining, and applications in genomics and single-cell analysis.
Keynote: On the Verge of Synthetic Biology Breakthroughs - September 7, 2024
Explore cutting-edge genomics and synthetic biology insights in Manolis Kellis' keynote address at iGEM OnTheVerge, delving into future possibilities and current advancements.
Sequence Data - Part 4
Explore advanced techniques for analyzing and interpreting sequence data, enhancing your bioinformatics skills and research capabilities.
Overcome Challenges in Cancer Research with xGen NGS Solutions for Oncology and MRD Research
Explore advanced NGS solutions for cancer and MRD research, enhancing library complexity and offering customizable hybridization capture approaches.