Gene Therapy and Genome Editing Technology
This article provides insights into the status, regulatory considerations, and delivery methods of gene therapy and genome editing technologies. It discusses approved gene therapies in the US, human genome editing in clinical applications, and the regulatory authority of the FDA over gene therapy. T
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Insights into Genome Assembly and Shotgun Sequencing
Explore the world of genome assembly, shotgun sequencing, and the fundamental concepts behind deriving genomes from large sets of sequencing reads. Learn about the complexity and core algorithms involved in contemporary genome assembly processes. Discover how the shotgun concept has revolutionized g
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Sudden Death and Cardiomyopathy Associated with LMNA in Nova Scotia Duck Tolling Retriever
A study on sudden death and cardiomyopathy in Nova Scotia Duck Tolling Retrievers due to LMNA association. The research includes genetic mapping, genotype verification, and functional predictions on Lamin A/C effects. Echocardiogram findings, pedigree data, genome-wide association study, whole-genom
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Perfect Precision with CNC Alignment Services - Optimize Your Machines
Enhance your CNC machine performance with our expert CNC alignment services. Our skilled technicians ensure precise alignment for optimal accuracy and efficiency. We use advanced technology to correct misalignments, reducing errors and downtime. Trust us to keep your machines running smoothly. Exper
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Understanding Genome-Wide Association Studies in Statistical Genetics Workshop
Explore the essentials of Genome-Wide Association Studies (GWAS) and genetic data quality control as presented by Daniel Howrigan in the 2023 workshop. Delve into the goals of GWAS, genetic data characteristics, SNP variations, and genotyping techniques. Gain insights into moving from trait heritabi
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Laser Alignment Training for Safety
This laser alignment training program focuses on exercises like wedge window alignment and beam splitter cube alignment to prevent laser eye injuries and control reflections. It covers techniques for safely setting up optics and aligning laser beams in a controlled environment.
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Understanding a Complex KMT2A Rearrangement in AML with Optical Genome Mapping
A case report explores the use of optical genome mapping (OGM) to unravel a complex KMT2A rearrangement in an AML patient. Traditional cytogenetic analyses identified translocations and rearrangements involving chromosomes 10 and 11, leading to the fusion of genes KMT2A and MLLT10. OGM technique, ut
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Understanding the Cancer Genome Atlas (TCGA) Project
The Cancer Genome Atlas (TCGA) project, initiated in 2005, aims to identify genetic mutations in cancer through genome sequencing. Supervised by the Center for Cancer Genomics, TCGA has expanded over the years, publishing numerous research articles and involving various tumor types. The project has
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Evaluating Genomic Science: Insight into Genome Canada's Mission and Impact
This conversation with Dr. Samantha Evans, Director of Evaluation at Genome Canada, delves into the importance of program evaluation in genomic science. Genome Canada aims to connect ideas, invest in science and technology, and maximize impacts across sectors. The evaluation process involves collect
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Fast and Accurate Short Read Alignment with Burrows-Wheeler Transform
The presentation discusses the challenges in short read alignment, introduces the Burrows-Wheeler Transform (BWT) algorithm, and compares it with other alignment algorithms. It explores exact and inexact matching approaches, presenting results and conclusions. The focus is on improving alignment spe
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Understanding Sequence Alignment in Genetics
Sequence alignment is the comparison of DNA or protein sequences to highlight similarities, often indicating a common ancestral sequence. This process is essential in determining homology and functional similarities between sequences. Types of alignment include global and local alignment, with chall
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Understanding Sequence Alignment and Tools in Bioinformatics
Explore the concepts of homology, orthologs, and paralogs in bioinformatics, along with different types of sequence alignment such as global, local, and semi-global. Learn about popular alignment tools like Blast and Fasta and how they are used for analyzing sequences. Dive into the world of NCBI an
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Electron Beam Lithography with Raith EBPG: Alignment Marks Guide
The use of alignment marks in electron-beam lithography is crucial for aligning different layers of lithography, enabling precise printing of intricate patterns like wires connecting pads. This guide explores the significance of alignment marks, common alignment strategies, differences in alignment
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Understanding Sequence Alignment Methods in Bioinformatics
Sequence alignment is crucial in bioinformatics for identifying similarities between DNA, RNA, or protein sequences. Methods like Pairwise Alignment and Multiple Sequence Alignment help in recognizing functional, structural, and evolutionary relationships among sequences. The Needleman-Wunsch algori
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Optical Alignment Using Beam Triangle Opti 521 Phil Scott
This presentation delves into the intricate process of optical alignment using a beam triangle, focusing on defining optical and mechanical axes, addressing alignment challenges, degrees of freedom for various elements, and the importance of setting up a beam triangle for accurate alignment. The con
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Alignment Scenarios for ILD/ILC Ties Behnke
The calibration and alignment scenarios for ILD/ILC presented at the meeting in Oshu City focus on the initial requirements for tracking, alignment precision, track-based alignment, track samples, vertex detector alignment, and Si tracker alignment techniques. The detailed specifications include lig
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Constructive Alignment in Teaching and Learning: A Comprehensive Guide
Constructive alignment emphasizes the importance of aligning learning outcomes, teaching activities, and assessments to enhance student learning. By clearly specifying learning outcomes, designing appropriate activities, and establishing assessment criteria with feedback, educators can foster constr
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Advancements in Genome Alignment and Sequencing Techniques
Genome alignment plays a crucial role in understanding biological processes and evolutionary history. With the rise of whole genome sequencing, methods such as constrained alignment and longest increasing subsequence have been employed for accurate variant detection. Tools like BLAST, hash tables, a
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Ultrafast and Memory-Efficient DNA Sequence Alignment Study
This study discusses the development of Bowtie, a tool for aligning short DNA sequences to the human genome. Bowtie offers ultrafast and memory-efficient alignment, outperforming previous methods like Maq and SOAP. The tool achieves high alignment speeds with a small memory footprint, making it suit
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Tasks of Alignment and Installation in CEPC Project
Tasks involved in the alignment and installation optimization of components in the Circular Electron Positron Collider (CEPC) project include control network construction, component installation, smooth alignment, and addressing any arising problems. The process is crucial for the successful operati
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Understanding EMBOSS Needle: Pairwise Sequence Alignment Tool
EMBOSS Needle is a pairwise sequence alignment tool that uses the Needleman-Wunsch algorithm to find the optimal global alignment between two input sequences. It is available online through EMBOSS and requires entering two protein/DNA sequences of the same length to generate alignment results, inclu
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Long-term Variation of Magnet Alignment in SPring-8 Storage Ring
This study focuses on the long-term monitoring and variation of magnet alignment in the SPring-8 storage ring. It includes detailed information on the main events of magnet alignment, monument surveys, magnet installations, and alignment monitoring techniques used over the years at the facility. The
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Technical Review on Beam Line Alignment at KEKB Facility
Detailed overview of the alignment strategies, measurements, and completion status of girder alignment using laser straight techniques at KEKB facility. The process involves laser trackers, micrometer measurements, and monitoring floor movement to ensure precise alignment for optimal equipment perfo
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Understanding Sequence Alignment and Scoring Matrices
In this content, we dive into the fundamentals of sequence alignment, Opt score computation, reconstructing alignments, local alignments, affine gap costs, space-saving measures, and scoring matrices for DNA and protein sequences. We explore the Smith-Waterman algorithm (SW) for local sequence align
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Understanding Multiple Sequence Alignment Methods and Motivation
Multiple Sequence Alignment (MSA) involves aligning three or more biological sequences to reveal evolutionary relationships and subtle similarities. Various methods like Dynamic, Greedy, Progressive, and Iterative approaches are used to overcome challenges in MSA. The motivation behind MSA includes
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Genome Sciences 373: Informatics Quiz, Python Dictionaries, and Conditional Statements Overview
Today's session covers topics such as Python dictionaries with in-class examples, iterating through dictionary entries, counting repeating characters in a string, and understanding if/elif/else statements. The session also includes a discussion on combining tests in Python and comparisons operators.
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Understanding Sequence Alignment in Next-Generation Sequencing Data
Sequence alignment plays a crucial role in analyzing Next-Generation Sequencing (NGS) data by identifying similarities between DNA, RNA, or protein sequences. Global and local alignment methods are used to arrange sequences and locate fragments derived from specific genes or transcripts. Challenges
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Understanding Multiple Sequence Alignment with PASTA Algorithm
Explore the PASTA algorithm for multiple sequence alignment, from installation to using the GUI for alignment and tree estimation. Learn about SAT and PASTA algorithms, the input process, and the steps involved in obtaining the best ML score alignment/tree pair. Dive into the PASTA GUI, initial alig
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Understanding Genetic Disorders and the Human Genome Project
The Human Genome Project, completed in 2003, aimed to identify all human genes and DNA sequences. Genetic disorders, like autosomal disorders and Huntington's disease, can result from mutations at different levels, affecting single genes, chromosomes, or multiple genes. Albinism and cystic fibrosis
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Evaluation of PacBio Sequencing to Improve Sunflower Genome Assembly
Presentation at the Sunflower Genome Consortium Meeting in San Diego discussed the use of PacBio sequencing to enhance the sunflower genome assembly, with evaluations on PacBio data's effectiveness at locus and genome scales. Results highlighted challenges and successes in improving assembly quality
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GenPIP: In-Memory Acceleration of Genome Analysis
GenPIP is an innovative system that accelerates genome analysis through tight integration of basecalling and read mapping. By utilizing chunk-based pipelines and early rejection techniques, GenPIP optimizes data processing, reducing wasted computation and data movement. The system outperforms existi
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Autonomous Detection of Vehicular Wheel Alignment Parameters
This research focuses on the autonomous detection of vehicular wheel alignment parameters conducted by Aaron Ameerali, Nadine Sangster, and Gerard Ragbir at the University of Trinidad & Tobago. The study addresses the importance of wheel alignment for proper road contact and maintenance, discussing
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Importance of Functional Annotation of Animal Genomes in NIH Research
Functional Annotation of Animal Genomes (FAANG) is crucial for associating sequence variation with quantitative phenotypes in domestic animals, serving as important models for human health, disease, and ecology. The NIH actively participates in various genome projects involving cattle, horses, and c
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Insights into NP-Hard Problems in Molecular Biology and Genetics
Understanding the complexity of NP-Hard Problems arising in molecular biology and genetics is crucial. These problems involve genome sequencing, global alignment of multiple genomes, identifying relations through genome comparison, discovering dysregulated pathways in human diseases, and finding spe
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Understanding the Morphology and Genome Organization of NDV
NDV, a pleomorphic virus, has an irregular spherical shape with filamentous features. Its genome consists of a single-stranded RNA with six genes arranged in a specific order. The virus contains a lipoprotein envelope with short spikes and a helical nucleocapsid core to protect the RNA. The genomic
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Understanding GWAS: A Brief Overview of Genetic Association Studies
GWAS, or Genome-Wide Association Studies, are a method used to map genes associated with traits or diseases by analyzing genetic markers throughout the genome. This process involves statistically testing the association between SNPs and traits using regression or chi-squared tests in a hypothesis-fr
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Understanding Whole Genome Sequencing in Public Health Training
This training activity conducted by the New York Integrated Food Safety Center of Excellence in October 2019 focuses on educating public health staff/students on the application of Whole Genome Sequencing (WGS) and whole genome multi-locus sequence typing (wgMLST) for subtyping. Through a mock case
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Understanding Cauliflower Mosaic Virus: Structure, Reproduction, and Genome
Cauliflower Mosaic Virus (CaMV) is a plant virus studied by Assistant Professor Kavita Basumatary at Goalpara College. The virus has a circular, double-stranded DNA genome of about 8000 bp in length with unique discontinuities. Reproduction involves the viral genome entering the host cell nucleus, w
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Understanding Genome Browsers and their Significance in Genomic Research
Genome browsers are essential tools for visualizing complex genome information, integrating sequence data with annotations in a user-friendly graphical interface. They enable exploration of chromosomal regions, regulatory elements, and comparative genomics across different organisms. Key examples in
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DNA Editing of Retrotransposons and Mammalian Genome Evolution
Large-scale DNA editing of retrotransposons plays a crucial role in accelerating mammalian genome evolution. Retrotransposons, accounting for half of the human genome, are mobile elements that can lead to mutations and genetic disorders but also serve as a reservoir for genetic innovation, rewiring
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