Daniel Howrigan, Data group leader at Neale Lab (MGH, Broad Institute), for a workshop on data QC and cleaning in GWAS. Learn about goals of GWAS, genetic data visualization, QC methods, and more.

2 views • 35 slides

Founded in 1982, the Nevada Restaurant Association is dedicated to promoting, protecting, and educating the thriving restaurant industry in Nevada. With a focus on offering resources, networking opportunities, and training, the association plays a crucial role in advancing and safeguarding the busin

0 views • 11 slides

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

3 views • 27 slides

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

2 views • 66 slides

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

0 views • 13 slides

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

0 views • 35 slides

The American Association for Chinese Studies (AACS) Newsletter for 2022-2023 provides insights into the association's activities, including board members, conference call for papers, budget requests, and member achievements. The President's message highlights the successful 64th convention in Denver

1 views • 16 slides

The lecture covers the transcription and translation processes of virus genomes, including the Baltimore classification system, transcription control in eukaryotes, and the role of transcription factors in gene expression. It explores how different viruses replicate based on their genome type and me

0 views • 14 slides

Genome assembly is a technique to assemble short DNA fragments into a organized format.

0 views • 15 slides

Developed by Genomics Education Programme, these slides focus on the patient choice consent model for whole genome sequencing in NHS Genomic Medicine Service. The model aims to ensure informed choices for genomic testing, including participation in the National Genomic Research Library. It covers se

0 views • 34 slides

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

3 views • 5 slides

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

0 views • 7 slides

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

0 views • 36 slides

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

0 views • 11 slides

DNA, the hereditary basis of life, was first discovered by Friedrich Miescher in 1869. It consists of chromosomes, plasmids, and organellar DNA, collectively known as the genome. Genes, sequences of DNA, encode proteins and RNA, essential for an organism's functions. The genome is divided into chrom

0 views • 17 slides

Uncover the fascinating journey of molecular biology, tracing key milestones from the discovery of DNA to the intricate structure of genes and genomes. Dive into historical breakthroughs, such as understanding the role of genes in producing proteins, the double helix structure of DNA, and the comple

2 views • 30 slides

Chromosomes are the carriers of genetic information in cells, containing genes made of DNA. Chromatin, composed of DNA wrapped around histone proteins, plays a crucial role in organizing genetic material. Humans have 23 pairs of chromosomes, and the Human Genome Project aims to map the human genome.

0 views • 21 slides

This content provides information about a Genome Informatics course, including course logistics, homework policies, and contact details. It also introduces fundamental concepts such as algorithms, their key features, and examples like finding the smallest number among inputs. The course emphasizes l

0 views • 30 slides

PhD student João Vitor Nomura is conducting a Genome-Wide Association study for drought tolerance in potatoes at the University of São Paulo and the University of Wisconsin-Madison. The research focuses on adapting potato varieties to extreme heat waves and improving food security. Different abiot

0 views • 19 slides

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.

0 views • 41 slides

Explore the intricate world of gene regulation and genomic data analysis through a comprehensive study presented at a faculty workshop in 2014. Delve into the evolution and classification of biology, the impact of genome sequencing on digitizing biology, and the potential of genetic information vari

0 views • 18 slides

The document presents insights into tentative (re)association for non-AP MLDs, focusing on addressing data delivery interruptions during roaming and association with new access points. It covers necessary actions before data transfer, open system authentication, association operations, and fast BSS

0 views • 17 slides

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

0 views • 37 slides

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

0 views • 15 slides

Genome projects generate large GFF files which require significant storage space. GPress offers a solution by compressing GFF files while allowing quick searches and random access. The framework addresses challenges faced by current GFF utilities, providing a more efficient approach to managing and

0 views • 24 slides

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

0 views • 28 slides

Knowledge-based approaches are crucial in genetic data analysis to enhance the accuracy and scope of genome-wide association studies (GWAS). Stochastic Relational AI (Star-AI) offers a solution by leveraging probability theory and First Order Logic to capture complex genetic interactions. By integra

0 views • 10 slides

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

0 views • 10 slides

Exploring the utility of non-recombining paternal ancestry information in Genome-Wide Association Studies (GWAS) through the analysis of Y chromosomal haplogroups. This review delves into the implications of using Y chromosome and mitochondrial DNA data in tracing human migrations, ancestry, bottlen

0 views • 27 slides

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

0 views • 24 slides

Obtain valuable insights into retrieving genome files for bioinformatics analysis utilizing multiple methods such as connecting via Finder, using Filezilla for FTP access, and executing curl commands on Xanadu. Learn how to access coding sequences, feature tables, nucleotide sequences, and encoded p

0 views • 38 slides

Viruses are small obligate intracellular parasites that require living hosts for multiplication. They lack ribosomes and metabolic enzymes, relying on host cells for replication. Viruses vary in size, shape, and genome organization, with classification based on morphology, physicochemical properties

0 views • 31 slides

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

0 views • 35 slides

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

0 views • 19 slides

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

0 views • 12 slides

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

0 views • 6 slides

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

0 views • 24 slides

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

0 views • 26 slides

Exploring the genetic basis of smoking behavior-related traits through a meta-analysis combining data from three large consortia across 58 different cohorts/datasets. The study investigates genetic variants associated with cigarettes per day, pack years, smoking initiation, and smoking cessation. Ov

0 views • 34 slides

Exploring the challenges of scaling Genome Wide Association Studies (GWAS) to millions of samples, covering topics like FastPCA, TeraStructure, and imputation with Eagle. The session delves into working with summary statistics, exemplified by PrediXan journal discussion, and outlines concepts and ex

0 views • 46 slides