Conférences  >  Sciences biologiques  >  Génomique et bio-informatique

Department of Experimental Biology, Faculty of Medicine of the University of Porto

The Essential Molecular Biology course covers the fundamental principles and techniques used in experimental research in the area of Molecular Biology. Essentially practical in nature, it aims at the learning of current genomics and proteomics techniques, as well as the acquisition of skills in laboratory experimentation required for scientific research in Biomedicine. An exciting way to learn the essential genomics and proteomics techniques used in experimental research in biomedicine: hands-on, practical, intensive.

Tél.: [+351 220426779];     Email.: laimm@med.up.pt

Molecular biology, genomics, proteomics, hands-on, laboratory work, practical

Fusion Conferences

This conference aims to include recent progress in translating human genetic discoveries into functional characterization of genome wide association study (GWAS) regions that encode risk for complex human diseases. This symposium will highlight a number of exemplary functional studies of GWAS loci, examine how single cell data can accelerate translation of genetic associations, and how we can expand our catalogs of causal genes using the new CRISPR-Cas9 screening tools.

Pharmacologie et développement des médicaments,    Pharmacogénétique, Médecine personnalisée

University of Granada

The IWBBIO 2024 (11th International Work-Conference on Bioinformatics and Biomedical Engineering) seeks to continue the good synergy obtained in the previous edition, providing a discussion forum for scientists, engineers, educators and students about the latest ideas and realizations in the foundations, theory, models and applications for interdisciplinary and multidisciplinary research encompassing disciplines of computer science, mathematics, statistics, biology, bioinformatics, and biomedicine. The aims of IWBBIO 2024 is to create a friendly environment that could lead to the establishment or strengthening of scientific collaborations and exchanges among attendees, and therefore, IWBBIO 2024 solicits high-quality original research papers (including significant work-in-progress) on any aspect of Bioinformatics, Biomedicine and Biomedical Engineering.

Email.: iwbbio@ugr.es

bioinformatics, bioimaging devices, biomedical, biomedical signal processing, biomedical computing, artificial intelligence, biotechnology,

Génie biomédical,    Médecine translationnelle, essais cliniques

Centro de Ciencias de Benasque Pedro Pascual

Sciencezo Planet

A cell’s hereditary material is comprised of nucleic acids, which allows living organisms to pass on the genetic information from one generation to next. The Nucleotides in both DNA and RNA are comprised up of a sugar, a nitrogen base, and a phosphate molecule. Nucleic acids are long chains of nucleotides joined together by phosphodiester bonds. Nucleic acids comprised of: deoxyribonucleic acid (DNA) and ribonucleic acid (RNA). DNA and RNA having slight difference in their chemical composition, yet play importantly different biological roles. In the proposed Nucleic Acids 2024, we will bring together various eminent researchers working on molecular biology (Nucleic Acids) to learn and share the latest advancements in the field of cutting-edge applications in biology, functional nucleic acids, basic principles, human health, and its related diseases. It is a broad audience gathering for exploring the advancement in RNA, Genome Dynamics, DNA damage and repair, maintenance and replication, structure and structure-function studies of nucleic acids and protein, innovative techniques at molecular and chemical level, and current aspects of CRISPR etc. which focus on its research and wider applications.

Email.: suzannewilliams@sciencezoplanet.com

Molecular Biology and Techniques, Genome Dynamics and Mutagenesis, Human Statistical Genetics, Molecular Genetics & Epigenetics, CRISPR Technology, DNA Replication & Recombination, DNA Damage and Repair, RNA Editing and Interference, Recombinant DNA Technology, RNA Processing and Protein Synthesis, Alternate Nucleic Acid Structures, Computational Molecular Biology, Personalized Medicines, Thermodynamics of Nucleic Acid, Sequencing & Microarrays, RNA Processing and Protein Synthesis

Biologie moléculaire,    Biologie des systèmes

EMBL Heidelberg

This course will provide training in genome editing and cell engineering in mammalian cells and mouse embryos using the highly efficient CRISPR/Cas9 system. Participants will learn design of CRISPR targets using bioinformatics tools, generation of gene knock-outs/knock-ins, and target validation using the most current technologies. The course will be split into two groups (mammalian cells OR mice) based on participants’ expertise. Please note that all participants are expected to engage in all sessions. Participants should plan for approximately 1 hour extra per day for self paced learning modules.

Email.: charlotte.courtney@embl.de

ecSeq Bioinformatics GmbH

The purpose of this workshop is to get a deeper understanding in Next-Generation Sequencing (NGS) with a special focus on bioinformatics issues. Advantages and disadvantages of current sequencing technologies and their implications on data analysis will be discovered. The participants will be trained on understanding their own NGS data, finding potential problems/errors therein and finally perform their first downstream analysis (variant calling). In the course we will use a real-life NGS dataset from the current market leader illumina. All workshop attendees will be enabled to perform important first tasks of NGS data analysis themselves. The course layout has been adapted to the needs of beginners in the field of NGS bioinformatics and allows scientists with no or little background in computer science to get a first hands-on experience in this new and fast evolving research topic.

Events Team;     Email.: events@ecseq.com

Next-Generation Sequencing, NGS, Illumina,

ecSeq Bioinformatics GmbH

The Single-Cell RNA-Seq Workshop is designed to provide a thorough introduction to the analysis of single-cell RNA sequencing data. Through a combination of lectures and hands-on exercises, participants will learn how to process, analyze and integrate single-cell data using industry-standard tools and techniques. Topics covered include sequencing technologies, data quality control, preprocessing, dimensional reduction, clustering, trajectory inference, differential expression analysis, and multi-sample integration. By the end of the workshop, attendees will have the skills and confidence to perform custom analyses and gain new insights into complex biological systems. This workshop is ideal for researchers and students with little or no prior experience in single-cell RNA-seq analysis, as well as those seeking to update their skills and knowledge.

Events Team;     Email.: events@ecseq.com

NGS, RNA, Nest-Generation Sequencing

Fusion Conferences

Chromatin is the template of life, the carrier of genetic information and the core regulator of fundamental processes such as gene expression and stem cell fate determination. Chromatin dysfunction on the other hand can trigger various diseases, including cancer. Although chromatin structure and function and the mechanisms of disease and their diagnostic and therapeutic approaches are the subject of many meetings, conferences bringing them together are less frequent. The boundaries among these various disciplines are disappearing and meeting on "Epigenetics: from mechanisms to disease" will focus on the discussion of the role of chromatin architecture, epigenetics, stem and single cell biology in cancer and other diseases. The talks will cover a broad range of topics, including chromosome organisation, long-range interactions, chromatin assembly, stem cell regulation/differentiation, RNA-based mechanisms, transcription regulation, DNA methylation and hydroxymethylation, exploiting the power of genome engineering technologies, single-cell approaches, cutting edge epigenomics and imaging approaches and novel cell systems such as organoids. Speakers have been selected to broadly reflect lessons learned from a variety of model organisms and experimental approaches.

EMBL Heidelberg

Before the genetic information stored in DNA can be used to direct cell growth and metabolism, it has to be transferred into RNA. Messenger RNAs (mRNAs) that code for proteins and noncoding RNAs are key components in the transmission of genetic information in all life forms – from viruses to complex mammalian organisms. Following the great success of the 2022 edition of this long-standing symposium, we are looking forward to returning in 2024, bringing together leaders in the RNA field, post-docs and students, with the aim of disseminating and discussing the most recent results. The programme will include topics on transcription, RNA processing and modification, mRNA export and localisation, mRNA surveillance and decay, translation, the activity of non-coding RNAs, the control of mRNA expression, and coupling among these processes.

Email.: iva.gavran@embl.de

ecSeq Bioinformatics GmbH

The purpose of the workshop is to introduce the concepts of bioinformatic pipeline development through the context of the open source Workflow Management System (WMS) Nextflow. The participants will be trained in the scripting, configuration and execution of example analysis pipelines based on current industry best-practices, and learn how to share them with other users. Finally, the participants will apply everything they have learned by implementing their own analysis pipelines from the ground up. By the end of the workshop all attendees will be enabled to build their own scalable, reproducible bioinformatic pipelines which can be run locally, on high-performance computing clusters or even in the cloud. The course layout has been adapted to the needs of beginners in the field of computational biology and allows scientists with little or no background in software development to get a first hands-on experience in this new and fast-evolving area of expertise. This instructor-led live online workshop has been newly designed for an engaging, interactive online learning experience.

Events Team;     Email.: events@ecseq.com

NGS, Next-Generation Sequencing, Nextflow, Data Analysis

Schloss Dagstuhl - Leibniz-Zentrum für Informatik

At the Dagstuhl Seminar on RNA Regulation and Multidimensional Transcriptomics, we will delve into the intersection of computational biology, deep learning, and RNA research. The event will explore how cutting-edge AI technologies are reshaping our understanding of RNA-based gene regulation and its role in health and disease.

Réseaux de neurones et intelligence artificielle, apprentissage automatique,    Mise en œuvre et applications de l'intelligence artificielle

Uventia Global

Impurities may have a negative effect on the efficacy, safety, and quality of pharmaceutical components and products. The successful development and manufacturing of novel medications now depend heavily on the assessment of the impurity profiles as well as the management and monitoring of those. The diligent identification of nitrosamines and other genotoxic contaminants should be established at every step of drug development in order to comply with growing regulatory requirements and prevent costly recalls. Our online meeting, which we organized in collaboration with industry professionals, aimed to showcase and discuss different perspectives on addressing the challenges caused by mutagenic impurities. We will go over drug impurity profiling techniques that follow regulatory guidelines, as well as useful tips for adhering to recent updates to ICH M7 and Q3D, new nitrosamine regulations, nitrosamine impurities determination and calculation, risk assessment for genotoxic impurities, analytical challenges, development of acceptance criteria and most recent developments in elemental impurity assessment.

Email.: info@uventia.com

GTIs, Genotoxic, Mutagenicity, Nitrosamines, Impurities, Regulatory Affairs, LC-MS, Mass Spectrometry, API, Process Chemistry, Drug Safety, Genetic, Toxicology

Spectroscopie de masse, chromatographie et résonance magnétique nucléaire,    Génétique et maladie génétique

ecSeq Bioinformatics GmbH

The purpose of this workshop is to get a deeper understanding in Next-Generation Sequencing (NGS) with a special focus on bioinformatics issues. Advantages and disadvantages of current sequencing technologies and their implications on data analysis will be discovered. The participants will be trained on understanding their own NGS data, finding potential problems/errors therein and finally perform their first downstream analysis (variant calling). In the course we will use a real-life NGS dataset from the current market leader illumina. All workshop attendees will be enabled to perform important first tasks of NGS data analysis themselves. The course layout has been adapted to the needs of beginners in the field of NGS bioinformatics and allows scientists with no or little background in computer science to get a first hands-on experience in this fast evolving research topic. The online course will make use of a web conferencing system. Hands-on NGS analysis will be performed in an interactive browser-based data analysis platform. Before the course, you will get a printed manuscript.

Events Team;     Email.: events@ecseq.com

NGS, Next-Generation Sequencing, Illumina, data analysis

Schloss Dagstuhl - Leibniz-Zentrum für Informatik

The progress in understanding genes and genomes has given a boost to the use of synthetic DNA for biological and technological applications. Synthetic nucleic acids play a central role in synthetic biology and in emerging therapeutic paradigms, e.g., genome editing and nucleic acid vaccines. DNA-based data storage is making significant progress, and thanks to its extreme data-density, its high durability and its timelessness, it is promising to be the next standard for data archival systems. Synthetic biology and the use of synthetic DNA for information storage applications bring important algorithmic and data analysis challenges. In synthetic biology, reagent and assay design are often driven by algorithmic approaches. Novel synthesis technologies offer cost-reduction by several orders of magnitude at the cost of increased error-rate, raising new coding-theoretic questions. This Dagstuhl Seminar aims to bring together leading biologists, chemists, engineers, computer/data scientists, and theoreticians working on synthetic biology and on DNA-based data storage, to enable joint work in small groups leading to discussing and exploring recent advancements and current challenges.

Biologie moléculaire,    Biologie des systèmes

Human Genetics and Genetical Disorders-2025 extend our immense pleasure and honor to invite you to attend the 2nd International Conference on Human Genetics and Genetical Disorders which is scheduled on April 14-16, 2024 in Paris, France. One of these directions was the need for genetic studies to identify genes and genetic markers of diagnostic, prognostic and therapeutic value Genetic processes work in combination with an organism's environment and experiences to influence development and behavior often referred to as nature versus nurture.

Event Manager;     Tél.: [+91-9100067998];     Email.: kristinefoster124@gmail.com

Genetic and Genomic Data Analysis and Interpretation Genetics of Neurological and Psychiatric Disorders Genome Engineering and Synthetic Biology Cytogenetic, Genome Variation and Architecture Functional Genomics, Medical Genetics and Gene Regulation Genetic Basis, Pathogenesis and Statistical Genetics Chromosomal Abnormalities Management of Genetic disease and New Treatments for Genetic Disorder Genome and Exome Sequencing Applications Genetic Cancer and Cystic Fibrosis Genetic Variation and Human Disease

Fusion

Laura Trundle, Director;     Email.: laura@fusion-conferences.com

DNA Damage Response, cancer biology, replication stress, cancer therapies, PARP inhibitors, BRCA, clinical development

Biologie moléculaire,    Cancérologie

Fusion

Felicity Harrap, Conference Manager ;     Email.: felicity@fusion-conferences.com

Nucleic Acids, DNA Replication, DNA Repair, RNA Structure & Function

Biologie,    Biologie moléculaire