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European Molecular Biology Organization – EMBO

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

Bioinformatics, NGS, Next Generation Sequencing, RNA

European Molecular Biology Organization – EMBO

Seqera

This premier event brings together leading experts, innovators, and researchers to showcase the latest breakthroughs in workflow management. There will be a hackathon and training sessions on May 21st and May 22nd and the Summit on May 23rd and May 24th.

Event organizers;     Email: summit@nextflow.io

nextflow, nf-core, pipeline, workflow, bioinformatics, data science

Klinisches Datenmanagement, E-Health,    Wissenschaftliches Rechnen und Datenwissenschaft

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

Bioinformatics, NGS, Next Generation Sequencing, Nextflow

ecSeq Bioinformatics GmbH

The purpose of this intense one-week summer course is to get a deep 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. You will be trained on understanding NGS data formats and handling potential problems/errors therein. In the summer school we will use a real-life RNA-seq dataset from the current market leader illumina. All students will be enabled to perform important first tasks of NGS data analysis themselves. The layout of the summer school 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. In the evenings there will be social events, like a conference dinner, or a guided city tour through Berlin. These are always great networking possibilities.

Events Team;     Email: events@ecseq.com

Bioinformatics, NGS, Next Generation Sequencing

Front Line Genomics Limited

The Festival of Genomics and Biodata is returning to Boston! Join us on Wednesday June 12th - Thursday June 13th 2024 at the Boston Convention & Exhibition Center for inspirational speakers, the latest research and clinical breakthroughs, cutting-edge technology and incredible networking opportunities. Free for 90% of attendees, the Festival is designed to help you return to work armed with dozens of new ideas and contacts, but also to keep you engaged, excited and proud of the difference your efforts make for patients. With 7 theatres of content, 150 speakers and an extensive range of topics there’s something for everyone!

Email: info@frontlinegenomics.com

Advanced Sequencing Technologies, AI, Cancer Diagnostics, Cancer Vaccines, Data Storage and Analysis, Drug Development, Epigenetics, Ethics, Gene Therapy, Genomic Medicine, Mental Health, Metagenomics, Microbiome, Multi-Omics, Newborn Screening, Patient Inclusion, Pharmacogenomics, Polygenic Risk Scores, Population Genomics, Precision Oncology, Rare Disease, RNA-Seq, Single-Cell & Spatial, Women's Health

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.

Tel.: [+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.

Pharmakologie und Arzneimittelentwicklung,    Pharmakogenomik, Personalisierte Medizin

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,

Medizintechnik,    Translationale Medizin, Klinische Studien

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

Molekularbiologie,    Systembiologie und mathematische Biologie

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.

Neuronale Netze und Künstliche Intelligenz, Maschinelles Lernen,    Implementierung und Anwendungen von künstlicher Intelligenz

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.

Molekularbiologie,    Systembiologie und mathematische Biologie