- Наступний запис:
- Durchführung nur auf Anfrage
- Загальна тривалість:
- in 5 Tagen
- Практика:
- Nein
- Мови навчання:
- Englisch
- Вид заходу:
- Weiterbildung
- Форма проведення:
- Präsenzveranstaltung
- Час проведення:
- Tagesveranstaltung
- Мінімальна кількість учасників:
- keine Angaben
- Максимальна кількість учасників:
- 12
- Ціна:
- 1 489 EUR - MwSt.-befreit, inkl. Lehrgangsmaterialien
- Вид документа про освіту:
- Zertifikat/Teilnahmebestätigung
- Випускний екзамен:
- Nein
- Спеціальність:
- keine Angaben
- Сертифікати курсу:
- Nicht zertifiziert
- Курс тільки для жінок:
- Nein
- Догляд за дітьми:
- Nein
- Посилання на курс:
- Zum Angebot auf der Anbieter-Webseite
- Інформаційна якість:
- Suchportal Standard Plus
- Цільові групи:
- keine Angaben
- Професійні вимоги:
- Grundsätzliche Kenntnisse der Molekularbiologie, besonders der Genetik/Genomik; von Molekular-/Sequenziertechnologien (PCR, DNA-Bibliotheken, Illumina-Sequenzierung)
- Технічні вимоги:
- Computer mit freiem Festplattenspeicherplatz von min. 30 GB; Linux (Ubuntu) oder Mac OSX als Betriebssystem; ein aktueller Browser (Firefox oder Chrome).
- Номенклатура агенцій з працевлаштування:
- keine Angaben
Зміст
In this online training course, you will learn the essential aspects of NGS data analysis and workflow management. This includes:
Handling large NGS datasets and understanding various data formats.
Building and applying complete DNA analysis workflows using Galaxy and Snakemake/Nextflow.
Starting with quality control and progressing to variant calling, you will create DNA workflows in Galaxy and later transfer these steps to script-based open-source workflow management systems like Snakemake or Nextflow.
Using these tools, you will develop reproducible and automated bioinformatics pipelines.
________________________________________
What Will You Achieve?
By the end of this training, you will have acquired:
A comprehensive understanding of NGS file formats (FASTQ, SAM/BAM, VCF).
Skills in managing and processing large NGS datasets.
Proficiency in navigating the command line using basic Bash commands.
Knowledge of using Conda, a software manager.
Experience in applying analytical software via the command line.
Competence in using open-source software for all analytical steps.
The ability to create a complete DNA analysis workflow in Galaxy (from quality control to variant calling).
Expertise to translate this knowledge into building reproducible and scalable workflows in Snakemake or Nextflow.
Certification: Upon successful completion of the course, you will receive a certificate from CQ Beratung+Bildung GmbH.
________________________________________
What Funding Options Are Available?
This training is AZAV-certified and eligible for funding under the employment promotion program.
It is part of the certified "Bioinformatics and Biostatistics" course and can be funded with a training voucher.
Program Number for Employment Agencies/Job Centers: 962/26/2024.
Additional funding opportunities for training and coaching can be found here.
________________________________________
Tips
Course Language: The training is conducted entirely in English. We offer language coaching to help you prepare for the course.
________________________________________
Who Is This Training For?
The course is designed for academics in the fields of:
Biology, Microbiology, Biochemistry, Chemistry, Medicine, Mathematics, and Physics.
________________________________________
Your Qualifications
Subject Knowledge Requirements:
Basic knowledge of molecular biology (especially genetics/genomics).
Fundamental understanding of sequencing technologies (PCR, DNA libraries, Illumina sequencing).
Experience with Linux/Bash, R, and/or Python.
Technical Requirements:
A computer with at least 30 GB of free storage space.
Operating System: Windows, Linux (Ubuntu/Virtual Machine), or Mac OSX.
An up-to-date browser (Firefox or Chrome).
Stable internet connection, webcam, speakers, and microphone. Ideally, two monitors or one large screen.
________________________________________
Your Motivation
Efficient and high-quality analysis of genomic data (DNA) is increasingly essential for addressing biological and medical research questions. Leveraging cutting-edge technologies like Next-Generation Sequencing (NGS), this training equips you with the bioinformatics skills needed to work with large datasets and tackle real-world challenges in genomics.
________________________________________
Topics and Course Outline
Module 1: NGS Data Analysis
Introduction to NGS data formats (FASTQ, SAM/BAM, VCF).
Processing and quality control of large datasets.
Module 2: Introduction to Command-Line Tools and Software Management
Basics of Bash commands and navigation.
Using software managers like Conda.
Module 3: Introduction to Workflow Management Systems
Creating DNA workflows in Galaxy.
Transferring workflows to Snakemake or Nextflow.
________________________________________
Technical Requirements
Computer with at least 30 GB of free storage space.
Operating System: Windows, Linux, or Mac OSX.
An up-to-date browser (Firefox or Chrome).
Stable internet connection, webcam, speakers, and microphone.
Ideally, two monitors or a large screen.
Ми не гарантуємо правильність інформації. Відповідальність за правильність даних несуть виключно освітні організації.
Дата першої публікації: 23.09.2023, дата останнього оновлення: 05.12.2024