BioDiscovery Group is conducting Workshops and eWorkshop since 2010. Till date we have successfully trained participants from several countries who were not only students but scientists, faculties, professor, company executives, etc. Till now we have conducted some great workshops in India as well as other countries please click here for all our upcoming as well as previous workshops and click here for the pictures of previous workshops.
We have launched 2 day training cum workshop Next Generation Sequencing Data Analysis (DNA-Seq, RNA-Seq & Chip-Seq) in New Delhi, India.
This 2-day training course will focus on the use of efficient technologies used in the next generation sequencing data analysis (DNA-Seq, RNA-Seq & Chip-Seq). The program will be conducted for 2 days for which participants have to bring their own laptop and for which the Linux environment will be provided by us so that student can use that for running NGS processes on their laptops. We will provide handouts (soft & hard copy both) along with the software and paper of technology. It will be extensive training program which will make the participants do all the processes on their Computer Systems (hands-on training) with complete learning of Next Generation Sequencing Data Analysis(DNA-Seq, RNA-Seq & Chip-Seq) process. The course will be of great help to students/ researchers/ scientists in learning this latest science and technology.
ONLY 15 SEATS | BRING YOUR LAPTOP HAVING WINDOWS OS WITH FOLLOWING SYSTEM CONFIGURATION
TOPICS
1. Basic Terminologies.
2. Introduction to file types in NGS.
3. What is Sequence alignment.
4. Introduction to Genome Analysis
5. Database and File Formats in NGS.
6. NCBI Genomics Library.
7. NCBI resources used in Next Generation Sequencing.
8. Introduction to analysis of Next Generation Sequencing Data.
9. What is the FASTQ format.
PRACTICAL APPLICATION
Hands-on exercises will be performed individually using software tools on your own laptops. No prior software experience is required.
1. Blasting into SRA.
2. Checking the quality of Sequence DNA, RNA.
3. Process Sequence Reads-Quality trimming read joining etc.
4. Aligning the sequences (DNA, RNA).
5. Gene Annotation.
6. Chip-Seq Sequencing of the reads.
7. DNA-Seq result Analysis.
8. RNA-Seq result Analysis.
9. Chip-Seq Sequencing result analysis
TARGET AUDIENCE | WHO SHOULD ATTEND
Scientists and Scholars with basic knowledge of Life Science and Genomics who would like to receive a comprehensive overview or refresher on the Next Generation Sequencing.
Academics: Bachelor/Masters Students, PhD, Research Scholars, Resident Doctors as well a Faculty from Microbiology, Molecular Biology, Biochemistry, Biotechnology, Immunology, Hematology, Pharmacy, Biomedical Technology, Genetics, Genomics, Proteomics, Bioinformatics, Animal & Plant Science and Life Sciences.
Professionals: Scientists from Biotechnology, Bioinformatics and Pharmaceutical industry and regulatory agencies. Hands-on exercises will be performed individually using software tools on your own laptops. (no prior experience required).
OUTCOME
Participants will
T & C
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