Bengaluru, India | 3 Day workshop in NGS Data Analysis (DNA-Seq, RNA-Seq & Chip-Seq) | Hands-On Practical sessions on SeqSysTM


ONLY 20 SEATS
25 AUGUST IS LAST DATE OF REGISTRATION

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. Click here for all our upcoming as well as previous workshops and click here for the pictures of previous workshops.

In our continuous efforts to make you learn by unique ways we have launched 3 day training cum workshop Next Generation Sequencing Data Analysis (DNA-Seq, RNA-Seq & Chip-Seq) at our Bengaluru office in Bengaluru, Karnataka, India.

This 3-day training course NGS Data Analysis (DNA-Seq, RNA-Seq & Chip-Seq) will focus on the use of efficient processes used in the technology. The general steps in a bioinformatics pipeline for NGS data analysis usually involves accessing the quality of the sequences, performing the QC, alignment with the reference sequence and generation of tables and graphs for the analysis of the results. The program covers all of these steps giving you complete learning of this latest technology.

It will be an extensive training program for which participants have to bring their own laptop and the Linux environment (SeqSysTM - for more details on this kindly write to jennifer@biodiscoverygroup.com) will be provided by us so the participants can use that for running the processes on their own computer systems- HANDS-ON with complete learning of Next Generation Sequencing Data Analysis (DNA-Seq, RNA-Seq & Chip-Seq). We will provide handouts (soft & hard copy both) along with the papers of technology to make you understand each aspect of technology.
The course will be of great help to students/ researchers/ faculty/scientists in learning this latest science and technology.

ONLY 20 SEATS | BRING YOUR LAPTOP HAVING WINDOWS OS WITH FOLLOWING SYSTEM CONFIGURATION

  • Processor – i3 or above (not older than 5th Generation).
  • RAM – 4 GB or above.
  • Hard Disk – 500 GB or above.

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
  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, Medicine, 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 as well as resident doctors.

Hands-on exercises will be performed individually using software tools on our device SeqSysTM on your own laptops. (no prior experience required). 

OUTCOME

Participants will
  • Be able to understand the technology behind the sequencing of human genome.
  • Learn to retrieve and check the quality of sequences.
  • Learn aligning the target sequence with reference sequence.
  • Learn sequence analysis.
  • Learn data analysis of our result based on different parameters.
  • Learn the overall concept of Next Generation Sequencing Data Analysis.

T & C
  • Only Windows OS is required for training & software installation.
  • While buying the ticket choose the right category of registration in which you fall, as the category in which you register, you will get certificate of that ONLY.
  • If you register under wrong category then your registration will be invalid and NO REFUND WILL BE MADE IN THIS CASE. This is your mistake and the company is not responsible for it.
  • Once you register we will send you Welcome email 5 days prior to the event. This email will have all detail of files, software, etc.
  • You need to follow the instructions in the welcome email and prepare your system accordingly.
  • If you do not turn up for training session on any day then NO CERTIFICATE WILL BE AWARDED TO YOU.
  • No refund will be made in any case.

For any queries feel free to write to us on workshops@biodiscoverygroup.com or call Mr Rishabh on +919538710056

Post a Comment

0 Comments