Next Generation Sequencing Data Analysis Courses
Next Generation Sequencing (NGS), a recently evolved technology, have served a lot in the research and development sector of our society. NGS methods are highly parallelized enabling to sequence thousands to millions of molecules simultaneously. This technology results into huge amount of data, which need to be analysed to conclude valuable information. Analysis of NGS data unravels important clues in quest for the treatment of various life-threatening diseases; improved crop varieties and other related scientific problems related to human welfare.
Participants will be introduced with its applicability to real-time data analysis problem. All our training content is as per industrial requirement and 100% practical exposure which will help candidate to make their better career in the field of bioinformatics.
More than 300+ candidates have taken this course and have successfully build their career in
Bioinformatics.
NGS data analysis now you can learn with your own datasets and you can learn NGS analysis to
implement for your paper publication or defense your thesis.
Hurry up and register soon...To become expert in Bioinformatics !
## 10% Discount if you register before 15th December, 2024. Hurry up!!
- RNASeq [R]
- RNASeq [D]
- scRNA-Seq
- ATAC-Seq
- lncRNA-Seq
- DNASeq
- ChipSeq
- MethylSeq
- miRNA-Seq
- PSI-Seq
- Whole Genome de novo Assembly
- Targeted metagenomics
- Whole Genome Metagenomics
- Metatranscriptomics
Available slots - 9:00 AM to 11:00 AM / 11:00 AM to 1:00 PM / 2:00 PM to 4:00 PM / 4:00 PM to 6:00 PM
Online(For online training candidate have to install Skype and AnyDesk)(it is same like offline)
Offline(For offline training candidate have to come to head office Pune and bring their own laptop)
All our training is one to one and 100% focus with individual candidate which provides 100% learning.
if other platform pacbio or nanopore or any other sequencing platform kindly write email to us.
Kindly note if custom requirement either to change the content or tools or raw data from candidate to be included during training in that case it will come under custom training and we request to send us email details accordingly.
Also candidate can learn with their own raw data as well as can also make all figures and tables as per the publication reports which will help to directly make reports with our expert team. Kindly note only custom based training will provide this feature and need to be discussed before registration.
Training can be started on any date as per the candidate convenience as its one to one training as well as its 100% interactive.
DNAseq Data Analysis
- Linux understanding and Installation of Linux and NGS tools
- Data Retrieval (NCBI SRA) & Introduction to data types
- Read Quality Check (FastQC & Cutadapt)
- Alignment of reads using reference Genome (BWA/Bowtie)
- Understanding Mapping Output(SAM/BAM, Samtools & Bedtools)
- Variant detection using GATK(germline and somatic variations)
- Visualization of variation with IGV browser
- Complete annotation and variant effect prediction(SNPEff, SNPDB / ensemble VEP )
- Predict the effects of coding non-synonymous variants on protein function
- CNV calling using BreakDancer(insertions, deletions, inversions, inter- and intra-chromosomal translocations)
- Additional 2hrs of support after completion of training
- server access if the candidate laptop/desktop will not support for analysis