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NGS Training Program

Learn NGS Data Analysis step-by-step with hands-on training. Cover quality control, alignment, variant calling, RNA-Seq, metagenomics, genome assembly, and data visualization using free tools like FastQC, BWA, GATK, and DESeq2.

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NGS Training Program

This NGS Data Analysis training provides a comprehensive, hands-on approach to mastering next-generation sequencing techniques. Learn data preprocessing, alignment, variant calling, RNA-Seq, metagenomics, genome assembly, and visualization using free tools, ensuring practical expertise.
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Note: Below modules are designed keeping high end industrial professionals into consideration. Please refer individual protocols below for affordable prices.

NGS Data Analysis Training Program

    Fee: Rs 65000/-
  1. Fee: Rs 65000

    Day 1 - 5: Introduction to NGS and Sequencing Platforms

    • Overview of NGS Technologies
    • Sequencing Platforms: Illumina, Ion Torrent, PacBio, Oxford Nanopore
    • Applications of NGS
    • Data Formats: FASTQ, SAM, BAM, VCF
    • Hands-on Practice: Downloading sample datasets from NCBI SRA
  2. Day 6 - 10: Quality Control of NGS Data

    • Quality Assessment Tools: FastQC
    • Trimming and Filtering: Trimmomatic, Cutadapt
    • Adapter Removal and Base Quality Filtering
    • Hands-on Practice: Running FastQC and Trimmomatic
  3. Day 11 - 15: Data Preprocessing and Alignment

    • Genome Indexing: Bowtie2, BWA
    • Sequence Alignment: Mapping reads to reference genome
    • Sorting and Indexing BAM files: SAMtools
    • Hands-on Practice: Aligning reads with BWA and analyzing BAM files
  4. Day 16 - 20: Post-Alignment Processing

    • Duplicate Removal: Picard Tools
    • Realignment and Base Recalibration: GATK Tools
    • Sorting and Indexing BAM files
    • Hands-on Practice: Processing aligned data using SAMtools and Picard
  5. Day 21 - 25: Variant Calling and Annotation

    • SNP and INDEL Calling: FreeBayes, VarScan
    • Variant Annotation: ANNOVAR, SnpEff
    • Filtration and Prioritization of Variants
    • Hands-on Practice: Calling variants using FreeBayes and annotating using ANNOVAR
  6. Day 26 - 30: RNA-Seq Data Analysis

    • Transcriptome Assembly: HISAT2, StringTie
    • Differential Gene Expression Analysis: DESeq2, edgeR
    • Functional Annotation and Pathway Analysis
    • Hands-on Practice: RNA-Seq alignment and expression analysis
  7. Day 31 - 35: Metagenomics Analysis

    • Taxonomic Classification: Kraken2, MetaPhlAn
    • Functional Annotation: HUMAnN
    • Microbial Community Profiling
    • Hands-on Practice: Analyzing metagenomics data using Kraken2
  8. Day 36 - 40: De Novo Assembly and Genome Annotation

    • Genome Assembly: SPAdes, Velvet
    • Scaffolding and Contig Merging
    • Annotation Tools: Prokka, MAKER
    • Hands-on Practice: Assembling genomes and performing annotation
  9. Day 41 - 45: Visualization and Data Interpretation

    • Genome Browsers: IGV, UCSC Genome Browser
    • Visualization Tools: Circos, Integrative Genomics Viewer
    • Hands-on Practice: Visualizing data and interpreting results
  10. Day 46 - 50: Reporting and Final Project

    • Summarizing Results and Findings
    • Project Presentation and Feedback
    • Generating Reports using MultiQC
    • Q&A and Certification

    • Contact for

Individual Protocols Under NGS Training Program

    Please contact on +91-7993084748 for more details

    Cant Come to Hyderabad or Chennai or Bangalore? No Problem, You can do it in Virtual / Online Mode




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