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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

    Kindly review the fees outlined for the individual protocols listed in this module.

  • 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
  • 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
  • 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
  • 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
  • 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
  • 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
  • Day 31 - 35: Metagenomics Analysis

    • Taxonomic Classification: Kraken2, MetaPhlAn
    • Functional Annotation: HUMAnN
    • Microbial Community Profiling
    • Hands-on Practice: Analyzing metagenomics data using Kraken2
  • 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
  • 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
  • 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 +91-8977624748 for more details

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




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