I will analyze ngs fastq data using fastqc and provide quality control report

Welcome to My Gig

I will professionally analyze your NGS sequencing data (FASTQ files) and provide a clear, easy-to-understand quality control report using FastQC.

This service helps you understand whether your sequencing data is good enough for downstream analysis like RNA-seq, variant calling, or genome studies.

What I Will Do?

• Overall sequence quality
• Per-sequence quality score distribution
• GC content analysis
• Sequence duplication levels
• Adapter contamination check
• Read length distribution
• Identification of warnings and failed modules

All results will be clearly explained, even if you are not a bioinformatician.

Tools I Use

• FastQC
• Linux (Ubuntu environment)
• Command-line based professional workflow

What You Will Receive

You will get:

• FastQC HTML report
• Quality plots (like per-sequence quality score graph)
• Simple explanation of PASS / WARN / FAIL
• Clear recommendation (Is your data usable or not?)

If needed, I will also guide you on next steps (trimming, filtering, or analysis).

Supported Data Types

• RNA-seq
• DNA-seq
• WGS / WES
• Illumina FASTQ files
• Single-end or Paired-end data

Why Choose Me

• Bioinformatics background
• Real research experience
• Clean and honest reporting
• Fast delivery