I will perform ngs data analysis
About this Gig
I provide professional NGS data analysis services, specializing in converting raw sequencing data (FASTQ) into high-quality variant results (VCF).
I will perform a complete and reliable pipeline using standard bioinformatics tools.
What I will do:
- FASTQ quality control (FastQC, fastp)
- Sequence alignment using BWA
- BAM processing with SAMtools
- Variant calling using GATK
- Clean and reproducible VCF output
What you will receive:
- Processed BAM files
- Final VCF file
- Summary of steps performed
️ Important:
- Suitable for research and academic datasets
- Large datasets may require additional time/resources
If you have specific requirements, feel free to contact me before placing an order.
Technology:
Jupyter Notebook
•
RStudio
Expertise:
Prediction
Programming language:
Python
•
R
•
SQL
FAQ
What data do you need?
FASTQ files and reference genome (if available)
Can you handle large datasets?
Yes, but large datasets may require additional time or resources.
What tools do you use?
BWA, SAMtools, GATK, FastQC, and fastp.
Will you provide interpretation?
Basic interpretation is included in the premium package.
