I will analyze your ngs genomic data including alignment and variant calling

Hello,

I provide bioinformatics analysis for next generation sequencing (NGS) data, combining a background in biochemistry and molecular biology with hands on experience in genomic data processing.

What I can help you with:

• Read alignment (raw FASTQ to aligned reads)
• Variant calling and annotation
• Quality control of sequencing data
• Genomic data cleaning and formatting
• Summary reports of findings

Who this is for:

• Researchers and labs working with sequencing data
• Biotech teams needing variant analysis support
• Anyone needing a second pass on genomic pipeline output

What you'll receive:

• Processed/aligned data
• Variant call output with annotation
• Plain-language summary of key findings
• Optional visualization of results

Send me details about your sequencing platform and data format before ordering so I can confirm the right approach.