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I will do ngs wes data analysis and somatic germline variant calling
Bioinformatics Expert for Reliable NGS Data Analysis
Hi, I'm Ranodip, a Bioinformatics and NGS Data Analyst with over 4 years of experience in multi-omics data analysis. I currently work at a leading genomics research institute in India, where I analyze...
About this Gig
I will perform high-quality Whole Exome Sequencing (WES) NGS data analysis from raw FASTQ files to annotated variants. I offer both germline variant calling and somatic variant calling (Tumor-normal paired or Tumor-only data). My workflow includes quality control, read alignment, duplicate marking, variant calling, filtering, annotation, coverage analysis, pathogenicity prediction, IGV validation, and candidate variant interpretation. I use industry-standard bioinformatics tools to deliver accurate, reproducible, and well-documented results for research and clinical projects.
Pricing (Per Sample):
- Basic: $5 per sample
- Standard: $8 per sample
- Premium: $12 per sample
Please contact me before placing an order to discuss your project requirements and choose the most suitable package. As I am new to Fiverr, I am excited to work with my first clients and am committed to providing high-quality service and timely delivery. I look forward to collaborating with you!
Technology:
Excel
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Other
Expertise:
Other
Programming language:
Python
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R
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SQL
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Other
FAQ
Do you offer custom bioinformatics analyses besides WES variant calling ?
Yes. I also provide custom bioinformatics and omics data analysis services based on your research requirements. Please contact me before placing an order so we can discuss your project and determine the best workflow.
What input files do you require?
I accept raw FASTQ files for WES analysis. If you have BAM, CRAM, or VCF files, please contact me first to discuss your requirements.
