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I will perform large scale cancer genomics and mutation analysis
Unlock genomic insights with expert NGS data analysis, Medical imaging analysis
Bioinformatics and Medical Imaging Analyst with expertise in NGS cancer mutation analysis, Bulk RNA-Seq, scRNA-Seq, gene expression profiling, pathway analysis, MRI/CT tumor identification, and 3D Sli...
About this Gig
Whether you need support for a research project, thesis, manuscript, grant proposal, or biotech investigation, I can provide reliable and reproducible cancer genomics analysis.
I am a bioinformatics researcher with expertise in cancer genomics, NGS, and large-scale multi-cohort analysis. I will help you analyze somatic mutations from cancer genome datasets using state-of-the-art bioinformatics workflows.
Services Offered:
- NGS data analysis.
- Mutation profiling across cancer cohorts
- Driver gene identification
- Significantly mutated gene analysis
- Development of custom pipelines using R, Perl, Java, and Linux shell
- Mutation frequency analysis
Why choose me?
- PhD in Bioinformatics
- Publications in high-impact journals (NAR, BMC)
- Professional and deliver in time.
Tools n Tech
- Samtools, Bedtools
- Quality Control (FastQC, MultiQC)
- Read Trimming (Trimmomatic, Cutadapt)
- Alignment (BWA, Bowtie2, STAR, HISAT2)
- Variant Calling (GATK, FreeBayes, DeepVariant)
- Functional Annotation (ANNOVAR, VEP, SnpEff)
- Visulisation (IGV, Circos(
- Workflow Automation (Snakemake, Nextflow)
Deliverables
- Clean processed datasets
- Publication-quality figures
- Detailed analysis report
- Reproducible scripts (R/Python)
