I will do genomics variant calling and gene annotation using gatk
About this Gig
Do you have genomic sequence data and need help with variant identification or gene annotation? I will perform clear, well-documented genomics analysis and deliver results you can use directly in your research or thesis.
What I offer:
- DNA sequence quality control and trimming (FastQC, Trimmomatic)
- Reference genome alignment (BWA, Bowtie2)
- SNP and indel variant calling (GATK, bcftools)
- Variant annotation and filtering (SnpEff, ANNOVAR)
- Gene finding and functional annotation (Prokka, BLAST)
- Manhattan plots, variant summary tables, and written report
All scripts (Python/Bash/R) are included so your analysis is fully reproducible. I work with human, plant, and microbial genomes.
Message me with your FASTQ or VCF files and organism details before ordering.
FAQ
What organisms do you support?
Human, animal, plant, and microbial genomes as long as a reference genome is available.
What input files do you need?
Raw FASTQ or an already aligned BAM/VCF file. I can work with either.
Will I get the scripts used?
Yes, all code is delivered so you can reproduce or extend the analysis yourself.
