- Hi, I’m John @Focyte
- A research scientist with 15+ years experience in the fields of cancer, immunology, and RNA biology
- I use R and Python to process and analyse genomic data
- Using Linux Command Line tools and Bash scripting I have worked with Next Generation Sequencing (NGS) pipeliens
- Through collaborations with data scientists I have also tried some feature selection methods and machine learning
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DNA-Variant-NF-Focyte
DNA-Variant-NF-Focyte PublicA Nextflow pipeline for processing and calling of variants: FASTA to VCF
Nextflow
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ATACseq
ATACseq PublicPipeline for analysing ATAC-seq data from raw fastq files to called genomic peaks
Shell
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