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ramsainanduri/README.md

MasterHead

Hi, I'm Ram Nanduri

Bioinformatics developer working with genomics, clinical diagnostics, and research software.

Website · LinkedIn


About me

I am a bioinformatics developer based in Lund, Sweden. I work with genomic data to study disease-related variation and help translate sequencing results into evidence that can be interpreted and used in a clinical setting.

My work involves examining patterns in DNA and RNA sequencing data, assessing their technical and biological plausibility, and developing methods to make the analysis more reliable. I am particularly interested in cancer genomics, variant interpretation, quality control, and the validation of computational approaches.

I also develop the software needed to support this work from reproducible analysis workflows to applications that help researchers and clinical teams explore, review, and report genomic findings. This means moving regularly between biological questions, computational methods, and software engineering.

Areas I work in

  • Cancer genomics and clinical sequencing
  • DNA and RNA variant analysis
  • Variant interpretation and reporting
  • Workflow development and validation
  • Research and clinical software development

Technical work

I primarily use Python for analysis and backend development, and Nextflow or Snakemake for reproducible workflows. For user-facing applications, I work with TypeScript and React. My development environment also includes databases, containers, Linux, HPC systems, testing, and CI/CD.


GitHub activity

GitHub statistics showing stars, commits, pull requests, issues, and contributions Most-used languages across public repositories

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  1. Reverse_Compliment Reverse_Compliment Public

    Shell 1

  2. split_multi_fasta split_multi_fasta Public

    Split multi fasta file into single fasta files

    Python 9 8

  3. subset_multifasta subset_multifasta Public

    Subset Multi Fasta

    Python

  4. bash-handbook bash-handbook Public

    Forked from denysdovhan/bash-handbook

    📖 For those who wanna learn Bash

    JavaScript 1

  5. SMD-Bioinformatics-Lund/PGxModule SMD-Bioinformatics-Lund/PGxModule Public

    PGxModule is an advanced Nextflow DSL2 workflow, designed to seamlessly integrate into your genomics pipeline. It empowers you to generate sample-specific reports with clinical guidelines, leveragi…

    Nextflow 1

  6. SMD-Bioinformatics-Lund/cll_genie SMD-Bioinformatics-Lund/cll_genie Public

    CLL Genie is a web application for managing LymphoTrack data, IMGT/V-QUEST analysis, IGHV mutation assessment, and clinical CLL reporting.

    Python 1