gatoravi - Overview

Skip to content

Navigation Menu

Sign in

Appearance settings

Hi, I'm Avinash

Computational biologist working at the intersection of genomics and software.

Languages: Python, R, C/C++

Projects

  • castools — command line tools for the CAS project
  • regtools — integrate DNA-seq and RNA-seq data to identify regulatory mutations
  • maury — R package to detect sample-swaps in NGS data
  • arnav — mutation calling using a site-specific binomial model
  • bam-parser-tutorial — parsing BAM files using htslib
  • mpileup2readcounts — per-nucleotide read counts from samtools mpileup

Links

Pinned Loading

  1. Forked from griffithlab/regtools

    Tools that integrate DNA-seq and RNA-seq data to help identify mutations that have a regulatory effect.

    C++

  2. An R package to detect sample-swaps in Next Generation Sequencing(NGS) data.

    R 2

  3. Mutation calling using a site-specific binomial model

    C 1

  4. A simple example of parsing BAM files using htslib

    C 12 2

  5. Get per-nucleotide readcounts from samtools mpileup

    C++ 5 6