Name: Nagarajan Paramasivam
Type: User
Company: DKFZ, NCT
Bio: Computational Biologist, cancer genomics
Twitter: naga_rna
Location: Heidelberg, Germany
Nagarajan Paramasivam's Projects
Allele-specific copy number estimation with whole genome sequencing
The DKFZ alignment workflow plugin originally developed at the eilslabs.
Bioinformatics data-mining
Application for making ENCODE Blacklists
Characterization of Germline variants
This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file.
Unsupervised subgroup classification based on consensus clustering
A basic Roddy plugin for computational oncology workflows
My CV built using RMarkdown and the pagedown package.
R notebooks for the code samples of the book "Deep Learning with R"
Docker container for running AnnotSV
A demo flask app in docker
A docker image for the ML
updated MNIST CNN script from rKeras
A series of Jupyter notebooks that walk you through the fundamentals of Machine Learning and Deep Learning in python using Scikit-Learn and TensorFlow.
A Platypus-based workflow for indel calling
A tiny scalar-valued autograd engine and a neural net library on top of it with PyTorch-like API. Based on Karpathy's micrograd
Python implementations of the k-modes and k-prototypes clustering algorithms, for clustering categorical data
Learning ML with different data sets
Lollipop-style mutation diagrams for annotating genetic variations.
fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
Bayesian haplotype-based mutation calling
Platypus based small variant calling on a single or multiple samples setting.
Materials and IPython notebooks for "Python for Data Analysis" by Wes McKinney, published by O'Reilly Media