Name: Hamid Ghaedi
Type: User
Company: Queens University
Bio: Passionate about genomic data science
Twitter: HaGhaedi
Location: Kingston, ON, Canada
Blog: https://www.biostars.org/u/49222/
Hamid Ghaedi's Projects
Pipeline to download, process and analyze TCGA bladder cancer ATAC-seq data on HPC environment
A collection of awk one-liner helpful in genomic data science
IHC based classifier to predict major subtypes of bladder cancer:
A deep learning approach to predict origin of cancer based on DNA methylation profile
Predict cancer tissue of origin using DNN-based methylation model
A Python library that helps data scientists to infer causation rather than observing correlation.
Steps into local deployment of cBioPortal using Docker on a Win machine
XGBoost classifiers to predict variant classification conflict
Production repo to accompany Deep Learning with Structured Data book from Manning: https://www.manning.com/books/deep-learning-with-structured-data
A repo on DNA-seq pipleine for somatic mutation calling and annotation
From RNA-seq raw reads to enriched pathways by DEGs
repo for sharing fils
Overview of GDC Harmonization Workflows
Harmony framework for connecting scRNA-seq data from discrete time points
Identification and annotation of HetExc regions in human genome hg38
Identifying regions in exomes with excess of heterozygotes
Using ESM-variant to identify critical residues in a protein, needed to assign PM1 criteria to a variant
R script to map gene name to each KEGG pathways and Modules
Course to get into Large Language Models (LLMs) with roadmaps and Colab notebooks.
Listing of papers about machine learning for proteins.
customization of the original package
Using SuperCell to define meta cell in sc datasets
Comprehensive tutorial for differential methylation analysis, differential variability analysis and integrative analysis
A worksheet for Modern Statistics for Modern Biology book
Somatic Mutation data Clustering
Mapping genes in the Oncomine Comprehensive Assay v3 (ocav3) to KEGG pathways
The snakemake workflow for whole-exome sequencing analysis and generating vcf files