Pretty 's Projects
List of software packages for single-cell data analysis, including RNA-seq, ATAC-seq, etc.
excel report generation using data from bcbio variant2 germline pipeline
ccfDNA Alignment pipeline with UMI calling. Snakemake workflow designed to align fastq reads, and call consensus on the barcoded reads tagged with UMI
š¢ Ready to learn! you will learn 10 skills as data scientist:š Machine Learning, Deep Learning, Data Cleaning, EDA, Learn Python, Learn python packages such as Numpy, Pandas, Seaborn, Matplotlib, Plotly, Tensorfolw, Theano...., Linear Algebra, Big Data, Analysis Tools and solve some real problems such as predict house prices.
Materials for the DeCART 2019 Summer School Data Visualization Course
Copy for learning
Python in 2 days for EVOP 2020 in Berlin
horizontal pileup
Intro to ChIPseq using HPC
Masks the genotype variants sites in FastQ reads
fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
Programming for Biology 2019
This is a walkthrough of the PFB2018 course taught at CSHL.
Config files for my GitHub profile.
Scanpy use cases.
Single cell current best practices tutorial case study for the paper:Luecken and Theis, "Current best practices in single-cell RNA-seq analysis: a tutorial"
sample-swap checking directly on BAMs/CRAMs for cancer data
scPrep/psuedotime with MAGIC and PHATE
TrajectoryNet: A Dynamic Optimal Transport Network for Modeling Cellular Dynamics
Training material based on webinar events