accessory scripts for processing varscan somatic/copynumber outputs.
MIT License
Statistics for this project are still being loaded, please check back later.
BS-Seeker3: An Ultra-fast, Versatile Pipeline for Mapping Bisulfite-treated Reads.
Alignment and antibody assembly pipelines for Croote et al. (Science, 2018)
Load numpy arrays and HDF5 files from VCF (variant call format)
Convenient plotting functions for working with variant call data.
Community-curated list of software packages and data resources for single-cell, including RNA-seq...
Single-cell analysis in Python. Scales to >1M cells.
BabelScan is a format independent data structure for holding different types of data from a scan ...
Add biological annotations to variants in a given VCF file.
SARS-CoV-2 analysis pipeline for short-read, paired-end illumina sequencing
Super sensitive mutation validator, uses sam/bam and vcf
See how pathogenic your mutations are according to AlphaMissense based on your 23andme raw data
Reliable, scalable, efficient demultiplexing for single-cell RNA sequencing