Skip to content
View kevinpryan's full-sized avatar

Highlights

  • Pro

Block or report kevinpryan

Block user

Prevent this user from interacting with your repositories and sending you notifications. Learn more about blocking users.

You must be logged in to block users.

Please don't include any personal information such as legal names or email addresses. Maximum 100 characters, markdown supported. This note will be visible to only you.
Report abuse

Contact GitHub support about this user’s behavior. Learn more about reporting abuse.

Report abuse
Showing results
R 1 Updated Jan 27, 2025

Our basic allele specific analysis pipeline for single nuclei data, based on nextflow

Java 2 Updated Feb 26, 2024

Accompanying codes for pan cancer atlas of intracellular tumor antigens

Python 2 Updated Feb 4, 2025
R 5 1 Updated Jul 5, 2024

dockerization of phlat hla typing tool

Shell 3 1 Updated Jul 25, 2022

Nextflow pipeline to run somatic alteration calling from single-cell data using SComatic

Nextflow 1 1 Updated Apr 29, 2024

DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.

Python 3,317 736 Updated Dec 9, 2024
Python 20 2 Updated Sep 27, 2024

Pipeline to detect HLA disruption from WES and RNAseq data

R 16 5 Updated Jan 10, 2025

Detection of chimeric transcripts (aka fusions) from barcoded single cell RNA-seq

Python 6 6 Updated Sep 26, 2019

Plot structural variant signals from many BAMs and CRAMs

Python 536 69 Updated Jul 13, 2024

The nimble & robust variant annotator

C# 174 44 Updated Apr 25, 2024

xHLA: Fast and accurate HLA typing from short read sequence data

Jupyter Notebook 108 52 Updated Oct 13, 2023
SCSS 550 227 Updated Mar 23, 2021

Deep semi-supervised complete cell deconvolution https://imsb-uke.github.io/DISSECT/

Jupyter Notebook 4 Updated Jan 8, 2025

AltAnalyze is a multi-functional and easy-to-use software package for automated single-cell and bulk gene and splicing analyses. Easy-to-use precompiled graphical user-interface versions available …

Python 100 31 Updated Jul 7, 2022

Long-read splice alignment with high accuracy

Python 61 10 Updated Sep 26, 2024

Splicing Neo Antigen Finder (SNAF) is an easy-to-use Python package to identify splicing-derived tumor neoantigens from RNA sequencing data, it further leverages both deep learning and hierarchical…

Python 46 9 Updated Jul 25, 2024

Snakemake pipeline for benchmarking cell-type deconvolution methods and deconvolving real bulk RNA-seq data with the use of scRNA-seq datasets

R 15 2 Updated Aug 1, 2024

Demultiplexing and debarcoding tool designed for LR-Split-seq data.

Python 22 4 Updated Oct 19, 2023

A program for the analysis of single cell nanopore long read data

Tcl 16 Updated Jul 11, 2024

R package for analysing single cell data

R 51 6 Updated Dec 8, 2022

LongSom tool for long-reads

Python 7 Updated Jan 13, 2025

This repository has the codes to reproduce the figures in our paper on single-cell long-read RNA sequencing data of patient-derived ccRCC organoids

HTML 1 Updated Jan 9, 2025

Calculation of the Percentage of Conserved Proteins following Qin, Xie et al. 2014 but using DIAMOND instead of BLASTP for alignments.

Nextflow 23 6 Updated Oct 24, 2024

Code Associated with the Nature Communications Publication entitled "Single-cell analysis reveals prognostic fibroblast subpopulations linked to molecular and immunological subtypes of lung cancer"

R 9 8 Updated Jan 3, 2023

Predictor of TCR-epitope interactions

Python 21 6 Updated Jan 16, 2025

Dockerfile for Kourami assembler for HLA haplotypes

Shell 1 Updated Oct 7, 2022

A script to run HLA typing tools from next generation sequencing data

Python 12 1 Updated Jan 4, 2023
Next