The complete sequence of a human genome

Box86 - Linux Userspace x86 Emulator with a twist, targeted at ARM Linux devices

NVR with realtime local object detection for IP cameras

A structural variation pipeline for short-read sequencing

A tutorial for DLS-2 migration

Collection of bioinformatics training materials

tools for working with genome variation graphs

Beatmup: image and signal processing library

E-Paper display for viewing sensor data from Home Assistant.

WebRTC/RTSP/RTMP/LL-HLS bridge for Wyze cams in a docker container

quickly set up your Plex dvr post processor

Remove commercials, add chapter markers, convert captions to subtitles, and compress files recorded from the Plex DVR

Workflow for germline short variant discovery using GATK4

My latest Hackintosh details and configuration 🍏

Strelka2 germline and somatic small variant caller

LIkelihood Ratio Interpretation of Clinical AbnormaLities

Scripts for implementing the Tractor pipeline

A tool set for short variant discovery in genetic sequence data.

This WDL pipeline implements data pre-processing and initial variant calling according to the GATK Best Practices for germline SNP and Indel discovery in human exome sequencing data.

Analysis of the penetrance of missense variants and tolerability of loss-of-function variants in PRNP

Shiny ClinVar web server source code

Repository for the GA4GH phenopacket schema

A library for reading text files over multiple cores.

Multivariate Analysis for the Behavioral Sciences: codes, datasets, examples, exercises, etc.

Method for detecting STR expansions from short-read sequencing data

Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms