Produce redistributable builds of Python

extract SV signal from a BAM

Structural variant toolkit for VCFs

don't get DUP'ed or DEL'ed by your putative SVs.

Tools for processing and analyzing structural variants.

Graph realignment tools for structural variants

DELLY2: Structural variant discovery by integrated paired-end and split-read analysis

structural variant calling and genotyping with existing tools, but, smoothly.

Structural variation caller using third generation sequencing

What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.

📖 Collection of naming guides for writing more consistent and readable codes

Automated generation of real Swagger/OpenAPI 2.0 schemas from Django REST Framework code.

Django multiple db test

Seamless integration between Django REST framework and Datatables.

Strelka2 germline and somatic small variant caller

The nimble & robust variant annotator

Structural variant and indel caller for mapped sequencing data

🎓 All things Vim!

👔 Online business card with a minimal landing page theme for any social media or online presence account: fork, edit, and go!

Python library to facilitate genome assembly, annotation, and comparative genomics

A curated list of awesome Kotlin related stuff Inspired by awesome-java.

A Latex template to share Wi-Fi credentials as business cards.

Google Analytics Proxy

Receive automatic email notifications before your Google Contacts birthday and other events!

Useful bash one-liners for bioinformatics.

A fast 23andMe DNA parser and inferrer for Python

GenomeWarp translates genetic variants from one genome assembly version to another.

A Python command-line and library that draws basic graphs in the terminal

Make Your Company Data Driven. Connect to any data source, easily visualize, dashboard and share your data.

Learn how to design large-scale systems. Prep for the system design interview. Includes Anki flashcards.