alkc
Currently incarnated as a Bioinformatician/Baker at @Clinical-Genomics-Lund
Lund University HospitalUnexpected input: '{' @ line 3225, column 16.
alkc's Stars
pallets/flask
The Python micro framework for building web applications.
bregman-arie/devops-exercises
Linux, Jenkins, AWS, SRE, Prometheus, Docker, Python, Ansible, Git, Kubernetes, Terraform, OpenStack, SQL, NoSQL, Azure, GCP, DNS, Elastic, Network, Virtualization. DevOps Interview Questions
bigskysoftware/htmx
</> htmx - high power tools for HTML
linexjlin/GPTs
leaked prompts of GPTs
doomemacs/doomemacs
An Emacs framework for the stubborn martian hacker
SawyerHood/draw-a-ui
Draw a mockup and generate html for it
a16z-infra/companion-app
AI companions with memory: a lightweight stack to create and host your own AI companions
pallets/quart
An async Python micro framework for building web applications.
rajasegar/awesome-htmx
Awesome things about htmx
Kalabasa/htmz
html with targeted manipulation zones
PyHAT-stack/awesome-python-htmx
A curated list of things related to python-based web development using htmx
Ensembl/ensembl-vep
The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants
licht1stein/obsidian.el
Obsidian Notes for Emacs
brentp/vcfanno
annotate a VCF with other VCFs/BEDs/tabixed files
olavolav/uniplot
Lightweight plotting to the terminal. 4x resolution via Unicode.
marty331/fasthtmx
FastAPI-HTMX Demo Project
pcingola/SnpEff
genome-in-a-bottle/giab_data_indexes
This repository contains data indexes from NIST's Genome in a Bottle project.
m-burst/flake8-pytest-style
A flake8 plugin checking common style issues or inconsistencies with pytest-based tests.
gforcada/flake8-isort
flake8 plugin that integrates isort
broadinstitute/gatk-sv
A structural variation pipeline for short-read sequencing
gagneurlab/drop
Pipeline to find aberrant events in RNA-Seq data, useful for diagnosis of rare disorders
edmondchuc/flask-htmx
A Flask extension to work with HTMX.
nf-core/raredisease
Call and score variants from WGS/WES of rare disease patients.
Illumina/SMNCopyNumberCaller
A copy number caller for SMN1 and SMN2 to enable SMA diagnosis and carrier screening with WGS
edmundmiller/nextflow-mode
Emacs major mode for Nextflow
genomic-medicine-sweden/nallo
A long-read (PacBio and ONT) analysis pipeline written in Nextflow
bejobioinformatics/tabixpy
Tabix reader written 100% in Python
genomic-medicine-sweden/pgx
Pharmacogenomics pipeline
rasmusab/ds-exploration-template
A template for a simple repo where your data science team can stash throwaway code