☆18Dec 18, 2023Updated 2 years ago
Alternatives and similar repositories for llms_from_dummies
Users that are interested in llms_from_dummies are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- An extensible Ruby on Rails web-service application and database for visualising HTGS data☆18Mar 7, 2014Updated 12 years ago
- Demonstrate A Drake Workflow Package☆29Mar 6, 2020Updated 6 years ago
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Feb 3, 2021Updated 5 years ago
- Easily run WDL workflows on GCP☆14Sep 28, 2021Updated 4 years ago
- hail-based pipelines for annotating variant callsets and exporting them to clickhouse☆23Aug 6, 2026Updated 3 weeks ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- Calculate AUC based on GWAS summary statistics only☆10Jun 29, 2018Updated 8 years ago
- Total copy number inference from single-cell RNA and ATAC sequing with cell clustering☆12Oct 31, 2024Updated last year
- Standard operating procedures for H3ABionet data processing and analyses☆11Aug 30, 2021Updated 5 years ago
- Benchmarking variant calling in polyploids☆16Nov 26, 2021Updated 4 years ago
- Run Python functions locally or in the cloud. Built for computational science.☆22Oct 4, 2023Updated 2 years ago
- ☆12Sep 27, 2023Updated 2 years ago
- ☆10Jul 23, 2020Updated 6 years ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Apr 23, 2019Updated 7 years ago
- Breast cancer risk prediction using genotyped data☆12Oct 11, 2018Updated 7 years ago
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- A set of Pyro models and functions to infer CNA from scRNA-seq data☆11Aug 14, 2023Updated 3 years ago
- Benchmark for evaluating LLM agents in bioinformatics☆32Aug 11, 2026Updated 2 weeks ago
- ☆15Aug 1, 2021Updated 5 years ago
- Integrated Variant Caller☆17Mar 15, 2018Updated 8 years ago
- A python tool for parsing pedigree files☆16Aug 29, 2017Updated 9 years ago
- Python wrapper for Caterva. Still preliminary.☆21Apr 10, 2023Updated 3 years ago
- scraping news articles from Quartz☆11Feb 9, 2021Updated 5 years ago
- Variant Effect Prediction for Python☆16Apr 5, 2017Updated 9 years ago
- ☆12Updated this week
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- ☆16Apr 10, 2024Updated 2 years ago
- ☆18Sep 23, 2024Updated last year
- A repository for the Petagraph project☆16Dec 11, 2025Updated 8 months ago
- Negative binomial maximum likelihood estimate implementation in Python using L-BFGS-B☆15Jan 27, 2022Updated 4 years ago
- ☆19Nov 30, 2021Updated 4 years ago
- This project is deprecated, please see strelka2 at https://github.com/Illumina/strelka☆37Feb 24, 2017Updated 9 years ago
- An experimental AI agent workflow.☆17Oct 11, 2025Updated 10 months ago
- Import and run CWL workflows on DNAnexus (alpha)☆13Sep 12, 2018Updated 7 years ago
- Method for performing genome-wide association like studies on neighborhoods identified on biological networks relevant for the phenotype …☆17Jun 28, 2023Updated 3 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- Extends miniwdl to run workflows on AWS Batch & EFS☆22Feb 5, 2024Updated 2 years ago
- Python interface to the GenoLogics LIMS server via its REST API.☆11Mar 30, 2022Updated 4 years ago
- ☆12Dec 10, 2024Updated last year
- ☆27May 22, 2025Updated last year
- Workflow for somatic variant calling of long read data☆27Updated this week
- A positive-unlabeled ensemble learning framework for disease gene prioritization.☆21Nov 10, 2025Updated 9 months ago
- Nextflow implementation of the GATK HaplotypeCaller pipeline☆13Dec 27, 2025Updated 8 months ago