awslabs / genomics-tertiary-analysis-and-machine-learning-using-amazon-sagemakerLinks
The Genomics Tertiary Analysis and Machine Learning Using Amazon SageMaker solution creates a scalable environment in AWS to develop machine learning models using genomics data, generate predictions, and evaluate model performance.
☆11Updated last year
Alternatives and similar repositories for genomics-tertiary-analysis-and-machine-learning-using-amazon-sagemaker
Users that are interested in genomics-tertiary-analysis-and-machine-learning-using-amazon-sagemaker are comparing it to the libraries listed below
Sorting:
- This guidance creates a scalable environment in AWS to prepare genomic, clinical, mutation, expression and imaging data for large-scale a…☆24Updated last year
- This solution provides a framework for Next Generation Sequencing (NGS) genomics secondary-analysis pipelines using AWS Step Functions an…☆39Updated last year
- Utilities for analyzing mutations and neoepitopes in patient cohorts☆20Updated 7 years ago
- An option to spin cost effective EMR clusters in AWS with Hail and JupyterNotebook installed☆16Updated 5 years ago
- In Silico Prediction of Novel Therapeutic Targets Using Gene – Disease Association Data☆18Updated 7 years ago
- Deconvolution of seed effects from gene effects in large scale RNAi screens☆11Updated 7 years ago
- AWS Quick Start Team☆24Updated 8 months ago
- This project contains the webapp sample integrated with AWS HealthOmics, which allows users such as admin and bioinformaticians to operat…☆19Updated 7 months ago
- provides common tools and lookup tables used primarily by the hgvs and uta packages☆22Updated 3 months ago
- ☆75Updated 3 weeks ago
- Tibanna helps you run your genomic pipelines on Amazon cloud (AWS). It is used by the 4DN DCIC (4D Nucleome Data Coordination and Integr…☆69Updated 2 months ago
- Code for the data processing pipeline☆17Updated 4 years ago
- ☆11Updated 3 years ago
- A cloud-based deployment of the 10x Genomics Cell Ranger software☆14Updated 5 years ago
- ALOFT, the Annotation Of Loss-of-Function Transcripts, provides extensive functional annotations to loss-of-function variants in the hum…☆19Updated 5 years ago
- Linter rules for Nextflow DSL scripts☆34Updated this week
- PRS-on-SPARK☆18Updated 4 years ago
- Railroadtracks is a Python package to handle connected computation steps for DNA and RNA Seq.☆14Updated 10 years ago
- iS-CellR: interactive graphical tool for analysis of single-cell RNAseq data☆24Updated 5 years ago
- R package with netDx software and data for examples☆12Updated 2 years ago
- Extends miniwdl to run workflows on AWS Batch & EFS☆22Updated last year
- Python library & CLI to create, view and edit PFB files☆11Updated this week
- Repository for development of the genomic module of the CDM.☆20Updated 6 years ago
- SEQSpark documentation☆18Updated 4 years ago
- Bayesian analysis of MPRA and other high-throughput genomic assays☆10Updated 4 years ago
- Introduction to single-cell RNA-Seq analysis workshop☆15Updated 8 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Updated 6 years ago
- ☆21Updated last year
- Simple and efficient access to genomic data for deep learning models.☆43Updated 5 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆21Updated 3 years ago