GoogleCloudPlatform / solutions-google-compute-engine-cluster-for-grid-engineLinks
Grid Engine on Compute Engine provides a shell script to manage a Compute Engine cluster along with instructions on how to install and configure Sun Grid Engine on the Compute Engine cluster
☆22Updated 8 years ago
Alternatives and similar repositories for solutions-google-compute-engine-cluster-for-grid-engine
Users that are interested in solutions-google-compute-engine-cluster-for-grid-engine are comparing it to the libraries listed below
Sorting:
- Examples for the Google Genomics Pipelines API.☆50Updated 8 years ago
- [Historical] Reproducible Analyses for Bioinformatics☆106Updated 6 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 9 years ago
- Run bcbio-nextgen genomic sequencing analyses using isolated containers and virtual machines☆68Updated 5 years ago
- The open source version of the Melbourne Genomics Health Alliance Exome Sequencing Pipeline☆33Updated 8 years ago
- Snakemake library for bioinformatics programs, with a focus on next-generation sequencing☆22Updated 10 years ago
- CRAM format specification and java API for read data.☆59Updated 7 years ago
- variant discovery and annotation using GATK and Ensembl☆17Updated 12 years ago
- A fast Python library for VCF files leveraging Cython for speed.☆52Updated 7 years ago
- A configurable de novo assembly pipeline☆28Updated 9 years ago
- Benchmarking toolkit for variant calling☆48Updated 5 years ago
- a wee tool for random access into BGZF files.☆86Updated 7 years ago
- vcf file manipulation☆22Updated 10 years ago
- [Bio in Docker] Symposium 2015☆21Updated 8 years ago
- Provides access to complex Bioinformatics software (even BioLinux!) in just one command.☆75Updated 8 years ago
- Tools for next-generation sequencing analysis☆89Updated 6 years ago
- Manage the visualization of large amounts of other people's [often messy] genomics data☆18Updated 9 years ago
- HPG Aligner is an ultrafast and highly sensitive Next-Generation Sequencing (NGS) mapper which supoprts both DNA and RNA alignment☆34Updated 8 years ago
- Tools for producing pseudo-cgh of next-generation sequencing data☆18Updated 9 years ago
- Scalable RNA-seq analysis☆73Updated 5 years ago
- Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)☆86Updated 8 years ago
- A collection of well-known bioinformatics programs.☆25Updated 10 years ago
- pre-process illumina reads☆19Updated 3 years ago
- A proof of concept RNA-Seq pipeline with Nextflow☆33Updated 5 years ago
- Core consonance utilities for scheduling, reporting on, and provisioning VMs for workflows☆14Updated 7 years ago
- Standalone C library for assembling Illumina short reads in small regions☆72Updated 3 years ago
- SevenBridges Python Api bindings☆46Updated 11 months ago
- Toil workflows for common genomic pipelines☆33Updated 6 years ago
- Docker images of bioinformatics software☆21Updated 8 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated this week