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edico genome dragen (9 results) showing 1 - 9

Free Trial

Starting from $10.35 to $22.10/hr for software + AWS usage fees

The DRAGEN Complete Suite* enables ultra-rapid analysis of Next Generation Sequencing (NGS) data for large data sets, such as whole genomes, exomes, and genes/panels. This application uses the DRAGEN Platform and includes highly-optimized algorithms for mapping, aligning, sorting, duplicate...

Linux/Unix, CentOS Version 7.5 - 64-bit Amazon Machine Image (AMI)

Free | 12 month subscription available.

This file contains the summary of over 7,200 MRSA genomes that have been assembled from raw sequence data. All raw sequence data are from NCBI.

  • Version 1.1.0
  • Sold by AEHRC

VariantSpark is a scalable toolkit for genome-wide association studies optimized for GWAS like datasets. Machine learning methods and, in particular, random forests (RFs) are a promising alternative to standard single SNP analyses in genome-wide association studies (GWAS) and from scalable to rare...

Linux/Unix, Ubuntu 18.04 - 64-bit Amazon Machine Image (AMI)

Storing and processing NGS data is a very challenging task because of big amount of data. At the same time the demand for higher sequencing throughput grows faster than IT industry is able to provide supporting infrastructure. We envision a world where a millions, if not billions, genetic samples...

Linux/Unix, Amazon Linux 2018.03 - 64-bit Amazon Machine Image (AMI)

Sentieon ( supplies award-winning software tools for secondary analysis of NGS data. Sentieon DNAseq and TNseq produce results identical to the Broad Institute's BWA-GATK HaplotypeCaller/MuTect/MuTect2 Best Practice Workflow by implementing the same mathematics but with...

Linux/Unix, Amazon Linux 2017.09 - 64-bit Amazon Machine Image (AMI)

We are all about innovation at Leap of Faith Technologies and are developing tools to help you develop and test your latest innovation in informatics. Our Genomic Archiving and Communication Systems (GACS) is available for you to use to speed the development of your latest innovation in genomics....

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Starting from $17.82 to $17.82/hr for software + AWS usage fees

Analyze more than 800,000 long reads of genomic data (about 102 GB) in 3 hours thanks to Huxelerate Hugenomic Nanopolish(*). Huxelerate Hugenomic Nanopolish enables ultra-fast signal-level analysis of large datasets of Oxford Nanopore Sequencing data. This AMI is a CentoOS Linux image and comes...

Linux/Unix, CentOS Centos 7 - 64-bit Amazon Machine Image (AMI)

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