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DRAGEN Complete Suite - Genome (approx. $15 per Genome)

DRAGEN Complete Suite - Genome (approx. $15 per Genome)

By: Edico Genome Latest Version: 2.2

This version has been removed and is no longer available to new customers.

Product Overview

**A new version of the DRAGEN Complete Suite is available under a standalone app for BOTH genomes and exomes. Please note that all latest versions will be released using that app moving forward.**

The DRAGEN Complete Suite (Genome)* enables ultra-rapid analysis of Next Generation Sequencing (NGS) data for large data sets, such as whole genomes. This application uses the DRAGEN Platform and includes highly-optimized algorithms for mapping, aligning, sorting, duplicate marking, and haplotype variant calling. The DRAGEN CS (Genome) includes a host of pipelines including our DRAGEN Germline V2 Pipeline, DRAGEN Somatic V2 Pipeline (T and T/N), DRAGEN Virtual Long Read Detection (VLRD), DRAGEN RNA Gene Fusion, DRAGEN Joint Genotyping Pipeline, and GATK Best Practices. The DRAGEN Germline V2 and DRAGEN Somatic V2 pipelines have greatly improved accuracy in calling SNPs and Indels compared to industry standard. This app also supports Illumina NovaSeq BCL conversion, download/upload of data streaming, and compressed reference hash tables for a more seamless and efficient workflow.

**Before running the DRAGEN Complete Suite (Genome), please be aware of the following limitations:
- This app does not support exome samples <22 gigabases, somatic tumor-only samples <40 gigabases, and somatic tumor-normal samples <80 gigabases. If a sample has these parameters, an output file will not be produced.*
- Mixture of single-end and paired-end input data is not supported.



Operating System

Linux/Unix, CentOS 7.2

Delivery Methods

  • Amazon Machine Image

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