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DRAGEN Complete Suite

By: Latest Version: 2.6.3
Linux/Unix
Linux/Unix

Product Overview

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 marking, and haplotype variant calling. The DRAGEN CS 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 Copy Number Variant (CNV) Pipeline, 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:
- Mixture of single-end and paired-end input data is not supported.

**Pricing Breakdown:
F1.2xlarge: $10.35 (DRAGEN) + $1.65 (Compute) = $12.00/hr
Per Genome: $12.00hr/0.8 genomes = $15
Per Exome: $12.00hr/5.45 exomes = $2
F1.16xlarge: $22.10 (DRAGEN) + $13.20 (Compute) = $35.30/hr
Per Genome: $35.30hr/1.76 genomes = $20
Per Exome: $35.30hr/12 exomes = $3

Version

2.6.3

By

Operating System

Linux/Unix, CentOS Version 7.2

Fulfillment Methods

  • Amazon Machine Image

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