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Data Analysis

eagle-i ID


Resource Type

  1. Data analysis service


  1. Fee for service
  2. Resource Description
    Finely-tuned and field-tested across hundreds of thousands of samples spanning flagship genomic initiatives, our tools are the industry-standard for genomic variant discovery. Coupled with the Broad-produced data used to train the tools, our outputs produce clean data with low false-positives and high sensitivity and specificity to discover causal variants. Sequence data analysis with the Picard Data Processing pipeline, VCF generation utilizing Genome Analysis Toolkit (GATK), Transcriptome analysis with TopHat & Star Aligner, GWAS array SNP and CNV analysis utilizing Birdsuite pipeline.
  3. Related Resource
  4. Related Resource
    Picard Data Processing pipeline
  5. Related Resource
    Genome Analysis Toolkit (GATK)
  6. Related Resource
  7. Related Resource
    Star Aligner
  8. Service Provided by
    Broad Institute Genomics Services
  9. Website(s)
Provenance Metadata About This Resource Record

Copyright © 2016 by the President and Fellows of Harvard College
The eagle-i Consortium is supported by NIH Grant #5U24RR029825-02 / Copyright 2016