Opal 5.5 Release Notes

Charlene Son-Rigby -

31 January 2018 

The Opal 5.5 adds features to Fabric's somatic offering. Fabric's oncology capabilities now include variant calling, annotation from cancer-specific databases, clinical curation from multiple providers, support for 2017 AMP scoring guidelines, and the ability to quickly create physician-ready clinical reports. 

This release also upgrades the annotation pipeline with the addition of the CIViC database for somatic curation content.

Feature Enhancements

Application:

  • Scoring History displays classifications of other SNVs in a gene, from the Classified Variant Database
  • Separate link outs for Alamut and IGV are now available. Please contact support@fabricgenomics.com to configure your workspace with these link outs
  • Dedicated clinical report pipeline for panel data has been deployed to speed creation of panel clinical reports

Somatic:

  • Annotations from the Clinical Interpretations of Variants in Cancer (CIViC) database are now available as Evidence and within the Gene Viewer. The Evidence column can now be displayed by as a default column for oncology tests
  • A new somatic workflow using CIViC curations is now available. 
 

Data Source & Algorithm Versions

Opal Pipeline 6.2.6 - 31 January 2018

  • 1000 Genomes phase 3 version 5 (downloaded May 2, 2013)
  • CADD v1.0
  • CIViC (downloaded January 17, 2018) 
  • ClinGen Dosage Sensitivity Project, ISCA Evidence (downloaded October 16, 2016)
  • ClinVar (2017-11 monthly XML release)
  • COSMIC v82
  • DGV Database of Genomic Variants (download May 15, 2016)
  • dbVar September 28, 2016 Release
  • dbNSFP version 2.9
  • dbSNP release 150
  • ENSEMBL version 83
  • ExAC 0.3 release
  • Exome Variant Server 6500 v0.0.30
  • Gene Ontology OBO  October 13, 2017
  • GeneSplicer  February 19, 2003
  • GERP++ 2010 release
  • Genome Reference Consortium Human Genome Build v37
  • GWAS catalogue (downloaded May 21, 2014)
  • HGNC and Entrez gene synonyms (downloaded August 9, 2017)
  • Human Phenotype Ontology1 build #133
  • Human Phenotype Ontology OBO October 5, 2017
  • MaxEntScan  September 25, 2003
  • MutationTaster (dbNSFP v2.9)
  • NNSplice v0.9
  • Omicia Score v2.0
  • OMIM (downloaded November 25, 2017)
  • PhastCons - phastCons46way (October 8, 2012)
  • PhenCode / LSDB (download April 30, 2014)
  • PhyloP - phyloP46way (December 1, 2009)
  • PolyPhen-2 v2.2.2 (dbNSFP v2.9)
  • RefSeq release 80/81 
  • SIFT (dbNSFP v2.9)
  • SiPhy v0.5
  • UMLS version 2017AA (May 8, 2017) 
  • VAAST Variant Prioritizer v1.1
  • VEP2 version v89

 

1Sebastian Köhler, Sandra C Doelken, Christopher J. Mungall, Sebastian Bauer, Helen V. Firth, et al. The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data. Nucl. Acids Res. (1 January 2014) 42 (D1): D966-D974 doi:10.1093/nar/gkt1026

2McLaren et. al. 2016 (doi:10.1186/s13059-016-)

 

Support Notes

1. Clinical reports can no longer be created using samples annotated with Opal Pipeline version 6.0.14 or older (samples annotated prior to July 8, 2017). 

 

 

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