Opal 5.3 Release Notes

Charlene Son-Rigby -

13 November 2017

The Opal 5.3 release upgrades the annotation pipeline with updates for ClinVar, OMIM, HPO and GO; and also contains various feature enhancements.

Feature Enhancements

Somatic:

  • Secondary analysis for somatic data now supported, using the Sentieon TNSeq algorithm.

Clinical Workflow and API:

  • Clinical Report 'Import Variants' and 'Export Variants for Confirmation' features are now available to all users in the workspace 
  • Clinical Report history can now be exported via the API.
 

Data Source & Algorithm Versions

Opal Pipeline 6.2.4 - November 13, 2017

  • 1000 Genomes phase 3 version 5 (downloaded May 2, 2013)
  • CADD v1.0
  • ClinGen Dosage Sensitivity Project, ISCA Evidence (downloaded October 16, 2016)
  • ClinVar (2017-10 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 October 10, 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-)

 

 

Have more questions? Submit a request

Comments