OpenEHR modeling for genomics in clinical practice
暂无分享,去创建一个
[1] Dipak Kalra,et al. The openEHR Foundation. , 2005, Studies in health technology and informatics.
[2] Guilherme Del Fiol,et al. Integrating Genomic Resources with Electronic Health Records using the HL7 Infobutton Standard , 2016, Applied Clinical Informatics.
[3] Christopher G Chute,et al. Practical considerations for implementing genomic information resources , 2016, Applied Clinical Informatics.
[4] Robert C. Green,et al. Clinical Genome Sequencing , 2013 .
[5] Simon M. Lin,et al. A Review on Genomics APIs , 2015, Computational and structural biotechnology journal.
[6] M. Levy,et al. Integrating cancer genomic data into electronic health records , 2016, Genome Medicine.
[7] Magalie S Leduc,et al. Clinical whole-exome sequencing for the diagnosis of mendelian disorders. , 2013, The New England journal of medicine.
[8] Wilko Spiering,et al. Diagnostic Clinical Genome and Exome Sequencing , 2014 .
[9] Birgit Funke,et al. College of American Pathologists' laboratory standards for next-generation sequencing clinical tests. , 2015, Archives of pathology & laboratory medicine.
[10] Gonçalo R. Abecasis,et al. The variant call format and VCFtools , 2011, Bioinform..
[11] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[12] M. Guyer,et al. Charting a course for genomic medicine from base pairs to bedside , 2011, Nature.
[13] Andrew G. Ury,et al. Storing and interpreting genomic information in widely deployed electronic health record systems , 2013, Genetics in Medicine.
[14] Michael R. Speicher,et al. A survey of tools for variant analysis of next-generation genome sequencing data , 2013, Briefings Bioinform..
[15] F. Cunningham,et al. The Ensembl Variant Effect Predictor , 2016, Genome Biology.
[16] Joshua L. Deignan,et al. ACMG clinical laboratory standards for next-generation sequencing , 2013, Genetics in Medicine.
[17] Gil Alterovitz,et al. SMART precision cancer medicine: a FHIR-based app to provide genomic information at the point of care , 2016, J. Am. Medical Informatics Assoc..
[18] Gil Alterovitz,et al. SMART on FHIR Genomics: facilitating standardized clinico-genomic apps , 2015, J. Am. Medical Informatics Assoc..
[19] W. Grody,et al. ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 , 2008, Genetics in Medicine.
[20] Keith Marsolo,et al. Practical considerations in genomic decision support: The eMERGE experience , 2015, Journal of pathology informatics.
[21] Leslie G Biesecker,et al. Diagnostic clinical genome and exome sequencing. , 2014, The New England journal of medicine.
[22] Mauricio O. Carneiro,et al. From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline , 2013, Current protocols in bioinformatics.
[23] Alice Virani,et al. Diagnostic clinical genome and exome sequencing. , 2014 .
[24] Raymond Dalgleish,et al. HGVS Recommendations for the Description of Sequence Variants: 2016 Update , 2016, Human mutation.