Standardized decision support in next generation sequencing reports of somatic cancer variants.
about
DoCM: a database of curated mutations in cancer.Molecular predictive markers in tumors of the gastrointestinal tractOrganizing knowledge to enable personalization of medicine in cancerSomatic cancer variant curation and harmonization through consensus minimum variant level dataNext-generation sequencing in clinical oncology: next steps towards clinical validationClinical Validation of Targeted Next Generation Sequencing for Colon and Lung Cancers.Validation and Application of a Custom-Designed Targeted Next-Generation Sequencing Panel for the Diagnostic Mutational Profiling of Solid Tumors.Clinical applicability and cost of a 46-gene panel for genomic analysis of solid tumours: Retrospective validation and prospective audit in the UK National Health Service.DGIdb 2.0: mining clinically relevant drug-gene interactions.Mutational Analysis of Extranodal NK/T-Cell Lymphoma Using Targeted Sequencing with a Comprehensive Cancer PanelTissue-based next generation sequencing: application in a universal healthcare system.A new generation of cancer genome diagnostics for routine clinical use: overcoming the roadblocks to personalized cancer medicine.Toward precision medicine in glioblastoma: the promise and the challenges.The ins and outs of molecular pathology reporting.Enteric neuropathies: Yesterday, Today and Tomorrow.The current state of clinical interpretation of sequence variants.Personalized oncogenomics in the management of gastrointestinal carcinomas-early experiences from a pilot study.Database of genomic biomarkers for cancer drugs and clinical targetability in solid tumors.A novel molecular diagnostics platform for somatic and germline precision oncology.The right drugs at the right time for the right patient: the MD Anderson precision oncology decision support platform.Personal Cancer Genome Reporter: variant interpretation report for precision oncology.From somatic variants towards precision oncology: Evidence-driven reporting of treatment options in molecular tumor boards.Genome editing: a tool for research and therapy: towards a functional understanding of variants for molecular diagnostics using genome editing.Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencing.Clinical validation of the Tempus xO assay.Artificial Intelligence Approach for Variant ReportingPrecision oncology: separating the wheat from the chaffThe prognostic effects of somatic mutations in ER-positive breast cancer
P2860
Q27942768-4DFBACB3-AB78-44C7-8927-282F616E7BFAQ28070583-24EDB48C-83AF-48C8-A5BC-7584140C4066Q28652806-1A7B5AEF-324F-473A-AF87-AA3A1871A196Q31140983-C6EB141B-49EC-4424-AD01-C251F9E0F569Q34774908-8E050939-7231-4DF6-B3D7-EEFBD79AF22BQ35772123-73F40BA1-7DAE-4FD9-8826-19C25CEB9D9BQ35996102-7473C93F-C0DB-4863-95D9-7EC207E786BBQ36279825-1CF59F62-4BBF-4B10-8171-0122A13491B6Q36434749-605F9659-9BD8-420C-B562-2E8EA5301754Q37324841-E62AE5AF-B67D-4874-97DF-638AC01F3B68Q37691479-C800B407-ED3E-4B58-B4E3-58FFBEFD44B9Q38433965-11D2EDEE-AFCA-40CC-8952-10AF2DE60FE6Q38454659-3E5249C8-56D9-405B-B8C9-BD8B216A0086Q38875985-0C7B9ECD-B87D-45FC-8849-70A80F58895EQ38886424-744D0A8A-9991-4EB1-8928-A66495D76F27Q38981093-2DDC04C5-8753-4FD2-91E2-BE9535157281Q39644315-42E8ECE8-B427-45D3-A2F4-F32E3B629AE0Q39988198-B442EA0E-AD5A-4380-8F91-53665B1FF22DQ41023790-CF621E5A-5583-4487-9070-914CF5C6EFF3Q42380390-CD6CC187-937C-4952-83C0-E9F4D50ACB1BQ47258949-50FB2C3C-3DF9-4B26-A129-3C8544C19733Q52354170-0CA4C665-EFE3-495C-AF42-D13822B236FEQ52423188-AF16B949-AEEC-417D-90EC-2CEDC2FC905EQ52611832-37BA6E52-C722-4F37-864D-503ADF536A8BQ55091748-84E16563-8B3B-48FC-A7EE-6B9CCD08446EQ58581733-358C2601-BA3E-4110-92C5-33F9B0FB5A1FQ58698377-A609E70D-0823-4C05-8871-0147C9C562A4Q58765339-F8FE58BC-1778-47A0-AE4B-65093EE4805B
P2860
Standardized decision support in next generation sequencing reports of somatic cancer variants.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Standardized decision support ...... ts of somatic cancer variants.
@en
type
label
Standardized decision support ...... ts of somatic cancer variants.
@en
prefLabel
Standardized decision support ...... ts of somatic cancer variants.
@en
P2093
P2860
P1433
P1476
Standardized decision support ...... ts of somatic cancer variants.
@en
P2093
A John Iafrate
Darrell Borger
Dora Dias-Santagata
Leif W Ellisen
Rodrigo Dienstmann
P2860
P304
P356
10.1016/J.MOLONC.2014.03.021
P577
2014-04-04T00:00:00Z