Q3141608 (Q3141608): Difference between revisions

From EU Knowledge Graph
Jump to navigation Jump to search
(‎Changed an Item: Edited by the infer coords bot - inferring coordinates from location)
(‎Changed an Item: Edited by the materialized bot - inferring region from the coordinates)
Property / contained in NUTS
 
Property / contained in NUTS: Cantabria / rank
 
Normal rank

Revision as of 13:43, 10 October 2021

Project Q3141608 in Spain
Language Label Description Also known as
English
No label defined
Project Q3141608 in Spain

    Statements

    0 references
    40,750.0 Euro
    0 references
    81,500.0 Euro
    0 references
    50.0 percent
    0 references
    1 January 2017
    0 references
    31 March 2020
    0 references
    FUNDACION INSTITUTO DE INVESTIGACION MARQUES DE VALDECILLA (IDIVAL)
    0 references
    0 references

    43°27'43.34"N, 3°48'35.89"W
    0 references
    39075
    0 references
    The aim of this Project is to characterize the genetic profile of a selected series of diffuse large B cell lymphoma patient samples by means of targeted exonic next generation sequencing. Diagnostic samples (tumor and normal DNA) from patients involved in three different clinical trials and a retrospective series of plasmablastic lymphoma cases will be analyzed using a targeted next generation sequencing approach, in order to identify markers associated with response to therapy. The samples are provided by three clinical trials from GELTAMO group (GEL-BRCAP21 (Nº EudraCT: 2012-005138-12), GEL-RCOMP 2013 (Nº EudraCT: 2013-001065-17) and LR-ESHAP (Nº EudraCT: 2010-018463-41). Plasmablastic lymphomas cases are obtained from biobank Valdecilla. Targeted exonic next generation sequencing will be performed using both normal and tumor DNA from patients. Library generation will be performed using a customized kit, developed in collaboration with Illumina, for this purpose. Sequencing will be done with MiSeq (Illumina) platform. In addition to his, we aim to develop a protocol for the accurate and sensitive detection of somatic mutations in the plasma of patients at diagnosis (circulating cell free tDNA) by means of digital PCR. This test may have an application in the screening and follow of patients with a suspicion or previously treated DLBCL, respectively. Next generation sequencing will also be used to explore the T cell repertoire in a selection of tumor samples with DLBCL and study its relationship with the mutational profiles, protein expression profiles and clinical outcome. (Spanish)
    0 references
    Santander
    0 references

    Identifiers

    PI16_01397
    0 references