2015
ARResT/AssignSubsets: a novel application for robust subclassification of chronic lymphocytic leukemia based on B cell receptor IG stereotypy
BYSTRÝ, Vojtěch; Andreas AGATHANGELIDIS; Vasileios BIKOS; Lesley Ann SUTTON; Panagiotis BALIAKAS et al.Základní údaje
Originální název
ARResT/AssignSubsets: a novel application for robust subclassification of chronic lymphocytic leukemia based on B cell receptor IG stereotypy
Autoři
BYSTRÝ, Vojtěch; Andreas AGATHANGELIDIS; Vasileios BIKOS; Lesley Ann SUTTON; Panagiotis BALIAKAS; Anastasia HADZIDIMITRIOU; Kostas STAMATOPOULOS a Nikos DARZENTAS
Vydání
Bioinformatics, Oxford, Oxford University Press, 2015, 1367-4803
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10600 1.6 Biological sciences
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 5.766
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14740/15:00086128
Organizační jednotka
Středoevropský technologický institut
UT WoS
EID Scopus
Klíčová slova anglicky
PATHOGENETIC IMPLICATIONS; IMMUNOGLOBULIN; GENES
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 5. 4. 2016 14:46, Mgr. Eva Špillingová
Anotace
V originále
Motivation: An ever-increasing body of evidence supports the importance of B cell receptor immunoglobulin (BcR IG) sequence restriction, alias stereotypy, in chronic lymphocytic leukemia (CLL). This phenomenon accounts for similar to 30% of studied cases, one in eight of which belong to major subsets, and extends beyond restricted sequence patterns to shared biologic and clinical characteristics and, generally, outcome. Thus, the robust assignment of new cases to major CLL subsets is a critical, and yet unmet, requirement. Results: We introduce a novel application, ARResT/AssignSubsets, which enables the robust assignment of BcR IG sequences from CLL patients to major stereotyped subsets. ARResT/AssignSubsets uniquely combines expert immunogenetic sequence annotation from IMGT/V-QUEST with curation to safeguard quality, statistical modeling of sequence features from more than 7500 CLL patients, and results from multiple perspectives to allow for both objective and subjective assessment. We validated our approach on the learning set, and evaluated its real-world applicability on a new representative dataset comprising 459 sequences from a single institution.
Návaznosti
| ED1.1.00/02.0068, projekt VaV |
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| 7E13008, projekt VaV |
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