Pavlos Antoniou
Pavlos Antoniou
Cyprus Institute of Neurology and Genetics
Patvirtintas el. paštas - Pagrindinis puslapis
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United Kingdom
K Schwarze, J Buchanan, JM Fermont, H Dreau, MW Tilley, JM Taylor, ...
Genetics in Medicine 22 (1), 85-94, 2020
Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project
P Robbe, N Popitsch, SJL Knight, P Antoniou, J Becq, M He, A Kanapin, ...
Genetics in Medicine 20 (10), 1196-1205, 2018
A comprehensive survey of congestion control protocols in wireless sensor networks
C Sergiou, P Antoniou, V Vassiliou
IEEE Communications Surveys & Tutorials 16 (4), 1839-1859, 2014
Congestion control in wireless sensor networks based on bird flocking behavior
P Antoniou, A Pitsillides, T Blackwell, A Engelbrecht, L Michael
Computer Networks 57 (5), 1167-1191, 2013
KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data
GAT Sacomoto, J Kielbassa, R Chikhi, R Uricaru, P Antoniou, MF Sagot, ...
BMC bioinformatics 13, 1-12, 2012
Bisulfite conversion of DNA: performance comparison of different kits and methylation quantitation of epigenetic biomarkers that have the potential to be used in non-invasive …
CA Leontiou, MD Hadjidaniel, P Mina, P Antoniou, M Ioannides, ...
PloS one 10 (8), e0135058, 2015
Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature
P Evangelidou, A Alexandrou, M Moutafi, M Ioannides, P Antoniou, ...
BioMed research international 2013 (1), 346762, 2013
Targeted deep sequencing reveals clinically relevant subclonal IgHV rearrangements in chronic lymphocytic leukemia
B Stamatopoulos, A Timbs, D Bruce, T Smith, R Clifford, P Robbe, A Burns, ...
Leukemia 31 (4), 837-845, 2017
Complex systems: A communication networks perspective towards 6G
C Sergiou, M Lestas, P Antoniou, C Liaskos, A Pitsillides
Ieee Access 8, 89007-89030, 2020
Clinical significance of TP53, BIRC3, ATM and MAPK-ERK genes in chronic lymphocytic leukaemia: data from the randomised UK LRF CLL4 trial
SJ Blakemore, R Clifford, H Parker, P Antoniou, E Stec-Dziedzic, ...
Leukemia 34 (7), 1760-1774, 2020
FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation
G Koumbaris, H Hatzisevastou-Loukidou, A Alexandrou, M Ioannides, ...
Human molecular genetics 20 (10), 1925-1936, 2011
Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features
P Robbe, KE Ridout, DV Vavoulis, H Dréau, B Kinnersley, N Denny, ...
Nature genetics 54 (11), 1675-1689, 2022
Conservative String Covering of Indeterminate Strings.
P Antoniou, M Crochemore, CS Iliopoulos, I Jayasekera, GM Landau
Stringology, 108-115, 2008
Classical and non-classical presentations of complement factor I deficiency: two contrasting cases diagnosed via genetic and genomic methods
AM Shields, AT Pagnamenta, AJ Pollard, OxClinWGS, JC Taylor, ...
Frontiers in immunology 10, 1150, 2019
Finding common motifs with gaps using finite automata
P Antoniou, J Holub, CS Iliopoulos, B Melichar, P Peterlongo
Implementation and Application of Automata: 11th International Conference …, 2006
Vibrational control of electron-transfer reactions: a feasibility study for the fast coherent transfer regime
P Antoniou, Z Ma, P Zhang, DN Beratan, SS Skourtis
Physical Chemistry Chemical Physics 17 (46), 30854-30866, 2015
Clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL
J Klintman, K Barmpouti, SJL Knight, P Robbe, H Dreau, R Clifford, ...
British journal of haematology 182 (3), 412-417, 2018
Mapping uniquely occurring short sequences derived from high throughput technologies to a reference genome
P Antoniou, JW Daykin, CS Iliopoulos, D Kourie, L Mouchard, SP Pissis
2009 9th International Conference on Information Technology and Applications …, 2009
Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencing
A Schuh, H Dreau, SJL Knight, K Ridout, T Mizani, D Vavoulis, R Colling, ...
Molecular Case Studies 4 (2), a002279, 2018
Whole-genome fetal and maternal DNA methylation analysis using MeDIP-NGS for the identification of differentially methylated regions
A Keravnou, M Ioannides, K Tsangaras, C Loizides, MD Hadjidaniel, ...
Genetics research 98, e15, 2016
Sistema negali atlikti operacijos. Bandykite vėliau dar kartą.
Straipsniai 1–20