VALLETTA, SIMONA
VALLETTA, SIMONA
DIPARTIMENTO DI SCIENZE DELLA SALUTE (attivo dal 01/10/2012 al 30/09/2015)
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
2014 Valletta, S
Whole-Exome Sequencing Data - Identifying Somatic Mutations
2014 Spinelli, R; Piazza, R; Pirola, A; Valletta, S; Roberta, R; Mogavero, A; Marega, M; KUNDANINGATTU RAMAN, H; GAMBACORTI PASSERINI, C
CEQer: A Graphical Tool for Copy Number and Allelic Imbalance Detection from Whole-Exome Sequencing Data
2013 Piazza, R; Magistroni, V; Pirola, A; Redaelli, S; Spinelli, R; Redaelli, S; Galbiati, M; Valletta, S; Giudici, G; Cazzaniga, G; GAMBACORTI PASSERINI, C
Identification of a Novel Splicing Mutation in Blast Crisis Transformation of Chronic Myeloid Leukemia Integrating Whole-exome and RNA-Seq data
2013 Spinelli, R; Pirola, A; Redaelli, S; Sharma, N; KUNDANINGATTU RAMAN, H; Valletta, S; Magistroni, V; Piazza, R; GAMBACORTI PASSERINI, C
Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases
2013 Spinelli, R; Pirola, A; Redaelli, S; Sharma, N; KUNDANINGATTU RAMAN, H; Valletta, S; Magistroni, V; Piazza, R; GAMBACORTI PASSERINI, C
Recurrent SETBP1 Mutations in Atypical Chronic Myeloid Leukemia
2013 Valletta, S; Piazza, R; Redaelli, S; Winkelmann, S; Spinelli, R; Pirola, A; Mologni, L; Donadoni, C; Papaemmanuil, E; Schnittger, S; Dong Wook, K; Boultwood, J; Rossi, F; Gaipa, G; DE MARTINI, G; Francia di Celle, P; Jang, H; Fantin, V; Bignell, G; Magistroni, V; Haferlach, T; Pogliani, E; Campbell, P; Chase, A; Tapper, W; Cross, N; GAMBACORTI PASSERINI, C
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
2013 Piazza, R; Valletta, S; Winkelmann, N; Redaelli, S; Spinelli, R; Pirola, A; Antolini, L; Mologni, L; Donadoni, C; Papaemmanuil, E; Schnittger, S; Kim, D; Boultwood, J; Rossi, F; Gaipa, G; DE MARTINI, G; di Celle, P; Jang, H; Fantin, V; Bignell, G; Magistroni, V; Haferlach, T; Pogliani, E; Campbell, P; Chase, A; Tapper, W; Cross, N; GAMBACORTI PASSERINI, C
A bioinformatics procedure to identify and annotate somatic mutations in whole-exome sequencing data
2012 Spinelli, R; Piazza, R; Pirola, A; Valletta, S; Rostagno, R; Mogavero, A; Marega, M; KUNDANINGATTU RAMAN, H; GAMBACORTI PASSERINI, C
FusionAnalyser: a new graphical, event-driven tool for fusion rearrangements discovery
2012 Piazza, R; Pirola, A; Spinelli, R; Valletta, S; Redaelli, S; Magistroni, V; GAMBACORTI PASSERINI, C
A computational procedure to identify and annotate somatic mutations in next-generation sequencing data
2011 Spinelli, R; Piazza, R; Pirola, A; Valletta, S; Rostagno, R; Mogavero, A; Marega, M; KUNDANINGATTU RAMAN, H; GAMBACORTI PASSERINI, C
CML Patients Present Additional Mutations in Cancer Related Genes When Tested At Diagnosis
2011 GAMBACORTI PASSERINI, C; Valletta, S; Stasia, A; Leeksma, A; Sharma, N; Rizzo, C; Pogliani, E; Pirola, A; Piazza, R
Identification of Novel Point Mutations in Splicing Sites by the Integration of Exome and RNA Sequencing Data in Myeloproliferative Diseases
2011 Spinelli, R; Piazza, R; Raman, H; Pirola, A; Valletta, S; Stasia, A; GAMBACORTI PASSERINI, C
Whole-Exome Sequencing of 8 Atypical Chronic Myeloid Leukaemia Patients
2011 Piazza, R; Valletta, S; Pirola, A; Raman, H; Spinelli, R; Cross, N; Cecchetti, C; Sortino, Z; GAMBACORTI PASSERINI, C
WHOLE-EXOME SEQUENCING OF A PHILADELPHIA NEGATIVE CHRONIC MYELOID LEUKEMIA PATIENT THROUGH THE EXON-CAPTURE TECHNIQUE
2010 Piazza, R; Spinelli, R; Pirola, A; Valletta, S; Rostagno, R; Mogavero, A; Marega, M; GAMBACORTI PASSERINI, C