KUNDANINGATTU RAMAN, HIMA

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DIPARTIMENTO DI SCIENZE DELLA SALUTE (attivo dal 01/10/2012 al 30/09/2015)

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Risultati 1 - 6 di 6 (tempo di esecuzione: 0.008 secondi).

Concomitant BCORL1 and BRAF Mutations in Vemurafenib-Resistant Melanoma Cells

2018 Mologni, L; Costanza, M; Sharma, G; Viltadi, M; Massimino, L; Citterio, S; Purgante, S; Raman, H; Pirola, A; Zucchetti, M; Piazza, R; Gambacorti-Passerini, C

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

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

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

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

Titolo	Tipologia	Data di pubblicazione	Autori
Concomitant BCORL1 and BRAF Mutations in Vemurafenib-Resistant Melanoma Cells	01 - Articolo su rivista	2018	Mologni, LCostanza, MSharma, GGViltadi, MMassimino, LCitterio, SPurgante, SRaman, HPirola, AZucchetti, MPiazza, RGambacorti-Passerini, C + -
Whole-Exome Sequencing Data - Identifying Somatic Mutations	03 - Contributo in libro	2014	SPINELLI, ROBERTAPIAZZA, ROCCO GIOVANNIPIROLA, ALESSANDRAVALLETTA, SIMONARoberta, RMOGAVERO, ANGELAMAREGA, MANUELAKUNDANINGATTU RAMAN, HIMAGAMBACORTI PASSERINI, CARLO + -
Identification of a Novel Splicing Mutation in Blast Crisis Transformation of Chronic Myeloid Leukemia Integrating Whole-exome and RNA-Seq data	02 - Intervento a convegno	2013	SPINELLI, ROBERTAPIROLA, ALESSANDRAREDAELLI, SARASHARMA, NITESH DEVINARAYANKUNDANINGATTU RAMAN, HIMAVALLETTA, SIMONAMAGISTRONI, VERAPIAZZA, ROCCO GIOVANNIGAMBACORTI PASSERINI, CARLO
Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases	01 - Articolo su rivista	2013	SPINELLI, ROBERTAPIROLA, ALESSANDRAREDAELLI, SARASHARMA, NITESH DEVINARAYANKUNDANINGATTU RAMAN, HIMAVALLETTA, SIMONAMAGISTRONI, VERAPIAZZA, ROCCO GIOVANNIGAMBACORTI PASSERINI, CARLO
A bioinformatics procedure to identify and annotate somatic mutations in whole-exome sequencing data	03 - Contributo in libro	2012	SPINELLI, ROBERTAPIAZZA, ROCCO GIOVANNIPIROLA, ALESSANDRAVALLETTA, SIMONAROSTAGNO, ROBERTAMOGAVERO, ANGELAMAREGA, MANUELAKUNDANINGATTU RAMAN, HIMAGAMBACORTI PASSERINI, CARLO
A computational procedure to identify and annotate somatic mutations in next-generation sequencing data	02 - Intervento a convegno	2011	SPINELLI, ROBERTAPIAZZA, ROCCO GIOVANNIPIROLA, ALESSANDRAVALLETTA, SIMONAROSTAGNO, ROBERTAMOGAVERO, ANGELAMAREGA, MANUELAKUNDANINGATTU RAMAN, HIMAGAMBACORTI PASSERINI, CARLO

Bicocca Open Archive

KUNDANINGATTU RAMAN, HIMA

Concomitant BCORL1 and BRAF Mutations in Vemurafenib-Resistant Melanoma Cells

Whole-Exome Sequencing Data - Identifying Somatic Mutations

Identification of a Novel Splicing Mutation in Blast Crisis Transformation of Chronic Myeloid Leukemia Integrating Whole-exome and RNA-Seq data

Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases

A bioinformatics procedure to identify and annotate somatic mutations in whole-exome sequencing data

A computational procedure to identify and annotate somatic mutations in next-generation sequencing data