Studying at the University of Verona

Here you can find information on the organisational aspects of the Programme, lecture timetables, learning activities and useful contact details for your time at the University, from enrolment to graduation.

The Study Plan includes all modules, teaching and learning activities that each student will need to undertake during their time at the University.
Please select your Study Plan based on your enrollment year.

1° Year

ModulesCreditsTAFSSD
8
A/B
BIO/09 ,BIO/16 ,BIO/17 ,MED/46
7
A/B
BIO/13 ,MED/03 ,MED/07 ,MED/46
7
A/B
FIS/07 ,ING-INF/06 ,ING-INF/07 ,MED/01

2° Year  activated in the A.Y. 2014/2015

ModulesCreditsTAFSSD
4
B
MED/06 ,MED/11 ,MED/13 ,MED/15
4
A/B
BIO/14 ,MED/46

3° Year  activated in the A.Y. 2015/2016

ModulesCreditsTAFSSD
6
A/B
IUS/07 ,MED/42 ,M-PSI/01 ,SECS-P/07 ,SPS/07
Prova finale
7
E
-
activated in the A.Y. 2014/2015
ModulesCreditsTAFSSD
4
B
MED/06 ,MED/11 ,MED/13 ,MED/15
4
A/B
BIO/14 ,MED/46

Legend | Type of training activity (TTA)

TAF (Type of Educational Activity) All courses and activities are classified into different types of educational activities, indicated by a letter.




S Placements in companies, public or private institutions and professional associations

Teaching code

4S000351

Credits

2

Language

Italian

Scientific Disciplinary Sector (SSD)

MED/46 - BIOTECHNOLOGY AND METHODS IN LABORATORY MEDICINE

Period

lez 3 anno 1 semestre TLB dal Oct 1, 2015 al Nov 27, 2015.

Location

VERONA

To show the organization of the course that includes this module, follow this link:  Course organization

Learning outcomes

The training objective is to provide adequate knowledge of the main diseases related to alterations of genes and theoretical principles of the techniques of cytogenetics and molecular genetics. Obtain adequate knowledge of the theoretical principles and applications of the techniques of detection of genetic alterations.

Program

Human genome organization, Genetic polymorphisms, Nucleic acid extraction, Nucleic acids labeling and quantification,
Gene amplification techniques: Signal Amplification, Target amplification ,
Chromosomal aberrations, Conventional cytogenetics, Molecular cytogenetics,
In situ hybridization FISH, Next generation Sequencing NGS,
QF PCR, Array CGH, MLPA PCR,
HLA typing, Genetic testing for clotting disorders, Tumor genetics,
Forensic genetics.
Pharmacogenetics, Genomic imprinting

Examination Methods

Oral and/or written reports

Students with disabilities or specific learning disorders (SLD), who intend to request the adaptation of the exam, must follow the instructions given HERE