%0 Journal Article %J Bioinformatics %D 2015 %T MultiMeta: an R package for meta-analyzing multi-phenotype genome-wide association studies. %A Vuckovic, D %A Gasparini, P %A Soranzo, N %A Iotchkova, V %X

UNLABELLED: As new methods for multivariate analysis of genome wide association studies become available, it is important to be able to combine results from different cohorts in a meta-analysis. The R package MultiMeta provides an implementation of the inverse-variance-based method for meta-analysis, generalized to an n-dimensional setting.

AVAILABILITY AND IMPLEMENTATION: The R package MultiMeta can be downloaded from CRAN.

CONTACT: dragana.vuckovic@burlo.trieste.it; vi1@sanger.ac.uk

SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

%B Bioinformatics %V 31 %P 2754-6 %8 2015 Aug 15 %G eng %N 16 %1 http://www.ncbi.nlm.nih.gov/pubmed/25908790?dopt=Abstract %R 10.1093/bioinformatics/btv222 %0 Journal Article %J Gene %D 2014 %T Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients. %A Vozzi, D %A Morgan, A %A Vuckovic, D %A D'Eustacchio, A %A Abdulhadi, K %A Rubinato, E %A Badii, R %A Gasparini, P %A Girotto, G %K Alleles %K Amino Acid Sequence %K Carrier Proteins %K Extracellular Matrix Proteins %K Female %K Genetic Testing %K GPI-Linked Proteins %K Hearing Loss %K Humans %K Italy %K Male %K Membrane Proteins %K Molecular Sequence Data %K Mutation %K Myosins %K Neoplasm Proteins %K Pedigree %K Qatar %K Sequence Analysis, DNA %K Serine Endopeptidases %K Untranslated Regions %X

Deafness is a really common disorder in humans. It can begin at any age with any degree of severity. Hereditary hearing loss is characterized by a vast genetic heterogeneity with more than 140 loci described in humans but only 65 genes so far identified. Families affected by hearing impairment would have real advantages from an early molecular diagnosis that is of primary relevance in genetic counseling. In this perspective, here we report a family-based approach employing Ion Torrent DNA sequencing technology to analyze coding and UTR regions of 96 genes related to hearing function and loss in a first series of 12 families coming from Italy and Qatar. Using this approach we were able to find the causative gene in 4 out of these 12 families (33%). In particular 5 novel alleles were identified in the following genes LOXHD1, TMPRSS3, TECTA and MYO15A already associated with hearing impairment. Our study confirms the usefulness of a targeted sequencing approach despite larger numbers are required for further validation and for defining a molecular epidemiology picture of hearing loss in these two countries.

%B Gene %V 542 %P 209-16 %8 2014 Jun 1 %G eng %N 2 %1 http://www.ncbi.nlm.nih.gov/pubmed/24657061?dopt=Abstract %R 10.1016/j.gene.2014.03.033