|
|
| (6 intermediate revisions by 3 users not shown) |
| Line 1: |
Line 1: |
| − | {{Bio
| + | #REDIRECT [[AltUser:Ernesto_Lowy_Gallego]] |
| − | |Name=Ernesto
| + | |
| − | |Surnames=Lowy Gallego
| + | |
| − | |Position=Bioinformatician
| + | |
| − | |Email_address=ernesto.lowy@crg.es
| + | |
| − | }}
| + | |
| − | '''Current Work at the CRG:'''<br>
| + | |
| − | | + | |
| − | I am involved in the data analysis of several projects that make use of the Next-Generation Sequencing technology for different purposes, such as:
| + | |
| − | * Polymorphism discovery in Whole Genome/Targeted resequencing experiments
| + | |
| − | * Functional Annotation
| + | |
| − | * De Novo assembly
| + | |
| − | | + | |
| − | For these sort of analyses I make use of the publicly available tools and I implement my own scripts depending on the customer needs
| + | |
| − | | + | |
| − | '''Past Activity:'''<br>
| + | |
| − | | + | |
| − | I completed my PhD in the field of Immunogenetics in 2003, then I decided to specialized myself in the field of Bioinformatics.
| + | |
| − | For this I joined the EMBL-EBI and collaborated in the Ensembl project, where I had the opportunity to work and familiarize with the Ensembl genomic data and more specifically with the predictions performed by the Ensembl automated genome analysis and annotation pipeline. Then, I joined the bioinformatics core of the Wellcome Trust Centre for Human Genetics (University of Oxford), where I worked providing bioinformatics support for scientists at the centre and for external customers. This support mainly consisted on the data analysis produced by the Next-Generation sequencing facility, database management, web development, statistical data analysis etc...
| + | |
