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title: Genome sequencing | Genomics conference | IX Symposium CRG Barcelona 2010

description: CRG Barcelona Two days of genomics conference during which the latest advances in genome sequencing technologies and their medical applications.

keywords: genome sequencing, genomics conference, genomic research, genomic medicine, crg barcelona

encoding: UTF-8

language: en-US

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Next generation technologies – Basics and applications

Applications of whole-genome sequencing

Bioinformatic prediction of non-redundant polymorphic inversions in the human genome

Allele-specific gene expression as a guide to genes with cis-acting regulatory epigenetic and genetic factors

Personal Genomes are Personalized

Characterization, through re-sequencing, of genetic variants associated with high altitude adaptation in North Caucasian ethnic groups

The case of the missing heritability: clues so far and mysteries remaining

Annotating and understanding human variation

A Tool for Reconstructing Sequences and Transcriptome Analysis using Next-Generation Sequencing Data

Structural Variation Analysis by Large-Scale Human Genome Sequencing

Applications of Single-Molecule, Real-Time (SMRT™) DNA Sequencing

Large-Scale Human Genome Sequencing Service for Advanced Disease Studies

Cellular population genomics in humans

The power of comparative genetics and genomics for finding genes of medical relevance

Filling up gaps in epigenomic maps: the active Aluome

Next-Generation Mendelian Genetics by Exome Sequencing

Next generation sequencing in the clinic

Using homozygosity mapping and exome sequencing to search for a gene causing a rare articular disease

Crohn disease, paradigm for the etiology of complex inflammatory disorders

Uncovering and understanding splicing through massively paralell sequencing

Terminal Osseous Dysplasia is Caused by a Single Recurrent Mutation in the FLNA gene

Exome re-sequencing of seven melanoma cell lines to characterize somatic mutations

Interrogating the architecture of cancer genomes

Disease epigenomics: Interpreting disease-associated non-coding variants using chromatin states and activity profiles across many human ENCODE cell types

IX Symposium CRG Barcelona 2010

U tags

I tags

images

file namealternative text
septiembre3
Paul Flicek at the IX CRG Annual Symposium
Victor Solovyev at the IX CRG Annual Symposium
Joris Veltman at the IX CRG Annual Symposium
Sara Ng at the IX CRG Annual Symposium
Mireia Jordà at the IX CRG Annual Symposium
Generalitat de Catalunya
Ministerio de ciencia e innovación
Universitat Pompeu Fabra
European Science Foundation
Ilumina

headers

H1

IX Symposium CRG Barcelona 2010 CRG Barcelona Two days of genomics conference during which the latest advances in genome sequencing technologies and their medical applications.

H2

News.A date with medical genomics

Event Description

Highlights Suscribe to RSS feed

Follow us on twitter

Genomics conference Programme

Genomics conference supported by

Genomics conference Twitter Feed: CRGenomica

H3

News.A date with medical genomics

Event Description

Highlights Suscribe to RSS feed

Follow us on twitter

Genomics conference Programme

Genomics conference supported by

Genomics conference Twitter Feed: CRGenomica

H4

H5

H6

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IX Symposium CRG Barcelona 2010 CRG Barcelona Two days of genomics conference during which the latest advances in genome sequencing technologies and their medical applications.
Home
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Paul Flicek at the IX CRG Annual Symposium
Doctor, which gene is making me sick?
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Victor Solovyev. “A Tool for Reconstructing Sequences and Transcriptome Analysis using Next-Generation Sequencing Data”
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Victor Solovyev at the IX CRG Annual Symposium
Joris Veltman at the IX CRG Annual Symposium
Sara Ng at the IX CRG Annual Symposium
Joris Veltman. “Next generation sequencing in the clinic”
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Mireia Jordà. “Filling up gaps in epigenomic maps: the active Aluome”
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Sarah Ng. “Next-Generation Mendelian Genetics by Exome Sequencing”
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Mireia Jordà at the IX CRG Annual Symposium
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