Variant prioritization

Similar documents
Variant association and prioritization

UKGTN Testing Criteria

Supplementary appendix

Phenotype Report. Num. Positions Not Called (Missing data) Num. Variants Assessed

Proposal form for the evaluation of a genetic test for NHS Service Gene Dossier/Additional Provider

Comprehensive genetic testing for hearing and vision loss

Genetic Defect Underlying Progressive Blindness Uncovered by Strand s Clinical Exome Test

Address City State Zip Phone. the hospital/facility:

Retinal dystrophies, genomic applications in diagnosis and prospects for therapy

Genetics and the Macular Dystrophies. George Anadiotis D.O. Medical Director Clinical and Biochemical Genetics Randall Children s Hospital

Next generation sequencing identified novel heterozygous nonsense mutation in CNGB1 gene associated with retinitis pigmentosa in a Chinese patient

GENE THERAPY FOR INHERITED RETINAL DISEASE

한국인망막색소변성증환자에서발견한복합이형접합 EYS 변이 1 예보고

RetNet panel. Microcornea, myopic chorioretinal atrophy, and telecanthus, (3), Autosomal recessive ADGRA No OMIM phenotype

Genes and mutations causing retinitis pigmentosa

Cleveland Clinic Laboratories

CilioPathy panel. 3-Jul-2018 (102 genen) Centrum voor Medische Genetica Gent. versie. OMIM gene ID

Cone-Rod Degeneration with Sensorineural Hearing Loss

Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome

Exceptional progress has been made during the past two decades in identifying genes

QLT Inc Rationale and Background for the development of QLT (Note: QLT is not approved for commercial use in any countries, worldwide)

Retinitis Pigmentosa: A Brief Review of the Genetic and Clinical Aspects of the Disease. Itia Dowdell

Usher Syndrome: When to Suspect it and How to Find It

Retinitis pigmentosa and allied conditions today: a paradigm of translational research

Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies

Corporate Medical Policy

Unravelling the genetic basis of simplex Retinitis Pigmentosa cases

Proposal form for the evaluation of a genetic test for NHS Service Gene Dossier

Cataract and optic disk drusen in a patient with glycogenosis and di George syndrome: clinical and molecular report

Utilization of the MiSeq in a clinical lab. Tony Krentz, PhD PreventionGenetics

Gene therapy for Inherited Retinal Diseases MD(Res) Thesis by Venki Sundaram

INDEX. Genetics. French poodle progressive rod-cone degeneration,

Symptoms, causes and treatment options of different IRDs

Investigation of the genetic cause and related phenotypes of rare early onset retinal dystrophies

PDF hosted at the Radboud Repository of the Radboud University Nijmegen

Genetics and Genomics: Applications to Developmental Disability

Advances in Drug Therapy for Usher Syndrome. Jennifer J. Lentz Usher Syndrome Family Conference July 11, 2015

The Genetics of Usher Syndrome

LUXTURNA (voretigene neparovec-rzyl)

The current status of molecular diagnosis of inherited retinal dystrophies

The Molecular Basis of Retinal Dystrophies in Pakistan

RETINITIS PIGMENTOSA A RARE GENETICAL DISORDER

Achromatopsia NGS 6 ATF6, CNGA3, CNGB3, GNAT2, PDE6C, PDE6H ARMS2, CFH Sequencing PAX6

Proposal form for the evaluation of a genetic test for NHS Service Gene Dossier

RNA-Seq guided gene therapy for vision loss. Michael H. Farkas

FOUNDATION OVERVIEW. Over the past four decades, the Foundation has raised $600 million to put an end to retinal degenerative diseases.

Usher syndrome Close to a cure? The Path to Clinical Trials

Top Pediatric Retinal Diseases you don t want to miss! Retinopathy of Prematurity (ROP) Aggressive, Posterior ROP (AP ROP)

SEEING HOPE. Newsletter. Living With LCA: Juliet s Story. So, Where Were You? From the Founder

Usher syndrome Close to a cure? The Path to Clinical Trials

The Pennsylvania State University. The Graduate School. Department of Neural and Behavioral Sciences

Insight into Leber congenital amaurosis: potential for gene therapy

GENETIC TESTING FOR RETINAL DISEASES. A resource for the inherited retinal disease community

Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis

RPE65-associated Leber Congenital Amaurosis

REQUEST FOR MOLECULAR GENETIC TESTING

Compound heterozygosity Yurii S. Aulchenko yurii [dot] aulchenko [at] gmail [dot] com. Thursday, April 11, 13

Genetic Testing for Biallelic RPE65 Variant-Associated Retinal Dystrophy

Achromatopsia NGS 6 ATF6, CNGA3, CNGB3, GNAT2, PDE6C, PDE6H ARMS2, CFH Sequencing PAX6 MLPA 1 PAX6

Applying structure-function to solve clinical cases

C ritical Review: Can individuals with hearing impairment associated with Usher Syndrome benefit from a cochlear implant?

REVIEW. Advances in Gene Therapy for Diseases of the Eye. j 563. Lolita Petit, 1 Hemant Khanna, 1,2 and Claudio Punzo 1,2, * INTRODUCTION

The global epidemic of obesity

SEEING HOPE. Newsletter. Living with LCA: Enzo s Story

Since the mapping of the first locus for autosomal

A so cilia network: cilia proteins start social networking

How the eye works. Causes of retinitis pigmentosa

Year 4 Results For a Phase 1 Trial of Voretigene Neparvovec in Biallelic RPE65- Mediated Inherited Retinal Disease

Research Article Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations

Recent Advances in Genetics of Retinal Dystrophies and Gene Therapy. Anita Agarwal, MD West Coast Retina San Francisco, CA

Kamron N Khan PhD, FRCOphth [1-3], Keren Carss [5], F. Lucy Raymond [5], Farrah Islam

Lesson Overview. Human Chromosomes. Lesson Overview. Human Chromosomes

Feedback of results. Report via to NTGMC inbox. Review by GMC clinician

Molecular scanning of the ABCA4 gene in Spanish patients with retinitis pigmentosa and Stargardt disease: Identification of novel mutations

Retinitis Pigmentosa: Causes, Tests, And Treatment Options By James Henry MA READ ONLINE

NIH Public Access Author Manuscript Kidney Int. Author manuscript; available in PMC 2011 September 1.

Prevalence of Hearing Impairment

Happy New Year! Dan Roberts. International Low Vision Support Group NEWSLETTER. This Month. In This Issue

Supplementary Figures. Supplementary Figure 1. Dinucleotide variant proportions. These are described and quantitated. for each lesion type.

Advances in assessing and managing vision impairment

The importance of electrophysiological and imaging methods in the diagnostics of inherited retinal degenerations: Genotype-phenotype correlations

11/14/2013. Progressive Eye Conditions. Agenda. Review from Sessions 1 and 2 Session 1 Review of Eye Conditions. Objectives

Heterotaxie PCD (Primaire ciliaire dyskinesie) panel

Genetic Testing for Hereditary Hearing Loss Section 2.0 Medicine Subsection 2.04 Pathology/Laboratory

Subject: Voretigene Neparvovec-rzyl (Luxturna) Injection

Diseases Caused by Defects in the Visual Cycle: Retinoids as Potential Therapeutic Agents

REGENCY'S MAUI KOA Genetic Vet Report by embarkvet.com Test Date: October 20, 2018 MULTIDRUG SENSITIVITY CHROMOSOME 14

Phosphorus. Diagnostics

Usher Syndrome and Progressive Hearing Loss

Prevalence and mode of inheritance of major genetic eye diseases in China

Leber congenital amaurosis (LCA; MIM ) is a severe,

Kenneth E. Pierce Jr., DVM A THESIS. Submitted to Michigan State University in partial fulfillment of the requirements for the degree of

INHERITED RETINAL DISEASE. The Rod/Cone Dichotomy. Case History/Entrance Skills. Health Assessment 9/4/18. Hereditary Retinal Diseases Epidemiology

Spotlight on childhood blindness

Molecular Diagnostic Testing by eyegene: Analysis of Patients With Hereditary Retinal Dystrophy Phenotypes Involving Central Vision Loss

Question 2: Which one of the following is the phenotypic monohybrid ratio in F2 generation? (a) 3:1 (b) 1:2:1 (c) 2:2 (d) 1:3 Solution 2: (a) 3 : 1

Lab Activity Report: Mendelian Genetics - Genetic Disorders

Understanding. Retinitis pigmentosa. and other inherited retinal dystrophies

Toward the Mutational Landscape of Autosomal Dominant Retinitis Pigmentosa: A Comprehensive Analysis of 258 Spanish Families

Transcription:

Variant prioritization University of Cambridge Marta Bleda Latorre Cambridge, UK mb2033@cam.ac.uk 30th September 2014 Research Assistant at the Department of Medicine University of Cambridge Cambridge, UK

The objective 2

And now what? Finding the mutations causative of diseases The simplest case: monogenic disease due to a single gene A C B D Controls E Cases 3

And now what? Finding the mutations causative of diseases Controls Cases Clear individual gene associations are difficult to find in some diseases Same phenotype can be due to different mutations and different genes (or combinat Many cases have to be used to obtain significant associations to many markers The only common element is the pathway (yet unknown) affected 4

Strategies Filtering using family information Network (Systems biology) approaches PPIs Gene regulatory elements (mirnas, Tfs) GO terms GWAS Burden tests for rare variants... 5

Using family information Families containing control and disease individuals can help us reduce the number of variants obtained Individuals from the same family less variability Filter variants present in healthy people 6

Using family information Dominant inheritance 7

Using family information Recessive homozygous 8

Using family information Recessive Compound heterozygosity 9

BierApp Bierapp.babelomics.org Marta Bleda Variant annotation 10

Using network information 11

Example with Inherited Retinal Dystrophie Prevalence 1 in 3000 Clinically and genetically very heterogeneous 190 GENES account for aprox. 50% of IRDs. Is genetic overlapping among IRDs related to protein int 12

Example with Inherited Retinal Dystrophie BBS ARL6, BBS2, BBS4, BBS5, BBS7, BBS9, BBS10, BBS12,, INPP5E, LZTFL1, MKKS, MKS1, SDCCAG8, TRIM32, TTC8 LCA LCA5, RD3 CACNA1F, CACNA2D4 CEP290 CABP4, CORD/COD CRB1, IMPDH1, BBS1 AIPL1, LRAT, MERTK, GUCY2D, RDH12, RPE65, RPGRIP1 SPATA7, TULP1 ADAM9, GUCA1A, HRG4/UNC119, KCNV2, PDE6H, PITPNM3, RAX2, RDH5, RIM1 CVD CNGA3, PDE6C BCP, GCP, RCP GNAT2 GRK1, GRM6, NYX, TRPM1 PDE6B, RHO, SAG CRX C2ORF71, C8ORF37, CA4,CERKL, CNGA1, CNGB1, DHDDS,EYS, FAM161A, RLBP1, IDH3B,KLHL7 SEMA4A IMPG2, MAK, NRL, PAP1, PDE6A, ABCA4, PDE6G, PRCD, PRF3, PRPF8, PRPF31 PROM1, RBP3, RGR, ROM1, RP1, RP2, PRPH2, SNRNP200, TOPORS, TTC8 RPGRFSCN2, ZNF513 CLRN1, GUCA1B USH2A C1QTNF5, EFEMP1, ELOVL4, HMNC1, RS1, TIMP3 MD CORD/COD RP BEST1 NR2E3 FZD4, KCNJ13, LRP5, NDP, TSPAN12, VCAN ABHD12, CDH23, CIB2, DFNB31, GPR98, HARS, MYO7A, PCDH15, USH1C, USH1G ERVR/EVR CVD NB LCA-Leber Congenital Amaurosis CORD/COD- Cone and cone-rod dystro. CVD- Colour Vision Defects MD- Macular Degeneration ERVR/EVR- Erosive and Exudative Vitreoretinopathies USH- Usher Syndrome RP- Retinitis Pigmentosa NB- Night Blindness BBS- Bardet-Biedl Syndrome USH 13

Example with Inherited Retinal Dystrophie Significant Clustering coefficient, p-value=0.0103 LCA BBS LCA-Leber Congenital Amaurosis CORD/COD- Cone and cone-rod dystro CVD- Colour Vision Defects MD- Macular Degeneration ERVR/EVR- Erosive and Exudative Vitreoretinopathies USH- Usher Syndrome RP- Retinitis Pigmentosa NB- Night Blindness BBS- Bardet-Biedl Syndrome CORD/COD NB RP CVD USH MD ERVR/EVR SNOW Tool. Minguez et al., NAR 2009 Implemented in Babelomics (http://www.babelomics.org) 14

SNOW The SNOW tool introduces protein-protein interaction data into the functio profiling of genomic data Evaluates role of the list within the interactome: identifies hubs in the proteins/genes (nodes) and evaluates the topological parameters of the within the interactome Evaluates the list s cooperative behavior as a functional module http://babelomics.bioinfo.cipf.es/functional.html 15

NetworkMiner Prioritizing disease candidate genes Scenario http://babelomics.bioinfo.cipf.es/functional.html You have: 1.a list of disease candidates (ranked by their populational frequency) 2.a list of genes that are known to be associated to the disease You want to see: which of your candidates are functionally related or interacting with the known disease genes NetworkMiner Study Tests whether any of the candidates is significantly located in the neighborhood of the known disease genes 16

NetworkMiner Prioritizing disease candidate genes Example: Genome-Wide Association Study in Bipolar Disorder Seed list: Genes associated to Bipolar Disorder Ranked list: Genes ranked according the association degree in a Case-Control Association Study Known Disease Gene (Elipse) Candidate (Circle) Intermediate (Square) 17

RENATO (REgulatory Network Analsis TOo Identifying common regulatory elements Sometimes, the problem is not in the gene but in its regulators http://renato.bioinfo.cipf.es Tool for the interpretation and visualization of transcriptional (TFs) and post-transcriptional (mirnas) regulatory information Designed to identify common regulatory elements in a list of genes RENATO maps these genes to the regulatory network, extracts the corresponding regulatory connections and evaluate each regulator for significant over-representation in the list. 18

THANK YOU. 19