Orit Levi

About Orit Levi

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So far Orit Levi has created 11 blog entries.

Webinar: Breaking the Interpretation Bottleneck

2020-06-22T07:54:26+00:00

Webinar: Breaking the interpretation bottleneck Examining the utility of an automated genomic interpretation algorithm in a clinical genetic lab Guest Division Director, Division of Clinical Genomics Interpretation Baylor Genetics Host Chief Science Officer Emedgene The utilization of exome and genome sequencing in clinical practice has become widespread in recent [...]

Webinar: Breaking the Interpretation Bottleneck2020-06-22T07:54:26+00:00

Webinar: Analytical validation of clinical whole genome sequencing

2020-06-22T07:55:45+00:00

#SideByScience Webinar: Analytical validation of clinical whole genome sequencing for germline disease diagnostics: Best practices and performance standards Speaker Co-Director, Centre for Genetic Medicine Associate Director, Department of Paediatric Laboratory Medicine SickKids Dr. Christian Marshall will present the findings of the Medical Genome Initiative, a consortium of leading [...]

Webinar: Analytical validation of clinical whole genome sequencing2020-06-22T07:55:45+00:00

Webinar: Genetics in Epilepsy – Early Steps on the Path to Precision Medicine

2020-06-22T07:56:37+00:00

#SideByScience Webinar Genetics in Epilepsy – Early Steps on the Path to Precision Medicine Annapurna Poduri, MD, MPH Speaker Associate Professor in Neurology, Harvard Medical School Director, Epilepsy Genetics Program Boston Children’s Hospital Date: June 25th, 2020 Time: 12:30PM ET Epilepsy diagnosis and care have changed [...]

Webinar: Genetics in Epilepsy – Early Steps on the Path to Precision Medicine2020-06-22T07:56:37+00:00

test webinar page

2020-06-22T09:10:30+00:00

This webinar presents the work of the Children’s Rare Disease Cohorts (CRDC) initiative at Boston Children’s Hospital, which integrates genomic, research, and clinical data to facilitate hospital-based analysis and reanalysis of genomic data to accelerate rates of discovery and patient diagnoses.

test webinar page2020-06-22T09:10:30+00:00

Breaking Genes
January 17th, 2019

2020-01-06T09:27:14+00:00

JANUARY 17TH, 2019 The shortest bi-weekly genomics research report in the world. Curated by the Emedgene Research Division. To Seq or not to Seq The results of BabySeq project, in which 159 newborns were sequenced to find genetic variants leading to increased risk of an actionable disease, proved [...]

Breaking Genes
January 17th, 2019
2020-01-06T09:27:14+00:00

2018 in Genomics: May you live in interesting times

2019-01-24T15:44:50+00:00

May you live in interesting times seems like an apt description for the year we’ve had in genomics. Significant advances in science, alongside ethical breaches and major privacy concerns. All the while, the sequencing march forward continues with more interest from countries, consumers and more insurance coverage. I polled the Emedgene team on the [...]

2018 in Genomics: May you live in interesting times2019-01-24T15:44:50+00:00

AI & Reanalysis: Close the gap on your past open cases

2018-12-06T14:36:43+00:00

Introduction Reanalysis. With demand for testing accelerating, this is quickly becoming a painful topic for labs. Every patient matters, and deserves the latest science can offer. But reanalyzing an ever-growing number of cases is unsustainable in the long run. If 50% of your cases are unsolved, and you revisit them every 6 or 12 months, [...]

AI & Reanalysis: Close the gap on your past open cases2018-12-06T14:36:43+00:00

Emedgene Wins Israeli Prime Minister’s
Innovation Award 2018

2018-11-22T08:54:07+00:00

It’s been an exciting week for Emedgene. We went from a packed booth at ASHG 2018 in San Diego, meeting some of our friends in leading genomics organizations. Straight to the awards ceremony for the Prime Minister Innovation Award for 2018. Overall, Israel is investing tremendous resources and attention to genomics. The Prime Minister office [...]

Emedgene Wins Israeli Prime Minister’s
Innovation Award 2018
2018-11-22T08:54:07+00:00

AI & Reanalysis: Close the gap on your past open cases

2018-12-06T14:36:53+00:00

Introduction Reanalysis. With demand for testing accelerating, this is quickly becoming a painful topic for labs. Every patient matters, and deserves the latest science can offer. But reanalyzing an ever-growing number of cases is unsustainable in the long run. If 50% of your cases are unsolved, and you revisit them every 6 or 12 months, [...]

AI & Reanalysis: Close the gap on your past open cases2018-12-06T14:36:53+00:00

What is AI? Learn how to separate the substance from the marketing hype

2018-07-23T09:05:50+00:00

Front Line Genomics have done an amazing job creating the Genomic Data 101: 2018 Edition. This thorough introduction to genomic data covers everything from generation, data analysis, storage and compression through use of AI to scale interpretation efforts. The exponential growth in genomic data has strained resources - from both a computing, infrastructure, storage and [...]

What is AI? Learn how to separate the substance from the marketing hype2018-07-23T09:05:50+00:00