Best exome sequencing podcasts we could find (Updated July 2017)   Exome sequencing public [search 0]

No series here

Try another search?

Broken tape
Loading …
 
This Genetics in Medicine podcast discusses the following article:Prenatal exome sequencing in anomalous fetuses: new opportunities and challengeshttps://www.nature.com/gim/journal/vaop/ncurrent/full/gim201733a.html
 
This Genetics in Medicine podcast discusses the following article:Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal developmenthttps://www.nature.com/gim/journal/vaop/ncurrent/full/gim201731a.html
 
A new technique called exome sequencing is a revolutionary way to look at our DNA. This, according to psychiatrist Stephen Sanders of the University of California, San Francisco School of Medicine. Basically, it allows researchers to determine the structure of all expressed genes in a genome and recently, it helped UCSF scientists find mutation ...…
 
The exome encompasses all protein coding regions, covers 2% of the human genome and contains majority of the disease-causing variants in inherited disorders. Whole exome sequencing (WES) represents a powerful tool to systematically detect the widest set of pathogenic variants in patients’ DNA. Blueprint Genetics provides high-quality WES and co ...…
 
Mike Murray and the crew over at Geisinger are making the implementation of genomic medicine look down right easy.In today’s interview, Mike explains GenomeFIRST Medicine, a program at the Geisinger Health System in Pennsylvania to offer care “that is based on an individual’s DNA sequence.” The healthcare provider boasts its own biobank and has ...…
 
For rare disease patients and their families, genome and exome sequencing may identify mutations that may be drivers of a condition, but nothing more. As families search for a name to put to a disease and look for treatments, finding others with the same condition and researchers working to understand and treat it becomes a critical part of the ...…
 
For rare disease patients and their families, genome and exome sequencing may identify mutations that may be drivers of a condition, but nothing more. As families search for a name to put to a disease and look for treatments, finding others with the same condition and researchers working to understand and treat it becomes a critical part of the ...…
 
S
Specialty Journals Author Interviews: Research in medicine, science & clinical practice for physicians, researchers, clinicians
 
Interview with Katherine A. Janeway, MD, MSc, author of Multicenter Feasibility Study of Tumor Molecular Profiling to Inform Therapeutic Decisions in Advanced Pediatric Solid Tumors: The Individualized Cancer Therapy (iCat) Study, and D. Williams Parsons, MD, PhD, author of Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing ...…
 
J
JAMA Oncology Author Interviews: Covering research, science, & clinical practice in oncology that improves the care of patients with cancer
 
Interview with Katherine A. Janeway, MD, MSc, author of Multicenter Feasibility Study of Tumor Molecular Profiling to Inform Therapeutic Decisions in Advanced Pediatric Solid Tumors: The Individualized Cancer Therapy (iCat) Study, and D. Williams Parsons, MD, PhD, author of Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing ...…
 
Interview with Katherine A. Janeway, MD, MSc, author of Multicenter Feasibility Study of Tumor Molecular Profiling to Inform Therapeutic Decisions in Advanced Pediatric Solid Tumors: The Individualized Cancer Therapy (iCat) Study, and D. Williams Parsons, MD, PhD, author of Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing ...…
 
Clinical exome sequencing is becoming more widely adopted every day. Based on the evidence offered hospitals, professional organizations, and even insurance companies are adopting and/or supporting the clinical exome for themselves. How might you convince someone who is still skeptical though? What evidence is available for the clinical and/or ...…
 
Christian Gund, genetic counselor at Ambry, interviews Megan Tucker, formerly a senior genetic counselor at St. Vincent Health in Indianapolis and current Program Director at Indiana State University. In this episode, Christian and Megan discuss the process of ordering exome sequencing from a clinical perspective including consenting the patien ...…
 
[Read the Article] Autism Spectrum Disorder (ASD) represents a diverse group of neurodevelopmental conditions. If researchers can better understand the genetics of ASD, it may be possible to identify and diagnose at-risk children sooner. A new study looked at the results of two newer genetic testing technologies, chromosomal microarray and whol ...…
 
J
JAMA Author Interviews: Covering research in medicine, science, & clinical practice. For physicians, researchers, & clinicians.
 
Interview with Bridget A. Fernandez, MD, author of Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
 
Matt Might came knocking on the door of genomic medicine out of pure necessity. After a four year diagnostic odyssey that led them to Duke University, Matt and his wife, Cristina, finally found out through exome sequencing that their son, Bertrand, was suffering from a rare disease known as NGLY1 deficiency. That was three years ago.…
 
Matt Might came knocking on the door of genomic medicine out of pure necessity. After a four year diagnostic odyssey that led them to Duke University, Matt and his wife, Cristina, finally found out through exome sequencing that their son, Bertrand, was suffering from a rare disease known as NGLY1 deficiency. That was three years ago.…
 
Originally Published December 5, 2014: Travis and Amol want you to recognize that: 1. Recognize whole exome sequencing is an important new method of identifying genetic mutations associated with disease. 2. Understand that the 4-year follow-up of the PROTECT AF study showed that left atrial appendage closure devices may be superior to warfarin ...…
 
T
This Week in Virology - MP3 Edition
 
Hosts: Vincent Racaniello, Dickson Despommier, Alan Dove, Rich Condit, and Kathy Spindler The TWiVsters explore mutations in the interferon pathway associated with severe influenza in a child, outbreaks of avian influenza in North American poultry farms, Ebolavirus infection of the eye weeks after recovery, and Ebolavirus stability on surfaces ...…
 
Christian Gund, genetic counselor at Ambry, gives a follow up to our previous Podcast where we discussed Ambry’s cohort paper on Exome Sequencing. In this episode, Christian gives an overview of other papers that Ambry has published since starting Exome Sequencing, as well as some of the interesting new discoveries that they’ve provide the scie ...…
 
A
AANEM Presents Nerve and Muscle Junction
 
Whole Exome Sequencing and the Clinical Impact of Sequencing Techniques by Dr. Daniel MacArthur, interviewed by Dr. Ted Burns.
 
As diagnostic clinical exome sequencing becomes more accessible and affordable, it’s clinical applications are undoubtedly expanding. This 1-hour* presentation will focus on providing clinicians with an overview of Ambry’s ExomeNext and ExomeNext-Rapid and will explore the utilization of this diagnostic tool in the clinical setting.…
 
In the hour, we explore the post diagnostic implications of whole exome sequencing as it pertains to clinical practice with some eye opening data from our two speakers Julie Cohen and Dr. Alejandro Iglesias. Julie is a Genetic Counselor at Kennedy Kreiger Institute in Baltimore Maryland, and Dr. Alejandro Iglesias has been a pediatrician and ge ...…
 
Genetic counselor Christian Gund hosts a Q&A session with genetic counselor Kelly Farwell Hagman, lead author for Ambry’s 2014 Genetics in Medicine publication about the family-centered power of exome sequencing.
 
Genetic counselor Christian Gund discusses the power of testing trios when doing exome sequencing, and why the technology is a family-centered analysis.
 
This week, Travis and Amol want you to recognize that: 1. Recognize whole exome sequencing is an important new method of identifying genetic mutations associated with disease. 2. Understand that the 4-year follow-up of the PROTECT AF study showed that left atrial appendage closure devices may be superior to warfarin in preventing strokes in pat ...…
 
J
JAMA Editors' Summary: On research in medicine, science, & clinical practice. For physicians, researchers, & clinicians.
 
Editor's Audio Summary by Howard Bauchner, MD, Editor in Chief of JAMA, the Journal of the American Medical Association, for the November 12, 2014 issue
 
The selective capture and sequencing of coding regions in the genome is a powerful and cost effective tool for researchers wanting to identify disease-causing mutations. Ambry Genetics has extensive experience with exome sequencing in both a research and clinical setting. As early adopters of NGS technology and advanced target enrichment techni ...…
 
A1-hour discussion of the role both clinical aCGH and exome sequencing play in the optimization of genetic diagnosis. The purpose of this webinar is to discuss the unique roles of microarray and diagnostic exome sequencing in the clinical diagnostic process, while also examining benefits, limitations, and detection rates of these tests.…
 
We discuss the revitalizing effects of young blood and how exome sequencing could help guide personalized cancer treatments.By Nature Medicine.
 
O
On Your Mind Neuroscience Podcast
 
This week on the On Your Mind Neuroscience Podcast: We walk the line between reality and science fiction this week with stories of reverse engineering an image from brain activity and compounds that can reverse aging. We’re also discussing a paper that uses gene network analysis and exome sequencing to study neurodegeneration…
 
This week: prostatectomy, prescription drug costs, exome sequencing for rare mutations Learning objectives – Amol, Nathan, and Travis discuss: 1. Understand that radical prostatectomy improved overall and disease free survival and decreased metastasis compared with watchful waiting in men with localized prostate cancer of intermediate grade. 2. ...…
 
A
AANEM Presents Nerve and Muscle Junction
 
Exome sequencing discussion by Michael Shy, MD and Stephan Zuchner, MD, and interviewed by Ted Burns, MD
 
T
This Week in Pediatric Oncology
 
April 05, 2012 Host Dr. Tim Cripe welcomes back co-host Dr. Lionel Chow to discuss somatic mutations in pediatric brain tumors. After recapping the consensus paper on molecular subgroups in medulloblastoma discussed in TWiPO episode 22 (Brain Tumor Round Robin) Dr Chow highlights the significance of the driver mutations in histone H3.3 in pedia ...…
 
In March of 2013, the ACMG, The American College of Medical Genetics and Genomics, issued a clinical laboratory guideline for the reporting of incidental findings observed through exome and genome sequencing, including the ethical implications of reporting these incidental findings.
 
P
Podcasts: Clinical Chemistry Podcast RSS
 
In March of 2013, the ACMG, The American College of Medical Genetics and Genomics, issued a clinical laboratory guideline for the reporting of incidental findings observed through exome and genome sequencing, including the ethical implications of reporting these incidental findings.
 
C. Gregory Elliott, MD, FCCP, and editorialist David Langlaben, MD, join CHEST Podcast Editor, D. Kyle Hogarth, MD, FCCP, to discuss the recent research of Dr. Elliott et al that determined the genetic mutations responsible for pulmonary capillary hemangiomatosis (PCH), a rare cause of pulmonary hypertension. The EIF2AK4 mutuations were found u ...…
 
Kip Harry interviews Gholson Lyon of the Cold Spring Harbor Laboratory on September 13, 2013. Dr. Lyon will be speaking during the Clinical Exome Sequencing conference at the Clinical Genomics & Informatics Europe Conference & Expo on December 4-6, in Lisbon, Portugal.Topics include:• Biology and Targeting of Cancer through Exome Sequencing• Te ...…
 
(June 7, 2013 - Insidermedicine) From Boston - Scientists have identified the genetic mutation that causes early puberty in boys and girls, according to a report published in the New England Journal of Medicine. Researchers conducted whole exome sequencing on 15 families and 40 individuals with central precocious puberty--a condition in which p ...…
 
(June 7, 2013 - Insidermedicine) From Boston - Scientists have identified the genetic mutation that causes early puberty in boys and girls, according to a report published in the New England Journal of Medicine. Researchers conducted whole exome sequencing on 15 families and 40 individuals with central precocious puberty--a condition in which p ...…
 
Speed
Series preference
1x
1x
Volume
100%
/

Google login Twitter login Classic login