This collection will give you access to select recordings of the 2017 Annual Meeting presentations and some of the associated pdf slides (see the topics tab for a complete list of the talks) .

Continuing education credit is no longer available.

The AMP 2017 Annual Meeting (November 16-18, 2017 in Salt Lake City, UT) showcased an impressive roster of speakers covering a wide range of topics in molecular diagnostics. The theme for the meeting was "Where Molecular Leads Medicine to Best Patient Care" and the presentations highlighted the true clinical utility of molecular diagnostics. In AMP 2017 Annual Meeting Highlights, catch up on the the most cutting-edge research in molecular pathology in topics ranging from CRISPR technologies, liquid biopsies, and the microbiome, to epigenetic roles in human disease, and new tools for interpreting the cancer genome. Click on the "Topics" tab for a list of the available presentations and click on the titles for more information about each session.

Duration:  13.25 hrs

If you have questions, please email AMPeducation@amp.org

Note: Join the AMP Family to purchase this content for a deep discount!

All sales are final. No refunds will be issued.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

AMP is the leading organization in the field of molecular diagnostics, and the AMP Annual meeting is the premier gathering of molecular professionals. As technologies change and new challenges arise, members and non-members alike rely on the AMP meeting to obtain the critical information needed to ensure that their patients receive the best care and best results.

This collection contains downloadable PDF slides of many of the presentations given during the AMP 2017 Annual Meeting. See the "topics" tab for a list of all the presentations for which slides are available.

The digital files (PDFs) for the AMP 2017 Annual Meeting are:

• Free for all AMP members until February 15, 2018. After February 15, 2018 (11:59PM EST), the price increases to $99.00.
• Free for Non-members who registered for the meeting. They will be emailed a coupon code valid until February 15, 2018.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

How to Access the Presentation Slides

1. On the menu to the right, click on "add to basket"
2. Log in using your AMP credentials.
3. The system will automatically check your membership status and provide the correct price. Add coupon code if applicable.
4. Check out.
5. Click here for instructions on how to access the presentation slides.

Join the AMP Family for a discount on this item.

Please note that this webinar was recorded in 2016. All AMPED^TM content is reviewed and approved annually by the Training & Education Committee as relevant and accurate, but new data may now be available and new studies may have since been published.

AMP Education is constantly updating these educational offerings, so keep checking back at educate.amp.org for new content, content updates, and information on cutting-edge molecular pathology research and applications.

This collection will give you access to the recordings of the presentations (listed below) and pdf slides only. CME/CMLE or SAM is not available for this collection

Description:

Did you miss out on joining us in Charlotte for the AMP 2016 Annual Meeting? Were you there but missed something you really wanted to see? We have you covered with the AMP 2016 Annual Meeting Highlights. Select presentations were recorded and are now available for online viewing.

Design, Validation, and Implementation of Effective Quality Control Materials for NGS/NIPS in a Clinical Laboratory

As tests for large numbers of rare genetic conditions come on-line in clinical laboratories, it is becoming increasing difficult to obtain high-quality, well-characterized human samples to use for the purposes of test development, validation, and ongoing proficiency testing. The first presentation will review how the CDC GeT-RM program is helping laboratories access samples for these purposes. Non-invasive prenatal screening (NIPS) for the common triploidies, Down (T21), Edward (T18) and Patau (T13) syndromes, as well as numerical abnormalities of the sex chromosomes, is now firmly established as an extremely valuable screening tool. However, there is currently no universally accepted or adopted proficiency test (PT) for NIPS. The second presentation will review the substantial challenges in developing PT for NIPS, and review progress in its development.

- Identify the sample resources available to laboratories through the Get-RM program.

- Explain the challenges and current progress toward developing PT samples for NIPS testing.

Development of Reference Materials for Proficiency Testing and Quality Assurance

Lisa V. Kalman, PhD, Centers for Disease Control and Prevention, Atlanta, GA, USA

External Proficiency Assessment of Prenatal Cell Free (cf )DNA Testing for Aneuploidy

Glenn E. Palomaki, PhD, Women & Infants Hospital, Providence, RI, USA

Duration: 1.5 hr

Recording Date: November 10, 2016

You might also be interested in:

• AMP 2018 Annual Meeting Recordings
• AMP 2017 Annual Meeting Highlights
• More on AMPED^TM

Note: Join the AMP Family to purchase many of the content for a deep discount!

Please note that this webinar was recorded in 2016. All AMPED^TM content is reviewed and approved annually by the Training & Education Committee as relevant and accurate, but new data may now be available and new studies may have since been published.

AMP Education is constantly updating these educational offerings, so keep checking back at educate.amp.org for new content, content updates, and information on cutting-edge molecular pathology research and applications.

This collection will give you access to the recordings of the presentations (listed below) and pdf slides only. CME/CMLE or SAM is not available for this collection

Description:

Did you miss out on joining us in Charlotte for the AMP 2016 Annual Meeting? Were you there but missed something you really wanted to see? We have you covered with the AMP 2016 Annual Meeting Highlights. Select presentations were recorded and are now available for online viewing.

A View from Across the Pond: European Models for Molecular Infectious Disase Testing

Speakers will highlight the differences and challenges of European molecular diagnostic approaches compared to those in the U.S. with respect to Clostridium difficile-associated disease and for high-risk HPV detection in cervical cancer screening.

- Outline differences between European diagnostic models compared to the US.

- Describe available tests that have been incorporated into European testing paradigms.

- Identify differences in patient outcomes observed using these different diagnostic practices

Testing Models for Clostridium difficile Infection Used in the UK

Mark Wilcox, MD, FRCPath, Leeds Teaching Hospital & University of Leeds, Leeds, West Yorkshire, UK

HPV Primary Screening: Challenges of Application and Implementation - and Priorities for Research

Kate Cuschieri, BSc, PhD, NHS Lothian, Edinburgh, United Kingdom

Duration: 1.5 hr

Recording Date: November 10, 2016

You might also be interested in:

• AMP 2018 Annual Meeting Recordings
• AMP 2017 Annual Meeting Highlights
• More on AMPED^TM

Note: Join the AMP Family to purchase many of the content for a deep discount!

The AMP 2016 Annual Meeting (November 10-12, 2016, Charlotte, North Carolina) showcased research in the latest advances in molecular medicine with the goal of enabling the highest quality health care.

The purchase of this product provides you with downloadable PDF slides of many of the AMP 2016 Annual Meeting presentations. See the "topics" tab for a list of all the presentations with slides available.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

This collection will give you access to select recordings from the AMP 2017 Global Congress. If you would like continuing education credit for the webinar, see the table below to purchase the collection + CME/CMLE or collection + SAM.

The AMP 2017 Global Congress in Berlin was a multi-disciplinary scientific program showcasing molecular technology with clinical applications in oncology, genetics, and infectious diseases. AMP Education has assembled the “AMP 2017 Global Congress Highlights,” which includes a selection of some of the most highly rated presentations and asked the speakers to record their talks from the meeting. This selection of excellent presentations includes:

Duration: 3.75 hr

Level of Instruction: Basic

You can purchase individual talks or purchase all of the AMP 2017 Global Congress Highlights for a discount.

• To purchase the entire series, click the "Add to Cart" button located on the right.
• To purchase individual talks, click on the "Purchase Individual Topics" button on the right, and select the particular talk(s) that you would like to purchase.

If you would like continuing education credit, click on the links below.

If you have questions, please email AMPeducation@amp.org

Note: Join the AMP Family to purchase this content for a deep discount!

All sales are final. No refunds will be issued.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

The AMP 2017 Global Congress (April 3-5, 2017 in Berlin, Germany) highlighted a multi-disciplinary scientific program showcasing molecular technology with clinical applications in oncology, genetics, and infectious diseases. The emphasis was on modern, user-friendly laboratory analytics supported by informatics tools to facilitate interpretation of actionable genomic test results.

The purchase of this product provides you with downloadable PDF slides of many of the presentations given during the AMP 2017 Global Congress. See the "topics" tab for a list of all the presentations with slides available.

The digital files (PDFs) for the AMP Global Congress 2017 Meeting are available free to meeting registrants for a limited time (three months) after the conference.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical, except that AMP authorizes you to view, copy, download and print for your own purposes.

AMP is the leading organization in the field of molecular diagnostics, and the AMP Annual meeting is the premier gathering of molecular professionals. As technologies change and new challenges arise, members and non-members alike rely on the AMP meeting to obtain the critical information needed to ensure that their patients receive the best care and best results.

This collection contains downloadable PDF slides of many of the presentations given during the AMP 2018 Annual Meeting and Expo. See the "topics" tab for a list of all the presentations for which slides are available.

The digital files (PDFs) for the AMP 2018 Annual Meeting are:

• Free for all AMP members until February 15, 2019. After February 15, 2019 (11:59PM EST), the price increases to $99.00.
• Free for Non-members who registered for the meeting. They will be emailed a coupon code valid until February 15, 2019.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

How to Access the Presentation Slides

1. On the menu to the right, click on "add to basket"
2. Log in using your AMP credentials.
3. The system will automatically check your membership status and provide the correct price. Add coupon code if applicable.
4. Check out.
5. Click here for instructions on how to access the presentation slides.

Join the AMP Family for a discount on this item.

This collection will give you access to the sessions recorded at the 2018 Annual Meeting presentations and the associated pdf slides (see the topics tab for a complete list of available talks).

If you would like continuing education credit, see the table below to purchase the collection + CME/CMLE or the collection + SAM.

AMP is the leading organization in the field of molecular diagnostics, and the AMP Annual meeting is the premier gathering of molecular professionals. As technologies change and new challenges arise, members and non-members alike rely on the AMP meeting to obtain the critical information needed to ensure that their patients receive the best care and best results.

Many of the sessions from the AMP Annual Meeting and Expo were recorded and this collection contains all the recorded sessions and downloadable PDF slides. See the "topics" tab for a list of all the presentations for which recordings and slides are available.

Duration: 49.25 hrs total

If you have questions, please email AMPeducation@amp.org

If you wish to obtain CME/CMLE or SAMs, click on the appropriate link to purchase the collection +CME/CMLE or +SAM.

* You may not submit SAMs and CME/CMLE credit for the same content.

Note: Join the AMP Family to purchase this content for a deep discount!

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

How to access the recordings

1. Click here for instructions on how to access the presentation slides.

Join the AMP Family for a discount on this item.

AMP hosted the Reference Materials forum to discuss genetic testing reference materials availability and needs (for test validation, quality control, and proficiency testing). Speakers presented a variety of current reference material development projects for molecular testing of inherited and acquired somatic genetic disorders followed by group discussion. 

This collection contains downloadable PDF slides of many of the presentations given during the Reference Material Forum Meeting which took place on October 30, 2018 in San Antonio, Texas. Click here for more details about the meeting.

The digital files (PDFs) for the Reference Material Forum Meeting are:

• Free for all AMP members.
• Free for Non-members who registered for the meeting. They will be emailed a coupon code valid until February 15, 2019.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

How to Access the Presentation Slides

1. On the menu to the right, click on "add to basket"
2. Log in using your AMP credentials.
3. The system will automatically check your membership status and provide the correct price. Add coupon code if applicable.
4. Check out.
5. To access the presentation slides, click on "My classroom" on the menu to the right.
6. Click on "AMP 2018 Reference Material Forum Meeting Presentations and Handouts.
7. Under "Resources", click on the PDF buttons to download the materials.

All sales are final. No refunds will be issued.

Join the AMP Family for a discount on this item.

This collection contains downloadable PDF slides of many of the presentations given during the AMP Global 2019 (May 16 - May 18, 2019).  Click here for more information about the meeting.

The digital files (PDFs) from AMP Global 2019 are:

• Free for all AMP members until August 31, 2019. After August 31, 2019 (12:00 PM EST), the price increases to $99.00.
• Free for Non-members who registered for the meeting. They will be emailed a coupon code valid until August 31, 2019.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

How to Purchase and Access the Presentation Slides

1. On the menu to the right, click on "add to basket"
2. Log in using your AMP credentials.
3. The system will automatically check your membership status and provide the correct price. Add coupon code if applicable.
4. Check out.
5. Click here for instructions on how to access the presentation slides.

You may also be interested in:

• AMP 2018 Annual Meeting Presentations and Handouts
• AMP 2018 Annual Meeting Recordings (CE Available)
• AMP Europe 2018: Handouts
• AMP Europe 2018: Presentation Recordings

Join the AMP Family for a discount on this item.

This course is designed for pathologists, residents, laboratory directors and technologists who have some prior exposure to molecular diagnostic testing. The course features introductory information about the state of the science as well as a series of case studies illustrating some of the most current principles and practices in the field of Molecular Pathology. Attendees from all career levels will benefit from this staple offering.

The objective of this course is to increase basic and applied pathology knowledge, focusing on the molecular diagnosis of disease and to facilitate knowledge acquisition regarding issues and challenges related to care and prevention. This course is designed to meet the participants' educational needs in the physician competency area of Medical Knowledge, as defined by the Accreditation Council for Graduate Medical Education (ACGME) and the American Board of Medical Specialties (ABMS), and to support participants' lifelong learning towards a goal of promoting patient safety and improving patient care.

Contemporary hot topics in the clinical molecular diagnostics laboratory will be introduced, followed by an overview of genomic testing to build the molecular diagnostic "toolkit." Short case presentations will demonstrate practical applications of a wide range of methodologies ranging from common commercial platforms to traditional amplification methods.

Duration: 5.25 hours

CME or SAMs is no longer available for this course

This online course includes all the recorded presentations, course materials, and case studies from the live 2018 Molecular Pathology Outreach Course held on October 31, 2018 in San Antonio, TX.

CME/CMLE and SAMs credit are available with the purchase of this course.

This course is designed to provide an overview of techniques and instrumentation used from the framework of the "Molecular Pathology/Molecular Diagnostic Toolkit." In this course, faculty members will present case studies to demonstrate the toolkit’s methodologies and technologies. Emphasis will be placed on molecular testing in the areas of clinical genetics, solid tumors, hematopathology, and infectious diseases. The application of novel technologies, such as next generation sequencing and informatics, will also be highlighted.

Visit the Program page for more information.

Audience: Pathologists, residents, laboratory directors and technologists who have little experience with molecular diagnostic testing.

Duration: 3.5 hrs

Maximum CME/CMLE credit available: 3.0 

Maximum SAM credit available: 3.0 

Last day to purchase course and claim credit: October 31, 2019

Note - registrants who attended the face-to-face course do not need to register for the online course to access the online materials.

CME/CMLE and SAM Credit:

How to claim credit: To earn credit, all learners must watch the lectures, achieve a minimum score of 80% on the online quiz, and complete an online survey. To access the quiz and the online survey, click "Submit credit" on the course homepage or click on "My Credit" on the menu to the left and then "submit credit" for the appropriate course.

CME/CMLE Credit

This activity was planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education through the joint providership of American Society for Clinical Pathology (ASCP) and the Association for Molecular Pathology (AMP). The ASCP is accredited by the ACCME to provide continuing medical education for physicians.

The ASCP designates this online educational activity for a maximum of 3.0 AMA PRA Category 1 Credit(s)TM. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

This continuing medical laboratory education activity is recognized by the ASCP for up to 3.0 hours of CMLE credit. ASCP CMLE credit hours meet the continuing education requirements for the ASCP Board of Certification Credential Maintenance Program (CMP) and state relicensure requirements for laboratory personnel. Participants should claim only the credit commensurate with the extent of their participation in the activity.

SAM Credit

This activity is approved by the American Board of Pathology for a maximum of 3.0 SAM Credits. Physicians should only claim credit commensurate with the extent of their participation in the activity. Participants must successfully complete the online exam (answering at least 80% of the questions correctly).

SAM edited by: Yi Ding, MD, PhD; Honey Reddi, PhD; Midhat Farooqi, PhD

* You may not submit SAMs and CME/CMLE credit for the same content.

All sales are final. No refunds will be issued.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

This online course includes all the recorded presentations, course materials, case studies, and tests from the live course held on May 16-19, 2019. CME/CMLE or SAMs is available with the purchase of this course until December 31, 2020.

This course features an intense update and review of molecular diagnostics for those prepping for the Molecular Genetic Pathology (MGP) Subspecialty Certification Exam as well as other certification exams, those who need a refresher, or anyone looking to add molecular testing to their current pathology practice. Participants have the opportunity to learn directly from recognized experts in the field of molecular pathology. Learn at your own pace and rewatch lectures as many times as you'd like.

Go here for more information on the course. 

Duration: 

The course will be available to purchase until December 31, 2020 (11:59PM Eastern), but please note that the course will also expire in your classroom on December 31, 2020. If you need access beyond December 31, please email AMPEducation@amp.org and we will consider a limited extension on a case-by-case basis. 

Note - registrants who attended the face-to-face course do not need to register for the online course to access the online materials.

CME/CMLE credit and SAMs credit are both available with the purchase of this course.

* You may not submit SAMs and CME/CMLE credit for the same content.

In support of improving patient care, this activity has been planned and implemented by Amedco LLC and Association for Molecular Pathology.  Amedco LLC is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.

Credit Designation Statement – Amedco LLC designates this enduring activity for a maximum of 20.75 AMA PRA Category 1 CreditsTM. Physicians should claim only the credit commensuratesam with the extent of their participation in the activity. 

SAM Credit: The AMP 2019 MGP Review Course is approved by the American Board of Pathology for up to 19.50 SAM credits. Physicians should claim only credit commensurate with the extent of their participation in the activity. Learners must pass the post-test with a score of 80% or higher and complete an evaluation form to receive a certificate of completion. Your chosen sessions must be attended in their entirety. Partial credit of individual sessions is not available.  If you are seeking continuing education credit for an accrediting board other than the ABP, it is your responsibility to contact your licensing/certification board to determine course eligibility for your licensing/certification requirement.

DISCLAIMER: AMP makes no guarantee or assurances that completion of its courses or participation in any educational activity will in any manner ensure a passing score on any certification examination or activity post-test, or achievement of certification status. The AMP Molecular Genetic Pathology review course is an educational program provided by the Association for Molecular Pathology, (AMP) and is not sponsored or endorsed by the American Board of Pathology (ABP) or the American Board of Medical Genetics (ABMG).

Note: Members of AMP can access this course for a deep discount. Join the AMP Family!

All sales are final. No refunds will be issued.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

This AMP certificate program contains 5.5 hours of lecture content, the associated pdf slides of the lectures, a post-course exam, and an AMP Certificate of Completion.

If you are interested in claiming CME/CMLE or SAM, see the table below to purchase the certificate program + CME/CMLE or the certificate program + SAM.

The ability to understand the world through the use of molecular tools has led to fascinating discoveries in the field of microbiology and infectious diseases. In this certificate program, participants will learn about the current state-of-the-art infectious disease topics with the emphasis on the key topics and advances in infectious disease testing and their impact on patient care practices and in public health. This certificate program will review updates on what's new in sexually transmitted disease (STD) care, rapid diagnostics point of care tests, metagenomics also known as microbiome and its impact of bacterial diversity (microbiome), and human health by using next- generation sequencing.

Click on the Topics Tab to see the talks that are included in the Certificate Program.

Target Audience: Clinical and research lab professionals at any level (clinical lab professional, researcher, educator, clinicians, graduate or undergraduate students)

This certificate program was planned and coordinated by the Content Directors:

• Preeti Pancholi, PhD, Ohio State University Wexner Medical Center
• Sophie S. Arbefeville, MD, University of Minnesota Medical Center

and supported by the Training & Education Committee

Duration: 5.5 hours

About AMP Certificate Programs: AMP Certificate Programs are thematically bundled packages containing some repurposed and some newly recorded content and does not necessarily build on previous recordings. It is designed to help you develop knowledge and skills needed for success in molecular pathology and diagnostics. Each program is reviewed, vetted, and curated by expert content directors. All certificate programs include a post-course final exam and an AMP Certificate of Completion. Some certificate programs are also available for CME/CMLE or SAMs credit. Click on the links on the table below to purchase AMP Certificate + CME/CMLE or AMP Certificate + SAM.

CME/CMLE or SAMs: If you wish to obtain CME/CMLE or SAMs, click on the appropriate link to purchase the collection +CME/CMLE or +SAM. These also contain the AMP Certificate of Completion

* You may not submit SAMs and CME/CMLE credit for the same content.

You might also be interested in:

• Microbiome and Predictive Response to Immunotherapy
• The Role of Genomic Susceptibility Testing in Predicting Antimicrobial Responses
• AMP 2018 Annual Meeting Recordings: Metagenomic Characterization of Molecular Scientists
• Other AMP Certificate Programs:
  • 2016 World Health Organization (WHO) Updates in Hematologic Malignancies (+AMP Certificate)
  • Circulating Tumor DNA Testing: Advances, Challenges, and Applications (+AMP Certificate)
• More on AMPEDTM

Note: Members of AMP can access this webinar for a discount. Join the AMP Family!

All sales are final. No refunds will be issued.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

Welcome to the Fellowship-in-Service-Examination 2019 brought to you by the Molecular Genetic Pathology (MGP) Program Directors and the Association for Molecular Pathology.

These exam questions were written by MGP faculty from many MGP-Fellowship institutions and cover the range of topics listed below. For each examination, a total of 45 questions populated from a question bank of nearly 250 questions will be randomly generated. At the end of the examination, you will receive your results along with the correct responses, an explanation of the correct choice, and references for further information. You will only receive this information for each question answered, so you are encouraged to answer all questions, regardless of whether or not you know the correct answer.

You are welcome to take the exam as many times as you like, but please note that participants will be charged a small administrative fee ($25 for AMP members, $50 for non-members) each time they take the exam.

Good luck!

MGP Category Codes (in alphabetical order):

1. Constitutional disorders

2. Hematopathology

3. Identity Testing and Histocompatability

4. Infectious disease

5. Informatics and Genomics

6. Laboratory Management, Regulatory, Ethical and Legal topics

7. Laboratory Test development and validation

8. Molecular Genetic Pathology principles and methods

9. Pharmacogenetics

10. Professionalism and Professional Development

11. Solid tumor, including inherited cancer syndromes

Professionalism Statement:

The Molecular Genetic Pathology Fellowship In-Service Exam was developed by the MGP Program Directors Council, the AMP Training and Education Committee and faculty from several Molecular Genetic Pathology Fellowship training programs as a tool to assess program performance and to identify areas of strength as well as those needing improvement. We hope that you find the Molecular Genetic Pathology Fellowship In-Service Exam to be a useful tool and rely on the participants to exemplify professionalism by not copying or sharing content, so that this resource continues to be a low-cost and useful tool to evaluate and improve MGP fellows training. 

DISCLAIMER: AMP makes no guarantee or assurances that completion of its courses or participation in any educational activity will in any manner ensure a passing score on any certification examination or activity post-test, or achievement of certification status. The Molecular Genetic Pathology Question Bank is an educational program provided by the Association for Molecular Pathology, (AMP) and is not sponsored or endorsed by the American Board of Pathology (ABP) or the American Board of Medical Genetics (ABMG).

How to Purchase:

1. Under the "Products" menu on the right, click the "add to basket" button.
2. Login with your AMP Member/Customer Username and Password. 
3. Proceed to "Checkout".
4. Provide your payment information by clicking “Edit my Billing Info”.
5. Save your billing information and click “Submit Order”.
6. You will receive a confirmation email from Peach New Media.

All sales are final. No refunds will be issued.

Note: Join the AMP Family to purchase this content for a discount!

Description:

A 28 year old male presents to the ED with complaints of weakness and decreased urine output...What tests should the physician run? How are the patient samples handled and analyzed in the lab?

Work through the case study and answer a series of questions to help diagnose, analyze and interpret the test results, and provide the patient with the best possible outcomes.
 

Level of Instruction: Basic

Audience: Primay Care Physicians, Residents

All sales are final. No refunds will be issued.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

This product will give you access to the webinar only. If you would like continuing education credit for the webinar, see the table below to purchase the webinar + CME/CMLE or webinar + SAM.

Description:

Recent advances in long-read sequencing technologies allows for a more complete identification of DNA and RNA associated with human disease. Two talks will be given to describe a few applications of these technologies.

The first talk will present nanopore sequencing of full-length cDNA from chronic lymphocytic leukemia (CLL) with and without mutation in a splicing factor, SF3B1. SF3B1 is one of the most frequently mutated genes in and is associated with poor patient prognosis. While alternative splicing patterns caused by mutations in SF3B1 using short-read sequencing are known, identifying the full-length isoform changes may better elucidate the functional consequences of these mutations. The talk will describe a computational workflow for transcript analysis called FLAIR (Full-Length Alternative Isoform analysis of RNA), novel findings, and remaining challenges with long-read sequencing approaches for alternative splicing analysis.

The second talk will present single-molecule real time sequencing of influenza. Infection by influenza virus can activate innate immune pathways that help control viral infection. However, these pathways are only rarely activated in single virus-infected cells. This webcast will describe how combining long-read sequencing with other single-cell techniques to determine how mutations in influenza virions affect whether infected cells activate innate immune pathways.
 

Speakers: Angela N. Brooks, PhD and Jesse D. Bloom, PhD

Moderator: Cecilia S. Yeung, MD

Duration: 1 hr

Level of Instruction: Basic

Click on the links below to purchase continuing education credit.

* You may not submit SAMs and CME/CMLE credit for the same content.

You may also be interested in:

• 2016 World Health Organization (WHO) Updates in Hematologic Malignancies (+AMP Certificate)
• Hot Topics in Infectious Diseases (+AMP Certificate)
• More on AMPED^TM

Note: Members of AMP can access this webinar at no cost. Join the AMP Family!

All sales are final. No refunds will be issued.

No digital files may be reproduced or transmitted in any form, by any means, electronic or mechanical. By purchasing a product, you agree to not share any of the course materials, including videos, downloadable slide presentations, outlines, manuscripts, etc. without explicit and written permission from AMP.

Please note that this webinar was recorded in 2016. All AMPED^TM content is reviewed and approved annually by the Training & Education Committee as relevant and accurate, but new data may now be available and new studies may have since been published.

AMP Education is constantly updating these educational offerings, so keep checking back at educate.amp.org for new content, content updates, and information on cutting-edge molecular pathology research and applications.

Description:

This presentation discusses current methods used to identify bacteria by 16S rRNA gene sequencing and fungi by use of the ITS (Internal Transcribed Spacers) and D1/D2 regions, including both technical and bioinformatic analyses. Additional content covers use of these methods to identify pathogens in primary samples, example cases and clinical reporting, potential application of next generation sequencing (NGS)-based methods, and considerations for labs developing and implemeting these assays.

Speaker: Lynn Bry, MD, PhD

Host: Colleen Kraft, MD

Duration: 40 min.

Level of Instruction: Intermediate

You might also be interested in:

• More on AMPED^TM

All sales are final. No refunds will be issued.

Note: Members of AMP can access this webinar at no cost. Join the AMP Family!

A Collaborative Educational Event Presented by AMP, PASCV and APHL

Description:

Laboratory diagnostics of HIV continue to evolve with antigen/antibody and molecular methods becoming increasingly more sensitive, specific, and rapid. Moreover, laboratory implementation of the CDC/APHL testing algorithm incorporating these assays may result in improved diagnosis of acute HIV but may also be challenging to interpret. The overall goal of this webinar is to discuss diagnostic methods for HIV and the current testing algorithm through the presentation of actual clinical cases. The webinar will conclude with a brief discussion of emerging or novel diagnostic methods and their impact on HIV diagnosis.

Speakers: Cecilia Perret MD & Benjamin Pinsky MD, PhD

Duration: 1 hr

Level of Instruction: Basic

Note:

Members of AMP can access this webinar at no cost. Join the AMP Family!

Members of PASCV can access this webinar at no cost from PASCV (www.pascv.org).

Members of APHL may be able to access this webinar from APHL (www.aphl.org).

Description:

HIV-1 exists within individuals as a complex mixture of variants often referred to as a quasispecies. During the past 10 years, there have been many studies of the distribution and clinical significance of "low-abundance" or "minority" drug-resistance variants present in plasma in proportions below 20% to 30% -- the limit of detection of standard genotypic resistance testing using dideoxy-terminator "Sanger" sequencing. HIV-1 "deep" sequencing using NGS technologies have been widely used in research settings to study the clinical significance of low-abundance drug resistance mutations. In addition, NGS is commercially available for several niche clinical applications such as determining HIV-1 tropism before using a CCR5 inhibitor.

In this webinar, Dr. Shafer will review the scenarios in which low-abundance HIV-1 drug-resistance mutations are most clinically relevant, the most influential studies of NGS for HIV-1 drug resistance testing, and the practical aspects of NGS that have so far slowed its widespread adoption for most routine HIV-1 genotypic resistance testing.

This content is now FREE for all but, continuing education credit is not available.

Speaker: Robert W. Shafer MD

Duration: 1.0 hrs.

Level of Instruction: Basic

Reviewed: March, 2018 

• The material presented is still relevant.

All sales are final. No refunds will be issued.

Members of AMP can access this webinar at no cost. Join the AMP Family!