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#ClinicalGenetics

Latest posts tagged with #ClinicalGenetics on Bluesky

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Posts tagged #ClinicalGenetics

A picture of PhenoTips' booth #417 at the ACMG conference. Parker Lachance, a white man in a dark suit with dark hair, and Connor McLeod, a white man with light brown hair and a light grey suit, speak to an anonymous conference attendee with her back turned to the camera.

A picture of PhenoTips' booth #417 at the ACMG conference. Parker Lachance, a white man in a dark suit with dark hair, and Connor McLeod, a white man with light brown hair and a light grey suit, speak to an anonymous conference attendee with her back turned to the camera.

#ACMGMtg26, don't miss your chance to explore the complete #GenomicHealthRecord at Booth #417!

Our team has thoroughly enjoyed sharing ideas with you during #MedicalGeneticsAwareness Week. We look forward to these continued conversations as we challenge the status quo of #ClinicalGenetics together.

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On tap: discussion of exome/genome coverage in adults, cancer MRI screening, adult mito workup, PRSs, ideas for future SIG events, and great conversation and connection making! 🧬

#MedicalGenetics #AdultGenetics #ClinicalGenetics @theacmg.bsky.social

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Postdoctoral Researcher in Clinical Genetics with a Focus on Molecular Hematology Do you want to contribute to top quality medical research? The postdoctoral position is based in Professor Richard Rosenquist Brandell’s research group in Clinical Genetics. Our group focuses on map

Are you interested in pursuing a #Postdoc in #Sweden?

@ki.se is hiring a Postdoctoral Researcher in #ClinicalGenetics with a Focus on Molecular Hematology.

Learn more and apply before February 23, 2026.

ki.varbi.com/en/what:job/...

#academicjobs #molecularhematology #cancerresearch

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Yep - another (potentially very useful!) tool in our kit - already helping prioritise variants for real patients. #Genomics #ClinicalGenetics

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What is risk in clinical genetics? Designing and piloting tools to evaluate risk in clinical genetics using failure modes and effects analysis - European Journal of Human Genetics European Journal of Human Genetics - What is risk in clinical genetics? Designing and piloting tools to evaluate risk in clinical genetics using failure modes and effects analysis

📢 New #ClinicalGenetics risk assessment tools across Europe to systematise risk evaluation & monitor adverse events. Pinpointing risk enables targeted interventions, helping reduce risk & improve care quality! 🧬
#Genetics #PatientSafety

www.nature.com/articles/s41...

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Parents across genetics, #oncology, and #prenatalcare see value in #genetictesting, but priorities differ. This highlights the need for setting-specific tools to measure personal utility. bit.ly/4nLLwTh #GIMO #PersonalUtility #ClinicalGenetics

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This latest review explores how expression quantitative trait loci are identified, analyzed, and tracked across different #Physiological stages and examines key data resources and their application in #Clinical #diseases. #medsky #ClinicalGenetics

#OpenAccess: www.sciencedirect.com/science/arti...

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#ClinicalGenetics #GeneticTesting #MedicalEducation #ShortCourse #CPD #HealthcareTraining #OnlineLearning #MBHG #GenomicMedicine #EthicsInGenetics

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The August 2025 issue of Genetics in Medicine, the ACMG's flagship journal, is now available at gimjournal.org/issue/S1098-....
Check it out! #genomics #medicalgenetics #clinicalgenetics #MedicalEducation

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Genseq was delighted to host a briefing session at Leinster House in conjunction with Oireachtas Health Committee member, Colm Burke TD. We look forward to continuing this important conversation.

#GeneticTesting #Genomics #GeneticTestingIreland #ClinicalGenetics #PrecisionMedicine

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It was our pleasure to host Amy, Nora, Serena, and Una from the Irish Cancer Society at our Cherrywood facility last Friday afternoon.

Thank you for the visit and for the important work you do every day.

#Genomics #ClinicalGenetics #CancerResearch #PatientSupport #IrishCancerSociety #genetics

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Wellcome Connecting Science 
Curating the Clinical Genome
Course dates: 11-13 June 2025

Registration deadlines
In person: 13 May
Virtual: 3 June

Wellcome Connecting Science Curating the Clinical Genome Course dates: 11-13 June 2025 Registration deadlines In person: 13 May Virtual: 3 June

Gain an understanding of how to maximise clinical data insights to improve patient care! #CCG2025

Register for an in-person place to join leading #genomics and #biodata experts at Curating the Clinical Genome 2025. #ClinicalGenetics

📅Deadline: 13 May

📎 More info: bit.ly/4gt4EB6
#ClinicalGenetics

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Recording a pedigree is a crucial part of the #genomics #clinicalgenetics consultation - but it's a pain in electronic health records. #PedigreeMD is a format I'm working on to rapidly & intuitively note down basic pedigree information in a simple text box/editor. github.com/shanemuk/ped...

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📢🧬 Happy #MedicalGeneticsAwareness week 🧬📢

This week, lets share knowledge, and raise #awareness about the importance of medical genetics in healthcare.
#ACMGmtg25 #LA #LosAngeles #IamaMedicalGeneticist #clinicalgenetics #hereditarydiseases #hereditarycancer #rarediseases

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Screenshot of Figure 2: Reclassification of VUS at 3 distinct transition points (ACMG/AMP, ACMG/AMP + SVI, and ENIGMA): A. The top section of the figure shows the number of variants n as bars on the y-axis and their classification into (benign, likely benign, and variants of uncertain significance [VUS]) in their corresponding color (green, light green, and yellow, respectively) at 3 distinct transition points t1, t2, and t3 (x-axis). The transition points refer to the initial interpretation and the 2 reanalysis: American College of Medical Genetics and Genomics/Association for Molecular Pathology (ACMG/AMP) 2015 (t1) represent the baseline VUS for this study. These variants were classified as VUS between January 2018 and November 2023. Sequence Variant Interpretation Working Group (SVI) recommendations from 2015 onward were considered, depending on the time of classification, eg, PM2 used as supporting evidence strength for all variants. ACMG/AMP + SVI (t2) lists variants that have been reclassified using new annotated data as of November 2023 (eg, ClinVar, BRCA Exchange, literature, and in-house data) and using all current recommendations from the SVI as of November 2023. Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Variant Curation Expert Panels (t3) are variants that have been reclassified based on the same new data as in t2 but using the ENIGMA specifications. The transient lines between the 3 bars, and the numbers indicate how many variants have changed from one class to another between 2 time points.

Screenshot of Figure 2: Reclassification of VUS at 3 distinct transition points (ACMG/AMP, ACMG/AMP + SVI, and ENIGMA): A. The top section of the figure shows the number of variants n as bars on the y-axis and their classification into (benign, likely benign, and variants of uncertain significance [VUS]) in their corresponding color (green, light green, and yellow, respectively) at 3 distinct transition points t1, t2, and t3 (x-axis). The transition points refer to the initial interpretation and the 2 reanalysis: American College of Medical Genetics and Genomics/Association for Molecular Pathology (ACMG/AMP) 2015 (t1) represent the baseline VUS for this study. These variants were classified as VUS between January 2018 and November 2023. Sequence Variant Interpretation Working Group (SVI) recommendations from 2015 onward were considered, depending on the time of classification, eg, PM2 used as supporting evidence strength for all variants. ACMG/AMP + SVI (t2) lists variants that have been reclassified using new annotated data as of November 2023 (eg, ClinVar, BRCA Exchange, literature, and in-house data) and using all current recommendations from the SVI as of November 2023. Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Variant Curation Expert Panels (t3) are variants that have been reclassified based on the same new data as in t2 but using the ENIGMA specifications. The transient lines between the 3 bars, and the numbers indicate how many variants have changed from one class to another between 2 time points.

ENIGMA VCEP guidelines significantly improve BRCA1/BRCA2 variant interpretation, reducing VUS rates and streamlining clinical diagnostics bit.ly/4bHELwk #GIMO #ACMGAMP #BRCA1 #BRCA2 #VUS #ColdSpot #VariantClassification #UCSCGenomeBrowser #ClinicalGenetics #SingleNucleotideVariant #SNV #ENIGMA

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Academic Europe - Bioinformatiker*in im Institut für Klinische Genetik

Job - Alert 🧫

🧬 BIOINFORMATIKER*IN IM INSTITUT FÜR KLINISCHE GENETIK

Deadline: 2025-03-21
Location: Germany, Dresden, Sachsen

www.academiceurope.com/job/?id=7048

#hiring #Bioinformatics #clinicalGenetics #biology #genetics #systemsbiology #phd

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Medical genetics students, residents & #geneticcounseling trainees – take the FREE monthly ACMG Student Challenge! Have fun and gain knowledge with our monthly questions about #clinicalgenetics & inborn errors of metabolism. Login and register: bit.ly/434rdbW #MedEd #medicalgenetics

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Absolutely brilliant news! The power of #science, #pharma, #clinicalgenetics and #genetherapy. A much needed good news story on the value of science, research and translation to medicines. 👏👏

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Unique | Understanding Rare Chromosome and Gene Disorders

We've been doing this for years in #ClinicalGenetics - once you get used to it, it's not hard, and brings great benefit. My current letters incorporate an edit of my Epic clinic note and a summary, plus patient info from Unique rarechromo.org if appropriate, copied electronically to GP, Paeds etc.

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🧬🖥️ Our study is different because we: a) Focus on whether a CNV disrupts exons or splice regions, b) Assess performance in key clinically relevant genes, c) Include widely available commercial software often omitted in academic papers but used in clinical labs. #ClinicalGenetics

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