
Jonathan Edgerley
@jon_omics
Clinical Scientist specialising in rare disease genomics within the @NWGLH. @NSHCS STP alumni.
ID: 990914826036793345
https://mft.nhs.uk/nwglh/ 30-04-2018 11:24:39
120 Tweet
156 Followers
240 Following

There are multiple high-throughput methods being used in COVID-19 Genomics UK (COG-UK) Consortium (PCR barcoding, CoronaHiT, CovidSeq, bait capture, RC-PCR) as well as rapid turnaround Oxford Nanopore methods.

Our manuscript exploring the value of SARS-CoV-2 Group Testing in Healthcare Settings has just been published in The Journal of Molecular Diagnostics. Great to collaborate with Bill Newman, Jamie Ellingford, DS Analytics, and colleagues from MFT NHS and The North West Genomic Laboratory Hub on this work. jmdjournal.org/article/S1525-…

Our article now accepted and available eLife - the journal The North West Genomic Laboratory Hub Evolution, Infection and Genomics (EIG) UoM elifesciences.org/articles/65453

"A collaboration between Evolution, Infection and Genomics (EIG) UoM and MFT NHS has applied new techniques to detect and track the transmission of Covid-19 in hospital." Now out at eLife - the journal! manchester.ac.uk/discover/news/…

A really nice summary of our work tracking #SARSCoV2 infections in hospitals. Evolution, Infection and Genomics (EIG) UoM The North West Genomic Laboratory Hub MFT Research and Innovation MFT NHS Hear more about this work in the #COVID19 session at #ESHG21 European Society of Human Genetics (ESHG) manchester.ac.uk/discover/news/… Jonathan Edgerley Dr Ryan George Stephen Ball John McDermott Bill Newman

Can you reduced exome interpretation workload and maintain diagnostic rates? @_lesliemolina investigates clinician-personalised virtual gene panels #OpenAccess here: ow.ly/qwoy50Evnk1 Bill Newman Jill CS Jamie Ellingford Sofia Douzgou Houge Suresh Somarathi Siddharth Banka The North West Genomic Laboratory Hub



📢👁️🧬 EyeG2P: an Ensembl Variant Effect Predictor plugin to automatically prioritise variants that cause inherited ophthalmic disorders from genomic datasets. Through TGMI working with EMBL-EBI The North West Genomic Laboratory Hub Evolution, Infection and Genomics (EIG) UoM David FitzPatrick Fiona Cunningham. Preprint:medrxiv.org/content/10.110… 1/4

Are you planning to attend #ESHG2021? Be sure to check out Jamie Ellingford's talk. Jamie will be presenting on the importance of genomic epidemiology to track #SARSCoV2 transmission through a hospital. Find out more: bit.ly/3jJOPu8 European Society of Human Genetics (ESHG)


📢 3 fully funded MRC PhD studentships available Evolution, Infection and Genomics (EIG) UoM The North West Genomic Laboratory Hub 📢 Please RT and share. Application deadline 12/11/2021. More details of projects available in the thread below.

Excellent work by Charlie Rowlands and Jamie Ellingford. Identifying best computational approaches for splicing variant prioritisation, highlighting importance of functional studies to aid accurate interpretation. Superbly presented at this afternoon’s The North West Genomic Laboratory Hub Educational Seminar.

Genomic tests don't always find a diagnosis for rare disease patients, but what if we look again? Our paper in Genetics in Medicine describes a #bioinformatics tool that can help #NHS labs to reanalyse genomic variants using the dynamic None database 🧬: sciencedirect.com/science/articl…

Considering a career in clinical #genomics? Thinking of applying for the National School of Healthcare Science STP? Or have you seen other roles we've advertised & want to know more? Join us Monday 24th January at the NWGLH Virtual Open day 2022. Sign up for FREE using the link: eventbrite.co.uk/e/nwglh-open-d…



📢 Thinking about applying to the National School of Healthcare Science Scientist Training Programme (STP) in Genomic Counselling? Find out more at our virtual open day on Wed 14th December 1-4pm. 📧 [email protected] or [email protected] to register.



❗️Reanalysis of arrayCGH datasets The North West Genomic Laboratory Hub uplifts genetic diagnoses❗️ We shortlisted CNVs from ~16,000 patients referred over a 7 year period. Of the shortlisted CNVs, 7.2% were reclassified as (likely)/pathogenic due to new evidence. George Burghel - جورج برغل Siddharth Banka medrxiv.org/content/10.110…

⏪Reanalysing historical arrayCGH data identifies new diagnoses⏪ Copy number losses overlap with disease genes that have been discovered since the time of first analysis George Burghel - جورج برغل Siddharth Banka Jake ⓥ Miller Jonathan Edgerley Chris Watt Ronnie Wright The North West Genomic Laboratory Hub pubmed.ncbi.nlm.nih.gov/38604752/