Interesting new findings by @LabWiller! We had a similar experience when we found Long QT in some of our volunteers. The paper has been published with open access at: https://t.co/GmV6rZPwNO #DataSavesLives
We tackled a somewhat similar return of results scenario in @vikinggenes, paper published with open access here: https://t.co/j9PslSRUKe #DataSavesLives
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. https://t.co/eD2LJstqrS https://t.co/Aff57z9zTe
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. https://t.co/ebGFKsXoK0
RT @shona_kerr: I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists a…
RT @shona_kerr: I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists a…
RT @shona_kerr: Paper published @SciReports https://t.co/w3mE52FB7z "Rare Ancestral Variant found in VIKING Health Study" https://t.co/Mche…
New from #The_MRC https://t.co/yx84FxiCia An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort
New from #CSO_Scotland https://t.co/yx84FxiCia An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort
RT @shona_kerr: Paper published @SciReports https://t.co/w3mE52FB7z "Rare Ancestral Variant found in VIKING Health Study" https://t.co/Mche…
RT @shona_kerr: Paper published @SciReports https://t.co/w3mE52FB7z "Rare Ancestral Variant found in VIKING Health Study" https://t.co/Mche…
Paper published @SciReports https://t.co/w3mE52FB7z "Rare Ancestral Variant found in VIKING Health Study" https://t.co/McheUySriY
RT @vikinggenes: The Director of the @mrc_hgu in Edinburgh, Prof Wendy Bickmore, commenting on a recently published research paper from @vi…
RT @vikinggenes: The Director of the @mrc_hgu in Edinburgh, Prof Wendy Bickmore, commenting on a recently published research paper from @vi…
The Director of the @mrc_hgu in Edinburgh, Prof Wendy Bickmore, commenting on a recently published research paper from @vikinggenes @ScottishGenomes https://t.co/0CMCborV3x
RT @shona_kerr: New paper by Kerr et al 😀 "An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a po…
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. https://t.co/LBR6NrwOsI
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort. https://t.co/PoayynWjZq
RT @wendy_bickmore: Showing the value, opportunities and challenges of genomics in isolate populations. Thank you to the people of the Nort…
RT @wendy_bickmore: Showing the value, opportunities and challenges of genomics in isolate populations. Thank you to the people of the Nort…
RT @wendy_bickmore: Showing the value, opportunities and challenges of genomics in isolate populations. Thank you to the people of the Nort…
RT @wendy_bickmore: Showing the value, opportunities and challenges of genomics in isolate populations. Thank you to the people of the Nort…
RT @wendy_bickmore: Showing the value, opportunities and challenges of genomics in isolate populations. Thank you to the people of the Nort…
RT @wendy_bickmore: Showing the value, opportunities and challenges of genomics in isolate populations. Thank you to the people of the Nort…
Showing the value, opportunities and challenges of genomics in isolate populations. Thank you to the people of the Northern Isles for their participation in this important project.
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort https://t.co/WOsRZ1t0kB
RT @shona_kerr: I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists a…
RT @shona_kerr: I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists a…
RT @shona_kerr: I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists a…
RT @shona_kerr: I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists a…
RT @shona_kerr: I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists a…
RT @vikinggenes: @shona_kerr and @hukwi from our team recently published a paper talking about detection of Long QT syndrome and feedback o…
@shona_kerr and @hukwi from our team recently published a paper talking about detection of Long QT syndrome and feedback of results to our VIKING Health Study - Shetland volunteers!
RT @l_klaric: One of my favourite stories is out! Read how we used a subset of our cohort that has WGS to identify a single individual carr…
One of my favourite stories is out! Read how we used a subset of our cohort that has WGS to identify a single individual carrying a long QT syndrome variant and "profited" from a high kinship in the cohort to detect 4 additional carriers in the rest of the
RT @shona_kerr: I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists a…
New paper by Kerr et al 😀 "An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research… https://t.co/Jq2tTKTDaJ
I'm pleased with this paper! Nice teamwork by the sequencing lab, bioinformaticians, statistical and clinical geneticists and some ethics too @vikinggenes @mrc_hgu @ScottishGenomes https://t.co/h23L1BhroG https://t.co/NZtPQgBWud