At London Calling 2023, @Carolinmsa talked about potential application of #nanopore sequencing for liquid biopsy analysis in children with cancer.
New data analysis tools such as those developed by @isidrolauscher's group are key for cancer detection.
https://t.co/9sv2pEee9d
I’ve been with @nanopore for 9 years, yet this Nanopore Day Copenhagen is the first time I’ll ever officially present our Applications work in my motherland. Awesome agenda showing use of nanopore sequencing in human clinical and translational research
https://t.co/lgKs0SQsm0
You can tell it’s been a busy week! A constant queue waiting for space on the GridION and P2 Solo. Excellent work from the whole team preparing 100’s of soil DNA and RNA samples for @nanopore sequencing.
Up and running with our first QC run 😀
We are working with @nanopore and @GenomicsEngland on the NHSE Pathfinder clinical long read #WGS programme.
@NorthThamesGLH @NEYGenomics
#ESHG2023 this morning at 9.40 on the ONT booth, @philres1 will take us on a bioinformatic tour de force using @nanopore data. All the things: ‘Single sample, haplotype-resolved genetic and epigenetic variation calling using nanopore sequencing'
Thinking about presenting #nanopore data at a conference? With ASHG submissions just around the corner don’t forget we offer bursaries, check out this link here: https://t.co/9p3atM2gqO
Looking very much forward to our Nanopore Day Stockholm on May 31st. Register to join for exciting user talks and the latest tech updates! ⬇️🧬⬇️
@nanopore@ngisweden
https://t.co/RusMCIxQ1N
Danny Miller (@danrdanny) #GRD23: Starts with his take home points
- long-read sequencing will fundamentally change clinical genetic testing
- will reduce barriers to accessing comprehensive testing
- this will happen even if the cost of generating other types of data falls to $0
The people were hungry for data at out data for breakfast session this morning at #aacr23!
Don’t worry if you missed the session. We are running another one at 9:30 tomorrow at booth 801.
At #AACR23 and interested in applications of long-read seq to cancer research? Stop by @hbelrick 's poster to learn more about our tool, #SAVANA, specifically designed for somatic SV calling! Poster LB080 at Section 34 today 9am-12:30pm! @AACR@emblebi