Real-time detection of 20 amino acids and discrimination of pathologically relevant peptides with functionalized nanopore.

@RudolfMeier15 @nanopore Hallo😅🌹

@The__Taybor Both

A fast and inexpensive automated tool to screen patients with AML for therapy-relevant genetic aberrations directly from routine, conventionally stained bone marrow smears.

Rapid nanopore metagenomic sequencing and predictive susceptibility testing of positive blood cultures from intensive care. doi: 

TALLSorts: a T-cell acute lymphoblastic leukemia subtype classifier using RNA-seq expression data.

@AdrienLeger2 @nanopore @logan_mulroney Congratulations for you and for us

@WilliamAird4 RDW+MCHC high=HS

@LaraUrban42 @MolSystBiol @EMBOPress @HelmholtzMunich @helmholtz_ai @PioneerCampus @TU_Muenchen @nanopore @Albert_Perlas @harika_urel @olga_francino @J_MartiCarreras @HernMoral @mugabre @ClaudiaFontsere @gringene_bio @tmarquesbonet @ZaneLibke Congratulations ❤

RT @LaraUrban42: It has never felt so wrong to be a German citizen; its leaders @Bundeskanzler @vonderleyen openly disregard human rights,…

Direct detection of target DNA from raw MinION signals using trainable neural networks, that can run without basecalling on a $100 single-board computer.

RT @mbeisen: I have been informed that I am being replaced as the Editor in Chief of @eLife for retweeting a @TheOnion piece that calls out…

@hemawaf @alnuaimi_hemonc No thrombocytopenia noted in these blood film🤔

My last particepate in ESCCA 2023 Utrecht-Netherlands 30.09.2023 Leukemia Immunophenotyping profiles in Yemen.

Great work. 👍 Commercially available MinION sequencing device, ofering a one-hour turnaround time from sample preparation to results.Directly detect cardiovascular disease-associated microRNA from human serum without extraction or amplifcation.

@LaraUrban42 @eLife @eLifeCommunity @mbeisen @PlantEvolution @Health_talents @helmholtz_ai @helmholtz_en @PioneerCampus @CGH_TUM Congratulations

First-ever #malaria vaccine.

CRISPR and single-cell sequencing pinpoint causal genetic variants for traits and diseases

The nanopore sequencing workflow is fast (feasible in under 5 hours) and cost-effective (100-150€ per sample), allowing fresh embryo transfer. Evaluation of nanopore sequencing on polar bodies for routine PGT-A.

Real-time molecular classification of leukemias