A stand-alone sequencing approach was accurate, cost effective and efficient for analyzing resistant pathogens and ...
You may have heard of the big names in the business, like Illumina, Oxford Nanopore Technologies ... next-generation sequencing (NGS) to more labs. The core components of the company’s genome ...
The details of the Oxford Nanopore Technologies (ONT) long-read DNA sequencing have been published previously (Kolmogorov et al., 2023; Billingsley et al., 2024) and uses the Napu (Nanopore Analysis ...
In this project we assessed the ability of an AlphaFold2-based linear epitope scan pipeline we call PAbFold ... with sequence information obtainable via various sequencing technologies such as next ...
A research team has achieved a gapless assembly of Syntrichia caninervis's genome, totaling 323.44 Mbp with an N50 value of ...
The use of nanopore sequencing for molecular diagnosis of PWS and AS has been explored by Yamada et al; however, to confirm heterodisomy parental data were still required. Here, we investigate ...
One in every 10 people worldwide is impacted by a rare genetic disease but about 50% of them remain undiagnosed despite rapid increases in genetic technology and testing.
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Long read sequencing reveals more genetic information while cutting time and cost of rare disease diagnosesThe typical approach for finding these variants uses a technique called short-read sequencing, which reads the genetic base pairs—combinations ... the Miga Lab using nanopore sequencing, a ...
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