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Advancing clinical interpretation from single cell sequencing datasets – Webinar

Novel tools for data analysis and clinical interpretation The clinical translation of single cell analysis approaches into routine practice represents […]

New tool merges single cell RNA-Seq and spatial data

A team has developed a new tool, called cell2location, that can resolve fine-grained cell types in spatial transcriptomic data. Spatial […]

New DNA sequencing technique sets world record

A team from Stanford Medicine has set a Guinness World Record for the fastest time to sequence a whole genome. […]

Sequencing of DNA in the bone marrow can predict leukaemia relapse

DNA sequencing-based detection of residual disease has been found to accurately predict which acute lymphoblastic leukaemia patients will eventually relapse. […]

RNA modifications provide new insights into disease brain states

Recently, researchers have used advanced microscopy to investigate the role that RNA modifications play in ‘synaptic tagging’ within the brain. […]

Discovering the importance of placental microRNAs

Researchers have carried out the most comprehensive profiling of human placental miRNA expression to date, in the hope of driving […]

Newborn genomic sequencing has no negative effect on families

A new study, published today in JAMA Pediatrics, has investigated the impact of newborn genomic sequencing (nGS) on parents. Their […]

Is nanopore sequencing the future?

Nanopore-based methods took over 25 years to fully materialise, which involved the collaboration of both academia and industry. It is […]

DNA Sequencing: How to Choose the Right Technology

Introduction It has been over 30 years since the first generation of DNA sequencing technology was developed in 1977. Since […]

What are ChIP-seq and bisulfite sequencing?

ChIP-seq protocol Chromatin immunoprecipitation sequencing, also known as ChIP-seq, is a method used to analyze protein interactions with DNA. Chromatin […]