At ASH's annual meeting, a study showed the potential for this method to inform the next treatment after patients relapse on BCMA- or GPRC5D-targeted therapy.

By inferring proliferation rates from single-cell genomics, SPRINTER enhances understanding of tumor evolution and identifies ...

allowing for much higher sequencing depth and higher sensitivity, which is crucial for detecting low-frequency mutations and single nucleotide polymorphisms (SNPs) (Dinis et al., 2016; Takayama et al.

scplotter is an R package that is built upon plotthis. It provides a set of functions to visualize single-cell sequencing data in an easy and efficient way.

Genome-wide association studies have identified thousands of genetic loci that are significantly associated with complex traits and diseases status. However, the functions/roles of the majority (~90%) ...

Here, we report a systematic transcriptional atlas to delineate molecular and cellular heterogeneity in GA using single-cell RNA sequencing (scRNA-seq). Design We performed unbiased transcriptome-wide ...

(Nasdaq: AZTA) announced the launch of a long-read Whole Genome Sequencing (WGS ... Subscribe for FREE "Clinical-grade long-read sequencing represents a monumental leap forward in the ability to ...

This study reveals distinct immune subpopulations associated with specific myeloma cell genotypes and highlights the central ...

Think of a genome as a living book with instructions for every cell in the body ... can sometimes be a very complex process. Whole genome sequencing (WGS) can help identify small changes in ...