This article provides a comprehensive analysis of the current landscape of computational tools for detecting copy number variations (CNVs) from single-cell RNA sequencing (scRNA-seq) data.
Recent advances in single-cell RNA sequencing (scRNA-seq) have revolutionized our ability to dissect the complex cellular ecosystems of human cancers at unprecedented resolution.
Single-cell sequencing has revolutionized biomarker discovery by revealing cellular heterogeneity and identifying novel cell-type-specific signatures with high resolution.
This article provides researchers, scientists, and drug development professionals with a definitive guide to the cross-platform validation of 10x Genomics Chromium and SMART-seq2 single-cell RNA sequencing technologies.
This article provides a comprehensive guide to single-cell RNA sequencing data normalization and highly variable gene (HVG) selection, critical steps that directly impact all downstream analyses.
This article provides a comprehensive guide for researchers and drug development professionals on integrating single-cell RNA sequencing (scRNA-seq) with flow cytometry to validate transcriptomic findings.
This article provides researchers, scientists, and drug development professionals with a comprehensive analysis of single-cell and bulk sequencing methodologies for investigating tumor heterogeneity.
This article provides a comprehensive examination of microfluidic technology for optimizing cell capture rates, a critical parameter for researchers and drug development professionals.
Single-cell RNA sequencing (scRNA-seq) has revolutionized biomedical research by revealing cellular heterogeneity, but its application is often constrained by the challenge of low input RNA.
The integrative analysis of single-cell genomic data across multiple patients is revolutionizing our understanding of cellular heterogeneity in health and disease.