This article provides a comprehensive comparison of full-length and 3'-end single-cell RNA sequencing protocols.
This article provides a detailed, comparative analysis of three leading long-read (Flye and Canu) and short-read (SPAdes) genome assemblers, tailored for researchers and professionals in genomics and drug development.
This comprehensive guide provides researchers, scientists, and drug development professionals with a complete workflow for performing genome assembly using Flye with Oxford Nanopore long-read data.
This guide provides a detailed exploration of the Flye assembler, a leading tool for de novo genome assembly from long-read sequencing data.
This definitive guide provides researchers, scientists, and drug development professionals with a detailed roadmap for developing and validating mass spectrometry-based biomarker assays aligned with current FDA expectations.
This article provides a comprehensive guide for researchers and drug development professionals on implementing FAIR (Findable, Accessible, Interoperable, Reusable) data principles in genomic annotation workflows.
This guide provides a detailed roadmap for researchers, scientists, and drug development professionals leveraging Fluorescence-Activated Cell Sorting (FACS) to isolate single cells for downstream single-cell RNA sequencing (scRNA-seq).
This comprehensive guide addresses the critical challenge of prioritizing causative variants from next-generation sequencing data in rare disease research.
This article provides a critical evaluation of the sensitivity of affinity-based (e.g., immunoassays) and mass spectrometry (MS)-based platforms for quantifying proteins and biomarkers.
This comprehensive beginner's guide to the Ensembl Variant Effect Predictor (VEP) walks researchers through the foundational concepts, practical application, troubleshooting, and validation of variant annotations.