The variables for NGS experiments: coverage, read length, multiplexing

NASCarD (Nanopore Adaptive Sampling with Carrier DNA): A rapid, PCR-free method for whole genome sequencing of pathogens in clinical samples

How many sequence reads do I need for my RNA-Seq samples?

Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer [PeerJ]

Making your science powerful : an introduction to NGS experimental design

Next-Generation Sequencing (NGS)- Definition, Types

Sequencing 101: Sequencing coverage - PacBio

Frontiers Methods to improve the accuracy of next-generation sequencing

MACE: The smart RNA-Seq alternative

How to calculate the coverage for a NGS experiment

The variables for NGS experiments: coverage, read length, multiplexing

Next Generation Sequencing: Principle, Steps Involved, and Applications • Microbe Online

Diagnostics, Free Full-Text

Guidelines for Validation of Next-Generation Sequencing–Based Oncology Panels: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists - ScienceDirect

What is mappable coverage?

NGS Experimental Design & Protocol Guidance