The variables for NGS experiments: coverage, read length, multiplexing
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Basics of NGS, Target Capture
Frontiers High-Quality Library Preparation for NGS-Based Immunoglobulin Germline Gene Inference and Repertoire Expression Analysis
CRISPECTOR provides accurate estimation of genome editing translocation and off-target activity from comparative NGS data
Single Cell Gene Expression Flex - 10x Genomics
NGS - Experimental Design
Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer [PeerJ]
Highlighting Clinical Metagenomics for Enhanced Diagnostic Decision-making: A Step Towards Wider Implementation - Computational and Structural Biotechnology Journal
Comparison of DNA Quantification Methods for Next Generation Sequencing
What is mappable coverage?
Single duplex DNA sequencing with CODEC detects mutations with high sensitivity
Identifying the best PCR enzyme for library amplification in NGS
NASCarD (Nanopore Adaptive Sampling with Carrier DNA): A rapid, PCR-free method for whole genome sequencing of pathogens in clinical samples
encore™ NGS Library System I and Multiplex System I
Multiplexed targeted next generation sequencing coverage
Depth of Coverage: The histograms depict the read depth by all called
