Single nucleotide variants| Oxford Nanopore Technologies
An integrated Asian human SNV and indel benchmark established using multiple sequencing methods | Scientific Reports
lizamathews/CAISC: README.md
Total RNA-seq−based SNV identification workflow for AD. Single and... | Download Scientific Diagram
AccuSomatic Amplification for Single Cell DNA Sequencing
Genes | Free Full-Text | Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing
SNV | RNA-Seq Blog
Application of high-throughput, high-depth, targeted single-nucleus DNA sequencing in pancreatic cancer | bioRxiv
SNP & SNV Genotyping | NGS & array techniques
Whole-genome sequencing of multiple myeloma reveals oncogenic pathways are targeted somatically through multiple mechanisms | Leukemia
Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing - ScienceDirect
Rare Disease Whole-Genome Sequencing
Genes | Free Full-Text | Improved SNV Discovery in Barcode-Stratified scRNA- seq Alignments
Experimental design for validating SNV identification in... | Download Scientific Diagram
Representative Sanger sequencing electropherogram at the position of de... | Download Scientific Diagram
Somatic variant calling from single-cell DNA sequencing data - ScienceDirect
Sanger sequencing of single nucleotide variant (SNV) in FDOV1 | Download Scientific Diagram
SNV calling from NGS data - Wikipedia
PicoPLEX single-cell DNA-seq: detection of CNV and SNV from single cells
Frontiers | Application of Next-Generation Sequencing to Reveal How Evolutionary Dynamics of Viral Population Shape Dengue Epidemiology
Flow diagram for the comparison of single nucleotide variant (SNV) detection performances of whole genome sequencing (WGS), whole exome sequencing (WES), and HaloPlex target enrichment sequencing (HES).
Systematic comparative analysis of single-nucleotide variant detection methods from single-cell RNA sequencing data | Genome Biology | Full Text
Example of validation by Sanger's sequencing of a SNV specific to... | Download Scientific Diagram
An integrated Asian human SNV and indel benchmark combining multiple sequencing methods | bioRxiv
Find SNVs
PHLI-seq: constructing and visualizing cancer genomic maps in 3D by phenotype-based high-throughput laser-aided isolation and sequencing | Genome Biology | Full Text
scSNV: accurate dscRNA-seq SNV co-expression analysis using duplicate tag collapsing | Genome Biology | Full Text
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program | Nature Communications
