Genes | Free Full-Text | TEfinder: A Bioinformatics Pipeline for Detecting New Transposable Element Insertion Events in Next-Generation Sequencing Data
Filtering of VCF Files
Validation of a Customized Bioinformatics Pipeline for a Clinical Next-Generation Sequencing Test Targeting Solid Tumor–Associated Variants - ScienceDirect
A) Distribution of RNA editing types with and without a filter for... | Download Scientific Diagram
Common examples where variant calling may prove erroneous. Forward... | Download Scientific Diagram
The effect of strand bias in Illumina short-read sequencing data | BMC Genomics | Full Text
QC with STAR and Qualimap | Introduction to RNA-Seq using high-performance computing - ARCHIVED
The use of technical replication for detection of low-level somatic mutations in next-generation sequencing | Nature Communications
Allele and strand bias for SNVs. This figure shows read distribution of... | Download Scientific Diagram
strand bias and orientation bias – GATK
Analysis of Assemblies and Alignments - Geneious Prime User Manual
Common artifacts in NGS alignments that gave rise to a false-positive... | Download Scientific Diagram
Heteroduplex finder | CCS Docs
Validation of a Customized Bioinformatics Pipeline for a Clinical Next-Generation Sequencing Test Targeting Solid Tumor–Associated Variants - ScienceDirect
Filtering of VCF Files
Analysis of Assemblies and Alignments - Geneious Prime User Manual
Aligned reads with strand biased errors. Hypothetical reads of two... | Download Scientific Diagram
HIV-1 Drug Resistance Assay Using Ion Torrent Next Generation Sequencing and On-Instrument End-to-End Analysis Software | Journal of Clinical Microbiology
Comparing a few SNP calling algorithms using low-coverage sequencing data | BMC Bioinformatics | Full Text
modules/lofreq_filter
UVC: universality-based calling of small variants using pseudo-neural networks | bioRxiv
Robust data storage in DNA by de Bruijn graph-based de novo strand assembly | Nature Communications
