Confluence Mobile - Integrated Genome Browser Help Pages
Frontiers | MATCHCLIP: locate precise breakpoints for copy number variation using CIGAR string by matching soft clipped reads
IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis | Scientific Reports
Manipulating NGS data with Galaxy - Galaxy Community Hub
ClipCrop: a tool for detecting structural variations with single-base resolution using soft-clipping information | BMC Bioinformatics | Full Text
Alignment with STAR | Introduction to RNA-Seq using high-performance computing - ARCHIVED
Soft-clipped reads vs. improperly aligned reads at a structural variant... | Download Scientific Diagram
Reads filtering · Issue #879 · igvteam/igv.js · GitHub
QC Fail Sequencing » Soft-clipping of reads may add potentially unwanted alignments to repetitive regions
Common sources of 5′end soft clipping and mismatches in 3′ end seq. (a)... | Download Scientific Diagram
![PDF] Socrates: identification of genomic rearrangements in tumour genomes by re-aligning soft clipped reads | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/16b34a01c549bc1b12b6c5a17e85e1db117f26e3/2-Figure1-1.png "PDF] Socrates: identification of genomic rearrangements in tumour genomes by re-aligning soft clipped reads | Semantic Scholar")
PDF] Socrates: identification of genomic rearrangements in tumour genomes by re-aligning soft clipped reads | Semantic Scholar
Sequencing artifacts derived from a library preparation method using enzymatic fragmentation | PLOS ONE
Confluence Mobile - Integrated Genome Browser Help Pages
The flow chart of TDNAscan pipeline. Types A and B of soft-clipped... | Download Scientific Diagram
QC Fail Sequencing » Soft-clipping of reads may add potentially unwanted alignments to repetitive regions
Hepatitis Delta Virus Genome RNA Synthesis Initiates at Position 1646 with a Nontemplated Guanosine | Journal of Virology
SoftSearch: Integration of Multiple Sequence Features to Identify Breakpoints of Structural Variations | PLOS ONE
Accurate Detection and Quantification of FLT3 Internal Tandem Duplications in Clinical Hybrid Capture Next-Generation Sequencing Data - ScienceDirect
VarDict: a novel and versatile variant caller for next-generation sequencing in cancer research. - Abstract - Europe PMC
Split Reads
A customized scaffolds approach for the detection and phasing of complex variants by next-generation sequencing | Scientific Reports
Challenges and importance of mid-sized deletion identification for genomic medicine - SeqOne Genomics
VarDict uses soft-clipped reads for local realignment to... | Download Scientific Diagram
