Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis | Scientific Reports
Left) Linked-read sequencing with the 10X Genomics Chromium platform... | Download Scientific Diagram
HLS-CATCH and TELL-Seq™: a new route to Targeted Long-Fragment Linked-Read Sequencing | Sage Science
Cancers | Free Full-Text | Comparison of Structural and Short Variants Detected by Linked-Read and Whole-Exome Sequencing in Multiple Myeloma
Linked Read Sequencing – 10X Genomics Chromium Technology | DNA Technologies Core
Haplotagging enables population-scale linked-read sequencing. a,... | Download Scientific Diagram
CATCH targeting and linked read sequencing of HMW DNA. (A) Overview of... | Download Scientific Diagram
![PDF] Droplet Barcode Sequencing for targeted linked-read haplotyping of single DNA molecules | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/b3d42728a61f19d438150b6aecf26131ed0bd7bc/5-Figure1-1.png "PDF] Droplet Barcode Sequencing for targeted linked-read haplotyping of single DNA molecules | Semantic Scholar")
PDF] Droplet Barcode Sequencing for targeted linked-read haplotyping of single DNA molecules | Semantic Scholar
Linked-read sequencing of gametes allows efficient genome-wide analysis of meiotic recombination | Nature Communications
Beyond the exome projects
Linked read technology for assembling large complex and polyploid genomes | BMC Genomics | Full Text
Haplotyping germline and cancer genomes with high-throughput linked-read sequencing | Nature Biotechnology
A new era of long-read sequencing for cancer genomics | Journal of Human Genetics
Identifying structural variants using linked-read sequencing data
Opportunities and challenges in long-read sequencing data analysis | Genome Biology | Full Text
Synthetic Long Read" Sequencing - France Génomique
Long-linked read sequencing application note - Revvity chemagen Technologie GmbH
Ultra-low input single tube linked-read library method enables short-read NGS systems to generate highly accurate and economical long-range sequencing information for de novo genome assembly and haplotype phasing | bioRxiv
Application of long-read sequencing to the detection of structural variants in human cancer genomes - ScienceDirect
10X genomics data and assembly with Supernova | UC Davis Bioinformatics Core December 2018 Genome Assembly workshop
Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing - ScienceDirect
Linked‐read sequencing enables haplotype‐resolved resequencing at population scale - Lutgen - 2020 - Molecular Ecology Resources - Wiley Online Library
Identifying rearrangements from linked reads. The workflow is... | Download Scientific Diagram
