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Automated Structural Variant Verification in Human Genomes using Single-Molecule Electronic DNA Mapping
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.gpb.2015.08.002openalex-snapshot
PacBio Sequencing and its Applications
inferredcites →https://doi.org/10.1016/j.gpb.2016.05.004openalex-snapshot
Oxford Nanopore MinION Sequencing and Genome Assembly
inferredcites →https://doi.org/10.1016/j.neucom.2008.04.024openalex-snapshot
Fusion of feature selection methods for pairwise scoring SVM
inferredcites →https://doi.org/10.1016/j.pbi.2017.02.002openalex-snapshot
The impact of third generation genomic technologies on plant genome assembly
inferredcites →https://doi.org/10.1023/a:1009715923555openalex-snapshot
A Tutorial on Support Vector Machines for Pattern Recognition
inferredcites →https://doi.org/10.1038/nature11632openalex-snapshot
An integrated map of genetic variation from 1,092 human genomes
inferredcites →https://doi.org/10.1038/nature14962openalex-snapshot
The UK10K project identifies rare variants in health and disease
inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot
A global reference for human genetic variation
inferredcites →https://doi.org/10.1038/nbt.2835openalex-snapshot
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
inferredcites →https://doi.org/10.1038/nmeth.3454openalex-snapshot
Assembly and diploid architecture of an individual human genome via single-molecule technologies
inferredcites →https://doi.org/10.1038/nrg3933openalex-snapshot
Genetic variation and the de novo assembly of human genomes
inferredcites →https://doi.org/10.1038/sdata.2016.25openalex-snapshot
Extensive sequencing of seven human genomes to characterize benchmark reference materials
inferredcites →https://doi.org/10.1063/1.4938732openalex-snapshot
Measurements of DNA barcode label separations in nanochannels from time-series data
inferredcites →https://doi.org/10.1073/pnas.0604040103openalex-snapshot
An algorithm for assembly of ordered restriction maps from single DNA molecules
inferredcites →https://doi.org/10.1073/pnas.1613365113openalex-snapshot
Deep sequencing of 10,000 human genomes
inferredcites →https://doi.org/10.1101/048603openalex-snapshot
Third-generation sequencing and the future of genomics
inferredcites →https://doi.org/10.1101/102764openalex-snapshot
Rapid Automated Large Structural Variation Detection in a Diploid Genome by NanoChannel Based Next-Generation Mapping
inferredcites →https://doi.org/10.1101/139840openalex-snapshot
High-Definition Electronic Genome Maps from Single Molecule Data
inferredcites →https://doi.org/10.1101/gr.214007.116openalex-snapshot
Discovery and genotyping of structural variation from long-read haploid genome sequence data
inferredcites →https://doi.org/10.1109/igarss.2015.7326952openalex-snapshot
The effect of mis-labeled training data on the accuracy of supervised image classification by SVM
inferredcites →https://doi.org/10.1186/s12864-016-2366-2openalex-snapshot
svclassify: a method to establish benchmark structural variant calls
inferredcites →https://doi.org/10.1186/s13742-015-0052-yopenalex-snapshot
Using optical mapping data for the improvement of vertebrate genome assemblies
inferredcites →https://doi.org/10.1534/genetics.115.183483openalex-snapshot
Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel Arrays
inferredcites →https://doi.org/10.18632/oncotarget.15802openalex-snapshot
Next generation mapping reveals novel large genomic rearrangements in prostate cancer
inferredcites →https://doi.org/10.3389/fbioe.2015.00092openalex-snapshot
Detection of Genomic Structural Variants from Next-Generation Sequencing Data
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.micres.2020.126665openalex-snapshot
Characterization of Lysinibacillus fusiformis strain S4C11: In vitro, in planta, and in silico analyses reveal a plant-beneficial microbe
inferred← citeshttps://doi.org/10.1038/s41557-023-01322-xopenalex-snapshot
Nanopore DNA sequencing technologies and their applications towards single-molecule proteomics
inferred← citeshttps://doi.org/10.1038/s41576-023-00590-0openalex-snapshot
Variant calling and benchmarking in an era of complete human genome sequences
inferred← citeshttps://doi.org/10.1038/s41587-020-0538-8openalex-snapshot
A robust benchmark for detection of germline large deletions and insertions
inferred← citeshttps://doi.org/10.1101/664623openalex-snapshot
A robust benchmark for germline structural variant detection
inferred← citeshttps://doi.org/10.1105/tpc.17.00514openalex-snapshot
Is It Ordered Correctly? Validating Genome Assemblies by Optical Mapping
inferred← citeshttps://doi.org/10.1186/s12864-019-6168-1openalex-snapshot
Assembly, annotation, and comparison of Macrophomina phaseolina isolates from strawberry and other hosts
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