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Critical length in long read resequencing

https://doi.org/10.1101/621862
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inferredcites →https://doi.org/10.1016/j.tibtech.2018.07.013openalex-snapshot
Single-Molecule Sequencing: Towards Clinical Applications
inferredcites →https://doi.org/10.1016/j.tibtech.2019.02.003openalex-snapshot
Newest Methods for Detecting Structural Variations
inferredcites →https://doi.org/10.1016/j.tig.2018.05.008openalex-snapshot
The Third Revolution in Sequencing Technology
inferredcites →https://doi.org/10.1038/nature13907openalex-snapshot
Resolving the complexity of the human genome using single-molecule sequencing
inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot
A global reference for human genetic variation
inferredcites →https://doi.org/10.1038/nature15394openalex-snapshot
An integrated map of structural variation in 2,504 human genomes
inferredcites →https://doi.org/10.1038/nbt.4060openalex-snapshot
Nanopore sequencing and assembly of a human genome with ultra-long reads
inferredcites →https://doi.org/10.1038/ncomms14061openalex-snapshot
Transient structural variations have strong effects on quantitative traits and reproductive isolation in fission yeast
inferredcites →https://doi.org/10.1038/s41467-017-01343-4openalex-snapshot
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
inferredcites →https://doi.org/10.1038/s41467-018-08148-zopenalex-snapshot
Multi-platform discovery of haplotype-resolved structural variation in human genomes
inferredcites →https://doi.org/10.1038/s41592-018-0001-7openalex-snapshot
Accurate detection of complex structural variations using single-molecule sequencing
inferredcites →https://doi.org/10.1038/s41592-018-0054-7openalex-snapshot
A synthetic-diploid benchmark for accurate variant-calling evaluation
inferredcites →https://doi.org/10.1093/bioinformatics/btq033openalex-snapshot
BEDTools: a flexible suite of utilities for comparing genomic features
inferredcites →https://doi.org/10.1093/bioinformatics/btr509openalex-snapshot
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
inferredcites →https://doi.org/10.1093/bioinformatics/btw286openalex-snapshot
SimLoRD: Simulation of Long Read Data
inferredcites →https://doi.org/10.1093/bioinformatics/btx057openalex-snapshot
cyvcf2: fast, flexible variant analysis with Python
inferredcites →https://doi.org/10.1093/bioinformatics/btx699openalex-snapshot
Mosdepth: quick coverage calculation for genomes and exomes
inferredcites →https://doi.org/10.1093/bioinformatics/bty191openalex-snapshot
Minimap2: pairwise alignment for nucleotide sequences
inferredcites →https://doi.org/10.1093/bioinformatics/bty841openalex-snapshot
BulkVis: a graphical viewer for Oxford nanopore bulk FAST5 files
inferredcites →https://doi.org/10.1093/gigascience/gix038openalex-snapshot
Alignment of 1000 Genomes Project reads to reference assembly GRCh38
inferredcites →https://doi.org/10.1093/gigascience/giz040openalex-snapshot
Duphold: scalable, depth-based annotation and curation of high-confidence structural variant calls
inferredcites →https://doi.org/10.1093/hmg/ddx287openalex-snapshot
The potential impact of nanopore sequencing on human genetics
inferredcites →https://doi.org/10.1093/hmg/ddy177openalex-snapshot
Long reads: their purpose and place
inferredcites →https://doi.org/10.1093/nar/gkx1098openalex-snapshot
Ensembl 2018
inferredcites →https://doi.org/10.1101/434118openalex-snapshot
Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome
inferredcites →https://doi.org/10.1101/gr.244939.118openalex-snapshot
Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome
inferredcites →https://doi.org/10.1109/mcse.2007.55openalex-snapshot
Matplotlib: A 2D Graphics Environment
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