Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data-Reference-Cited by-同舟云学术

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Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data

Published:2018-01 Issue:1 Volume:28 Page:144-144
ISSN:1088-9051
Container-title:Genome Research
language:en
Short-container-title:Genome Res.

Author:

Huddleston John,Chaisson Mark J.P.,Steinberg Karyn Meltz,Warren Wes,Hoekzema Kendra,Gordon David,Graves-Lindsay Tina A.,Munson Katherine M.,Kronenberg Zev N.,Vives Laura,Peluso Paul,Boitano Matthew,Chin Chen-Shin,Korlach Jonas,Wilson Richard K.,Eichler Evan E.

Publisher

Cold Spring Harbor Laboratory

Subject

Genetics (clinical),Genetics

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A national pilot study: Clinical long-read sequencing of chromosomal rearrangements;2023-12-17

2. Hidden biases in germline structural variant detection;Genome Biology;2021-12

3. SENSV: Detecting Structural Variations with Precise Breakpoints using Low-Depth WGS Data from a Single Oxford Nanopore MinION Flowcell;2021-04-21

4. Comparison of Structural and Short Variants Detected by Linked-Read and Whole-Exome Sequencing in Multiple Myeloma;Cancers;2021-03-10

5. The third generation sequencing: the advanced approach to genetic diseases;Translational Pediatrics;2020-04

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