Skip navigation
Search
Sciety application settings
Home
Groups
Explore
Newsletter
About
Log In
Sign Up
Full characterization of unresolved structural variation through long-read sequencing and optical genome mapping
Griet De Clercq
Lies Vantomme
Barbara Dewaele
Bert Callewaert
Olivier Vanakker
Sandra Janssens
Bart Loeys
Mojca Strazisar
Wouter De Coster
Joris Robert Vermeesch
Annelies Dheedene
Björn Menten
Read the full article
See related articles
Listed in
This article is not in any list yet, why not save it to one of your lists.
Log in to save this article
Abstract
No abstract available
Article activity feed
Version published to 10.1038/s41598-024-80068-z
Nov 25, 2024
Version published to 10.1101/2024.07.18.24310562 on medRxiv
Jul 19, 2024
Related articles
Long Read Genome Sequencing Elucidates Diverse Functional Consequences of Structural and Repeat Variation in Autism
This article has 11 authors:
Milad Mortazavi
James Guevara
Joshua Diaz
Stephen Tran
Helyaneh Ziaei Jam
Sergey Batalov
Matthew Bainbridge
Aaron D Besterman
Melissa Gymrek
Abraham A Palmer
Jonathan Sebat
Characterization of Rare Genomic Structural Variants Across 2,981 Genomes Reveals Significant Involvements in Recessive Conditions
This article has 12 authors:
Zirui Dong
Keying Li
Chi Chun Chan
Jia Zheng
Mengmeng Shi
Wenbin He
Matthew Hoi Kin Chau
Ye Cao
Juan Du
Yvonne Ka Yin Kwok
Yue-Qiu Tan
Kwong Wai Choy
Complementarity of long-read sequencing and optical genome mapping in Parkinson’s disease
This article has 18 authors:
André Fienemann
Theresa Lüth
Susen Schaake
Carolin Gabbert
Marius Möller
Hauke Busch
Katja Lohmann
Jonas A. Gustafson
Danny E. Miller
Kensuke Daida
Manabu Funayama
Nobutaka Hattori
Samia Ben Sassi
Faycel Hentati
Matthew J. Farrer
Kristian K. Ullrich
Christine Klein
Joanne Trinh
Site navigation links
Home
Groups
Explore
Newsletter
About
Log In
Sign Up