Literature DB >> 31747936

Structural variant calling: the long and the short of it.

Medhat Mahmoud1, Nastassia Gobet2,3, Diana Ivette Cruz-Dávalos3,4, Ninon Mounier3,5, Christophe Dessimoz6,7,8,9,10, Fritz J Sedlazeck11.   

Abstract

Recent research into structural variants (SVs) has established their importance to medicine and molecular biology, elucidating their role in various diseases, regulation of gene expression, ethnic diversity, and large-scale chromosome evolution-giving rise to the differences within populations and among species. Nevertheless, characterizing SVs and determining the optimal approach for a given experimental design remains a computational and scientific challenge. Multiple approaches have emerged to target various SV classes, zygosities, and size ranges. Here, we review these approaches with respect to their ability to infer SVs across the full spectrum of large, complex variations and present computational methods for each approach.

Entities:  

Keywords:  De novo assembly; Gene fusion; Hybrid; Long-read; Mapping; RNA-Seq; Short-read; Structural variant (SV) detection

Year:  2019        PMID: 31747936     DOI: 10.1186/s13059-019-1828-7

Source DB:  PubMed          Journal:  Genome Biol        ISSN: 1474-7596            Impact factor:   13.583


  104 in total

Review 1.  Towards improved genetic diagnosis of human differences of sex development.

Authors:  Emmanuèle C Délot; Eric Vilain
Journal:  Nat Rev Genet       Date:  2021-06-03       Impact factor: 53.242

2.  Characterization of intermediate-sized insertions using whole-genome sequencing data and analysis of their functional impact on gene expression.

Authors:  Saeideh Ashouri; Jing Hao Wong; Hidewaki Nakagawa; Mihoko Shimada; Katsushi Tokunaga; Akihiro Fujimoto
Journal:  Hum Genet       Date:  2021-05-12       Impact factor: 4.132

3.  Characterization of the poll allele in Brahman cattle using long-read Oxford Nanopore sequencing.

Authors:  Harrison J Lamb; Elizabeth M Ross; Loan T Nguyen; Russell E Lyons; Stephen S Moore; Ben J Hayes
Journal:  J Anim Sci       Date:  2020-05-01       Impact factor: 3.159

4.  Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluation.

Authors:  Olivier Quenez; Kevin Cassinari; Sophie Coutant; François Lecoquierre; Kilan Le Guennec; Stéphane Rousseau; Anne-Claire Richard; Stéphanie Vasseur; Emilie Bouvignies; Jacqueline Bou; Gwendoline Lienard; Sandrine Manase; Steeve Fourneaux; Nathalie Drouot; Virginie Nguyen-Viet; Myriam Vezain; Pascal Chambon; Géraldine Joly-Helas; Nathalie Le Meur; Mathieu Castelain; Anne Boland; Jean-François Deleuze; Isabelle Tournier; Françoise Charbonnier; Edwige Kasper; Gaëlle Bougeard; Thierry Frebourg; Pascale Saugier-Veber; Stéphanie Baert-Desurmont; Dominique Campion; Anne Rovelet-Lecrux; Gaël Nicolas
Journal:  Eur J Hum Genet       Date:  2020-06-26       Impact factor: 4.246

5.  Targeted long-read sequencing identifies missing disease-causing variation.

Authors:  Danny E Miller; Arvis Sulovari; Tianyun Wang; Hailey Loucks; Kendra Hoekzema; Katherine M Munson; Alexandra P Lewis; Edith P Almanza Fuerte; Catherine R Paschal; Tom Walsh; Jenny Thies; James T Bennett; Ian Glass; Katrina M Dipple; Karynne Patterson; Emily S Bonkowski; Zoe Nelson; Audrey Squire; Megan Sikes; Erika Beckman; Robin L Bennett; Dawn Earl; Winston Lee; Rando Allikmets; Seth J Perlman; Penny Chow; Anne V Hing; Tara L Wenger; Margaret P Adam; Angela Sun; Christina Lam; Irene Chang; Xue Zou; Stephanie L Austin; Erin Huggins; Alexias Safi; Apoorva K Iyengar; Timothy E Reddy; William H Majoros; Andrew S Allen; Gregory E Crawford; Priya S Kishnani; Mary-Claire King; Tim Cherry; Jessica X Chong; Michael J Bamshad; Deborah A Nickerson; Heather C Mefford; Dan Doherty; Evan E Eichler
Journal:  Am J Hum Genet       Date:  2021-07-02       Impact factor: 11.025

6.  Optical genome mapping enables constitutional chromosomal aberration detection.

Authors:  Tuomo Mantere; Kornelia Neveling; Céline Pebrel-Richard; Marion Benoist; Guillaume van der Zande; Ellen Kater-Baats; Imane Baatout; Ronald van Beek; Tony Yammine; Michiel Oorsprong; Faten Hsoumi; Daniel Olde-Weghuis; Wed Majdali; Susan Vermeulen; Marc Pauper; Aziza Lebbar; Marian Stevens-Kroef; Damien Sanlaville; Jean Michel Dupont; Dominique Smeets; Alexander Hoischen; Caroline Schluth-Bolard; Laïla El Khattabi
Journal:  Am J Hum Genet       Date:  2021-07-07       Impact factor: 11.025

7.  Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases.

Authors:  Shilpa Nadimpalli Kobren; Dustin Baldridge; Matt Velinder; Joel B Krier; Kimberly LeBlanc; Cecilia Esteves; Barbara N Pusey; Stephan Züchner; Elizabeth Blue; Hane Lee; Alden Huang; Lisa Bastarache; Anna Bican; Joy Cogan; Shruti Marwaha; Anna Alkelai; David R Murdock; Pengfei Liu; Daniel J Wegner; Alexander J Paul; Shamil R Sunyaev; Isaac S Kohane
Journal:  Genet Med       Date:  2021-02-12       Impact factor: 8.822

Review 8.  Beyond monogenetic rare variants: tackling the low rate of genetic diagnoses in predominantly antibody deficiency.

Authors:  Emily S J Edwards; Julian J Bosco; Samar Ojaimi; Robyn E O'Hehir; Menno C van Zelm
Journal:  Cell Mol Immunol       Date:  2020-08-17       Impact factor: 11.530

9.  Samplot: a platform for structural variant visual validation and automated filtering.

Authors:  Jonathan R Belyeu; Murad Chowdhury; Joseph Brown; Brent S Pedersen; Michael J Cormier; Aaron R Quinlan; Ryan M Layer
Journal:  Genome Biol       Date:  2021-05-25       Impact factor: 13.583

Review 10.  Towards population-scale long-read sequencing.

Authors:  Wouter De Coster; Matthias H Weissensteiner; Fritz J Sedlazeck
Journal:  Nat Rev Genet       Date:  2021-05-28       Impact factor: 53.242

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