Literature DB >> 30938757

Structural variant analysis for linked-read sequencing data with gemtools.

S U Greer1, H P Ji1,2.   

Abstract

SUMMARY: Linked-read sequencing generates synthetic long reads which are useful for the detection and analysis of structural variants (SVs). The software associated with 10× Genomics linked-read sequencing, Long Ranger, generates the essential output files (BAM, VCF, SV BEDPE) necessary for downstream analyses. However, to perform downstream analyses requires the user to customize their own tools to handle the unique features of linked-read sequencing data. Here, we describe gemtools, a collection of tools for the downstream and in-depth analysis of SVs from linked-read data. Gemtools uses the barcoded aligned reads and the Megabase-scale phase blocks to determine haplotypes of SV breakpoints and delineate complex breakpoint configurations at the resolution of single DNA molecules. The gemtools package is a suite of tools that provides the user with the flexibility to perform basic functions on their linked-read sequencing output in order to address even more questions.
AVAILABILITY AND IMPLEMENTATION: The gemtools package is freely available for download at: https://github.com/sgreer77/gemtools. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Mesh:

Year:  2019        PMID: 30938757      PMCID: PMC6821325          DOI: 10.1093/bioinformatics/btz239

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  4 in total

1.  Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases.

Authors:  Stephanie U Greer; Lincoln D Nadauld; Billy T Lau; Jiamin Chen; Christina Wood-Bouwens; James M Ford; Calvin J Kuo; Hanlee P Ji
Journal:  Genome Med       Date:  2017-06-19       Impact factor: 11.117

2.  Haplotype-resolved and integrated genome analysis of the cancer cell line HepG2.

Authors:  Bo Zhou; Steve S Ho; Stephanie U Greer; Noah Spies; John M Bell; Xianglong Zhang; Xiaowei Zhu; Joseph G Arthur; Seunggyu Byeon; Reenal Pattni; Ishan Saha; Yiling Huang; Giltae Song; Dimitri Perrin; Wing H Wong; Hanlee P Ji; Alexej Abyzov; Alexander E Urban
Journal:  Nucleic Acids Res       Date:  2019-05-07       Impact factor: 16.971

3.  Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562.

Authors:  Bo Zhou; Steve S Ho; Stephanie U Greer; Xiaowei Zhu; John M Bell; Joseph G Arthur; Noah Spies; Xianglong Zhang; Seunggyu Byeon; Reenal Pattni; Noa Ben-Efraim; Michael S Haney; Rajini R Haraksingh; Giltae Song; Hanlee P Ji; Dimitri Perrin; Wing H Wong; Alexej Abyzov; Alexander E Urban
Journal:  Genome Res       Date:  2019-02-08       Impact factor: 9.043

4.  Haplotyping germline and cancer genomes with high-throughput linked-read sequencing.

Authors:  Grace X Y Zheng; Billy T Lau; Michael Schnall-Levin; Mirna Jarosz; John M Bell; Christopher M Hindson; Sofia Kyriazopoulou-Panagiotopoulou; Donald A Masquelier; Landon Merrill; Jessica M Terry; Patrice A Mudivarti; Paul W Wyatt; Rajiv Bharadwaj; Anthony J Makarewicz; Yuan Li; Phillip Belgrader; Andrew D Price; Adam J Lowe; Patrick Marks; Gerard M Vurens; Paul Hardenbol; Luz Montesclaros; Melissa Luo; Lawrence Greenfield; Alexander Wong; David E Birch; Steven W Short; Keith P Bjornson; Pranav Patel; Erik S Hopmans; Christina Wood; Sukhvinder Kaur; Glenn K Lockwood; David Stafford; Joshua P Delaney; Indira Wu; Heather S Ordonez; Susan M Grimes; Stephanie Greer; Josephine Y Lee; Kamila Belhocine; Kristina M Giorda; William H Heaton; Geoffrey P McDermott; Zachary W Bent; Francesca Meschi; Nikola O Kondov; Ryan Wilson; Jorge A Bernate; Shawn Gauby; Alex Kindwall; Clara Bermejo; Adrian N Fehr; Adrian Chan; Serge Saxonov; Kevin D Ness; Benjamin J Hindson; Hanlee P Ji
Journal:  Nat Biotechnol       Date:  2016-02-01       Impact factor: 54.908

  4 in total
  4 in total

Review 1.  Structural variation in the sequencing era.

Authors:  Steve S Ho; Alexander E Urban; Ryan E Mills
Journal:  Nat Rev Genet       Date:  2019-11-15       Impact factor: 53.242

2.  Starfish infers signatures of complex genomic rearrangements across human cancers.

Authors:  Lisui Bao; Xiaoming Zhong; Yang Yang; Lixing Yang
Journal:  Nat Cancer       Date:  2022-07-14

3.  Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).

Authors:  Catherine Rehder; Lora J H Bean; David Bick; Elizabeth Chao; Wendy Chung; Soma Das; Julianne O'Daniel; Heidi Rehm; Vandana Shashi; Lisa M Vincent
Journal:  Genet Med       Date:  2021-04-29       Impact factor: 8.822

4.  Linked-Read Whole Genome Sequencing Solves a Double DMD Gene Rearrangement.

Authors:  Maria Elena Onore; Annalaura Torella; Francesco Musacchia; Paola D'Ambrosio; Mariateresa Zanobio; Francesca Del Vecchio Blanco; Giulio Piluso; Vincenzo Nigro
Journal:  Genes (Basel)       Date:  2021-01-21       Impact factor: 4.096

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.