Genome-wide reconstruction of complex structural variants using read clouds
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Genome-wide reconstruction of complex structural variants using read clouds
Authors
Keywords
-
Journal
NATURE METHODS
Volume 14, Issue 9, Pages 915-920
Publisher
Springer Nature
Online
2017-07-17
DOI
10.1038/nmeth.4366
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Haplotyping germline and cancer genomes with high-throughput linked-read sequencing
- (2016) Grace X Y Zheng et al. NATURE BIOTECHNOLOGY
- Punctuated copy number evolution and clonal stasis in triple-negative breast cancer
- (2016) Ruli Gao et al. NATURE GENETICS
- Read clouds uncover variation in complex regions of the human genome
- (2015) Alex Bishara et al. GENOME RESEARCH
- An integrated map of structural variation in 2,504 human genomes
- (2015) Peter H. Sudmant et al. NATURE
- Cell-lineage heterogeneity and driver mutation recurrence in pre-invasive breast neoplasia
- (2015) Ziming Weng et al. Genome Medicine
- The Architecture and Evolution of Cancer Neochromosomes
- (2014) Dale W. Garsed et al. CANCER CELL
- Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing
- (2014) Sasan Amini et al. NATURE GENETICS
- LUMPY: a probabilistic framework for structural variant discovery
- (2014) Ryan M Layer et al. GENOME BIOLOGY
- Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes
- (2013) Lixing Yang et al. CELL
- Punctuated Evolution of Prostate Cancer Genomes
- (2013) Sylvan C. Baca et al. CELL
- Genome evolution during progression to breast cancer
- (2013) D. E. Newburger et al. GENOME RESEARCH
- Phenotypic impact of genomic structural variation: insights from and for human disease
- (2013) Joachim Weischenfeldt et al. NATURE REVIEWS GENETICS
- The genome sequence of the colonial chordate, Botryllus schlosseri
- (2013) Ayelet Voskoboynik et al. eLife
- DELLY: structural variant discovery by integrated paired-end and split-read analysis
- (2012) T. Rausch et al. BIOINFORMATICS
- IDBA-UD: a de novo assembler for single-cell and metagenomic sequencing data with highly uneven depth
- (2012) Y. Peng et al. BIOINFORMATICS
- Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells
- (2012) Brock A. Peters et al. NATURE
- Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration
- (2012) Colby Chiang et al. NATURE GENETICS
- Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development
- (2011) Philip J. Stephens et al. CELL
- Estimation of rearrangement phylogeny for cancer genomes
- (2011) C. D. Greenman et al. GENOME RESEARCH
- Characterizing complex structural variation in germline and somatic genomes
- (2011) Aaron R. Quinlan et al. TRENDS IN GENETICS
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started