Related references
Note: Only part of the references are listed.Fast and accurate long-read assembly with wtdbg2
Jue Ruan et al.
NATURE METHODS (2020)
Accurate detection of complex structural variations using single-molecule sequencing
Fritz J. Sedlazeck et al.
NATURE METHODS (2018)
LongISLND: in silico sequencing of lengthy and noisy datatypes
Bayo Lau et al.
BIOINFORMATICS (2016)
Extensive sequencing of seven human genomes to characterize benchmark reference materials
Justin M. Zook et al.
SCIENTIFIC DATA (2016)
Complex and multi-allelic copy number variation in human disease
Christina L. Usher et al.
BRIEFINGS IN FUNCTIONAL GENOMICS (2015)
Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms
Alexej Abyzov et al.
NATURE COMMUNICATIONS (2015)
AGE: defining breakpoints of genomic structural variants at single-nucleotide resolution, through optimal alignments with gap excision
Alexej Abyzov et al.
BIOINFORMATICS (2011)
CNVnator: An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing
Alexej Abyzov et al.
GENOME RESEARCH (2011)
A Human Genome Structural Variation Sequencing Resource Reveals Insights into Mutational Mechanisms
Jeffrey M. Kidd et al.
CELL (2010)
Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library
Hugo Y. K. Lam et al.
NATURE BIOTECHNOLOGY (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)