Hehir-Kwa JY, Marschall T, Kloosterman WP, et al. A high-quality human reference panel reveals the complexity and distribution of genomic structural variants. Nature Communications. 2016;7(1): 12989
The study of variation found in DNA is fundamental in human genetic studies. Single nucleotide polym...
Structural variants (SVs) rearrange large segments of DNA1 and can have profound consequences in evo...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
Structural variation (SV) represents a major source of differences between individual human genomes ...
Structural variation (SV) represents a major source of differences between individual human genomes ...
Structural variants are implicated in numerous diseases and make up the majority of varying nucleoti...
© 2015 Macmillan Publishers Limited. All rights reserved. Structural variants are implicated in nume...
Abstract Background Several genomes have now been seq...
© 2020, The Author(s). Structural variants (SVs) rearrange large segments of DNA1 and can have profo...
A key goal of whole-genome sequencing for studies of human genetics is to interrogate all forms of v...
Genomic variation extends from single nucleotide variants to large chromosomal rearrangements, but t...
The study of variation found in DNA is fundamental in human genetic studies. Single nucleotide polym...
Structural variants (SVs) rearrange large segments of DNA1 and can have profound consequences in evo...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
Structural variation (SV) represents a major source of differences between individual human genomes ...
Structural variation (SV) represents a major source of differences between individual human genomes ...
Structural variants are implicated in numerous diseases and make up the majority of varying nucleoti...
© 2015 Macmillan Publishers Limited. All rights reserved. Structural variants are implicated in nume...
Abstract Background Several genomes have now been seq...
© 2020, The Author(s). Structural variants (SVs) rearrange large segments of DNA1 and can have profo...
A key goal of whole-genome sequencing for studies of human genetics is to interrogate all forms of v...
Genomic variation extends from single nucleotide variants to large chromosomal rearrangements, but t...
The study of variation found in DNA is fundamental in human genetic studies. Single nucleotide polym...
Structural variants (SVs) rearrange large segments of DNA1 and can have profound consequences in evo...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...