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A Streamlined Method for Detecting Structural Variants in Cancer Genomes by Short Read Paired-End Sequencing
Mijušković M,
Brown SM,
Tang Z,
Lindsay CR,
Efstathiadis E,
et al.
(2012)
A Streamlined Method for Detecting Structural Variants in Cancer Genomes by Short Read Paired-End Sequencing.
PLOS ONE 7(10): e48314.
https://doi.org/10.1371/journal.pone.0048314