Papers: 10.3390/diagnostics11040708
https://doi.org/10.3390/diagnostics11040708
Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH
Cited by: 4
Author(s): Marcel Kucharík, Jaroslav Budiš, Michaela Hýblová, Gabriel Minárik, Tomáš Szemes
Published: over 5 years ago
Software Mentions 1
pypi: CNVkit
Copy number variation toolkit for high-throughput sequencing.Papers that mentioned: 161
Very Likely Science (65)