Papers: 10.1186/s12920-018-0404-4

https://doi.org/10.1186/s12920-018-0404-4

Clinical analysis of germline copy number variation in DMD using a non-conjugate hierarchical Bayesian model

Cited by: 2
Author(s): Velina Kozareva, Clayton Stroff, Maxwell Silver, Jonathan F. Freidin, Nigel F. Delaney
Published: about 8 years ago

Software Mentions 2

cran: ExomeDepth
Calls Copy Number Variants from Targeted Sequence Data
Papers that mentioned: 112
Very Likely Science (75)
pypi: CNVkit
Copy number variation toolkit for high-throughput sequencing.
Papers that mentioned: 161
Very Likely Science (65)