An open API service providing mapping between scientific papers and software projects that are mentioned in them.

Papers: 10.3390/genes12091427

https://doi.org/10.3390/genes12091427

CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations

Cited by: 14
Author(s): Béryl Royer‐Bertrand, Katarina Cisarova, Florence Niel-Bütschi, Lauréane Mittaz-Crettol, Heidi Fodstad, Andrea Superti‐Furga
Published: almost 4 years ago

Software Mentions 1

cran: ExomeDepth
Calls Copy Number Variants from Targeted Sequence Data
Papers that mentioned: 112
Very Likely Science (75)