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

Papers: 10.1186/s12864-016-2374-2

https://doi.org/10.1186/s12864-016-2374-2

cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data

Cited by: 26
Author(s): Pubudu Samarakoon, Hanne Sørmo Sorte, Asbjørg Stray-Pedersen, Olaug K. Rødningen, Torbjørn Rognes, Robert Lyle
Published: over 9 years ago

Software Mentions 2

bioconductor: DECIPHER
Tools for curating, analyzing, and manipulating biological sequences
Papers that mentioned: 415
Very Likely Science (98)
cran: ExomeDepth
Calls Copy Number Variants from Targeted Sequence Data
Papers that mentioned: 112
Very Likely Science (75)