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

Papers: 10.1186/s13073-020-0712-0

https://doi.org/10.1186/s13073-020-0712-0

A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Cited by: 37
Author(s): Ramakrishnan Rajagopalan, Jill R. Murrell, Minjie Luo, Laura K. Conlin
Published: over 5 years ago

Software Mentions 3

cran: ES
Edge Selection
Papers that mentioned: 323
Very Likely Science (75)
cran: ExomeDepth
Calls Copy Number Variants from Targeted Sequence Data
Papers that mentioned: 112
Very Likely Science (75)
pypi: liftover
Package for converting between genome build coordinates
Papers that mentioned: 34
Very Likely Science (80)