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

Papers: 10.1186/s13023-020-1311-2

https://doi.org/10.1186/s13023-020-1311-2

Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations

Cited by: 20
Author(s): Xiaoyu Yu, Yun Lin, Jingying Xu, Tuanjie Che, Lin Li, Tao Yang, Hao Wu
Published: over 5 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)