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

Papers: 10.3390/genes12081282

https://doi.org/10.3390/genes12081282

A Novel Missense Mutation in TNNI3K Causes Recessively Inherited Cardiac Conduction Disease in a Consanguineous Pakistani Family

Cited by: 5
Author(s): Shafaq Ramzan, Stephanie Tennstedt, Muhammad Tariq, Sheraz Khan, Hafiza Noor Ul Ayan, Aamir Ali, Matthias Munz, Holger Thiele, Asad Aslam Korejo, Abdul Razzaq Mughal, Syed Zahid Jamal, Peter Nürnberg, Shahid Mahmood Baig, Jeanette Erdmann, Ilyas Ahmad
Published: almost 4 years ago

Software Mentions 4

cran: ExomeDepth
Calls Copy Number Variants from Targeted Sequence Data
Papers that mentioned: 112
Very Likely Science (75)
cran: Platypus
Single-Cell Immune Repertoire and Gene Expression Analysis
Papers that mentioned: 218
Very Likely Science (85)
pypi: Platypus
A minimal language
Papers that mentioned: 218
Very Likely Science (65)
pypi: trajectory
Trajectory data lossy compression format based on Google's Encoded Polyline Algorithm Format
Papers that mentioned: 1
Very Likely Science (90)