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

Papers: 10.1186/s13073-020-00791-w

https://doi.org/10.1186/s13073-020-00791-w

Best practices for variant calling in clinical sequencing

Cited by: 136
Author(s): Daniel C. Koboldt
Published: almost 5 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: Lumpy
Papers that mentioned: 60
Very Likely Science (65)
pypi: Platypus
A minimal language
Papers that mentioned: 218
Very Likely Science (65)