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

Papers: 10.1186/s13073-021-00841-x

https://doi.org/10.1186/s13073-021-00841-x

ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data

Cited by: 29
Author(s): André E. Minoche, Ben Lundie, Greg Peters, Thomas Ohnesorg, Mark Pinese, David M. Thomas, Andreas Zankl, Tony Roscioli, Nicole Schönrock, Sarah Kummerfeld, Leslie Burnett, Marcel E. Dinger, Mark J. Cowley
Published: over 4 years ago

Software Mentions 3

cran: ART
Aligned Rank Transform for Nonparametric Factorial Analysis
Papers that mentioned: 580
Very Likely Science (85)
pypi: Lumpy
Papers that mentioned: 60
Very Likely Science (65)
pypi: svviz
A read visualizer for structural variants
Papers that mentioned: 6
Very Likely Science (100)