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

Papers: 10.1371/journal.pone.0226694

https://doi.org/10.1371/journal.pone.0226694

AlleleProfileR: A versatile tool to identify and profile sequence variants in edited genomes

Cited by: 4
Author(s): Arne A.N. Bruyneel, Alexandre R. Colas, Ioannis Karakikes, Mark Mercola
Published: over 5 years ago

Software Mentions 9

bioconductor: CrispRVariants
Tools for counting and visualising mutations in a target location
Papers that mentioned: 18
Very Likely Science (90)
cran: config
Manage Environment Specific Configuration Values
Papers that mentioned: 33
Very Likely Science (77)
cran: fasta
Fast Adaptive Shrinkage/Thresholding Algorithm
Papers that mentioned: 848
Very Likely Science (60)
cran: matlab
'MATLAB' Emulation Package
Papers that mentioned: 666
Very Likely Science (75)
cran: Rcpp
Seamless R and C++ Integration
Papers that mentioned: 152
Very Likely Science (100)
pypi: config
A hierarchical, easy-to-use, powerful configuration module for Python
Papers that mentioned: 33
Very Likely Science (65)
pypi: CRISPResso
Software pipeline for the analysis of CRISPR-Cas9 genome editing outcomes from deep sequencing data
Papers that mentioned: 43
Very Likely Science (100)
pypi: fasta
The fasta python package enables you to deal with biological sequence files easily.
Papers that mentioned: 848
Very Likely Science (80)
pypi: matlab
Matlab for python
Papers that mentioned: 666
Very Likely Science (65)