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

Papers: 10.1038/s41598-021-93878-2

https://doi.org/10.1038/s41598-021-93878-2

Benchmarking germline CNV calling tools from exome sequencing data

Cited by: 27
Author(s): Veronika Gordeeva, Е. И. Шарова, Konstantin Babalyan, Rinat Sultanov, Vadim M. Govorun, Georgij Arapidi
Published: about 4 years ago

Software Mentions 4

bioconductor: CODEX
A Normalization and Copy Number Variation Detection Method for Whole Exome Sequencing
Papers that mentioned: 72
Very Likely Science (93)
bioconductor: exomeCopy
Copy number variant detection from exome sequencing read depth
Papers that mentioned: 7
Very Likely Science (100)
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)