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

Papers: 10.1038/s41598-021-94292-4

https://doi.org/10.1038/s41598-021-94292-4

Prevalence of cancer susceptibility variants in patients with multiple Lynch syndrome related cancers

Cited by: 7
Author(s): Yoon Young Choi, Su‐Jin Shin, Jae Eun Lee, Lisa Madlensky, Seung Tae Lee, Ji Soo Park, Jeong-Hyeon Jo, Hyun Ki Kim, Daniela Nachmanson, Xiaojun Xu, Sung Hoon Noh, Jae‐Ho Cheong, Olivier Harismendy
Published: about 4 years ago

Software Mentions 4

cran: ExomeDepth
Calls Copy Number Variants from Targeted Sequence Data
Papers that mentioned: 112
Very Likely Science (75)
pypi: bcbio-nextgen
Best-practice pipelines for fully automated high throughput sequencing analysis
Papers that mentioned: 43
Very Likely Science (100)
pypi: CNVkit
Copy number variation toolkit for high-throughput sequencing.
Papers that mentioned: 161
Very Likely Science (65)
pypi: for
Papers that mentioned: 1,226
Very Likely Science (65)