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A simple method to estimate the in-house limit of detection for genetic mutations with low allele frequencies in whole-exome sequencing analysis by next-generation sequencing

Crossref DOI link: https://doi.org/10.1186/s12863-020-00956-x

Published Online: 2021-02-18

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Miura, Takumi

Yasuda, Satoshi

Sato, Yoji https://orcid.org/0000-0002-9889-1272
Funding

Funding for this research was provided by:

Japan Agency for Medical Research and Development (JP17mk0104044, JP20mk0104118)

Japan Ministry of Health, Labor and Welfare (Promotion of acquisition of international standards such as innovative medical equipment)
License Information

Text and Data Mining valid from 2021-02-18

Version of Record valid from 2021-02-18
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Article History

Received: 25 June 2020

Accepted: 16 December 2020

First Online: 18 February 2021

Ethics approval and consent to participate

: Not applicable.

: Not applicable.

: The authors declare no competing or financial interests.

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