← Evidence map

TrialGenomics

exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels.

B Maranhao et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

14 papers cite it

2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
cites it
Full record →Abstract, authors, funding and every citing paper · PMID 24603341