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

Concepedia

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

DOI Full Paper Access

24

Citations

27

References

2014

Year

Bruno Maranhao, Pooja Biswas, Jacque L. Duncan, Kari Branham, G.A. Silva, Muhammad Asif Naeem, S. N. Khan, Sheikh Riazuddin, J. Fielding Hejtmancik, John R. Heckenlively,

Rapid IdentificationNext-generation SequencingGeneticsPathologyOmicsDisease Gene IdentificationGenomicsMedicineBioinformaticsVariant Interpretation

References

	Year	Citations

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