grant

Novel bioinformatics methods for prioritizing disease-causing INDELs [ 2014 - 2017 ]

Also known as: Discriminating disease-causing from neutral insertion/deletions in human genetic variations

Research Grant

[Cite as http://purl.org/au-research/grants/nhmrc/1059775]

Brief description This project will build a bioinformatics diagnostic tool for the detection of small insertions and deletions (INDELs) in the human genome, which are the second most abundant class of human genetic variations. INDELs are implicated in many human diseases. Thus, the assessment of INDELs is critical for understanding disease etiology, disease susceptibility, and for interpreting personal genome sequencing data. The goal is to improve disease diagnosis and prevention.

Funding Amount $AUD 351,664.73

Funding Scheme Project Grants

Notes Standard Project Grant

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