Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data.
Suyash S. ShringarpureRasika A. MathiasRyan D. HernandezTimothy D. O'ConnorZachary A. SzpiechPublished in: Bioinform. (2017)
Keyphrases
- data sets
- data collection
- data processing
- database
- small number
- synthetic data
- training data
- data samples
- complex data
- raw data
- sensor data
- data analysis
- high quality
- image data
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- data sources
- prior knowledge
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- clustering algorithm
- end users
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- noisy data
- historical data
- xml documents