Assessing the reproducibility of exome copy number variations predictions.
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A Path to Implement Precision Child Health Cardiovascular MedicineA rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism.CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability.Ximmer: A system for improving accuracy and consistency of CNV calling from exome data
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Assessing the reproducibility of exome copy number variations predictions.
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scientific article published on 08 August 2016
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Assessing the reproducibility of exome copy number variations predictions.
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Assessing the reproducibility of exome copy number variations predictions.
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Assessing the reproducibility of exome copy number variations predictions.
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Assessing the reproducibility of exome copy number variations predictions.
@nl
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Assessing the reproducibility of exome copy number variations predictions.
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Assessing the reproducibility of exome copy number variations predictions.
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P2860
P1433
P1476
Assessing the reproducibility of exome copy number variations predictions.
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P2093
Celine S Hong
Larry N Singh
P2860
P2888
P356
10.1186/S13073-016-0336-6
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2016-08-08T00:00:00Z
P6179
1028740342