Analysis and annotation of whole-genome or whole-exome sequencing-derived variants for clinical diagnosis.
about
Detailed comparison of two popular variant calling packages for exome and targeted exon studiesUse of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.Genomic architecture of pharmacological efficacy and adverse events.A de novo splice site mutation in EHMT1 resulting in Kleefstra syndrome with pharmacogenomics screening and behavior therapy for regressive behaviors.Successful Application of Whole Genome Sequencing in a Medical Genetics Clinic.Diagnosis of Pyruvate Kinase Deficiency.CoVaCS: a consensus variant calling system.
P2860
Q34285275-68147C2B-18AA-4562-8B8D-1B2234E7ECDBQ35648306-E7A59167-52A0-4119-A946-4491A941F0C2Q38292930-DE249043-1C44-48CA-A3DC-6E32F8133E79Q42293521-BFF0F63A-091C-45B6-8819-940EEAE15222Q46225649-3C1DB578-679C-4287-89B3-E10AA8893C14Q46812430-09ACC7F5-01F2-4949-A506-3A85C55DE4FAQ48104036-870552E2-A0DE-47E3-8289-5E328CE50CED
P2860
Analysis and annotation of whole-genome or whole-exome sequencing-derived variants for clinical diagnosis.
description
2013 nî lūn-bûn
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name
Analysis and annotation of who ...... riants for clinical diagnosis.
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Analysis and annotation of who ...... riants for clinical diagnosis.
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type
label
Analysis and annotation of who ...... riants for clinical diagnosis.
@en
Analysis and annotation of who ...... riants for clinical diagnosis.
@nl
prefLabel
Analysis and annotation of who ...... riants for clinical diagnosis.
@en
Analysis and annotation of who ...... riants for clinical diagnosis.
@nl
P2860
P1476
Analysis and annotation of who ...... riants for clinical diagnosis.
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P2093
Elizabeth A Worthey
P2860
P304
Unit 9.24.
P356
10.1002/0471142905.HG0924S79
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2013-10-18T00:00:00Z