about
Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays.Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expressionGenomic copy number variation in Mus musculusGenome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.Extensive load of somatic CNVs in the human placenta.Copy number variation profile in the placental and parental genomes of recurrent pregnancy loss families.Post-zygotic genomic changes in glutamate and dopamine pathway genes may explain discordance of monozygotic twins for schizophrenia.Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.
P2860
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P2860
description
2012 nî lūn-bûn
@nan
2012 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
HD-CNV: hotspot detector for copy number variants.
@ast
HD-CNV: hotspot detector for copy number variants.
@en
HD-CNV: hotspot detector for copy number variants.
@nl
type
label
HD-CNV: hotspot detector for copy number variants.
@ast
HD-CNV: hotspot detector for copy number variants.
@en
HD-CNV: hotspot detector for copy number variants.
@nl
prefLabel
HD-CNV: hotspot detector for copy number variants.
@ast
HD-CNV: hotspot detector for copy number variants.
@en
HD-CNV: hotspot detector for copy number variants.
@nl
P2093
P2860
P356
P1433
P1476
HD-CNV: hotspot detector for copy number variants
@en
P2093
Jenna L Butler
Kathleen A Hill
Marjorie Elizabeth Osborne Locke
P2860
P304
P356
10.1093/BIOINFORMATICS/BTS650
P407
P50
P577
2012-11-04T00:00:00Z