Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencing

PLoS ONE

Volumn 9, Issue 12, 2014, Pages

  Szelinger, Szabolcs ^a,b   Malenica, Ivana ^a   Corneveaux, Jason J ^a   Siniard, Ashley L ^a   Kurdoglu, Ahmet A ^a   Ramsey, Keri M ^a   Schrauwen, Isabelle ^a,c   Trent, Jeffrey M ^a   Narayanan, Vinodh ^a,d   Huentelman, Matthew J ^a   Craig, David W ^a  

^a TRANSLATIONAL GENOMICS RESEARCH INSTITUTE   (United States)

^b ARIZONA STATE UNIVERSITY   (United States)

^c UNIVERSITY OF ANTWERP   (Belgium)

^d BARROW NEUROLOGICAL INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; MESSENGER RNA;

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CHROMOSOME DELETION X; CHROMOSOME XM; CHROMOSOME XP; COMPUTER MODEL; CONTROLLED STUDY; CORRELATION COEFFICIENT; CYTOGENETICS; DNA METHYLATION; EPIGENETICS; EXOME; FAMILY STUDY; FEMALE; GENE; GENE DELETION; GENE EXPRESSION; GENE FREQUENCY; GENE IDENTIFICATION; GENE SEQUENCE; HDHD1 GENE; HETEROZYGOSITY; HIGH THROUGHPUT SCREENING; HOMOZYGOSITY; HUMAN; HUMAN CELL; MI4767 GENE; MILD COGNITIVE IMPAIRMENT; MOLECULAR BIOLOGY; NUCLEOTIDE SEQUENCE; PCSK1N GENE; PHENOTYPE; PLXNA3 GENE; PNPLA4 GENE; RNA SEQUENCE; SCHOOL CHILD; SEGREGATION ANALYSIS; SIMULATION; SINGLE NUCLEOTIDE POLYMORPHISM; STS GENE; VCX GENE; VCX3A GENE; WHOLE EXOME SEQUENCING; X CHROMOSOME; X CHROMOSOME INACTIVATION; ALLELIC IMBALANCE; COMPUTER SIMULATION; GENETICS; HIGH THROUGHPUT SEQUENCING; NEUROLOGIC DISEASE; PROCEDURES; SEQUENCE ANALYSIS; YOUNG ADULT;

ADOLESCENT; ALLELIC IMBALANCE; CHILD; CHROMOSOMES, HUMAN, X; COMPUTER SIMULATION; EXOME; FEMALE; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; NERVOUS SYSTEM DISEASES; RNA, MESSENGER; SEQUENCE ANALYSIS, RNA; SEQUENCE DELETION; X CHROMOSOME INACTIVATION; YOUNG ADULT;

EID: 84917691516     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0113036     Document Type: Article

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