These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 24561482)

  • 61. ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing.
    Fan J; Hu J; Xue C; Zhang H; Susztak K; Reilly MP; Xiao R; Li M
    PLoS Genet; 2020 May; 16(5):e1008786. PubMed ID: 32392242
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Interaction between the Xce locus and imprinting of the paternal X chromosome in mouse yolk-sac endoderm.
    Rastan S; Cattanach BM
    Nature; 1983 Jun 16-22; 303(5918):635-7. PubMed ID: 6855908
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Accuracy of RNA-Seq and its dependence on sequencing depth.
    Cai G; Li H; Lu Y; Huang X; Lee J; Müller P; Ji Y; Liang S
    BMC Bioinformatics; 2012; 13 Suppl 13(Suppl 13):S5. PubMed ID: 23320920
    [TBL] [Abstract][Full Text] [Related]  

  • 64. A multitask clustering approach for single-cell RNA-seq analysis in Recessive Dystrophic Epidermolysis Bullosa.
    Zhang H; Lee CAA; Li Z; Garbe JR; Eide CR; Petegrosso R; Kuang R; Tolar J
    PLoS Comput Biol; 2018 Apr; 14(4):e1006053. PubMed ID: 29630593
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Differential expression analysis of RNA sequencing data by incorporating non-exonic mapped reads.
    Chen HI; Liu Y; Zou Y; Lai Z; Sarkar D; Huang Y; Chen Y
    BMC Genomics; 2015; 16 Suppl 7(Suppl 7):S14. PubMed ID: 26099631
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Exploring the gonad transcriptome of two extreme male pigs with RNA-seq.
    Esteve-Codina A; Kofler R; Palmieri N; Bussotti G; Notredame C; Pérez-Enciso M
    BMC Genomics; 2011 Nov; 12():552. PubMed ID: 22067327
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Have humans lost control: The elusive X-controlling element.
    Peeters SB; Yang C; Brown CJ
    Semin Cell Dev Biol; 2016 Aug; 56():71-77. PubMed ID: 26849907
    [TBL] [Abstract][Full Text] [Related]  

  • 68. A mixture model for expression deconvolution from RNA-seq in heterogeneous tissues.
    Li Y; Xie X
    BMC Bioinformatics; 2013; 14 Suppl 5(Suppl 5):S11. PubMed ID: 23735186
    [TBL] [Abstract][Full Text] [Related]  

  • 69. DAFS: a data-adaptive flag method for RNA-sequencing data to differentiate genes with low and high expression.
    George NI; Chang CW
    BMC Bioinformatics; 2014 Mar; 15():92. PubMed ID: 24685233
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Allelic imbalance metre (Allim), a new tool for measuring allele-specific gene expression with RNA-seq data.
    Pandey RV; Franssen SU; Futschik A; Schlötterer C
    Mol Ecol Resour; 2013 Jul; 13(4):740-5. PubMed ID: 23615333
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Mapping the mouse Allelome reveals tissue-specific regulation of allelic expression.
    Andergassen D; Dotter CP; Wenzel D; Sigl V; Bammer PC; Muckenhuber M; Mayer D; Kulinski TM; Theussl HC; Penninger JM; Bock C; Barlow DP; Pauler FM; Hudson QJ
    Elife; 2017 Aug; 6():. PubMed ID: 28806168
    [TBL] [Abstract][Full Text] [Related]  

  • 72. ASElux: an ultra-fast and accurate allelic reads counter.
    Miao Z; Alvarez M; Pajukanta P; Ko A
    Bioinformatics; 2018 Apr; 34(8):1313-1320. PubMed ID: 29186329
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Xce haplotypes show modified methylation in a region of the active X chromosome lying 3' to Xist.
    Courtier B; Heard E; Avner P
    Proc Natl Acad Sci U S A; 1995 Apr; 92(8):3531-5. PubMed ID: 7536936
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Variant phasing and haplotypic expression from long-read sequencing in maize.
    Wang B; Tseng E; Baybayan P; Eng K; Regulski M; Jiao Y; Wang L; Olson A; Chougule K; Buren PV; Ware D
    Commun Biol; 2020 Feb; 3(1):78. PubMed ID: 32071408
    [TBL] [Abstract][Full Text] [Related]  

  • 75. A statistical method for detecting differentially expressed SNVs based on next-generation RNA-seq data.
    Fu R; Wang P; Ma W; Taguchi A; Wong CH; Zhang Q; Gazdar A; Hanash SM; Zhou Q; Zhong H; Feng Z
    Biometrics; 2017 Mar; 73(1):42-51. PubMed ID: 27276420
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Evaluation of logistic regression models and effect of covariates for case-control study in RNA-Seq analysis.
    Choi SH; Labadorf AT; Myers RH; Lunetta KL; Dupuis J; DeStefano AL
    BMC Bioinformatics; 2017 Feb; 18(1):91. PubMed ID: 28166718
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Genetic and parent-of-origin influences on X chromosome choice in Xce heterozygous mice.
    Chadwick LH; Willard HF
    Mamm Genome; 2005 Sep; 16(9):691-9. PubMed ID: 16245026
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Improved haplotype inference by exploiting long-range linking and allelic imbalance in RNA-seq datasets.
    Berger E; Yorukoglu D; Zhang L; Nyquist SK; Shalek AK; Kellis M; Numanagić I; Berger B
    Nat Commun; 2020 Sep; 11(1):4662. PubMed ID: 32938926
    [TBL] [Abstract][Full Text] [Related]  

  • 79. A model based criterion for gene expression calls using RNA-seq data.
    Wagner GP; Kin K; Lynch VJ
    Theory Biosci; 2013 Sep; 132(3):159-64. PubMed ID: 23615947
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Comprehensive analysis of imprinted genes in maize reveals allelic variation for imprinting and limited conservation with other species.
    Waters AJ; Bilinski P; Eichten SR; Vaughn MW; Ross-Ibarra J; Gehring M; Springer NM
    Proc Natl Acad Sci U S A; 2013 Nov; 110(48):19639-44. PubMed ID: 24218619
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.