-
1
-
-
56349112904
-
Global survey of genomic imprinting by transcriptome sequencing
-
Babak T., et al. Global survey of genomic imprinting by transcriptome sequencing. Curr. Biol. 2008, 18(22):1735-1741.
-
(2008)
Curr. Biol.
, vol.18
, Issue.22
, pp. 1735-1741
-
-
Babak, T.1
-
2
-
-
58149357315
-
Validating discovered Cis-acting regulatory genetic variants: application of an allele specific expression approach to HapMap populations
-
Campino S., et al. Validating discovered Cis-acting regulatory genetic variants: application of an allele specific expression approach to HapMap populations. PLoS One 2008, 3(12):e4105.
-
(2008)
PLoS One
, vol.3
, Issue.12
-
-
Campino, S.1
-
3
-
-
70349910898
-
Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data
-
Degner J.F., et al. Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data. Bioinformatics 2009, 25(24):3207-3212.
-
(2009)
Bioinformatics
, vol.25
, Issue.24
, pp. 3207-3212
-
-
Degner, J.F.1
-
4
-
-
55449125813
-
Modifier effects between regulatory and protein-coding variation
-
Dimas A.S., et al. Modifier effects between regulatory and protein-coding variation. PLoS Genet. 2008, 4(10):e1000244.
-
(2008)
PLoS Genet.
, vol.4
, Issue.10
-
-
Dimas, A.S.1
-
5
-
-
77952982347
-
Natural selection on cis and trans regulation in yeasts
-
Emerson J.J., et al. Natural selection on cis and trans regulation in yeasts. Genome Res. 2010, 20(6):826-836.
-
(2010)
Genome Res.
, vol.20
, Issue.6
, pp. 826-836
-
-
Emerson, J.J.1
-
6
-
-
70149112830
-
Tissue effect on genetic control of transcript isoform variation
-
Kwan T., et al. Tissue effect on genetic control of transcript isoform variation. PLoS Genet. 2009, 5(8):e1000608.
-
(2009)
PLoS Genet.
, vol.5
, Issue.8
-
-
Kwan, T.1
-
7
-
-
79953303842
-
RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression
-
Lalonde E., et al. RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression. Genome Res. 2011, 21(4):545-554.
-
(2011)
Genome Res.
, vol.21
, Issue.4
, pp. 545-554
-
-
Lalonde, E.1
-
8
-
-
84859210032
-
Fast gapped-read alignment with Bowtie 2
-
Langmead B., Salzberg S.L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 2012, 9(4):357-359.
-
(2012)
Nat. Methods
, vol.9
, Issue.4
, pp. 357-359
-
-
Langmead, B.1
Salzberg, S.L.2
-
9
-
-
79955046277
-
Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment
-
Lau K.C., et al. Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment. Clin. Chim. Acta 2011, 412(11-12):952-957.
-
(2011)
Clin. Chim. Acta
, vol.412
, Issue.11-12
, pp. 952-957
-
-
Lau, K.C.1
-
10
-
-
77950458649
-
Transcriptome genetics using second generation sequencing in a Caucasian population
-
Montgomery S.B., et al. Transcriptome genetics using second generation sequencing in a Caucasian population. Nature 2010, 464(7289):773-777.
-
(2010)
Nature
, vol.464
, Issue.7289
, pp. 773-777
-
-
Montgomery, S.B.1
-
11
-
-
78650428373
-
Statistical inference of allelic imbalance from transcriptome data
-
Nothnagel M., et al. Statistical inference of allelic imbalance from transcriptome data. Hum. Mutat. 2011, 32(1):98-106.
-
(2011)
Hum. Mutat.
, vol.32
, Issue.1
, pp. 98-106
-
-
Nothnagel, M.1
-
12
-
-
80052279867
-
Risk alleles for chronic hepatitis B are associated with decreased mRNA expression of HLA-DPA1 and HLA-DPB1 in normal human liver
-
O'Brien T.R., et al. Risk alleles for chronic hepatitis B are associated with decreased mRNA expression of HLA-DPA1 and HLA-DPB1 in normal human liver. Genes Immun. 2011, 12(6):428-433.
-
(2011)
Genes Immun.
, vol.12
, Issue.6
, pp. 428-433
-
-
O'Brien, T.R.1
-
13
-
-
77954763156
-
Genome-wide allele-specific analysis: insights into regulatory variation
-
Pastinen T. Genome-wide allele-specific analysis: insights into regulatory variation. Nat. Rev. Genet. 2010, 11(8):533-538.
-
(2010)
Nat. Rev. Genet.
, vol.11
, Issue.8
, pp. 533-538
-
-
Pastinen, T.1
-
14
-
-
29644446630
-
Mapping common regulatory variants to human haplotypes
-
Pastinen T., et al. Mapping common regulatory variants to human haplotypes. Hum. Mol. Genet. 2005, 14(24):3963-3971.
-
(2005)
Hum. Mol. Genet.
, vol.14
, Issue.24
, pp. 3963-3971
-
-
Pastinen, T.1
-
15
-
-
77950460661
-
Understanding mechanisms underlying human gene expression variation with RNA sequencing
-
Pickrell J.K., et al. Understanding mechanisms underlying human gene expression variation with RNA sequencing. Nature 2010, 464(7289):768-772.
-
(2010)
Nature
, vol.464
, Issue.7289
, pp. 768-772
-
-
Pickrell, J.K.1
-
16
-
-
40149090710
-
Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression
-
Serre D., et al. Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression. PLoS Genet. 2008, 4(2):e1000006.
-
(2008)
PLoS Genet.
, vol.4
, Issue.2
-
-
Serre, D.1
-
17
-
-
80053522581
-
A powerful and flexible statistical framework for testing hypotheses of allele-specific gene expression from RNA-seq data
-
Skelly D.A., et al. A powerful and flexible statistical framework for testing hypotheses of allele-specific gene expression from RNA-seq data. Genome Res. 2011, 21(10):1728-1737.
-
(2011)
Genome Res.
, vol.21
, Issue.10
, pp. 1728-1737
-
-
Skelly, D.A.1
-
18
-
-
55449112185
-
Genome-wide associations of gene expression variation in humans
-
Stranger B.E., et al. Genome-wide associations of gene expression variation in humans. PLoS Genet. 2005, 1(6):e78.
-
(2005)
PLoS Genet.
, vol.1
, Issue.6
-
-
Stranger, B.E.1
-
19
-
-
33846978695
-
Relative impact of nucleotide and copy number variation on gene expression phenotypes
-
Stranger B.E., et al. Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science 2007, 315(5813):848-853.
-
(2007)
Science
, vol.315
, Issue.5813
, pp. 848-853
-
-
Stranger, B.E.1
-
20
-
-
61449218868
-
Targeted screening of cis-regulatory variation in human haplotypes
-
Verlaan D.J., et al. Targeted screening of cis-regulatory variation in human haplotypes. Genome Res. 2009, 19(1):118-127.
-
(2009)
Genome Res.
, vol.19
, Issue.1
, pp. 118-127
-
-
Verlaan, D.J.1
-
21
-
-
84858625881
-
A common HLA-DPA1 variant is associated with hepatitis B virus infection but fails to distinguish active from inactive Caucasian carriers
-
Vermehren J., et al. A common HLA-DPA1 variant is associated with hepatitis B virus infection but fails to distinguish active from inactive Caucasian carriers. PLoS One 2012, 7(3):e32605.
-
(2012)
PLoS One
, vol.7
, Issue.3
-
-
Vermehren, J.1
-
22
-
-
78049259700
-
Computational analysis of whole-genome differential allelic expression data in human
-
Wagner J.R., et al. Computational analysis of whole-genome differential allelic expression data in human. PLoS Comput. Biol. 2010, 6(7):e1000849.
-
(2010)
PLoS Comput. Biol.
, vol.6
, Issue.7
-
-
Wagner, J.R.1
-
23
-
-
77956637896
-
Genetics and beyond-the transcriptome of human monocytes and disease susceptibility
-
Zeller T., et al. Genetics and beyond-the transcriptome of human monocytes and disease susceptibility. PLoS One 2010, 5(5):e10693.
-
(2010)
PLoS One
, vol.5
, Issue.5
-
-
Zeller, T.1
|