Supplementary Fig 1D from Single Nucleotide Polymorphism–Based Genome-Wide Chromosome Copy Change, Loss of Heterozygosity, and Aneuploidy in Barrett's Esophagus Neoplastic Progression

Autor: Brian J. Reid, Kevin L. Gunderson, Dmitry Pokholok, Daniel A. Peiffer, Jessica Arnaudo, Carlo C. Maley, Patricia L. Blount, Carissa A. Sanchez, Patricia C. Galipeau, Xiaohong Li

Supplementary Fig 1C from Single Nucleotide Polymorphism–Based Genome-Wide Chromosome Copy Change, Loss of Heterozygosity, and Aneuploidy in Barrett's Esophagus Neoplastic Progression

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03486f75df0baf85fbf0e54712ed56d4
https://doi.org/10.1158/1940-6207.22523226.v1

Supplementary Table S1 from Deletion at Fragile Sites Is a Common and Early Event in Barrett's Esophagus

Autor: Peter S. Rabinovitch, Kevin L. Gunderson, Brian J. Reid, Carlo C. Maley, Carissa A. Sanchez, Robert Odze, Dimitry Pokholok, Daniel A. Peiffer, Michael T. Barrett, Rumen Kostadinov, Lisa A. Lai

Supplementary Table S1.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54876211c5202922ccccf686548b39bf
https://doi.org/10.1158/1541-7786.22519026

Supplementary Table 2 from Single Nucleotide Polymorphism–Based Genome-Wide Chromosome Copy Change, Loss of Heterozygosity, and Aneuploidy in Barrett's Esophagus Neoplastic Progression

Autor: Brian J. Reid, Kevin L. Gunderson, Dmitry Pokholok, Daniel A. Peiffer, Jessica Arnaudo, Carlo C. Maley, Patricia L. Blount, Carissa A. Sanchez, Patricia C. Galipeau, Xiaohong Li

Supplementary Table 2 from Single Nucleotide Polymorphism–Based Genome-Wide Chromosome Copy Change, Loss of Heterozygosity, and Aneuploidy in Barrett's Esophagus Neoplastic Progression

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::793c1cfabe02455c54f40dd9d4d9f4d7
https://doi.org/10.1158/1940-6207.22523217.v1

Power to detect risk alleles using genome-wide tag SNP panels.

Autor: Michael A Eberle, Pauline C Ng, Kenneth Kuhn, Lixin Zhou, Daniel A Peiffer, Luana Galver, Karine A Viaud-Martinez, Cynthia Taylor Lawley, Kevin L Gunderson, Richard Shen, Sarah S Murray

Publikováno v: PLoS Genetics, Vol 3, Iss 10, Pp 1827-1837 (2007)

Advances in high-throughput genotyping and the International HapMap Project have enabled association studies at the whole-genome level. We have constructed whole-genome genotyping panels of over 550,000 (HumanHap550) and 650,000 (HumanHap650Y) SNP lo

Externí odkaz: https://doaj.org/article/6f35ed976e6e4f0ebdc90c7bbf139a85

Sequences of 95 human MHC haplotypes reveal extreme coding variation in genes other than highly polymorphic HLA class I and II

Autor: Steven Norberg, Kevin L. Gunderson, Jill A. Hollenbach, Weihua Chang, Peter Parham, Paul Norman, Lisbeth A. Guethlein, Melissa Won, Neda Nemat-Gorgani, Claudia Alicata, Emily E. Wroblewski, Laurent Abi-Rached, Mostafa Ronaghi, Tamsen Dunn, Tobias Mann, Thomas Royce

Publikováno v: Genome Research
Genome Research, Cold Spring Harbor Laboratory Press, 2017, 27 (5), pp.813-823. ⟨10.1101/gr.213538.116⟩
Genome Research, 2017, 27 (5), pp.813-823. ⟨10.1101/gr.213538.116⟩

The most polymorphic part of the human genome, the MHC, encodes over 160 proteins of diverse function. Half of them, including the HLA class I and II genes, are directly involved in immune responses. Consequently, the MHC region strongly associates w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7841edf98dcee156bb6be77c169cf3e3
https://doi.org/10.1101/gr.213538.116